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Continuation or reintroduction of bevacizumab beyond progression to first-line therapy in metastatic colorectal cancer: final results of the randomized BEBYP trial.
Masi, G; Salvatore, L; Boni, L; Loupakis, F; Cremolini, C; Fornaro, L; Schirripa, M; Cupini, S; Barbara, C; Safina, V; Granetto, C; Fea, E; Antonuzzo, L; Boni, C; Allegrini, G; Chiara, S; Amoroso, D; Bonetti, A; Falcone, A.
Afiliação
  • Masi G; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa. Electronic address: gl.masi@tin.it.
  • Salvatore L; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa.
  • Boni L; Clinical Trials Coordinating Center, AOU Careggi/Istituto Toscano Tumori, Firenze.
  • Loupakis F; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa.
  • Cremolini C; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa.
  • Fornaro L; Division of Medical Oncology, Azienda USL 2 di Lucca, Istituto Toscano Tumori, Lucca.
  • Schirripa M; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa.
  • Cupini S; Division of Medical Oncology, Azienda USL 6 di Livorno, Istituto Toscano Tumori, Livorno.
  • Barbara C; Division of Medical Oncology, Azienda USL 6 di Livorno, Istituto Toscano Tumori, Livorno.
  • Safina V; Division of Medical Oncology, Azienda USL 6 di Livorno, Presidio Ospedaliero di Piombino, Istituto Toscano Tumori, Piombino.
  • Granetto C; Division of Medical Oncology, Ospedale S. Croce e Carle, Cuneo.
  • Fea E; Division of Medical Oncology, Ospedale S. Croce e Carle, Cuneo.
  • Antonuzzo L; Division of Medical Oncology 1, Azienda Ospedaliero-Universitaria Careggi, Istituto Toscano Tumori, Firenze.
  • Boni C; Division of Medical Oncology, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia.
  • Allegrini G; Division of Medical Oncology, Azienda USL 5 di Pisa, Ospedale Felice Lotti, Istituto Toscano Tumori, Pontedera.
  • Chiara S; Division of Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria San Martino-Istituto Nazionale Ricerca Cancro, Genova.
  • Amoroso D; Division of Medical Oncology, Ospedale della Versilia, Istituto Toscano Tumori, Lido di Camaiore.
  • Bonetti A; Division of Medical Oncology, AULSS 21 Legnago, Ospedale Mater Salutis, Legnago, Italy.
  • Falcone A; Division of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Pisa.
Ann Oncol ; 26(4): 724-730, 2015 Apr.
Article em En | MEDLINE | ID: mdl-25600568
ABSTRACT

BACKGROUND:

The combination of bevacizumab with fluorouracil-based chemotherapy is a standard first-line treatment option in metastatic colorectal cancer (mCRC). We studied the efficacy of continuing or reintroducing bevacizumab in combination with second-line chemotherapy after progression to bevacizumab-based first-line therapy. PATIENTS AND

METHODS:

In this phase III study, patients with mCRC treated with fluoropyrimidine-based first-line chemotherapy plus bevacizumab were randomized to receive in second-line mFOLFOX-6 or FOLFIRI (depending on first-line regimen) with or without bevacizumab. The primary end point was progression-free survival. To detect a hazard ratio (HR) for progression of 0.70 with an α and ß error of 0.05 and 0.20, respectively, 262 patients were required.

RESULTS:

In consideration of the results of the ML18147 trial, the study was prematurely stopped. Between April 2008 and May 2012, a total of 185 patients were randomized. Bevacizumab-free interval was longer than 3 months in 43% of patients in chemotherapy alone arm and in 50% of patients in the bevacizumab arm. At a median follow-up of 45.3 months, the median progression-free survival was 5.0 months in the chemotherapy group and 6.8 months in the bevacizumab group [adjusted HR = 0.70; 95% confidence interval (CI) 0.52-0.95; stratified log-rank P = 0.010]. Subgroup analyses showed a consistent benefit in all subgroups analyzed and in particular in patients who had continued or reintroduced bevacizumab. An improved overall survival was also observed in the bevacizumab arm (adjusted HR = 0.77; 95% CI 0.56-1.06; stratified log-rank P = 0.043). Responses (RECIST 1.0) were similar in the chemotherapy and bevacizumab groups (17% and 21%; P = 0.573). Toxicity profile was consistent with previously reported data.

CONCLUSIONS:

This study demonstrates that the continuation or the reintroduction of bevacizumab with second-line chemotherapy beyond first progression improves the outcome and supports the use of this strategy in the treatment of mCRC. ClinicalTrials.gov number NCT00720512.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Hepáticas Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Hepáticas Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article