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

被引:388
作者
Van Cutsem, Eric [2 ]
de Haas, Sanne [3 ]
Kang, Yoon-Koo [4 ]
Ohtsu, Atsushi [5 ]
Tebbutt, Niall C. [6 ]
Xu, Jian Ming [7 ]
Yong, Wei Peng [8 ]
Langer, Bernd [9 ]
Delmar, Paul [3 ]
Scherer, Stefan J. [9 ]
Shah, Manish A. [1 ,10 ]
机构
[1] New York Presbyterian Hosp, Weill Cornell Med Coll, New York, NY 10021 USA
[2] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
[3] F Hoffmann La Roche & Co Ltd, CH-4002 Basel, Switzerland
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Seoul, South Korea
[5] Hosp East, Natl Canc Ctr, Kashiwa, Chiba, Japan
[6] Austin Hlth, Heidelberg, Vic, Australia
[7] PLA 307 Hosp, Beijing, Peoples R China
[8] Natl Univ Singapore Hosp, Singapore 117548, Singapore
[9] Genentech Inc, San Francisco, CA 94080 USA
[10] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, New York, NY USA
关键词
PACLITAXEL PLUS BEVACIZUMAB; ENDOTHELIAL GROWTH-FACTOR; DOUBLE-BLIND; PATIENTS PTS; GEMCITABINE; POLYMORPHISMS; HER-2/NEU; RECEPTORS; C-ERBB-2; PLACEBO;
D O I
10.1200/JCO.2011.39.9824
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:2119 / 2127
页数:9
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