Overview of studies and trials of tailored-ablation approaches using the identification of patient-specific biomarkers
Study (year of publication) . | Patients . | Description . | Primary endpoint . | Outcome . |
---|---|---|---|---|
STAR AF II (2015)82,115 | Persistent AF patients (n = 589) | Multicentre, prospective, single-blind, randomized trial Three ablation strategies:
| During FU (3 months blanking period) freedom from AF recurrence (documented episode >30 s) after a single ablation procedure, with or without AADs | 18 months FU No significant differences in success rates between the three ablation strategies; 49, 46, and 59% of the patients experienced recurrences, respectively (P = 0.15) |
DECAAF II (2022)116,117 | Persistent AF patients (n = 843) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (90 day blanking period) first recurrence of AF, atrial flutter or AT (documented episode ≥30 s) after a single ablation procedure or repeat ablation | 12–18 months FU No significant difference in success rates between Group 1 and Group 2, 57.0 and 53.9%, respectively (P = 0.63) |
STABLE-SR-II (2022)118 | Persistent AF patients (n = 300) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) freedom from AF or AT (documented episode >30 s) after a single ablation procedure without the use of AADs | 18 months FU No significant difference in success rates between both ablation strategies, 67.2 and 67.4%, respectively. (P = 0.52) |
ERASE-AF (2022)119 | Persistent AF patients (n = 324) | Multicentre, prospective, open-label, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) first recurrence of AF or AT (documented episode >30 s) after a single ablation procedure | 12 months FU Significantly higher success rate in the PVI + low voltage area ablation group compared with the PVI only group, 65 vs. 50%, respectively (log rank P = 0.006) |
FLOW-AF (2024)120 | Persistent and long-standing persistent AF patients (n = 85) | Multicentre, prospective, open-label, randomized trial Two (redo) ablation strategies:
| (Secondary effectiveness endpoint) During FU (3 month blanking period) freedom from AF, AT, or atrial flutter | 12 months FU Higher success rate in the PVI in combination with EGF-guided ablation group compared with the PVI only group, 51 vs. 14% (P = 0.103) |
Study (year of publication) . | Patients . | Description . | Primary endpoint . | Outcome . |
---|---|---|---|---|
STAR AF II (2015)82,115 | Persistent AF patients (n = 589) | Multicentre, prospective, single-blind, randomized trial Three ablation strategies:
| During FU (3 months blanking period) freedom from AF recurrence (documented episode >30 s) after a single ablation procedure, with or without AADs | 18 months FU No significant differences in success rates between the three ablation strategies; 49, 46, and 59% of the patients experienced recurrences, respectively (P = 0.15) |
DECAAF II (2022)116,117 | Persistent AF patients (n = 843) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (90 day blanking period) first recurrence of AF, atrial flutter or AT (documented episode ≥30 s) after a single ablation procedure or repeat ablation | 12–18 months FU No significant difference in success rates between Group 1 and Group 2, 57.0 and 53.9%, respectively (P = 0.63) |
STABLE-SR-II (2022)118 | Persistent AF patients (n = 300) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) freedom from AF or AT (documented episode >30 s) after a single ablation procedure without the use of AADs | 18 months FU No significant difference in success rates between both ablation strategies, 67.2 and 67.4%, respectively. (P = 0.52) |
ERASE-AF (2022)119 | Persistent AF patients (n = 324) | Multicentre, prospective, open-label, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) first recurrence of AF or AT (documented episode >30 s) after a single ablation procedure | 12 months FU Significantly higher success rate in the PVI + low voltage area ablation group compared with the PVI only group, 65 vs. 50%, respectively (log rank P = 0.006) |
FLOW-AF (2024)120 | Persistent and long-standing persistent AF patients (n = 85) | Multicentre, prospective, open-label, randomized trial Two (redo) ablation strategies:
| (Secondary effectiveness endpoint) During FU (3 month blanking period) freedom from AF, AT, or atrial flutter | 12 months FU Higher success rate in the PVI in combination with EGF-guided ablation group compared with the PVI only group, 51 vs. 14% (P = 0.103) |
AAD, antiarrhythmic drug; AF, atrial fibrillation; AT, atrial tachycardia; CFAE, complex fractionated atrial electrogram; CPVI, circumferential pulmonary vein isolation; EGF, electrographic flow; FU, follow-up; MRI, magnetic resonance imaging; PEERP, pacing at the end of the effective refractory period; PVI, pulmonary vein isolation.
Overview of studies and trials of tailored-ablation approaches using the identification of patient-specific biomarkers
Study (year of publication) . | Patients . | Description . | Primary endpoint . | Outcome . |
---|---|---|---|---|
STAR AF II (2015)82,115 | Persistent AF patients (n = 589) | Multicentre, prospective, single-blind, randomized trial Three ablation strategies:
| During FU (3 months blanking period) freedom from AF recurrence (documented episode >30 s) after a single ablation procedure, with or without AADs | 18 months FU No significant differences in success rates between the three ablation strategies; 49, 46, and 59% of the patients experienced recurrences, respectively (P = 0.15) |
DECAAF II (2022)116,117 | Persistent AF patients (n = 843) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (90 day blanking period) first recurrence of AF, atrial flutter or AT (documented episode ≥30 s) after a single ablation procedure or repeat ablation | 12–18 months FU No significant difference in success rates between Group 1 and Group 2, 57.0 and 53.9%, respectively (P = 0.63) |
STABLE-SR-II (2022)118 | Persistent AF patients (n = 300) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) freedom from AF or AT (documented episode >30 s) after a single ablation procedure without the use of AADs | 18 months FU No significant difference in success rates between both ablation strategies, 67.2 and 67.4%, respectively. (P = 0.52) |
ERASE-AF (2022)119 | Persistent AF patients (n = 324) | Multicentre, prospective, open-label, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) first recurrence of AF or AT (documented episode >30 s) after a single ablation procedure | 12 months FU Significantly higher success rate in the PVI + low voltage area ablation group compared with the PVI only group, 65 vs. 50%, respectively (log rank P = 0.006) |
FLOW-AF (2024)120 | Persistent and long-standing persistent AF patients (n = 85) | Multicentre, prospective, open-label, randomized trial Two (redo) ablation strategies:
| (Secondary effectiveness endpoint) During FU (3 month blanking period) freedom from AF, AT, or atrial flutter | 12 months FU Higher success rate in the PVI in combination with EGF-guided ablation group compared with the PVI only group, 51 vs. 14% (P = 0.103) |
Study (year of publication) . | Patients . | Description . | Primary endpoint . | Outcome . |
---|---|---|---|---|
STAR AF II (2015)82,115 | Persistent AF patients (n = 589) | Multicentre, prospective, single-blind, randomized trial Three ablation strategies:
| During FU (3 months blanking period) freedom from AF recurrence (documented episode >30 s) after a single ablation procedure, with or without AADs | 18 months FU No significant differences in success rates between the three ablation strategies; 49, 46, and 59% of the patients experienced recurrences, respectively (P = 0.15) |
DECAAF II (2022)116,117 | Persistent AF patients (n = 843) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (90 day blanking period) first recurrence of AF, atrial flutter or AT (documented episode ≥30 s) after a single ablation procedure or repeat ablation | 12–18 months FU No significant difference in success rates between Group 1 and Group 2, 57.0 and 53.9%, respectively (P = 0.63) |
STABLE-SR-II (2022)118 | Persistent AF patients (n = 300) | Multicentre, prospective, single-blind, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) freedom from AF or AT (documented episode >30 s) after a single ablation procedure without the use of AADs | 18 months FU No significant difference in success rates between both ablation strategies, 67.2 and 67.4%, respectively. (P = 0.52) |
ERASE-AF (2022)119 | Persistent AF patients (n = 324) | Multicentre, prospective, open-label, randomized trial Two ablation strategies:
| During FU period (3 months blanking period) first recurrence of AF or AT (documented episode >30 s) after a single ablation procedure | 12 months FU Significantly higher success rate in the PVI + low voltage area ablation group compared with the PVI only group, 65 vs. 50%, respectively (log rank P = 0.006) |
FLOW-AF (2024)120 | Persistent and long-standing persistent AF patients (n = 85) | Multicentre, prospective, open-label, randomized trial Two (redo) ablation strategies:
| (Secondary effectiveness endpoint) During FU (3 month blanking period) freedom from AF, AT, or atrial flutter | 12 months FU Higher success rate in the PVI in combination with EGF-guided ablation group compared with the PVI only group, 51 vs. 14% (P = 0.103) |
AAD, antiarrhythmic drug; AF, atrial fibrillation; AT, atrial tachycardia; CFAE, complex fractionated atrial electrogram; CPVI, circumferential pulmonary vein isolation; EGF, electrographic flow; FU, follow-up; MRI, magnetic resonance imaging; PEERP, pacing at the end of the effective refractory period; PVI, pulmonary vein isolation.
This PDF is available to Subscribers Only
View Article Abstract & Purchase OptionsFor full access to this pdf, sign in to an existing account, or purchase an annual subscription.