4.2 Article

A Randomized Phase II Study of Perioperative Chemotherapy Plus Bevacizumab Versus Postoperative Chemotherapy Plus Bevacizumab in Patients With Upfront Resectable Hepatic Colorectal Metastases

Journal

CLINICAL COLORECTAL CANCER
Volume 19, Issue 3, Pages E140-E150

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.clcc.2020.03.004

Keywords

Bevacizumab; Liver resection; Metastatic colorectal cancer; Perioperative chemotherapy; Resectable

Categories

Funding

  1. Roche [4-2012-0166]

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It remains controversial whether patients with resectable colorectal liver metastases gain a survival benefit from perioperative chemotherapy with bevacizumab. We found that the overall survival was improved, but it did not affect progression-free survival from our randomized clinical trial. Patients with high carcinoembryonic antigen levels or over 2 liver metastases may benefit from the overall survival of perioperative chemotherapy. Introduction: Whether patients with resectable colorectal liver metastases (CRLM) gain a survival benefit from perioperative chemotherapy remains controversial. The benefit of including bevacizumab in chemotherapy also remains unclear. Material and Methods: Seventy-six patients with CRLM were randomly assigned to either 6 cycles of FOLFOX (folinic acid, 5-fluorouracil, and oxaliplatin)/FOLFIRI (folinic acid, 5-fluorouracil, and irinotecan) with bevacizumab before and after surgery or 12 cycles after surgery. Progression-free survival (PFS) was estimated using the Kaplan-Meier method and compared by the log-rank test. Results: The median PFS of all patients was 37.4 months at 5.4 years follow-up, and the median overall survival (OS) was not reached. The PFS between the perioperative group and the postoperative group did not reveal a statistical difference (P = .280). The OS was significantly better in the perioperative group (hazard ratio [HR], 0.60; 95% confidence interval [CI],) 0.35-1.02; P = .049). In subgroup patients with carcinoembryonic antigens (CEA) >= 5 ng/mL or those with over 2 liver metastases, perioperative group had longer OS than postoperative group (CEA: HR, 0.49; 95% CI, 0.25-0.93; P = .030; number of livermetastases: HR, 0.55; 95% CI, 0.30-0.99; P = .049). The largest liver metastases size, disease-free interval, and sidedness did not affect PFS or OS. There was no difference between the 2 groups in postoperative complications with bevacizumab or adverse events during chemotherapy. Conclusions: In patients with resectable CRLMs, perioperative chemotherapy had no effect on PFS, but improved OS. Patients with high CEA levels or over 2 liver metastases may benefit from perioperative chemotherapy. (C) 2020 The Author(s). Published by Elsevier Inc.

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