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Treatments after progression to first-line FOLFOXIRI and bevacizumab in metastatic colorectal cancer: a pooled analysis of TRIBE and TRIBE2 studies by GONO.

Authors :
Rossini, Daniele
Lonardi, Sara
Antoniotti, Carlotta
Santini, Daniele
Tomasello, Gianluca
Ermacora, Paola
Germani, Marco Maria
Bergamo, Francesca
Ricci, Vincenzo
Caponnetto, Salvatore
Moretto, Roberto
Zaniboni, Alberto
Pietrantonio, Filippo
Buonadonna, Angela
Ritorto, Giuliana
Masi, Gianluca
Latiano, Tiziana Pia
Rapisardi, Stefania
Falcone, Alfredo
Cremolini, Chiara
Source :
British Journal of Cancer; 2021, Vol. 124 Issue 1, p183-190, 8p
Publication Year :
2021

Abstract

<bold>Background: </bold>FOLFOXIRI/bevacizumab (bev) is a first-line regimen of proven activity and efficacy in metastatic colorectal cancer. The upfront exposure to three cytotoxics raises concerns about the efficacy of treatments after progression.<bold>Methods: </bold>We performed a pooled analysis of treatments after progression to upfront FOLFOXIRI/bev in patients enrolled in two randomised Phase 3 studies (TRIBE and TRIBE2) that compared FOLFOXIRI/bev to doublets (FOLFOX or FOLFIRI)/bev. Response rate, progression-free survival (2nd PFS) and overall survival (2nd OS) during treatments after progression were assessed. The RECIST response in first line and the oxaliplatin and irinotecan-free interval (OIFI) were investigated as potential predictors of benefit from FOLFOXIRI ± bev reintroduction.<bold>Results: </bold>Longer 2nd PFS was reported in patients receiving FOLFOXIRI ± bev reintroduction compared to doublets ± bev or other treatments (6.1 versus 4.4 and 3.9 months, respectively, P = 0.013), and seems limited to patients achieving a response during first line (6.9 versus 4.2 and 4.7 months, respectively, P = 0.005) and an OIFI ≥ 4 months (7.2 versus 6.5 and 4.6 months, respectively, P = 0.045).<bold>Conclusions: </bold>First-line FOLFOXIRI/bev does not impair the administration of effective second-line therapies. First-line response and longer OIFI seem associated with improved response and 2nd PFS from FOLFOXIRI ± bev reintroduction, without impacting 2nd OS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
124
Issue :
1
Database :
Complementary Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
147907139
Full Text :
https://doi.org/10.1038/s41416-020-01089-9