REVERCE: a randomized phase II study of regorafenib followed by cetuximab versus the reverse sequence for previously treated metastatic colorectal cancer patients

被引:69
作者
Shitara, K. [1 ]
Yamanaka, T. [2 ]
Denda, T. [3 ]
Tsuji, Y. [4 ]
Shinozaki, K. [5 ]
Komatsu, Y. [6 ]
Kobayashi, Y. [7 ]
Furuse, J. [8 ]
Okuda, H. [9 ]
Asayama, M. [10 ]
Akiyoshi, K. [11 ]
Kagawa, Y. [12 ]
Kato, T. [13 ]
Oki, E. [14 ]
Ando, T. [15 ]
Hagiwara, Y. [16 ]
Ohashi, Y. [17 ]
Yoshino, T. [1 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
[2] Yokohama City Univ, Dept Biostat, Sch Med, Yokohama, Kanagawa, Japan
[3] Div Gastroenterol, Chiba Canc Ctr, Chiba, Japan
[4] Tonan Hosp, Dept Med Oncol, Sapporo, Hokkaido, Japan
[5] Hiroshima Prefectural Hosp, Div Clin Oncol, Hiroshima, Japan
[6] Hokkaido Univ Hosp, Div Canc Chemotherapy, Ctr Canc, Sapporo, Hokkaido, Japan
[7] Kushiro Rosai Hosp, Dept Med Oncol, Kushiro, Japan
[8] Kyorin Univ, Dept Med Oncol, Fac Med, Tokyo, Japan
[9] Keiyukai Sapporo Hosp, Dept Med Oncol, Sapporo, Hokkaido, Japan
[10] Saitama Canc Ctr, Dept Gastroenterol, Saitama, Japan
[11] Osaka City Gen Hosp, Dept Clin Oncol, Osaka, Japan
[12] Kansai Rosa Hosp, Dept Surg, Amagasaki, Hyogo, Japan
[13] Natl Hosp Org Osaka Natl Hosp, Dept Surg, Osaka, Japan
[14] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Sci, Fukuoka, Fukuoka, Japan
[15] Univ Tsukuba, Sch Med, Tsukuba, Ibaraki, Japan
[16] Univ Tokyo, Sch Publ Hlth, Dept Biostat, Tokyo, Japan
[17] Chuo Univ, Fac Sci & Engn, Dept Integrated Sci & Engn Sustainable Soc, Tokyo, Japan
关键词
colorectal cancer; cetuximab; regorafenib; liquid biomarkers; randomized phase II; ACQUIRED-RESISTANCE; RAS MUTATIONS; PLUS IRINOTECAN; OPEN-LABEL; 1ST-LINE; CHEMOTHERAPY; MULTICENTER; BEVACIZUMAB; THERAPY; FOLFIRI;
D O I
10.1093/annonc/mdy526
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: The objective of this randomized phase II trial was to evaluate efficacy and safety of the therapeutic sequence of regorafenib followed by cetuximab, compared with cetuximab followed by regorafenib, as the current standard sequence for metastatic colorectal cancer patients. Patients and methods: Patients with KRAS exon 2 wild-type metastatic colorectal cancer after failure of fluoropyrimidine, oxaliplatin, and irinotecan were randomized to receive sequential treatment with regorafenib followed by cetuximab 6 irinotecan (R-C arm), or the reverse sequence [cetuximab 6 irinotecan followed by regorafenib (C-R arm)]. The primary end point was overall survival (OS). Key secondary end points included progression-free survival (PFS) with initial treatment (PFS1), PFS with second treatment (PFS2), safety, and quality of life. Exploratory end points included serial biomarker analyses, including oncogenic alterations from circulating tumor DNA or multiple serum or plasma proteins. Results: One-hundred one patients were randomized and eligible for efficacy analysis. Sequential treatment was successful in 86% patients in both arms. Median OS for R-C and C-R was 17.4 and 11.6months, respectively (P 1/4 0.0293), with a hazard ratio (HR) of 0.61 for OS [95% confidence interval (CI) 0.39-0.96]. The HR for PFS1 (regorafenib in R-C versus cetuximab in C-R) was 0.97 (95% CI 0.611.54), and PFS2 (C in R-C versus R in C-R) was 0.29 (95% CI 0.17-0.50). No unexpected safety signals were observed. The quality of life scores during the entire treatment period was not significantly different between the two arms. Circulating biomarker analyses showed emerging oncogenic alterations in RAS, BRAF, EGFR, HER2, and MET, which weremore commonly detected after cetuximab than after regorafenib. Conclusions: The therapeutic sequence of regorafenib followed by cetuximab suggests a longer OS than the current standard sequence.
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页码:259 / 265
页数:7
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