Phase 3 trial of sequential versus combination treatment in colorectal cancer: The C-cubed study.

Ryo Inada, Takeshi Nagasaka, Mototsugu Shimokawa, Hitoshi Ojima, Shingo Noura, Hiroaki Tanioka, Yoshinori Munemoto, Yasuhiro Shimada, Keiichiro Ishibashi, Yoshiaki Shindo, Hideyuki Mishima, Masasumi Okajima, Yoshiyuki Yamaguchi

Journal: European journal of cancer (Oxford, England : 1990) 2022;169():166-178

PMID: 35569283

Abstract

BACKGROUND

An optimal treatment strategy using oxaliplatin and bevacizumab for metastatic colorectal cancer has not been defined. We investigated whether the sequential treatment using fluoropyrimidines with bevacizumab followed by the addition of oxaliplatin at first progression was better than a combination treatment using fluoropyrimidines and oxaliplatin with bevacizumab.

METHODS

In the sequential treatment, the escalation from fluoropyrimidines plus bevacizumab to fluoropyrimidines plus oxaliplatin with bevacizumab was recommended in case of progressive disease. Time to failure of strategy was the primary end-point, whereas the secondary end-points were overall survival, progression-free survival, overall response rate and safety.

RESULTS

Three hundred patients with previously untreated metastatic colorectal cancer were randomised to receive either the sequential treatment (n = 151) or the combination treatment (n = 149). The sequential treatment was superior to the combination treatment about time to failure of strategy (15.2 months; 95% CI, 12.5-17.2 months vs. 7.8 months: 95% CI, 6.3-9.5 months; P < 0.001). However, the median overall survival was 27.5 (95% CI, 24.4 to 32.7) months in the sequential treatment and 27.0 (95% CI, 22.8 to 36.0) months in the combination treatment (hazard ratio, 0.92; 95% CI, 0.66 to 1.28; P = 0.61). The overall response rate was 33.1% in the sequential treatment arm and 51.7% in the combination treatment.

CONCLUSIONS

The findings support the extension of the sequential treatment starting from fluoropyrimidine plus bevacizumab to selected patients who do not need an objective response to the threatening disease.

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Address: Department of Gastroenterological Surgery, Kochi Health Sciences Centre, Kochi, Kochi, Japan; Department of Surgery, Kansai Medical University, Hirakata, Osaka, Japan.; Department of Clinical Oncology, Kawasaki Medical School Hospital, Kurashiki, Okayama, Japan; Department of Gastroenterological Surgery, Okayama University Hospital, Okayama, Okayama, Japan. Electronic address: [email protected].; Department of Biostatistics, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan; Cancer Biostatistics Laboratory, Clinical Research Institute, National Hospital Organisation Kyushu Cancer Centre, Fukuoka, Fukuoka, Japan.; Department of Gastroenterological Surgery, Gunma Prefectural Cancer Centre, Ota, Gunma, Japan.; Department of Surgery, Osaka Rosai Hospital, Sakai, Osaka, Japan; Department of Surgery, Toyonaka Municipal Hospital, Toyonaka, Osaka, Japan.; Department of Clinical Oncology, Kawasaki Medical School Hospital, Kurashiki, Okayama, Japan.; Department of Surgery, Fukui-ken Saiseikai Hospital, Fukui, Fukui, Japan.; Division of Clinical Oncology, Kochi Health Sciences Centre, Kochi, Kochi, Japan.; Department of Digestive Tract and General Surgery, Saitama Medical Centre, Saitama Medical University, Kawagoe, Saitama, Japan.; Department of Gastroenterological Surgery, Nakadori General Hospital, Akita, Akita, Japan.; Cancer Centre, Aichi Medical University, Nagakute, Aichi, Japan.; Department of Surgery, Hiroshima City Hospital, Hiroshima, Hiroshima, Japan.

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