First-line cetuximab versus bevacizumab for RAS and BRAF wild-type metastatic colorectal cancer: a systematic review and meta-analysis

被引:19
作者
Zheng, Bobo [1 ]
Wang, Xin [2 ]
Wei, Mingtian [1 ]
Wang, Quan [3 ]
Li, Jiang [4 ,5 ]
Bi, Liang [1 ]
Deng, Xiangbing [1 ]
Wang, Ziqiang [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Gastrointestinal Surg, Chengdu 610041, Sichuan, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Gastroenterol, Xian 710061, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp, Digest Dis Hosp, Xian 710032, Shaanxi, Peoples R China
[4] Chinese Acad Med Sci, Natl Canc Ctr, Canc Hosp, Beijing 100021, Peoples R China
[5] Peking Union Med Coll, Beijing 100021, Peoples R China
关键词
First line; Cetuximab; Bevacizumab; Wild type; Metastatic colorectal cancer; CHEMOTHERAPY PLUS BEVACIZUMAB; TUMOR RESPONSE; OPEN-LABEL; SURVIVAL; FLUOROURACIL; LEUCOVORIN; THERAPY; PANITUMUMAB; IRINOTECAN; CONSENSUS;
D O I
10.1186/s12885-019-5481-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A first-line biologic treatment for metastatic colorectal cancer (mCRC) is still controversial. We, therefore, performed a meta-analysis to determine the efficacy of first-line cetuximab versus bevacizumab for RAS and BRAF wild-type mCRC. Methods: In March 2018, an electronic search of the following biomedical databases was performed: PubMed, EMBASE, Cochrane Library, ClinicalTrials.gov and Web of Knowledge. Randomized controlled trials (RCTs) and prospective or observational cohort studies (OCSs) were included. Subgroup analyses of all RCTs were performed in all outcomes. All statistical analyses were performed using RevMan software 5.3. Results: Two RCTs and three OCSs, involving a total 2576 patients, were included. The meta-analysis reported that cetuximab was associated with a longer overall survival (OS) [HR 0.89, 95% CI (0.81-0.98); p = 0.02], a higher ORR [RR 1.11, 95% CI (1.03-1.19); p = 0.006], higher complete response [RR 3.21, 95% CI (1.27-8.12); p= 0.01] and a greater median depth of response than bevacizumab. However, no significant difference was observed between cetuximab and bevacizumab groups for PFS, DCR, partial response, progressive disease, curative intent metastasectomy, EORR and incidence of grade 3 or higher adverse events. In the subgroup meta-analyses of the RCTs, inconsistent results compared to the main analysis, however, were found, in the ORR, DCR and curative intent metastasectomy. Conclusions: The current evidence indicates that compared to bevacizumab treatment, cetuximab provides a clinically relevant effect in first-line treatment against mCRC, at the cost of having lower stable disease.
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页数:12
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