A systematic review of gemcitabine and taxanes combination therapy randomized trials for metastatic breast cancer

被引:4
|
作者
Hu, Qian [1 ]
Jiang, Jun-xia [1 ]
Luo, Long [1 ,2 ]
Yang, Xing [1 ]
Lin, Xiao [1 ]
Dinglin, Xiao-xiao [1 ]
Zhang, Wei [3 ]
Wu, Jun-yan [4 ]
Yao, He-rui [1 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Oncol, Guangzhou 510120, Peoples R China
[2] Yiyang Cent Hosp Hunan Prov, Dept Oncol, Yiyang 413000, Hunan, Peoples R China
[3] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Breast Tumor Ctr, Guangzhou 510120, Peoples R China
[4] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Pharmaceut Dept, Guangzhou 510120, Peoples R China
来源
SPRINGERPLUS | 2014年 / 3卷
关键词
Metastatic breast cancer; Gemcitabine; Taxanes; Systematic review; SINGLE-AGENT THERAPY; COOPERATIVE ONCOLOGY GROUP; PHASE-II TRIAL; PLUS DOCETAXEL; 1ST-LINE CHEMOTHERAPY; PRETREATED PATIENTS; PACLITAXEL; METAANALYSIS; MANAGEMENT;
D O I
10.1186/2193-1801-3-293
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: Gemcitabine/taxanes-based combination shows anti-tumor activity for the treatment of metastatic breast cancer, but there is a debate regarding the advantages of gemcitabine and taxanes regimens as a first-line or second-line treatment for metastatic breast cancer. Here we conducted a systematic review and meta-analysis to compare the efficacy and toxicity for patients receiving chemotherapy with or without GT-based regimens. Methods: The randomized controlled trials were performed by searching Pubmed, MEDLINE, EMBASE, and conference proceedings. We identified eight randomized controlled trials and then extracted and combined the data using to calculate hazard ratios (HR). The primary outcomes were progression-free survival (PFS) and time to progression (TTP). The secondary outcomes were overall survival (OS) and acute toxicity. A meta-analysis was performed using Review Manager Version 4.2. Results: Eight eligible trails were identified. These studies involved 2234 patients with metastatic breast cancer, (1122 patients received GT-based combination regimen and 1112 patients received a regimen without the combination). A fixed-effects model meta-analysis showed that ORR and TTP are superior for GT-treated patients ORR (OR = 1.28, 95% CI 1.07-1.53), TTP (HR = 0.80; 95% CI 0.71-0.89). And GT-based combination significantly improved OS in the first-line subgroup (HR = 0.84; 95% CI 0.71-0.99). However, there were significant differences regarding acute hematological toxicity, particularly thrombocytopenia. Conclusion: Gemcitabine/taxanes-treated patients with metastatic breast cancer showed a significant improvement in the ORR, TTP and OS (first-line background) compared to patients not treated with the combination regimen.
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页数:11
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