Phase II study of combination chemotherapy with irinotecan and cetuximab for pretreated metastatic colorectal cancer harboring wild-type KRAS

被引:0
|
作者
Kohei Shitara
Tomoya Yokota
Daisuke Takahari
Takashi Shibata
Takashi Ura
Setsuo Utsunomiya
Yoshitaka Inaba
Hidekazu Yamaura
Yozo Sato
Mina Najima
Hiroki Kawai
Masahiro Tajika
Akira Sawaki
Yasushi Yatabe
Kei Muro
机构
[1] Aichi Cancer Center Hospital,Department of Clinical Oncology
[2] Nagoya Kyoritsu Hospital,Department of Gastroenterology
[3] Aichi Cancer Center Hospital,Department of Diagnostic and Interventional Radiology
[4] Aichi Cancer Center Hospital,Department of Gastroenterology
[5] Aichi Cancer Center,Department of Pathology and Molecular Diagnostics
来源
Investigational New Drugs | 2011年 / 29卷
关键词
Colorectal cancer; Chemotherapy; Irinotecan; Cetuximab;
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学科分类号
摘要
The aim of this study was to prospectively evaluate the efficacy of combination irinotecan and cetuximab chemotherapy in patients with pretreated metastatic colorectal cancer harboring wild-type KRAS. Patients with metastatic colorectal cancer that had progressed after chemotherapy with irinotecan, oxaliplatin, and fluoropyrimidine were included. KRAS status was evaluated using the Cycleave PCR method; only patients without KRAS mutations were included. Cetuximab was administered initially at 400 mg/m2 followed by weekly 250 mg/m2 infusions. Irinotecan was administered biweekly. From October 2008 to April 2009, a total of 30 patients were enrolled. The objective response rate was 30.0% (95% confidence interval [CI], 14.7–49.4%) and the disease control rate (complete response, partial response, or stable disease) was 80.0% (95% CI, 61.4–92.3%). Among the 15 patients with stable disease, 11 patients experienced >10% tumor shrinkage. Median progression-free survival was 5.8 months (95% CI, 4.1–7.6). Median overall survival was not reached at a median follow-up of 10.1 months. Grade 2 skin toxicity was observed in 23 patients, while no grade 3 skin toxicity was observed. Combined irinotecan and cetuximab is effective for pretreated metastatic wild-type KRAS colorectal cancer.
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页码:688 / 693
页数:5
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