Different doses of bevacizumab in combination with chemotherapy for advanced colorectal cancer: a meta-analysis and Bayesian analysis

被引:0
|
作者
Deng, Jia [1 ]
Zeng, Xinglin [2 ]
Hu, Wenting [1 ]
Yue, Tinghui [1 ]
Luo, Zicheng [1 ]
Zeng, Lian [1 ]
Li, Ping [3 ]
Chen, Jiang [3 ]
机构
[1] Guizhou Univ Tradit Chinese Med, Coll Clin Med, Guiyang, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Coll Clin Med, Chengdu, Peoples R China
[3] Guizhou Univ Tradit Chinese Med, Colorectal & Anal Surg, Affiliated Hosp 1, 71 Baoshan North Rd, Guiyang 550001, Peoples R China
关键词
Bevacizumab; Chemotherapy; Advanced colorectal cancer; Meta-analysis; Bayesian analysis; OXALIPLATIN-BASED CHEMOTHERAPY; 1ST-LINE TREATMENT; PLUS BEVACIZUMAB; PHASE-II; OPEN-LABEL; FLUOROURACIL; LEUCOVORIN; CAPECITABINE; EFFICACY; FOLFIRI;
D O I
10.1007/s00384-023-04442-5
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
ObjectiveThe aim of the present study was to explore the incremental benefit of bevacizumab (Bev) in the treatment of advanced colorectal cancer (CRC) with different doses.MethodsA literature search of eight electronic databases (China National Knowledge Infrastructure, Wanfang databases, Chinese Biomedical Database, VIP medicine information, Cochrane Library, MEDLINE, PubMed, and EMBASE) was conducted from database creation to December 2022. Randomized controlled trials (RCTs) that compared Bev at various dosages + chemotherapy (CT) versus placebo (or blank control) + CT were selected. The overall survival (OS), progression-free survival (PFS), overall response rate (ORR; complete response [CR] + partial response [PR]), and grade >= 3 adverse events (AEs) were integrated first by pooled analysis. The likelihood of ideal dosage of Bev was then ranked using random effects within Bayesian analysis.ResultsTwenty-six RCTs involving 18,261 patients met the inclusion criteria. OS increased significantly after using 5 mg (HR: 0.87, 95% CI 0.75 to 1.00) and 10 mg dosages of Bev (HR: 0.75, 95% CI 0.66 to 0.85) with CT, but statistical significance was not attained for the 7.5 mg dose (HR: 0.95, 95% CI 0.83 to 1.08). A significantly increased in PFS with doses of 5 mg (HR: 0.69, 95% CI 0.58 to 0.83), 7.5 mg (HR: 0.81, 95% CI 0.66 to 1.00), and 10 mg (HR: 0.60, 95% CI 0.53 to 0.68). ORR distinctly increased after 5 mg (RR: 1.34, 95% CI 1.15 to 1.55), 7.5 mg (RR: 1.25, 95% CI 1.05 to 1.50), and10 mg (RR: 2.27, 95% CI 1.82 to 2.84) doses were administered. Grade >= 3 AEs increased clearly in 5 mg (RR: 1.11, 95% CI 1.04 to 1.20) compared to 7.5 mg (RR: 1.05, 95% CI 0.82 to 1.35) and 10 mg (RR: 1.15, 95% CI 0.98 to 1.36). Bayesian analysis demonstrated that 10 mg Bev obtained the maximum time of OS (HR: 0.75, 95% CrI 0.58 to 0.97; probability rank = 0.05) indirectly compared to 5 mg and 7.5 mg Bev. Compared with 5 mg and 7.5 mg Bev, 10 mg Bev also holds the longest duration for PFS (HR: 0.59, 95% CrI 0.43 to 0.82; probability rank = 0.00). In terms of ORR, 10 mg Bev holds the maximum frequency (RR: 2.02, 95% CrI 1.52 to 2.66; probability rank = 0.98) in comparison to 5 mg and 7.5 mg Bev clearly. For grade >= 3 AEs, 10 mg Bev has the maximum incidence (RR: 1.15, 95% CrI 0.95 to 1.40, probability rank = 0.67) in comparison to other doses of Bev.ConclusionThe study suggests that 10 mg dose Bev could be more effective in treating advanced CRC in efficacy, but 5 mg Bev could be more safer in terms of safety.
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页数:19
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