Phase III Trial Assessing Bevacizumab in Stages II and III Carcinoma of the Colon: Results of NSABP Protocol C-08

Author:

Allegra Carmen J.1,Yothers Greg1,O'Connell Michael J.1,Sharif Saima1,Petrelli Nicholas J.1,Colangelo Linda H.1,Atkins James N.1,Seay Thomas E.1,Fehrenbacher Louis1,Goldberg Richard M.1,O'Reilly Seamus1,Chu Luis1,Azar Catherine A.1,Lopa Samia1,Wolmark Norman1

Affiliation:

1. From the National Surgical Adjuvant Breast and Bowel Project; Graduate School of Public Health, University of Pittsburgh; and Allegheny General Hospital, Pittsburgh, PA; University of Florida, Gainesville; and Florida Cancer Specialists–Sarasota, FL; Helen F. Graham Cancer Center at Christiana Care, Newark, DE; Southeast Cancer Control Consortium–Community Clinical Oncology Program (CCOP), Goldsboro, NC; Atlanta Cancer Care Regional CCOP, Atlanta, GA; Kaiser Permanente Northern California, Vallejo, CA;...

Abstract

Purpose The National Surgical Adjuvant Breast and Bowel Project C-08 trial was designed to investigate the safety and efficacy of adding bevacizumab to modified FOLFOX6 (mFOLFOX6; ie, infusional/bolus fluorouracil, leucovorin, and oxaliplatin) for the adjuvant treatment of patients with stages II to III colon cancer. Methods Patients received mFOLFOX6 every 2 weeks for 26 weeks alone or modified as FOLFOX6 + bevacizumab (5 mg/kg every 2 weeks for 52 weeks [ie, experimental group]). The primary end point was disease-free survival (DFS). Results Among 2,672 analyzed patients, demographic factors were well balanced by treatment. With a median follow-up of 35.6 months, the addition of bevacizumab to mFOLFOX6 did not result in an overall significant increase in DFS (hazard ratio [HR], 0.89; 95% CI, 0.76 to 1.04; P = .15). The point estimates for 3-year DFS for the overall population were 77.4% and 75.5% for the experimental and control arms, respectively. For patients with stages II and III diseases, these same estimates were 87.4% and 84.7%, respectively, for stage II and 74.2% and 72.4%, respectively, for stage III. Exploratory analyses found that the effect of bevacizumab on DFS was different before and after a 15-month landmark (time-by-treatment interaction P value < .0001). Bevacizumab had a strong effect before the landmark (HR, 0.61; 95% CI, 0.48 to 0.78; P < .001) but no significant effect after (HR, 1.22; 95% CI, 0.98 to 1.52; P = .076). Conclusion Bevacizumab for 1 year with mFOLFOX6 does not significantly prolong DFS in stages II and III colon cancer. However, a significant but transient effect during bevacizumab exposure was observed in the experimental arm. We postulate that this observation reflects a biologic effect during bevacizumab exposure. Given the lack of improvement in DFS, the use of bevacizumab cannot be recommended for use in the adjuvant treatment of patients with colon cancer.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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