Bevacizumab in Combination With Chemotherapy As First-Line Therapy in Advanced Gastric Cancer: A Biomarker Evaluation From the AVAGAST Randomized Phase III Trial

Author:

Van Cutsem Eric1,de Haas Sanne1,Kang Yoon-Koo1,Ohtsu Atsushi1,Tebbutt Niall C.1,Ming Xu Jian1,Peng Yong Wei1,Langer Bernd1,Delmar Paul1,Scherer Stefan J.1,Shah Manish A.1

Affiliation:

1. Eric Van Cutsem, University Hospital Gasthuisberg, Leuven, Belgium; Sanne de Haas and Paul Delmar, F. Hoffmann-La Roche, Basel, Switzerland; Yoon-Koo Kang, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea; Atsushi Ohtsu, National Cancer Center Hospital East, Kashiwa, Chiba, Japan; Niall C. Tebbutt, Austin Health, Heidelberg, Victoria, Australia; Jian Ming Xu, PLA 307 Hospital, Fengtai District, Beijing, China; Wei Peng Yong, National University Hospital, Singapore; Bernd...

Abstract

Purpose The AVAGAST study showed that adding bevacizumab to chemotherapy in patients with advanced gastric cancer improves progression-free survival and tumor response rate but not overall survival. To examine the hypothesis that angiogenic markers may have predictive value for bevacizumab efficacy in gastric cancer, AVAGAST included a prospective, mandatory biomarker program. Patients and Methods Patients with previously untreated, locally advanced or metastatic gastric cancer were randomly assigned to bevacizumab (n = 387) or placebo (n = 387) in combination with chemotherapy. Blood and tumor tissue samples were collected at baseline. Prespecified biomarkers included plasma vascular endothelial growth factor-A (VEGF-A), protein expression of neuropilin-1, and VEGF receptors-1 and -2 (VEGFR-1 and VEGFR-2). Correlations between biomarkers and clinical outcomes were assessed by using a Cox proportional hazards model. Results Plasma was available from 712 patients (92%), and tumor samples were available from 727 patients (94%). Baseline plasma VEGF-A levels and tumor neuropilin-1 expression were identified as potential predictors of bevacizumab efficacy. Patients with high baseline plasma VEGF-A levels showed a trend toward improved overall survival (hazard ratio [HR], 0.72; 95% CI, 0.57 to 0.93) versus patients with low VEGF-A levels (HR, 1.01; 95% CI, 0.77 to 1.31; interaction P = .07). Patients with low baseline expression of neuropilin-1 also showed a trend toward improved overall survival (HR, 0.75; 95% CI, 0.59 to 0.97) versus patients with high neuropilin-1 expression (HR, 1.07; 95% CI, 0.81 to 1.40; interaction P = .06). For both biomarkers, subgroup analyses demonstrated significance only in patients from non-Asian regions. Conclusion Plasma VEGF-A and tumor neuropilin-1 are strong biomarker candidates for predicting clinical outcome in patients with advanced gastric cancer treated with bevacizumab.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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