Randomized Controlled Trial of Cetuximab Plus Chemotherapy for Patients With KRAS Wild-Type Unresectable Colorectal Liver-Limited Metastases

被引:343
作者
Ye, Le-Chi [1 ]
Liu, Tian-Shu [1 ]
Ren, Li [1 ]
Wei, Ye [1 ]
Zhu, De-Xiang [1 ]
Zai, Sheng-Yong [1 ]
Ye, Qing-Hai [1 ]
Yu, Yiyi [1 ]
Xu, Bo [1 ]
Qin, Xin-Yu [1 ]
Xu, Jianmin [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai 200032, Peoples R China
关键词
1ST-LINE TREATMENT; CANCER; RESECTION; RESECTABILITY; FLUOROURACIL; LEUCOVORIN; GUIDELINES; MUTATIONS; CONSENSUS; SELECTION;
D O I
10.1200/JCO.2012.44.8308
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To assess the effects of cetuximab plus chemotherapy as first-line treatment for unresectable colorectal liver metastases (CLMs). Patients and Methods After resection of their primary tumors, patients with KRAS wild-type synchronous nonresectable liver-limited metastases from colorectal cancer were randomly assigned to receive chemotherapy (FOLFIRI [fluorouracil, leucovorin, and irinotecan] or mFOLFOX6 [modified fluorouracil, leucovorin, and oxaliplatin]) plus cetuximab (arm A) or chemotherapy alone (arm B). The primary end point was the rate of patients converted to resection for liver metastases. Secondary end points included tumor response and survival. Results The intent-to-treat population comprised 138 patients; 70 patients were randomly assigned to arm A and 68 to arm B. After a median of 25.0 months of follow-up, the 3-year overall survival (OS) rate and median survival time (MST) for all patients were 30% and 24.4 months, respectively. The R0 resection rates for liver metastases were 25.7% (18 of 70 patients) in arm A and 7.4% (five of 68 patients) in arm B, which were significantly different (P < .01). Patients in arm A had improved objective response rates (57.1% v 29.4%; P < .01), increased 3-year OS rate (41% v 18%; P = .013) and prolonged MST (30.9 v 21.0 months; P = .013) compared with those in arm B. In addition, in arm A, patients who had resection of liver metastases had a significantly improved MST (46.4 v 25.7 months; P < .01) compared with those who did not undergo surgery. Conclusion For patients with initially unresectable KRAS wild-type CLMs, cetuximab combined with chemotherapy improved the resectability of liver metastases and improved response rates and survival compared with chemotherapy alone. (c) 2013 by American Society of Clinical Oncology
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页码:1931 / 1938
页数:8
相关论文
共 32 条
[1]  
Abdalla EK, 2004, ANN SURG, V239, P818, DOI 10.1097/01.sla.0000128305.90650.71
[2]   Chemotherapy and surgery: new perspectives on the treatment of unresectable liver metastases [J].
Adam, R .
ANNALS OF ONCOLOGY, 2003, 14 :13-16
[3]   Is the Clinical Risk Score for Patients with Colorectal Liver Metastases Still Useable in the Era of Effective Neoadjuvant Chemotherapy? [J].
Ayez, Ninos ;
Lalmahomed, Zarina S. ;
van der Pool, Anne E. M. ;
Vergouwe, Yvonne ;
van Montfort, Kees ;
de Jonge, Jeroen ;
Eggermont, Alexander M. M. ;
IJzermans, Jan N. M. ;
Verhoef, Cornelis .
ANNALS OF SURGICAL ONCOLOGY, 2011, 18 (10) :2757-2763
[4]   Cetuximab with chemotherapy (CT) as first-line treatment for metastatic colorectal cancer (mCRC): Analysis of the CRYSTAL and OPUS studies according to KRAS and BRAF mutation status [J].
Bokemeyer, C. ;
Kohne, C. ;
Rougier, P. ;
Stroh, C. ;
Schlichting, M. ;
Van Cutsem, E. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
[5]   Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study [J].
Bokemeyer, C. ;
Bondarenko, I. ;
Hartmann, J. T. ;
de Braud, F. ;
Schuch, G. ;
Zubel, A. ;
Celik, I. ;
Schlichting, M. ;
Koralewski, P. .
ANNALS OF ONCOLOGY, 2011, 22 (07) :1535-1546
[6]   Selection of patients for resection of hepatic colorectal metastases: Expert consensus statement [J].
Charnsangavej, Chusilp ;
Clary, Bryan ;
Fong, Yuman ;
Grothey, Axel ;
Pawlik, Timothy M. ;
Choti, Michael A. .
ANNALS OF SURGICAL ONCOLOGY, 2006, 13 (10) :1261-1268
[7]   Trends in long-term survival following liver resection for hepatic colorectal metastases [J].
Choti, MA ;
Sitzmann, JV ;
Tiburi, MF ;
Sumetchotimetha, W ;
Rangsin, R ;
Schulick, RD ;
Lillemoe, KD ;
Yeo, CJ ;
Cameron, JL .
ANNALS OF SURGERY, 2002, 235 (06) :759-765
[8]   Chemotherapy-Associated Hepatotoxicity: Do We Need to Be Concerned? [J].
Choti, Michael A. .
ANNALS OF SURGICAL ONCOLOGY, 2009, 16 (09) :2391-2394
[9]   Drug therapy: EGFR antagonists in cancer treatment [J].
Ciardiello, Fortunato ;
Tortora, Giampaolo .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (11) :1160-1174
[10]   Chemotherapy permits resection of metastatic colorectal cancer: experience from Intergroup N9741 [J].
Delaunoit, T ;
Alberts, SR ;
Sargent, DJ ;
Green, E ;
Goldberg, RM ;
Krook, J ;
Fuchs, C ;
Ramanathan, RK ;
Williamson, SK ;
Morton, RF ;
Findlay, BP .
ANNALS OF ONCOLOGY, 2005, 16 (03) :425-429