Abstract

OBJECTIVES

The coronavirus disease 2019 (COVID-19) pandemic resulted in unprecedented tolls on both economies and human life. Healthcare resources needed to be reallocated away from the care of patients and towards supporting the pandemic response. In this systematic review, we explore the impact of resource allocation during the COVID-19 pandemic on the screening, diagnosis, management and outcomes of patients with lung cancer during the pandemic.

METHODS

PubMed and Embase were systematically searched for articles investigating the impact of the COVID-19 pandemic on patients with lung cancer. Of the 1605 manuscripts originally screened, 47 studies met the inclusion criteria.

RESULTS

Patients with lung cancer during the pandemic experienced reduced rates of screening, diagnostic testing and interventions but did not experience worse outcomes. Population-based modelling studies predict significant increases in mortality for patients with lung cancer in the years to come.

CONCLUSIONS

Reduced access to resources during the pandemic resulted in reduced rates of screening, diagnosis and treatment for patients with lung cancer. While significant differences in outcomes were not identified in the short term, ultimately the effects of the pandemic and reductions in cancer screening will likely be better delineated in the coming years. Future consideration of the long-term implications of resource allocation away from patients with lung cancer with an attempt to provide equitable access to healthcare and limited interruptions of patient care may help to provide the best care for all patients during times of limited resources.

OBJECTIVES

Lung cancer is among the leading causes of death worldwide and is the leading cause of cancer deaths [1]. With an incidence of 11.4% of new cancer cases and annual cancer mortality of 18.0%, lung cancer carries a significant burden on patient survival, quality of life, and strain on the healthcare system [1]. Despite this, early detection of resectable disease is potentially curative. Surgery, in conjunction with chemotherapy, radiotherapy and in recent years, immunotherapy, form a cornerstone in the management of this complex disease [1–3].

The severe acute respiratory syndrome coronavirus 2 or coronavirus disease 2019 (COVID-19) pandemic was first encountered at the end of 2019. There have been 650 million infections, 6.6 million deaths and a surge in hospital admissions that overwhelmed healthcare systems globally since the first reported cases in 2019 [4]. In an attempt to respond to the increasingly limited resources available, governments and policymakers were required to make decisions regarding resource allocation. As transmission characteristics, mutagenicity and short- and long-term outcomes were largely unknown, there was understandable caution taken when making these decisions during the early phases of the COVID-19 pandemic [5–7]. Cautionary resource allocation resulted in personal protective equipment, ventilators, hospital beds and staffing being redirected towards the pandemic response.

Surgical programs internationally were significantly impacted by resource redirection and constraints [5, 6]. In many countries and across a broad range of specialties, elective cases were reduced or halted altogether at times, with only emergent cases proceeding and patients otherwise being placed on ever-growing waiting lists. The resulting delay in care for patients who needed non-emergent care caused disease progression, potentially inferior surgical outcomes, and has tragically resulted in the progression to unresectable disease in some cases [2, 8].

Considering the necessity of early detection and intervention, patients with lung cancer are at increased risk for adverse outcomes with delayed screening, diagnosis and treatment [5, 8, 9]. Upstaging of early to advanced-stage lung cancer has the potential to significantly reduce a patient’s survival and impair their quality of life [5]. The purpose of this systematic review was to consolidate and appraise the literature investigating resource allocation during the COVID-19 pandemic and to explore the impact of resource allocation on the diagnosis, management and outcomes of lung cancer.

METHODS

Literature search strategy

Two authors systematically searched the PubMed and Embase databases. The search terms used were ‘lung, thoracic, cancer, malignancy, oncology, COVID-19, pandemic, screening, surgery, delay’ individually or in combination. The search was conducted including literature published from 1 January 2019 to 30 November 2022. The reference lists of identified manuscripts were screened to identify additional articles. Data were extracted from articles by 2 authors based on prespecified outcomes as detailed below.

Eligibility criteria and data extraction

The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines and a published explanation of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were referenced in structuring and conducting this systematic review [10, 11]. This review included retrospective and prospective studies examining the toll of resource allocation during the COVID-19 pandemic on the screening, diagnosis, management and outcomes of patients with lung cancer internationally. The inclusion criteria for this systematic review were studies published since 2019 investigating screening, diagnosis, management and postoperative outcomes of patients with lung cancer in relation to resource allocation and reduced available resources as a result of the COVID-19 pandemic. Case reports or series, reviews, abstracts without an associated full text, studies focusing on an era prior to the COVID-19 pandemic or studies investigating outcomes of conditions other than lung cancer were excluded from this study. Initial screening of 1605 manuscript titles and abstracts was performed by 2 authors. Once relevant manuscripts were identified, 92 full texts were reviewed, and 47 were included in this review (Fig. 1 and Table 1).

Study flow chart based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
Figure 1:

Study flow chart based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.

Table 1:

Characteristics of included studies

Study nameStudy typeStudy organizationYears data collectedStudy populationLocationOutcomes
Bertolaccini and Spaggiari [39]Retrospective, single centreHub-and-spokes system for oncological care2019–2020Patients with thoracic malignancyItalyThoracic oncologic surgical activity
Bertolaccini et al. [23]Retrospective, single centre
  • Group 1: baseline (January–July 2019)

  • Group 2: January–July 2020

  • Group 3: January–July 2021

2019–2021Lung cancer patient undergoing lobectomyItalyDisease stage
Bhalla et al. [29]Prospective, multicentre
  • Group 1: baseline (December 2019)

  • Group 2: pandemic period (July 2020)

2019–2020Adult patients with a current or history of hematological malignancy or invasive solid tumourUSACancer care delivery (number of in-person outpatient visits, telehealth visits and pandemic-related delays of oncologic care)
Cantini et al. [5]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Newly diagnosed lung cancer patientItalyLung cancer diagnosis and access to treatment
Ciriaco et al. [38]Retrospective, single centreDescription of COVID-related changes in NSCLC treatment2019–2020Patients with NSCLC lung cancerItalyThoracic oncologic surgical activity
Conibear et al. [2]Retrospective, multicentre
  • Group 1: baseline (2019)—33 091 patients

  • Group 2: pandemic (2020)—31 371 patients

2019–2020Patients with lung cancer; RCRDUKLung cancer diagnosis, stage at presentation, treatment, survival
Degeling et al. [47]Population-based modeling study
  • Baseline scenario

  • Stage shift scenario

2019Patients with stage I breast, colorectal and lung cancer and T1 melanomaAustraliaImpact of cancer care delays
Dolan et al. [18]Retrospective, single centre
  • Group 1: baseline (2019)—375 patients

  • Group 2: pandemic (March–May 2020)—58 patients

2019–2020Patients with NSCLC lung cancerUSAThoracic oncologic surgical activity
Englum et al. [9]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with prostate, lung, bladder and colorectal cancerUSACancer-related health care encounters, diagnostic or screening procedures, new cancer diagnoses
Flores et al. [8]Retrospective, single centreMonthly case average compared between baseline (2018–2019) to the pandemic period (2020–2021)2018–2021Patients with lung cancerUSARates of lung cancer diagnosis, disease stage
Fu et al. [32]Retrospective, single centre
  • Group 1: baseline (2015–2019)—2054 patients

  • Group 2: pandemic (2020)—397 patients

2015–2020Patients with lung cancerChinaLung cancer diagnosis; subjective patient outcomes
Fujita et al. [33]Retrospective, single centre
  • Group 1: no treatment delay—150 patients

  • Group 2: treatment delay—15 patients

2020Patients with lung cancerJapanLung cancer treatment; subjective patient outcomes
Geukens et al. [45]Retrospective, multicentre928 patients2020–2021Patients with malignancyBelgiumMortality
Gokce et al. [41]Retrospective, single centre35 patients2020–2021Patients with NSCLC lung cancerTurkeyLung cancer surgery outcomes
Hilzenrat et al. [15]Observational, multicentreElectronic survey distributed to CATS members2019–2020Patients with lung cancerCanadaSurgical lung cancer care
Kasymjanova et al. [20]Retrospective, single centre
  • Group 1: baseline (March 2019–February 2020)

  • Group 2: pandemic (March 2020–February 2021)

2019–2021Patients with lung cancerCanadaLung cancer diagnosis and treatment
Keogh et al. [21]Retrospective, single centre
  • Group 1: baseline (January 2019–February 2020)—330 patients

  • Group 2: pandemic (March 2020–February 2021)—320 patients

2019–2021Patients with NSCLC lung cancerCanadaLung cancer diagnosis, stage, treatment, outcomes
Leclère et al. [40]Retrospective, single centre115 patients2020Patients with NSCLC lung cancer undergoing surgical resectionFrancePostoperative occurrence of COVID-19
London et al. [17]Retrospective, multicentre
  • Group 1: baseline (January–April 2019)

  • Group 2: pandemic (January–April 2020)

2019–2020Patients with malignancy; CCRN databaseUSARates of lung cancer diagnosis
Lou et al. [12]Retrospective, single centre
  • Group 1: pre-pandemic period (2016–2019)

  • Group 2: pandemic (2020)

2016–2020Patients undergoing screening for lung, colorectal and breast cancerUSACancer-related screening and diagnosis
Malagón et al. [48]Population-based modeling studyModel of cancer incidence, stage at diagnosis and survival2020–2021Patients with malignancy; Canadian Cancer RegistryCanadaImpact of cancer care delays
Maringe et al. [49]Population-based modeling study29 305 patients2010–2015Patients with breast, colorectal, esophageal and lung cancer; NHS databaseUKImpact of cancer care delays
Martínez-Hernández et al. [37]Retrospective, multicentre, questionnaireElectronic survey sent to SPECT members2019–2020Patients with lung cancerSpainLung cancer management
Morais et al. [26]Retrospective, multicentre, propensity-matched
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalLung cancer management
Morais et al. [27]Retrospective, single centre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalCancer-related screening and diagnosis
Pasello et al. [30]Retrospective, multicentre
  • Group 1: baseline (March–April 2019)

  • Group 2: pandemic (March–April 2020)

2019–2020Patients with lung cancer; two centresItalyLung cancer management
Patt et al. [7]Retrospective, multicentre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancy; Medicare FFS claimsUSACancer-related screening and diagnosis
Peacock et al. [24]Retrospective, multicentre
  • Group 1: baseline (April 2019)

  • Group 2: pandemic (April 2020)

2019–2020Patients with malignancy; Belgian Cancer RegistryBelgiumRates of lung cancer diagnosis
Peer et al. [42]Retrospective, single centre113 patients2020Patients with NSCLC lung cancer undergoing surgical resectionIsraelLung cancer surgical outcomes
Piwkowski et al. [25]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients with lung cancer undergoing surgery; PNLCR databasePolandLung cancer stage and surgical outcomes
Priou et al. [28]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with lung cancerFranceLung cancer diagnosis, stage, treatment and outcomes
Ramanakumar et al. [22]Retrospective, multicentre
  • Group 1: baseline (averages of 2018, 2019, 2020)

  • Group 2: pandemic (April 2020–March 2021)

2018–2021Patients with lung, breast, colorectal and prostate cancerCanadaRates of newly diagnosed malignancy
Sato et al. [16]Retrospective, multicentre
  • Group 1: baseline (2014–2019)

  • Group 2: pandemic (2020)

2014–2020Patients with thoracic malignancyJapanLung cancer diagnosis, stage, treatment and outcomes
Seitlinger et al. [41]Prospective, multicentre731 patients2020Patients undergoing thoracic oncologic surgeryFrance, Germany, Italy, CanadaThoracic oncologic surgery outcomes
Sha et al. [3]Retrospective, single centreTotal patients: 1612020Patients with lung cancerChinaDelays in cancer-related care
Shipe et al. [50]Population-based modeling studyImmediate versus delayed surgical resectionPatients with suspicious lung nodules <2 cmUSAImpact of cancer care delays; 5-year survival
Sud et al. [51]Population-based modeling studyModel of cancer progression during COVID-19-induced delays in care2013–2017Patients with malignancy UKHazard ratios of cancer progression, 5-year reduction in survival
Taylor et al. [36]Observational, interview and questionnaire based30 patients2020Patients with lung cancerUKLung cancer quality of care and quality of life
Terashima et al. [34]Retrospective, single centre
  • Group 1: baseline (March 2018–March 2019)—82 patients

  • Group 2: pandemic (March 2020–March 2021)—75 patients

2018–2021Patients with lung cancerJapanLung cancer pre-visit, pre-diagnosis and pre-treatment time
Teteh et al. [35]Observational, single centre41 participants2020Patients enrolled in a randomized trial of self‐management intervention for lung cancer surgery preparation/recoveryUSASubjective outcomes of lung cancer surgery preparation/recovery
Uematsu et al. [43]Observational, questionnaire-basedQuestionnaire sent to 14 facilities in the Kanagawa General Thoracic Surgery Study Group2020Patients with lung cancerJapanLung cancer diagnosis and resource allocation
Van Haren et al. [12]Retrospective, single centre
  • Group 1: baseline (January 2017–February 2020)

  • Group 2: pandemic (March–July 2020)

2017–2020Patients undergoing screening for lung cancerUSACancer-related screening and diagnosis
Villena-Vargas et al. [19]Retrospective, single centre
  • Group 1: baseline (January 2020–March 2020)—57 patients

  • Group 2: pandemic (March 2020–June 2020)—42 patients

2020Patients with NSCLC lung cancerUSAOutcomes of lung cancer surgery
Walker et al. [14]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients undergoing screening for breast, cervical, colorectal and lung cancerCanadaCancer-related screening and diagnosis
Walter et al. [31]Observational, questionnaire-basedQuestionnaire sent to 245 patients2020Patients with thoracic malignancyGermanySubjective delays in thoracic malignancy diagnosis and treatment
Yu et al. [46]Retrospective, single centre, propensity-matched
  • Group 1: baseline (September 2019–November 2019)

  • Group 2: pandemic (December 2019–February 2020)

2019–2020Patients with NSCLC lung cancerChinaLung cancer treatment and outcomes
Zhang et al. [6]Retrospective, single centre
  • Group 1: baseline (February–July 2019)

  • Group 2: pandemic (February–July 2020)

2019–2020Patients with lung cancerChinaCancer-related screening and diagnosis
Study nameStudy typeStudy organizationYears data collectedStudy populationLocationOutcomes
Bertolaccini and Spaggiari [39]Retrospective, single centreHub-and-spokes system for oncological care2019–2020Patients with thoracic malignancyItalyThoracic oncologic surgical activity
Bertolaccini et al. [23]Retrospective, single centre
  • Group 1: baseline (January–July 2019)

  • Group 2: January–July 2020

  • Group 3: January–July 2021

2019–2021Lung cancer patient undergoing lobectomyItalyDisease stage
Bhalla et al. [29]Prospective, multicentre
  • Group 1: baseline (December 2019)

  • Group 2: pandemic period (July 2020)

2019–2020Adult patients with a current or history of hematological malignancy or invasive solid tumourUSACancer care delivery (number of in-person outpatient visits, telehealth visits and pandemic-related delays of oncologic care)
Cantini et al. [5]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Newly diagnosed lung cancer patientItalyLung cancer diagnosis and access to treatment
Ciriaco et al. [38]Retrospective, single centreDescription of COVID-related changes in NSCLC treatment2019–2020Patients with NSCLC lung cancerItalyThoracic oncologic surgical activity
Conibear et al. [2]Retrospective, multicentre
  • Group 1: baseline (2019)—33 091 patients

  • Group 2: pandemic (2020)—31 371 patients

2019–2020Patients with lung cancer; RCRDUKLung cancer diagnosis, stage at presentation, treatment, survival
Degeling et al. [47]Population-based modeling study
  • Baseline scenario

  • Stage shift scenario

2019Patients with stage I breast, colorectal and lung cancer and T1 melanomaAustraliaImpact of cancer care delays
Dolan et al. [18]Retrospective, single centre
  • Group 1: baseline (2019)—375 patients

  • Group 2: pandemic (March–May 2020)—58 patients

2019–2020Patients with NSCLC lung cancerUSAThoracic oncologic surgical activity
Englum et al. [9]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with prostate, lung, bladder and colorectal cancerUSACancer-related health care encounters, diagnostic or screening procedures, new cancer diagnoses
Flores et al. [8]Retrospective, single centreMonthly case average compared between baseline (2018–2019) to the pandemic period (2020–2021)2018–2021Patients with lung cancerUSARates of lung cancer diagnosis, disease stage
Fu et al. [32]Retrospective, single centre
  • Group 1: baseline (2015–2019)—2054 patients

  • Group 2: pandemic (2020)—397 patients

2015–2020Patients with lung cancerChinaLung cancer diagnosis; subjective patient outcomes
Fujita et al. [33]Retrospective, single centre
  • Group 1: no treatment delay—150 patients

  • Group 2: treatment delay—15 patients

2020Patients with lung cancerJapanLung cancer treatment; subjective patient outcomes
Geukens et al. [45]Retrospective, multicentre928 patients2020–2021Patients with malignancyBelgiumMortality
Gokce et al. [41]Retrospective, single centre35 patients2020–2021Patients with NSCLC lung cancerTurkeyLung cancer surgery outcomes
Hilzenrat et al. [15]Observational, multicentreElectronic survey distributed to CATS members2019–2020Patients with lung cancerCanadaSurgical lung cancer care
Kasymjanova et al. [20]Retrospective, single centre
  • Group 1: baseline (March 2019–February 2020)

  • Group 2: pandemic (March 2020–February 2021)

2019–2021Patients with lung cancerCanadaLung cancer diagnosis and treatment
Keogh et al. [21]Retrospective, single centre
  • Group 1: baseline (January 2019–February 2020)—330 patients

  • Group 2: pandemic (March 2020–February 2021)—320 patients

2019–2021Patients with NSCLC lung cancerCanadaLung cancer diagnosis, stage, treatment, outcomes
Leclère et al. [40]Retrospective, single centre115 patients2020Patients with NSCLC lung cancer undergoing surgical resectionFrancePostoperative occurrence of COVID-19
London et al. [17]Retrospective, multicentre
  • Group 1: baseline (January–April 2019)

  • Group 2: pandemic (January–April 2020)

2019–2020Patients with malignancy; CCRN databaseUSARates of lung cancer diagnosis
Lou et al. [12]Retrospective, single centre
  • Group 1: pre-pandemic period (2016–2019)

  • Group 2: pandemic (2020)

2016–2020Patients undergoing screening for lung, colorectal and breast cancerUSACancer-related screening and diagnosis
Malagón et al. [48]Population-based modeling studyModel of cancer incidence, stage at diagnosis and survival2020–2021Patients with malignancy; Canadian Cancer RegistryCanadaImpact of cancer care delays
Maringe et al. [49]Population-based modeling study29 305 patients2010–2015Patients with breast, colorectal, esophageal and lung cancer; NHS databaseUKImpact of cancer care delays
Martínez-Hernández et al. [37]Retrospective, multicentre, questionnaireElectronic survey sent to SPECT members2019–2020Patients with lung cancerSpainLung cancer management
Morais et al. [26]Retrospective, multicentre, propensity-matched
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalLung cancer management
Morais et al. [27]Retrospective, single centre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalCancer-related screening and diagnosis
Pasello et al. [30]Retrospective, multicentre
  • Group 1: baseline (March–April 2019)

  • Group 2: pandemic (March–April 2020)

2019–2020Patients with lung cancer; two centresItalyLung cancer management
Patt et al. [7]Retrospective, multicentre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancy; Medicare FFS claimsUSACancer-related screening and diagnosis
Peacock et al. [24]Retrospective, multicentre
  • Group 1: baseline (April 2019)

  • Group 2: pandemic (April 2020)

2019–2020Patients with malignancy; Belgian Cancer RegistryBelgiumRates of lung cancer diagnosis
Peer et al. [42]Retrospective, single centre113 patients2020Patients with NSCLC lung cancer undergoing surgical resectionIsraelLung cancer surgical outcomes
Piwkowski et al. [25]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients with lung cancer undergoing surgery; PNLCR databasePolandLung cancer stage and surgical outcomes
Priou et al. [28]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with lung cancerFranceLung cancer diagnosis, stage, treatment and outcomes
Ramanakumar et al. [22]Retrospective, multicentre
  • Group 1: baseline (averages of 2018, 2019, 2020)

  • Group 2: pandemic (April 2020–March 2021)

2018–2021Patients with lung, breast, colorectal and prostate cancerCanadaRates of newly diagnosed malignancy
Sato et al. [16]Retrospective, multicentre
  • Group 1: baseline (2014–2019)

  • Group 2: pandemic (2020)

2014–2020Patients with thoracic malignancyJapanLung cancer diagnosis, stage, treatment and outcomes
Seitlinger et al. [41]Prospective, multicentre731 patients2020Patients undergoing thoracic oncologic surgeryFrance, Germany, Italy, CanadaThoracic oncologic surgery outcomes
Sha et al. [3]Retrospective, single centreTotal patients: 1612020Patients with lung cancerChinaDelays in cancer-related care
Shipe et al. [50]Population-based modeling studyImmediate versus delayed surgical resectionPatients with suspicious lung nodules <2 cmUSAImpact of cancer care delays; 5-year survival
Sud et al. [51]Population-based modeling studyModel of cancer progression during COVID-19-induced delays in care2013–2017Patients with malignancy UKHazard ratios of cancer progression, 5-year reduction in survival
Taylor et al. [36]Observational, interview and questionnaire based30 patients2020Patients with lung cancerUKLung cancer quality of care and quality of life
Terashima et al. [34]Retrospective, single centre
  • Group 1: baseline (March 2018–March 2019)—82 patients

  • Group 2: pandemic (March 2020–March 2021)—75 patients

2018–2021Patients with lung cancerJapanLung cancer pre-visit, pre-diagnosis and pre-treatment time
Teteh et al. [35]Observational, single centre41 participants2020Patients enrolled in a randomized trial of self‐management intervention for lung cancer surgery preparation/recoveryUSASubjective outcomes of lung cancer surgery preparation/recovery
Uematsu et al. [43]Observational, questionnaire-basedQuestionnaire sent to 14 facilities in the Kanagawa General Thoracic Surgery Study Group2020Patients with lung cancerJapanLung cancer diagnosis and resource allocation
Van Haren et al. [12]Retrospective, single centre
  • Group 1: baseline (January 2017–February 2020)

  • Group 2: pandemic (March–July 2020)

2017–2020Patients undergoing screening for lung cancerUSACancer-related screening and diagnosis
Villena-Vargas et al. [19]Retrospective, single centre
  • Group 1: baseline (January 2020–March 2020)—57 patients

  • Group 2: pandemic (March 2020–June 2020)—42 patients

2020Patients with NSCLC lung cancerUSAOutcomes of lung cancer surgery
Walker et al. [14]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients undergoing screening for breast, cervical, colorectal and lung cancerCanadaCancer-related screening and diagnosis
Walter et al. [31]Observational, questionnaire-basedQuestionnaire sent to 245 patients2020Patients with thoracic malignancyGermanySubjective delays in thoracic malignancy diagnosis and treatment
Yu et al. [46]Retrospective, single centre, propensity-matched
  • Group 1: baseline (September 2019–November 2019)

  • Group 2: pandemic (December 2019–February 2020)

2019–2020Patients with NSCLC lung cancerChinaLung cancer treatment and outcomes
Zhang et al. [6]Retrospective, single centre
  • Group 1: baseline (February–July 2019)

  • Group 2: pandemic (February–July 2020)

2019–2020Patients with lung cancerChinaCancer-related screening and diagnosis

CATS: Canadian Association of Thoracic Surgeons; CCRN: COVID and Cancer Research Network; COVID: coronavirus disease 2019; FFS: fee for service; NHS: National Health Service; NSCLC: non-small-cell lung cancer; PNLCR: Polish National Lung Cancer Registry; RCRD: Rapid Cancer Registration Dataset; SPECT: Spanish Thoracic Surgery Society.

Table 1:

Characteristics of included studies

Study nameStudy typeStudy organizationYears data collectedStudy populationLocationOutcomes
Bertolaccini and Spaggiari [39]Retrospective, single centreHub-and-spokes system for oncological care2019–2020Patients with thoracic malignancyItalyThoracic oncologic surgical activity
Bertolaccini et al. [23]Retrospective, single centre
  • Group 1: baseline (January–July 2019)

  • Group 2: January–July 2020

  • Group 3: January–July 2021

2019–2021Lung cancer patient undergoing lobectomyItalyDisease stage
Bhalla et al. [29]Prospective, multicentre
  • Group 1: baseline (December 2019)

  • Group 2: pandemic period (July 2020)

2019–2020Adult patients with a current or history of hematological malignancy or invasive solid tumourUSACancer care delivery (number of in-person outpatient visits, telehealth visits and pandemic-related delays of oncologic care)
Cantini et al. [5]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Newly diagnosed lung cancer patientItalyLung cancer diagnosis and access to treatment
Ciriaco et al. [38]Retrospective, single centreDescription of COVID-related changes in NSCLC treatment2019–2020Patients with NSCLC lung cancerItalyThoracic oncologic surgical activity
Conibear et al. [2]Retrospective, multicentre
  • Group 1: baseline (2019)—33 091 patients

  • Group 2: pandemic (2020)—31 371 patients

2019–2020Patients with lung cancer; RCRDUKLung cancer diagnosis, stage at presentation, treatment, survival
Degeling et al. [47]Population-based modeling study
  • Baseline scenario

  • Stage shift scenario

2019Patients with stage I breast, colorectal and lung cancer and T1 melanomaAustraliaImpact of cancer care delays
Dolan et al. [18]Retrospective, single centre
  • Group 1: baseline (2019)—375 patients

  • Group 2: pandemic (March–May 2020)—58 patients

2019–2020Patients with NSCLC lung cancerUSAThoracic oncologic surgical activity
Englum et al. [9]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with prostate, lung, bladder and colorectal cancerUSACancer-related health care encounters, diagnostic or screening procedures, new cancer diagnoses
Flores et al. [8]Retrospective, single centreMonthly case average compared between baseline (2018–2019) to the pandemic period (2020–2021)2018–2021Patients with lung cancerUSARates of lung cancer diagnosis, disease stage
Fu et al. [32]Retrospective, single centre
  • Group 1: baseline (2015–2019)—2054 patients

  • Group 2: pandemic (2020)—397 patients

2015–2020Patients with lung cancerChinaLung cancer diagnosis; subjective patient outcomes
Fujita et al. [33]Retrospective, single centre
  • Group 1: no treatment delay—150 patients

  • Group 2: treatment delay—15 patients

2020Patients with lung cancerJapanLung cancer treatment; subjective patient outcomes
Geukens et al. [45]Retrospective, multicentre928 patients2020–2021Patients with malignancyBelgiumMortality
Gokce et al. [41]Retrospective, single centre35 patients2020–2021Patients with NSCLC lung cancerTurkeyLung cancer surgery outcomes
Hilzenrat et al. [15]Observational, multicentreElectronic survey distributed to CATS members2019–2020Patients with lung cancerCanadaSurgical lung cancer care
Kasymjanova et al. [20]Retrospective, single centre
  • Group 1: baseline (March 2019–February 2020)

  • Group 2: pandemic (March 2020–February 2021)

2019–2021Patients with lung cancerCanadaLung cancer diagnosis and treatment
Keogh et al. [21]Retrospective, single centre
  • Group 1: baseline (January 2019–February 2020)—330 patients

  • Group 2: pandemic (March 2020–February 2021)—320 patients

2019–2021Patients with NSCLC lung cancerCanadaLung cancer diagnosis, stage, treatment, outcomes
Leclère et al. [40]Retrospective, single centre115 patients2020Patients with NSCLC lung cancer undergoing surgical resectionFrancePostoperative occurrence of COVID-19
London et al. [17]Retrospective, multicentre
  • Group 1: baseline (January–April 2019)

  • Group 2: pandemic (January–April 2020)

2019–2020Patients with malignancy; CCRN databaseUSARates of lung cancer diagnosis
Lou et al. [12]Retrospective, single centre
  • Group 1: pre-pandemic period (2016–2019)

  • Group 2: pandemic (2020)

2016–2020Patients undergoing screening for lung, colorectal and breast cancerUSACancer-related screening and diagnosis
Malagón et al. [48]Population-based modeling studyModel of cancer incidence, stage at diagnosis and survival2020–2021Patients with malignancy; Canadian Cancer RegistryCanadaImpact of cancer care delays
Maringe et al. [49]Population-based modeling study29 305 patients2010–2015Patients with breast, colorectal, esophageal and lung cancer; NHS databaseUKImpact of cancer care delays
Martínez-Hernández et al. [37]Retrospective, multicentre, questionnaireElectronic survey sent to SPECT members2019–2020Patients with lung cancerSpainLung cancer management
Morais et al. [26]Retrospective, multicentre, propensity-matched
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalLung cancer management
Morais et al. [27]Retrospective, single centre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalCancer-related screening and diagnosis
Pasello et al. [30]Retrospective, multicentre
  • Group 1: baseline (March–April 2019)

  • Group 2: pandemic (March–April 2020)

2019–2020Patients with lung cancer; two centresItalyLung cancer management
Patt et al. [7]Retrospective, multicentre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancy; Medicare FFS claimsUSACancer-related screening and diagnosis
Peacock et al. [24]Retrospective, multicentre
  • Group 1: baseline (April 2019)

  • Group 2: pandemic (April 2020)

2019–2020Patients with malignancy; Belgian Cancer RegistryBelgiumRates of lung cancer diagnosis
Peer et al. [42]Retrospective, single centre113 patients2020Patients with NSCLC lung cancer undergoing surgical resectionIsraelLung cancer surgical outcomes
Piwkowski et al. [25]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients with lung cancer undergoing surgery; PNLCR databasePolandLung cancer stage and surgical outcomes
Priou et al. [28]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with lung cancerFranceLung cancer diagnosis, stage, treatment and outcomes
Ramanakumar et al. [22]Retrospective, multicentre
  • Group 1: baseline (averages of 2018, 2019, 2020)

  • Group 2: pandemic (April 2020–March 2021)

2018–2021Patients with lung, breast, colorectal and prostate cancerCanadaRates of newly diagnosed malignancy
Sato et al. [16]Retrospective, multicentre
  • Group 1: baseline (2014–2019)

  • Group 2: pandemic (2020)

2014–2020Patients with thoracic malignancyJapanLung cancer diagnosis, stage, treatment and outcomes
Seitlinger et al. [41]Prospective, multicentre731 patients2020Patients undergoing thoracic oncologic surgeryFrance, Germany, Italy, CanadaThoracic oncologic surgery outcomes
Sha et al. [3]Retrospective, single centreTotal patients: 1612020Patients with lung cancerChinaDelays in cancer-related care
Shipe et al. [50]Population-based modeling studyImmediate versus delayed surgical resectionPatients with suspicious lung nodules <2 cmUSAImpact of cancer care delays; 5-year survival
Sud et al. [51]Population-based modeling studyModel of cancer progression during COVID-19-induced delays in care2013–2017Patients with malignancy UKHazard ratios of cancer progression, 5-year reduction in survival
Taylor et al. [36]Observational, interview and questionnaire based30 patients2020Patients with lung cancerUKLung cancer quality of care and quality of life
Terashima et al. [34]Retrospective, single centre
  • Group 1: baseline (March 2018–March 2019)—82 patients

  • Group 2: pandemic (March 2020–March 2021)—75 patients

2018–2021Patients with lung cancerJapanLung cancer pre-visit, pre-diagnosis and pre-treatment time
Teteh et al. [35]Observational, single centre41 participants2020Patients enrolled in a randomized trial of self‐management intervention for lung cancer surgery preparation/recoveryUSASubjective outcomes of lung cancer surgery preparation/recovery
Uematsu et al. [43]Observational, questionnaire-basedQuestionnaire sent to 14 facilities in the Kanagawa General Thoracic Surgery Study Group2020Patients with lung cancerJapanLung cancer diagnosis and resource allocation
Van Haren et al. [12]Retrospective, single centre
  • Group 1: baseline (January 2017–February 2020)

  • Group 2: pandemic (March–July 2020)

2017–2020Patients undergoing screening for lung cancerUSACancer-related screening and diagnosis
Villena-Vargas et al. [19]Retrospective, single centre
  • Group 1: baseline (January 2020–March 2020)—57 patients

  • Group 2: pandemic (March 2020–June 2020)—42 patients

2020Patients with NSCLC lung cancerUSAOutcomes of lung cancer surgery
Walker et al. [14]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients undergoing screening for breast, cervical, colorectal and lung cancerCanadaCancer-related screening and diagnosis
Walter et al. [31]Observational, questionnaire-basedQuestionnaire sent to 245 patients2020Patients with thoracic malignancyGermanySubjective delays in thoracic malignancy diagnosis and treatment
Yu et al. [46]Retrospective, single centre, propensity-matched
  • Group 1: baseline (September 2019–November 2019)

  • Group 2: pandemic (December 2019–February 2020)

2019–2020Patients with NSCLC lung cancerChinaLung cancer treatment and outcomes
Zhang et al. [6]Retrospective, single centre
  • Group 1: baseline (February–July 2019)

  • Group 2: pandemic (February–July 2020)

2019–2020Patients with lung cancerChinaCancer-related screening and diagnosis
Study nameStudy typeStudy organizationYears data collectedStudy populationLocationOutcomes
Bertolaccini and Spaggiari [39]Retrospective, single centreHub-and-spokes system for oncological care2019–2020Patients with thoracic malignancyItalyThoracic oncologic surgical activity
Bertolaccini et al. [23]Retrospective, single centre
  • Group 1: baseline (January–July 2019)

  • Group 2: January–July 2020

  • Group 3: January–July 2021

2019–2021Lung cancer patient undergoing lobectomyItalyDisease stage
Bhalla et al. [29]Prospective, multicentre
  • Group 1: baseline (December 2019)

  • Group 2: pandemic period (July 2020)

2019–2020Adult patients with a current or history of hematological malignancy or invasive solid tumourUSACancer care delivery (number of in-person outpatient visits, telehealth visits and pandemic-related delays of oncologic care)
Cantini et al. [5]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Newly diagnosed lung cancer patientItalyLung cancer diagnosis and access to treatment
Ciriaco et al. [38]Retrospective, single centreDescription of COVID-related changes in NSCLC treatment2019–2020Patients with NSCLC lung cancerItalyThoracic oncologic surgical activity
Conibear et al. [2]Retrospective, multicentre
  • Group 1: baseline (2019)—33 091 patients

  • Group 2: pandemic (2020)—31 371 patients

2019–2020Patients with lung cancer; RCRDUKLung cancer diagnosis, stage at presentation, treatment, survival
Degeling et al. [47]Population-based modeling study
  • Baseline scenario

  • Stage shift scenario

2019Patients with stage I breast, colorectal and lung cancer and T1 melanomaAustraliaImpact of cancer care delays
Dolan et al. [18]Retrospective, single centre
  • Group 1: baseline (2019)—375 patients

  • Group 2: pandemic (March–May 2020)—58 patients

2019–2020Patients with NSCLC lung cancerUSAThoracic oncologic surgical activity
Englum et al. [9]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with prostate, lung, bladder and colorectal cancerUSACancer-related health care encounters, diagnostic or screening procedures, new cancer diagnoses
Flores et al. [8]Retrospective, single centreMonthly case average compared between baseline (2018–2019) to the pandemic period (2020–2021)2018–2021Patients with lung cancerUSARates of lung cancer diagnosis, disease stage
Fu et al. [32]Retrospective, single centre
  • Group 1: baseline (2015–2019)—2054 patients

  • Group 2: pandemic (2020)—397 patients

2015–2020Patients with lung cancerChinaLung cancer diagnosis; subjective patient outcomes
Fujita et al. [33]Retrospective, single centre
  • Group 1: no treatment delay—150 patients

  • Group 2: treatment delay—15 patients

2020Patients with lung cancerJapanLung cancer treatment; subjective patient outcomes
Geukens et al. [45]Retrospective, multicentre928 patients2020–2021Patients with malignancyBelgiumMortality
Gokce et al. [41]Retrospective, single centre35 patients2020–2021Patients with NSCLC lung cancerTurkeyLung cancer surgery outcomes
Hilzenrat et al. [15]Observational, multicentreElectronic survey distributed to CATS members2019–2020Patients with lung cancerCanadaSurgical lung cancer care
Kasymjanova et al. [20]Retrospective, single centre
  • Group 1: baseline (March 2019–February 2020)

  • Group 2: pandemic (March 2020–February 2021)

2019–2021Patients with lung cancerCanadaLung cancer diagnosis and treatment
Keogh et al. [21]Retrospective, single centre
  • Group 1: baseline (January 2019–February 2020)—330 patients

  • Group 2: pandemic (March 2020–February 2021)—320 patients

2019–2021Patients with NSCLC lung cancerCanadaLung cancer diagnosis, stage, treatment, outcomes
Leclère et al. [40]Retrospective, single centre115 patients2020Patients with NSCLC lung cancer undergoing surgical resectionFrancePostoperative occurrence of COVID-19
London et al. [17]Retrospective, multicentre
  • Group 1: baseline (January–April 2019)

  • Group 2: pandemic (January–April 2020)

2019–2020Patients with malignancy; CCRN databaseUSARates of lung cancer diagnosis
Lou et al. [12]Retrospective, single centre
  • Group 1: pre-pandemic period (2016–2019)

  • Group 2: pandemic (2020)

2016–2020Patients undergoing screening for lung, colorectal and breast cancerUSACancer-related screening and diagnosis
Malagón et al. [48]Population-based modeling studyModel of cancer incidence, stage at diagnosis and survival2020–2021Patients with malignancy; Canadian Cancer RegistryCanadaImpact of cancer care delays
Maringe et al. [49]Population-based modeling study29 305 patients2010–2015Patients with breast, colorectal, esophageal and lung cancer; NHS databaseUKImpact of cancer care delays
Martínez-Hernández et al. [37]Retrospective, multicentre, questionnaireElectronic survey sent to SPECT members2019–2020Patients with lung cancerSpainLung cancer management
Morais et al. [26]Retrospective, multicentre, propensity-matched
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalLung cancer management
Morais et al. [27]Retrospective, single centre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancyPortugalCancer-related screening and diagnosis
Pasello et al. [30]Retrospective, multicentre
  • Group 1: baseline (March–April 2019)

  • Group 2: pandemic (March–April 2020)

2019–2020Patients with lung cancer; two centresItalyLung cancer management
Patt et al. [7]Retrospective, multicentre
  • Group 1: baseline (March–July 2019)

  • Group 2: pandemic (March–July 2020)

2019–2020Patients with malignancy; Medicare FFS claimsUSACancer-related screening and diagnosis
Peacock et al. [24]Retrospective, multicentre
  • Group 1: baseline (April 2019)

  • Group 2: pandemic (April 2020)

2019–2020Patients with malignancy; Belgian Cancer RegistryBelgiumRates of lung cancer diagnosis
Peer et al. [42]Retrospective, single centre113 patients2020Patients with NSCLC lung cancer undergoing surgical resectionIsraelLung cancer surgical outcomes
Piwkowski et al. [25]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients with lung cancer undergoing surgery; PNLCR databasePolandLung cancer stage and surgical outcomes
Priou et al. [28]Retrospective, multicentre
  • Group 1: baseline (2018–2019)

  • Group 2: pandemic (2020)

2018–2020Patients with lung cancerFranceLung cancer diagnosis, stage, treatment and outcomes
Ramanakumar et al. [22]Retrospective, multicentre
  • Group 1: baseline (averages of 2018, 2019, 2020)

  • Group 2: pandemic (April 2020–March 2021)

2018–2021Patients with lung, breast, colorectal and prostate cancerCanadaRates of newly diagnosed malignancy
Sato et al. [16]Retrospective, multicentre
  • Group 1: baseline (2014–2019)

  • Group 2: pandemic (2020)

2014–2020Patients with thoracic malignancyJapanLung cancer diagnosis, stage, treatment and outcomes
Seitlinger et al. [41]Prospective, multicentre731 patients2020Patients undergoing thoracic oncologic surgeryFrance, Germany, Italy, CanadaThoracic oncologic surgery outcomes
Sha et al. [3]Retrospective, single centreTotal patients: 1612020Patients with lung cancerChinaDelays in cancer-related care
Shipe et al. [50]Population-based modeling studyImmediate versus delayed surgical resectionPatients with suspicious lung nodules <2 cmUSAImpact of cancer care delays; 5-year survival
Sud et al. [51]Population-based modeling studyModel of cancer progression during COVID-19-induced delays in care2013–2017Patients with malignancy UKHazard ratios of cancer progression, 5-year reduction in survival
Taylor et al. [36]Observational, interview and questionnaire based30 patients2020Patients with lung cancerUKLung cancer quality of care and quality of life
Terashima et al. [34]Retrospective, single centre
  • Group 1: baseline (March 2018–March 2019)—82 patients

  • Group 2: pandemic (March 2020–March 2021)—75 patients

2018–2021Patients with lung cancerJapanLung cancer pre-visit, pre-diagnosis and pre-treatment time
Teteh et al. [35]Observational, single centre41 participants2020Patients enrolled in a randomized trial of self‐management intervention for lung cancer surgery preparation/recoveryUSASubjective outcomes of lung cancer surgery preparation/recovery
Uematsu et al. [43]Observational, questionnaire-basedQuestionnaire sent to 14 facilities in the Kanagawa General Thoracic Surgery Study Group2020Patients with lung cancerJapanLung cancer diagnosis and resource allocation
Van Haren et al. [12]Retrospective, single centre
  • Group 1: baseline (January 2017–February 2020)

  • Group 2: pandemic (March–July 2020)

2017–2020Patients undergoing screening for lung cancerUSACancer-related screening and diagnosis
Villena-Vargas et al. [19]Retrospective, single centre
  • Group 1: baseline (January 2020–March 2020)—57 patients

  • Group 2: pandemic (March 2020–June 2020)—42 patients

2020Patients with NSCLC lung cancerUSAOutcomes of lung cancer surgery
Walker et al. [14]Retrospective, multicentre
  • Group 1: baseline (2019)

  • Group 2: pandemic (2020)

2019–2020Patients undergoing screening for breast, cervical, colorectal and lung cancerCanadaCancer-related screening and diagnosis
Walter et al. [31]Observational, questionnaire-basedQuestionnaire sent to 245 patients2020Patients with thoracic malignancyGermanySubjective delays in thoracic malignancy diagnosis and treatment
Yu et al. [46]Retrospective, single centre, propensity-matched
  • Group 1: baseline (September 2019–November 2019)

  • Group 2: pandemic (December 2019–February 2020)

2019–2020Patients with NSCLC lung cancerChinaLung cancer treatment and outcomes
Zhang et al. [6]Retrospective, single centre
  • Group 1: baseline (February–July 2019)

  • Group 2: pandemic (February–July 2020)

2019–2020Patients with lung cancerChinaCancer-related screening and diagnosis

CATS: Canadian Association of Thoracic Surgeons; CCRN: COVID and Cancer Research Network; COVID: coronavirus disease 2019; FFS: fee for service; NHS: National Health Service; NSCLC: non-small-cell lung cancer; PNLCR: Polish National Lung Cancer Registry; RCRD: Rapid Cancer Registration Dataset; SPECT: Spanish Thoracic Surgery Society.

RESULTS

Impact of COVID-19 on lung cancer screening

In an analysis of the Veteran Affairs Healthcare System in the USA, Englum et al. reported an overall decrease in new cancer diagnoses by 13% and a 10% decrease in screening chest computed tomography (CT) scans [9]. An analysis of the Medicare fee-for-service population from 2019–2020 indicated a 74% and 58% reduction in lung cancer screening and lung biopsy rates at the peak of the pandemic, respectively [7]. Furthermore, Van Haren et al. noted a significant increase in the ‘no-show rate’ and a decrease in the number of low-dose CT scans for patients scheduled for lung cancer screening. Subsequently, there was a significant increase in lung nodules suspicious for malignancy (Lung-RADS 4) upon resumption of screening [12]. Interestingly, 1 retrospective, single-centre study from the USA reported no difference in screening chest CTs during the pandemic period [13].

A multicentre study in Canada reported a 23% absolute reduction in screening and an increased rate of higher Lung-RADS categories in January–March 2020 compared to baseline (16.7% vs 12.8%) [14]. Additionally, a survey completed by 59% of the Canadian Association of Thoracic Surgeons reported essentially unchanged access to CT during the pandemic. However, 87%, 85% and 63% of surgeons reported ‘somewhat less’ or ‘much less’ access to flexible bronchoscopy, linear endobronchial ultrasound and pulmonary function tests, respectively [15].

Finally, a retrospective, multicentre study in Japan analysing patients with thoracic malignancies also reported a reduction in lung cancer screening [16].

Impact of COVID-19 on lung cancer rates & presentation

An analysis of the COVID and Cancer Research Network in the USA between 2019 and 2020 indicated a 39.1% reduction in new lung cancer diagnoses [17]. Flores et al. reported a 50% reduction in the proportion of stage 0/I/II lung cancers and a 179% increase in the proportion of stage III/IV lung cancers during the first lockdown. Similarly, they note a further 50% decrease and a 130% increase for the same during 2021 [8]. Additionally, a retrospective, single-centre US study indicated significantly increased tumour size at presentation during the pandemic [18]. Lou et al. [13] reported a significant decrease in new lung cancer diagnoses in 2020 but, interestingly, there was no change in stage at presentation. Similarly, in their retrospective, single-centre analysis of patients with non-small-cell lung cancer (NSCLC), Villena-Vargas et al. [19] also reported no significant difference in tumour pathologic stage at presentation.

One Canadian study indicated a 35% decrease in new lung cancer diagnoses along with an increased stage at diagnosis during the pandemic [20]. An analysis of solely NSCLC patients at a different Canadian centre indicated no significant difference in the number of patient referrals, baseline patient characteristics or tumour pathologic state [21]. Another Canadian centre reported a 5–34% underestimation of the incidence of stage-specific lung cancer during the first wave of the pandemic corresponding to the temporary suspension of local screening programs [22].

In Italy, Cantini et al. [5] reported a reduction in the number of newly diagnosed cases of lung cancer during the pandemic as well as an increased likelihood of stage IV disease. Another Italian study indicated a significant increase in the number of patients with IB–IIB disease and no difference in the number of patients with advanced-stage disease [23].

An analysis of the Belgian Cancer Registry from 2019 to 2020 indicated a 33% reduction in new lung cancer diagnoses [24]. The Polish National Lung Cancer Registry noted an increased rate of patients with more advanced pathological stage during the pandemic [25]. Similarly, a retrospective analysis of a single centre in Portugal reported a 21.5% reduction in new lung cancer diagnoses and an increased diagnosis of advanced-stage cancer [26]. A propensity-matched multicentre study in Portugal also indicated a 20% reduction in new lung cancer diagnoses [27].

The results of the National Lung Cancer Audit (NLCA) in the UK indicated a 4% absolute increase in patients with lung cancer presenting emergently. However, contrasting with some of the previous results, there was no difference in the proportion of patients with advanced (stage IV) disease [2]. A retrospective, multicentre analysis in France also indicated a 32% decrease in new lung cancer diagnoses but no significant difference in the initial tumour stage [28].

In China, Zhang et al. [6] reported that 47.6% of lung cancers were diagnosed incidentally, 34.2% based on symptoms and 18.2% physical exam during the pandemic, with the average tumour volume of the patients diagnosed by screening significantly smaller than in those diagnosed by symptoms or physical exam. A retrospective, multicentre study in Japan analysing patients with thoracic malignancies reported a 3.2% increase in the number of metastatic lung tumour surgeries during the pandemic [16].

Delays in lung cancer care during the COVID-19 pandemic

A multicentre study from the USA reported that delays in imaging and diagnostic procedures were more likely with lung cancer than other solid tumours and hematological malignancies [29]. Interestingly, in another US study, Lou et al. [13] reported a reduced time-to-treatment for lung cancer during the pandemic, with more patients undergoing surgical resection.

The analysis of patients with lung cancer at a single centre in Canada did not report delays in the initiation of chemotherapy and radiation treatment; however, they did note increased delays to surgical intervention [20].

In Italy, Pasello et al. reported reductions in outpatient visits, patient enrolment in clinical trials and end-of-life cancer systemic treatments, as well as increased tumour processing times during the pandemic [30]. However, another Italian study reported no differences in the interval between symptom onset and radiological/cytohistological diagnosis, treatment start and first radiological revaluation [5]. Similarly, the NLCA in the UK reported no difference in median time from diagnosis to treatment between 2019 and 2020 [2].

In a survey sent to 245 patients in Germany, 57–70% reported unavailability of respiratory/physical therapy, as well as delays or cancellations of appointments for tumour‐directed therapy, imaging and follow‐up care in 18.9%, 13.6% and 14.8% of patients, respectively [31].

In a single-centre analysis of 161 patients in China, delayed follow-up care and discontinued or delayed cancer treatment were noted in 59% and 9% of patients, respectively. Eighteen percent of patients with delayed care exhibited progressive disease upon reassessment [3]. In a nationwide survey, Fu et al. [32] reported that patient concerns included long waiting times for outpatient services, inpatient beds, physical examinations or operations.

The results of a single-centre analysis in Japan noted pandemic-related delays in lung cancer treatment in 9.1% of patients [33]. Similarly, Terashima et al. [34] identified increases in pre-visit time, surgery wait time, as well as reductions in surgery for lung cancer and increased rates of advanced disease.

Teteh et al. [35] surveyed patients and caregivers on their perspectives on care during the pandemic, identifying themes of delayed treatment, isolation, psychological distress and financial burden. In addition to that noted above, another survey reported mixed feelings regarding virtual care [36].

Surgical intervention for lung cancer during the coronavirus disease 2019 pandemic

A retrospective, single-centre analysis of lung cancer surgical outcomes in the USA reported no significant differences in postoperative complications, 30, 60 or 90-day mortality, between pre-pandemic and pandemic patient populations [18]. In their analysis of American patients with NSCLC, Villena-Vargas et al. reported no significant difference in 90-day postoperative morbidity or mortality. However, there was a 40% mortality rate associated with COVID-19 infections within 90 days of surgery [19].

A Canadian study reported increased utilization of radiosurgery as the first definitive treatment with a corresponding decrease in systemic treatment and surgery [20]. This was as a result of recommendations to utilize available treatments as alternatives to surgery. The reductions in surgical capacity were attributed to reductions in operating room hours, lack of medical staff and long waiting lists for surgery. An analysis of solely NSCLC patients at another Canadian site reported no difference in surgical mortality or hospital length of stay during the pandemic as compared to the pre-pandemic baseline [21].

The NLCA in the UK reported a 5% absolute reduction in patients with NSCLC undergoing surgical intervention [2]. Survey results of the Spanish Society of Thoracic Surgeons indicated a 96% reduction in thoracic surgical activity between 2019 and 2020 [37]. In their description of thoracic oncological surgical activity in multiple centres in Italy, Ciriaco et al. note a 50% reduction in thoracic surgery beds during the pandemic but no decrease in the number of surgical procedures. They describe a ‘hub and spokes’ approach to surgical care for patients with NSCLC [38]. The hub and spoke model refers to the establishment of ‘spoke’ centres where patients are initially seen and evaluated, following which they can be referred to a central ‘hub’ which is specialized in the treatment of lung cancers and ideally COVID-free to prevent interruptions of care. A similar hub and spoke model was described by Bertolaccini and Spaggiari [39] in the management of lung cancer in the Lombardy region of Italy. In a retrospective analysis of 115 patients with NSCLC undergoing surgical resection at a single centre in France, Leclère et al. report no immediate difference in oncologic outcomes. The rate of postoperative COVID-19 infection at 1 month was 5%. In patients with postoperative COVID-19 infection, they did observe an increased rate of readmission, but no significant increase in 30-day morbidity or mortality [40]. An analogous study consisting of 35 NSCLC patients undergoing surgical resection at a single centre in Turkey from 2020 to 2021 reported 0% and 14% rates of postoperative mortality and morbidity, respectively. There was no significant difference in complications in patients with a preoperative history of COVID-19 [41]. Finally, utilizing the Polish National Lung Cancer Registry, Piwkowski et al. [25] reported a 20.5% overall reduction in the number of lung cancer procedures, with no difference in rates of in-hospital mortality and decreased hospital length of stay during the pandemic.

A retrospective analysis of 113 patients with NSCLC undergoing surgical resection at a single centre in Israel noted postoperative complications slightly higher than other studies at 30.9% [42].

In a survey sent to 14 facilities in the Kanagawa General Thoracic Surgery Study Group, Uematsu et al. [43] reported a 22% reduction in total surgical case volume with a 6% and 14% reduction in lung cancer surgery at all institutions and those placed under restriction, respectively. A similar study carried out in China reported a 57% reduction in lung cancer surgery during the pandemic.

Finally, a multicentre study consisting of 731 patients undergoing thoracic oncologic surgery in France, Germany, Italy and Canada, reported 3%, 1.2% and 0.5% rates of overall mortality, COVID-19 infection and readmission [44].

Lung cancer outcomes during the coronavirus disease 2019 pandemic

According to the NLCA in the UK, there was a reduction in median survival from 2019 to 2020 (306 vs 316 days) [2].

In a retrospective, study consisting of 928 patients at 19 different hospitals across Belgium, there was a trend towards higher mortality in patients with lung cancer as compared to other solid organ cancers (27.6% vs 20.8%, P = 0.062) [45].

However, a retrospective, propensity-matched study in Portugal from 2019 to 2020 indicated no difference in crude, age-adjusted, stage-adjusted and propensity-matched hazard ratios for short-term mortality with lung cancer treatment overall during the pandemic. Of note, a significantly higher hazard ratio for mortality was observed in patients with stage III cancer [27].

A retrospective, multicentre analysis of patients with lung cancer in France over the same period also reported no significant difference in rates of 6-month mortality following systemic anticancer therapy or surgical intervention. However, they did note increased mortality in patients with COVID-19 who received systemic anticancer therapy [28].

In a propensity-matched study of 196 patients with NSCLC in China between 2019 and 2020, Yu et al. noted an increased rate of therapy discontinuation and non-surgical treatment for late-stage patients, but no difference in surgical treatment, discontinued therapy, cancer progression and mortality for early-stage patients [46].

Modelling of the impact of COVID-19-related delays in lung cancer care

In a population-based modelling study by Degeling et al., there is an estimated 8.3% and 16.0% probability of cancer progression with 3- and 6-month treatment delays, respectively. Three- and 6-month delays in care are estimated to result in 11 and 43 excess deaths, as well as 98 and 373 life-years lost at 10 years, respectively [47].

A similar study focusing on the Canadian population estimated a 1.1% relative mortality increase with 3082 excess deaths and 42 472 life-years lost due to the pandemic-related diagnostic and treatment delays for lung cancer [48].

An analysis from the UK estimated a 4.8–5.3% increase in lung cancer mortality 5 years after diagnosis [49].

Interestingly, an American study analysing the impact of immediate versus delayed (>3 months from diagnosis) surgical resection in patients with suspicious lung nodules <2 cm estimated no significant difference in 5-year survival for the overall patient population. However, survival is estimated to be significantly greater with delayed resection if the probability of COVID-19 infection is >13% [50].

Limitations

The literature published to date on resource allocation and outcomes during the COVID-19 pandemic is variable with heterogeneous studies and trends identified. Additionally, while negative implications for postoperative outcomes were not consistently identified, this may have been due to insufficient follow-up to date requiring longer-term studies on the outcomes of patients with lung cancer as the pandemic progresses. Furthermore, relatively few studies published data on the outcomes of these patients making it difficult to identify trends in the outcomes of these patients. Follow-up and presentation of the data for patients with lung cancer identified during or after the pandemic will be required to identify the impact on their outcomes over the long term.

CONCLUSIONS

This systematic review aimed to summarize the literature investigating the impact of resource allocation towards the COVID-19 pandemic on patients with lung cancer. Several interesting trends were identified in the literature published to date. First, rates of screening and diagnostic testing were reduced during the pandemic secondary to reduced access to these resources [7, 9, 12–16]. Second, investigations across the literature identified mixed results in the presentation of patients with lung cancer with several studies identifying decreased incidence of early-stage lung cancer, with a correlated increased incidence of late-stage disease [2, 5, 8, 13, 17–28]. Patients found to have lung cancer during the pandemic experienced reduced rates of in-person assessments, increased time to intervention and reduced follow-up [3, 13, 20, 29–33]. These differences in findings are likely multifactorial including the fact that many of these studies were published in different regions of the world where the impact and timing of the various waves of the pandemic differed, there were differing responses to the pandemic from governments and healthcare authorities, and there are diverse healthcare systems with contrasting priorities and resource utilization. Among patients undergoing surgical intervention for lung cancers during the pandemic, there were few differences identified in postoperative outcomes [18, 19, 21, 25, 28, 40–42, 45, 46]. Finally, when accounting for the above disruptions in screening, assessments, diagnostics and interventions, studies aimed at modelling the impact of these changes predict significant increases in mortality for patients with lung cancer in the years to come [47–50].

The findings of this review highlight the consequences of changes in healthcare resource allocation during the COVID-19 pandemic. The studies identified in this review highlight the impact of the pandemic on screening, diagnostic testing and surgical interventions, but interestingly, did not identify consistently significantly worse outcomes for patients [7–9, 13–16, 18, 20, 22]. While the pandemic had implications over the past 2 years on screening and diagnosis, the outcomes included in many of the published studies did not differ significantly. Reduced screening in the first year of the pandemic may have affected the incidence of lung cancer but not postoperative outcomes as many cases of lung cancer would have been undiagnosed. However, the indirectly related delayed presentation will affect morbidity and mortality in the years to come. As previously asymptomatic cases progress we will likely see a shift in staging to more advanced lung cancer. This stage shift will not only affect lung cancer survival rates but shift care from surgery for early-stage cancer to either multimodality treatment protocols or palliation further magnifying the impact of the COVID-19 pandemic on lung cancer resources in the future years. Due to these factors, a relatively small number of studies published data on outcomes of patients. This is likely related to the prolonged course of lung cancer developing over months or years. While we are able to appreciate differences in screening and management, data on outcomes will require years to clearly identify. Future investigations focusing on the outcomes of these patients will be required to follow their progress over time.

Given the recently identified impacts on patient outcomes and the significant implications for patients with lung cancer in the future, several considerations are required in the late stages of this pandemic and in future scenarios where resources may be scarce. While the pandemic certainly required mobilization and diversion of significant healthcare resources, an over-emphasis on the pandemic without concurrent consideration of non-COVID patients, such as those with lung cancer, may result in lasting impacts on those patients. As patients with lung cancer develop more advanced disease, prolonged treatment with worse prognoses will likely result in additional strain on healthcare resources. Referral to evidence based and guideline recommendations may help to identify key areas that are pivotal to the management of patients with lung cancer, and other conditions. While care during the pandemic in the included studies was infrequently compared to guideline recommendations for screening or management, the delay or cessation of screening and management of lung cancer likely delayed care well past guideline recommendations in many cases. As we are able to retrospectively analyse the efficacy of resource allocation and the unintended side effects, in future times when resources are scarce the implications of resource diversion must be considered for all patients to ensure optimal use of resources. This will mitigate the long-term effects of resource diversion and reallocation preventing further draining of healthcare resources to treat potentially preventable suboptimal outcomes.

Through reflecting on the pandemic response, we are able to understand the implications of specific decisions in order to guide future decision-making in times of limited resources. Future decisions regarding resource allocations should consider the impact on all patients, including the long-term results of progressive diseases not being identified or treated optimally. These decisions should be guided by past trends to provide optimal care to all patients.

As the COVID-19 pandemic placed enormous strains on global healthcare systems, resource allocation away from most sectors of healthcare to battle the pandemic was required. While significant resources were necessary to combat the pandemic, the shift of resources away from other areas of healthcare has had detrimental impacts on non-COVID patients. The findings of this review suggest that patients with lung cancer have been shown to experience reduced rates of screening, diagnosis and interventions during the pandemic. While significant differences in postoperative outcomes were not identified, the effects of the pandemic and reductions in cancer screening will likely be identified in the years to come. Future consideration of the long-term implications of resource allocation away from patients with lung cancer with an attempt to provide equitable access to healthcare and to limit the interruptions of patient care may help provide the best care for all patients during times of limited resources.

FUNDING

This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.

Conflict of interest: Eric L.R. Bédard discloses a financial relationship with Hoffman La Roche and Astra Zeneca. The other authors report no conflicts of interest.

DATA AVAILABILITY

The data that supports the findings of this study are available within the article and its supplements.

Author contributions

Ryaan EL-Andari: Conceptualization; Data curation; Investigation; Writing—original draft. Nicholas M. Fialka: Conceptualization; Data curation; Investigation; Writing—original draft. Uzair Jogiat: Conceptualization; Investigation; Writing—review & editing. Bryce Laing: Conceptualization; Investigation; Writing—review & editing. Eric L.R. Bédard: Conceptualization; Investigation; Writing—review & editing. Jayan Nagendran: Conceptualization; Investigation; Writing—original draft.

Reviewer information

Interdisciplinary CardioVascular and Thoracic Surgery thanks Mohsen Ibrahim and the other, anonymous reviewer(s) for their contribution to the peer review process of this article.

REFERENCES

1

Sung
H
,
Ferlay
J
,
Siegel
RL
,
Laversanne
M
,
Soerjomataram
I
,
Jemal
A
et al.
Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
.
CA Cancer J Clin
2021
;
71
:
209
49
.

2

Conibear
J
,
Nossiter
J
,
Foster
C
,
West
D
,
Cromwell
D
,
Navani
N.
The National Lung Cancer Audit: the impact of COVID-19
.
Clin Oncol (R Coll Radiol)
2022
;
34
:
701
7
.

3

Sha
Z
,
Chang
K
,
Mi
J
,
Liang
Z
,
Hu
L
,
Long
F
et al.
The impact of the COVID-19 pandemic on lung cancer patients
.
Ann Palliat Med
2020
;
9
:
3373
8
.

4

Dong
E
,
Du
H
,
Gardner
L.
An interactive web-based dashboard to track COVID-19 in real time
.
Lancet Infect Dis
2020
;
20
:
533
4
.

5

Cantini
L
,
Mentrasti
G
,
Russo
GL
,
Signorelli
D
,
Pasello
G
,
Rijavec
E
et al.
Evaluation of COVID-19 impact on DELAYing diagnostic-therapeutic pathways of lung cancer patients in Italy (COVID-DELAY study): fewer cases and higher stages from a real-world scenario
.
ESMO Open
2022
;
7
:
100406
.

6

Zhang
Y
,
Li
J
,
Li
ZK
,
Yang
X
,
Bai
J
,
Liu
L
et al.
Impact of coronavirus disease 2019 on clinical characteristics in patients with lung cancer: a large single-centre retrospective study
.
Front Oncol
2021
;
11
:
693002
6
.

7

Patt
D
,
Gordan
L
,
Diaz
M
,
Okon
T
,
Grady
L
,
Harmison
M
et al.
Impact of COVID-19 on cancer care: how the pandemic is delaying cancer diagnosis and treatment for american seniors
.
JCO Clin Cancer Inform
2020
;
4
:
1059
71
.

8

Flores
R
,
Alpert
N
,
McCardle
K
,
Taioli
E.
Shift in lung cancer stage at diagnosis during the COVID-19 pandemic in New York City
.
Transl Lung Cancer Res
2022
;
11
:
1514
6
.

9

Englum
BR
,
Prasad
NK
,
Lake
RE
,
Mayorga-Carlin
M
,
Turner
DJ
,
Siddiqui
T
et al.
Impact of the COVID-19 pandemic on diagnosis of new cancers: a national multicenter study of the Veterans Affairs Healthcare System
.
Cancer
2022
;
128
:
1048
56
.

10

Liberati
A
,
Altman
DG
,
Tetzlaff
J
,
Mulrow
C
,
Gotzsche
PC
,
Ioannidis
JPA
et al.
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration
.
BMJ
2009
;
339
:
b2700
.

11

Moher
D
PRISMA Group
Liberati
A
,
Tetzlaff
J
,
Altman
DG.
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement
.
BMJ
2009
;
339
:
b2535
.

12

Van Haren
RM
,
Delman
AM
,
Turner
KM
,
Waits
B
,
Hemingway
M
,
Shah
SA
et al.
Impact of the COVID-19 pandemic on lung cancer screening program and subsequent lung cancer
.
J Am Coll Surg
2021
;
232
:
600
5
.

13

Lou
J
,
Kooragayala
K
,
Williams
JP
,
Sandilos
G
,
Butchy
M. V
,
Yoon-Flannery
K
et al.
The early impact of the COVID-19 pandemic on lung, colorectal, and breast cancer screening and treatment at a tertiary cancer center
.
Am J Clin Oncol
2022
;
45
:
381
90
.

14

Walker
MJ
,
Meggetto
O
,
Gao
J
,
Espino-Hernández
G
,
Jembere
N
,
Bravo
CA
et al.
Measuring the impact of the COVID-19 pandemic on organized cancer screening and diagnostic follow-up care in Ontario, Canada: a provincial, population-based study
.
Prev Med
2021
;
151
:
106586
.

15

Hilzenrat
RA
,
Deen
SA
,
Yee
J
,
Grant
KA
,
Ashrafi
AS
,
Coughlin
S
et al.
Thoracic surgeon impressions of the impact of the covid-19 pandemic on lung cancer care—lessons from the first wave in Canada
.
Curr Oncol
2021
;
28
:
940
9
.

16

Sato
Y
,
Yamamoto
H
,
Ikeda
N
,
Konishi
H
,
Endo
S
,
Okada
Y
et al.
The impact of COVID-19 on thoracic surgical procedures in Japan: analysis of data from the National Clinical Database
.
Lung Cancer
2022
;
172
:
127
35
.

17

London
JW
,
Fazio-Eynullayeva
E
,
Palchuk
MB
,
Sankey
P
,
McNair
C.
Effects of the COVID-19 pandemic on cancer-related patient encounters
.
JCO Clin Cancer Inform
2020
;
4
:
657
65
.

18

Dolan
DP
,
Lee
DN
,
Polhemus
E
,
Kucukak
S
,
de León
LE
,
Wiener
D
et al.
Report on lung cancer surgery during COVID-19 pandemic at a high volume US institution
.
J Thorac Dis
2022
;
14
:
2874
9
.

19

Villena-Vargas
J
,
Lutton
EM
,
Mynard
N
,
Nasar
A
,
Voza
F
,
Chow
O
et al.
Safety of lung cancer surgery during COVID-19 in a pandemic epicenter
.
J Thorac Cardiovasc Surg
2022
;
164
:
378
85
.

20

Kasymjanova
G
,
Anwar
A
,
Cohen
V
,
Sultanem
K
,
Pepe
C
,
Sakr
L
et al.
The impact of COVID-19 on the diagnosis and treatment of lung cancer at a canadian academic center: a retrospective chart review
.
Curr Oncol
2021
;
28
:
4247
55
.

21

Keogh
JAJ
,
Chhor
AD
,
Begum
H
,
Akhtar-Danesh
N
,
Finley
C.
Impact of the COVID-19 pandemic on non–small-cell lung cancer pathologic stage and presentation
.
Can J Surg
2022
;
65
:
E496
E503
.

22

Ramanakumar
A. V
,
Annie
B
,
Frederic
L
,
Christine
B
,
Cathy
R
,
Jean
L.
Evaluating the impact of COVID-19 on cancer declarations in Quebec, Canada
.
Cancer Med
2022
;
12
:
6260
9
.

23

Bertolaccini
L
,
Ciani
O
,
Prisciandaro
E
,
Sedda
G
,
Spaggiari
L.
Lung cancer stage distribution from before COVID-19 through 18 months of the pandemic: the experience of a large-volume oncological referral centre
.
Eur J Surg Oncol
2022
;
48
:
470
1
.

24

Peacock
HM
,
Tambuyzer
T
,
Verdoodt
F
,
Calay
F
,
Poirel
HA
,
de Schutter
H
et al.
Decline and incomplete recovery in cancer diagnoses during the COVID-19 pandemic in Belgium: a year-long, population-level analysis
.
ESMO Open
2021
;
6
:
100197
.

25

Piwkowski
C
,
Gabryel
P
,
Orłowski
TM
,
Kowalewski
J
,
Kużdżał
J
,
Rzyman
W.
The impact of the COVID-19 pandemic on surgical treatment of lung cancer
.
Pol Arch Intern Med
2022
;
132
:
18
20
.

26

Morais
S
,
Antunes
L
,
Rodrigues
J
,
Fontes
F
,
Bento
MJ
,
Lunet
N.
The impact of the coronavirus disease 2019 pandemic on the diagnosis and treatment of cancer in Northern Portugal
.
Eur J Cancer Prev
2022
;
31
:
204
14
.

27

Morais
S
,
Antunes
L
,
Rodrigues
J
,
Fontes
F
,
Bento
MJ
,
Lunet
N.
The impact of the COVID-19 pandemic on the short-term survival of patients with cancer in Northern Portugal
.
Int J Cancer
2021
;
149
:
287
96
.

28

Priou
S
Assistance Publique – Hôpitaux de Paris (AP-HP) Cancer Group
Lamé
G
,
Zalcman
G
,
Wislez
M
,
Bey
R
,
Chatellier
G
,
Cadranel
J.
Influence of the SARS-CoV-2 outbreak on management and prognosis of new lung cancer cases, a retrospective multicentre real-life cohort study
.
Eur J Cancer
2022
;
173
:
33
40
.

29

Bhalla
S
,
Bakouny
Z
,
Schmidt
AL
,
Labaki
C
,
Steinharter
JA
,
Tremblay
DA
et al.
Care disruptions among patients with lung cancer: a COVID-19 and cancer outcomes study
.
Lung Cancer
2021
;
160
:
78
83
.

30

Pasello
G
,
Menis
J
,
Pilotto
S
,
Frega
S
,
Belluomini
L
,
Pezzuto
F
et al.
How the COVID-19 pandemic impacted on integrated care pathways for lung cancer: the parallel experience of a COVID-spared and a COVID-dedicated center
.
Front Oncol
2021
;
11
:
669786
8
.

31

Walter
J
,
Sellmer
L
,
Kahnert
K
,
Kiefl
R
,
Syunyaeva
Z
,
Kauffmann-Guerrero
D
et al.
Consequences of the COVID-19 pandemic on lung cancer care and patient health in a German lung cancer center: results from a cross-sectional questionnaire
.
Respir Res
2022
;
23
:
18
.

32

Fu
R
,
Wu
L
,
Zhang
C
,
Chu
Q
,
Hu
J
,
Lin
G
et al.
Real-world scenario of patients with lung cancer amid the coronavirus disease 2019 pandemic in the People’s Republic of China
.
JTO Clin Res Rep
2020
;
1
:
100053
.

33

Fujita
K
,
Ito
T
,
Saito
Z
,
Kanai
O
,
Nakatani
K
,
Mio
T.
Impact of COVID-19 pandemic on lung cancer treatment scheduling
.
Thorac Cancer
2020
;
11
:
2983
6
.

34

Terashima
T
,
Tsutsumi
A
,
Iwami
E
,
Kuroda
A
,
Nakajima
T
,
Eguchi
K.
Delayed visit and treatment of lung cancer during the coronavirus disease 2019 pandemic in Japan: a retrospective study
.
J Int Med Res
2022
;
50
:
030006052210973
.

35

Teteh
DK
,
Barajas
J
,
Ferrell
B
,
Zhou
Z
,
Erhunmwunsee
L
,
Raz
DJ
et al.
The impact of the COVID-19 pandemic on care delivery and quality of life in lung cancer surgery
.
J Surg Oncol
2022
;
126
:
407
16
.

36

Taylor
S
,
Stanworth
M
,
Eastwood
C
,
Gomes
F
,
Khatoon
B
,
Yorke
J.
Understanding the experiences of lung cancer patients during the COVID-19 pandemic: a qualitative interview study
.
Qual Life Res
2022
;
32
:
701
11
.

37

Martínez-Hernández
NJ
,
Silva
UC
,
Sánchez
AC
,
de la Cruz
JLCC
,
Carillo
AO
,
Sarceda
JRJ
et al.
Effect of covid-19 on thoracic oncology surgery in Spain: a Spanish thoracic surgery society (sect) survey
.
Cancers (Basel)
2021
;
13
:
1
18
.

38

Ciriaco
P
,
Carretta
A
,
Bandiera
A
,
Muriana
P
,
Negri
G.
Perspective: did Covid-19 change non-small cell lung cancer surgery approach?
Front Surg
2021
;
8
:
662592
5
.

39

Bertolaccini
L
,
Spaggiari
L.
Reorganization of thoracic surgery activity in a national high-volume comprehensive cancer centre in the Italian epicentre of coronavirus disease 2019
.
Eur J Cardiothorac Surg
2020
;
58
:
210
2
.

40

Leclère
JB
Thoracic Surgery Units of Paris Public Hospitals
Fournel
L
,
Etienne
H
,
Al Zreibi
C
,
Onorati
I
,
Roussel
A
et al.
Maintaining surgical treatment of non-small cell lung cancer during the COVID-19 pandemic in Paris
.
Ann Thorac Surg
2021
;
111
:
1682
8
.

41

Gokce
A
,
Hatipoglu
M
,
Akboga
SA
,
Sezen
AI
,
Akkas
Y
,
Kocer
B.
Critical care for lung cancer patients: surgical treatment during COVID-19 pandemic
.
Bratisl Lek Listy
2022
;
123
:
125
8
.

42

Peer
M
,
Azzam
S
,
Kolodii
M
,
Abramov
Y
,
Shaylor
R
,
Verenkin
V
et al.
Major pulmonary resection for non-small cell lung carcinoma during the COVID-19 pandemic—single Israeli Center cross-sectional study
.
J Clin Med
2022
;
11
:
1
9
.

43

Uematsu
S
,
Saji
H
,
Kitami
A
,
Ito
H
,
Tajiri
M
,
Shiomi
K
et al.
Impact of the first surge of the coronavirus disease pandemic on general thoracic surgery practices in Kanagawa: a questionnaire survey by the Kanagawa General Thoracic Surgical Study Group
.
Gen Thorac Cardiovasc Surg
2022
;
70
:
265
72
.

44

Seitlinger
J
,
Wollbrett
C
,
Mazzella
A
,
Schmid
S
,
Guerrera
F
,
Banga Nkomo
D
et al.
Safety and feasibility of thoracic malignancy surgery during the COVID-19 pandemic
.
Ann Thorac Surg
2021
;
112
:
1870
6
.

45

Geukens
T
,
Brandão
M
,
Laenen
A
,
Collignon
J
,
Van Marcke
C
,
Louviaux
I
et al.
Changes in anticancer treatment plans in patients with solid cancer hospitalized with COVID-19: analysis of the nationwide BSMO-COVID registry providing lessons for the future
.
ESMO Open
2022
;
7
:
100610
.

46

Yu
M
,
Cheng
Y
,
Zhang
R
,
Wen
T
,
Huai
S
,
Wei
X
et al.
Evaluating treatment strategies for non-small cell lung cancer during COVID-19: a propensity score matching analysis
.
Medicine (Baltimore)
2022
;
101
:
E30051
.

47

Degeling
K
,
Baxter
NN
,
Emery
J
,
Jenkins
MA
,
Franchini
F
,
Gibbs
P
et al.
An inverse stage-shift model to estimate the excess mortality and health economic impact of delayed access to cancer services due to the COVID-19 pandemic
.
Asia Pac J Clin Oncol
2021
;
17
:
359
67
.

48

Malagón
T
McGill Task Force on the Impact of COVID-19 on Cancer Control and Care
Yong
JHE
,
Tope
P
,
Miller
WH
,
Franco
EL.
Predicted long-term impact of COVID-19 pandemic-related care delays on cancer mortality in Canada
.
Int J Cancer
2022
;
150
:
1244
54
.

49

Maringe
C
,
Spicer
J
,
Morris
M
,
Purushotham
A
,
Nolte
E
,
Sullivan
R
et al.
The impact of the COVID-19 pandemic on cancer deaths due to delays in diagnosis in England, UK: a national, population-based, modelling study
.
Lancet Oncol
2020
;
21
:
1023
34
.

50

Shipe
ME
,
Haddad
DN
,
Deppen
SA
,
Kozower
BD
,
Grogan
EL.
Modeling the impact of delaying the diagnosis of non-small cell lung cancer during COVID-19
.
Ann Thorac Surg
2021
;
112
:
248
54
.

51

Sud
A
, ,
Jones
ME
,
,
Broggio
J
,
,
Loveday
C
,
,
Torr
B
,
,
Garrett
A
et al.
Collateral damage: the impact on outcomes from cancer surgery of the COVID-19 pandemic
.
Annals of Oncology
2020
;
31
:
1065
74
.

ABBREVIATIONS

    ABBREVIATIONS
     
  • COVID-19

    Coronavirus disease 2019

  •  
  • CT

    Computed tomography

  •  
  • NLCA

    National Lung Cancer Audit

  •  
  • NSCLC

    Non-small-cell lung cancer

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.