Abstract

BackgroundAlthough chemotherapy for metastatic colorectal cancer (mCRC) has improved, the standard chemotherapy regimens for patients with RAS wild-type mCRC remain debated. This study aimed to compare S-1 and oxaliplatin (SOX) + bevacizumab (B-mab) with SOX + cetuximab (C-mab) in patients with previously untreated recurrent advanced CRC with wild-type KRAS.MethodsThis randomized phase II, open-label, multicenter study compared the efficacy and safety of SOX+B-mab with SOX+C-mab in patients with previously untreated advanced CRC with wild-type KRAS. Between February 2012 and October 2016, 45 patients were enrolled.ResultsOverall response rates were 59.1 and 43.5% (p = 0.29) and disease control rates were 90.9 and 91.3% (p = 0.96) in the SOX+B-mab and SOX+C-mab groups, respectively. Median overall survival (OS) was 25.3 and 15.5 months (HR = 0.607, p = 0.167) and median progression-free survival (PFS) were 11.7 and 5.5 months (HR = 0.558, p = 0.077) in the SOX+B-mab and SOX+C-mab groups, respectively. The OS and PFS of patients with early tumor shrinkage (ETS) were not significantly different in the SOX+B-mab group. However, they were significantly better when ETS was ≥20 in the SOX+C-mab group (p = 0.032 and p = 0.003, respectively).ConclusionsThe efficacy and safety of SOX+B-mab and SOX+C-mab for wild-type KRAS recurrent advanced CRC as first-line chemotherapy were almost the same. Consideration of the treatment strategy based on ETS may improve patient prognosis, especially in patients receiving the SOX+C-mab regimen.Trial registrationUMIN Clinical Trials Registry (UMIN000006706).Date of registration: NOV/11/2011.URL of trial registry record:https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007920

Highlights

  • Chemotherapy for metastatic colorectal cancer has improved, the standard chemotherapy regimens for patients with RAS wild-type mCRC remain debated

  • Consideration of the treatment strategy based on early tumor shrinkage (ETS) may improve patient prognosis, especially in patients receiving the S-1 and oxaliplatin (SOX)+C-mab regimen

  • A phase III trial of irinotecan/5-FU/leucovorin (FOLFIRI) or oxaliplatin/5-FU/leucovorin with bevacizumab or cetuximab for patients with KRAS wild-type untreated mCRC (CALGB/SWOG80405), in which the primary endpoint was overall survival (OS), showed no significant difference in the combination of chemotherapy with cetuximab or bevacizumab, but it showed a trend toward longer OS in cetuximabtreated patients versus bevacizumab-treated patients with Oxaliplatin/ 5-FU/leucovorin (FOLFOX) [5]

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Summary

Introduction

Chemotherapy for metastatic colorectal cancer (mCRC) has improved, the standard chemotherapy regimens for patients with RAS wild-type mCRC remain debated. Clinical outcomes in patients with metastatic colorectal cancer (mCRC) have improved over the last decade in particular and the median OS for patients with mCRC is over 30 months and more than double that of 20 years ago, the standard-of-care chemotherapy regimens for patients with RAS wild-type mCRC remain debated [4]. A phase III trial of irinotecan/5-FU/leucovorin (FOLFIRI) or oxaliplatin/5-FU/leucovorin (mFOLFOX6) with bevacizumab or cetuximab for patients with KRAS wild-type untreated mCRC (CALGB/SWOG80405), in which the primary endpoint was OS, showed no significant difference in the combination of chemotherapy with cetuximab or bevacizumab, but it showed a trend toward longer OS in cetuximabtreated patients versus bevacizumab-treated patients with FOLFOX [5]. A post-hoc analysis of tumor dynamics in the final RAS wild-type subgroup showed a 7.5-month benefit in OS with cetuximab (hazard ratio [HR] 0.7) [7]

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