Table 2.

First‐line treatment outcomes in a cohort of GEA patients treated with second‐line FOLFIRI + ram

Treatment featuren = 29, n (%)
First‐line therapy
FOLFOX/XELOX backbone23 (79.3)
FOLFOX + trastuzumab2 (6.8)
FOLFOX + experimental agent (trial)12 (41.3)
Other 5FU + platinum6 (20.7)
5FU + platinum‐containing triplets6 (20.7)
FLOT3 (10.3)
DOF1 (3.4)
Modified DCF1 (3.4)
ECX + placebo/experimental agent (trial)1 (3.4)
Duration of 1L therapy, median (range), mo7 (2–12)
Objective response to 1L
Complete response1 (3.4)
Partial response13 (44.8)
Stable disease10 (34.4)
Progressive disease3 (10.3)
Unknown or nonmeasurable2 (6.9)
Maximal neuropathy grade
06 (20.7)
112 (41.4)
211 (37.9)
Treatment featuren = 29, n (%)
First‐line therapy
FOLFOX/XELOX backbone23 (79.3)
FOLFOX + trastuzumab2 (6.8)
FOLFOX + experimental agent (trial)12 (41.3)
Other 5FU + platinum6 (20.7)
5FU + platinum‐containing triplets6 (20.7)
FLOT3 (10.3)
DOF1 (3.4)
Modified DCF1 (3.4)
ECX + placebo/experimental agent (trial)1 (3.4)
Duration of 1L therapy, median (range), mo7 (2–12)
Objective response to 1L
Complete response1 (3.4)
Partial response13 (44.8)
Stable disease10 (34.4)
Progressive disease3 (10.3)
Unknown or nonmeasurable2 (6.9)
Maximal neuropathy grade
06 (20.7)
112 (41.4)
211 (37.9)

Denotes participation in a first line clinical trial. Total 45% (13/29) patients were treated on a first line clinical trial

Abbreviations: 1L, first‐line; 5FU, fluoropyrimidine; DCF, docetaxel, cisplatin, 5‐fluorouracil; DOF, docetaxel, oxaliplatin, 5‐fluorouracil; ECX, epirubicin, cisplatin, and capecitabine.

Table 2.

First‐line treatment outcomes in a cohort of GEA patients treated with second‐line FOLFIRI + ram

Treatment featuren = 29, n (%)
First‐line therapy
FOLFOX/XELOX backbone23 (79.3)
FOLFOX + trastuzumab2 (6.8)
FOLFOX + experimental agent (trial)12 (41.3)
Other 5FU + platinum6 (20.7)
5FU + platinum‐containing triplets6 (20.7)
FLOT3 (10.3)
DOF1 (3.4)
Modified DCF1 (3.4)
ECX + placebo/experimental agent (trial)1 (3.4)
Duration of 1L therapy, median (range), mo7 (2–12)
Objective response to 1L
Complete response1 (3.4)
Partial response13 (44.8)
Stable disease10 (34.4)
Progressive disease3 (10.3)
Unknown or nonmeasurable2 (6.9)
Maximal neuropathy grade
06 (20.7)
112 (41.4)
211 (37.9)
Treatment featuren = 29, n (%)
First‐line therapy
FOLFOX/XELOX backbone23 (79.3)
FOLFOX + trastuzumab2 (6.8)
FOLFOX + experimental agent (trial)12 (41.3)
Other 5FU + platinum6 (20.7)
5FU + platinum‐containing triplets6 (20.7)
FLOT3 (10.3)
DOF1 (3.4)
Modified DCF1 (3.4)
ECX + placebo/experimental agent (trial)1 (3.4)
Duration of 1L therapy, median (range), mo7 (2–12)
Objective response to 1L
Complete response1 (3.4)
Partial response13 (44.8)
Stable disease10 (34.4)
Progressive disease3 (10.3)
Unknown or nonmeasurable2 (6.9)
Maximal neuropathy grade
06 (20.7)
112 (41.4)
211 (37.9)

Denotes participation in a first line clinical trial. Total 45% (13/29) patients were treated on a first line clinical trial

Abbreviations: 1L, first‐line; 5FU, fluoropyrimidine; DCF, docetaxel, cisplatin, 5‐fluorouracil; DOF, docetaxel, oxaliplatin, 5‐fluorouracil; ECX, epirubicin, cisplatin, and capecitabine.

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