Network meta-analysis of eribulin versus other chemotherapies used as second- or later-line treatment in locally advanced or metastatic breast cancer

被引:4
作者
Zhao, Qi [1 ]
Hughes, Rachel [2 ]
Neupane, Binod [3 ]
Mickle, Kristin [4 ]
Su, Yun [5 ]
Chabot, Isabelle [6 ]
Betts, Marissa [4 ]
Kadambi, Ananth [2 ]
机构
[1] Eisai Inc, Global Value & Access, Woodcliff Lake, NJ USA
[2] Evidera, Evidence Synth Modeling & Commun, San Francisco, CA 94111 USA
[3] Evidera, Evidence Synth Modeling & Commun, Montreal, PQ, Canada
[4] Evidera, Evidence Synth Modeling & Commun, Waltham, MA USA
[5] Eisai Inc, Global Value & Access, Woodcliff Lake, NJ USA
[6] Univ Montreal, Fac Pharm, Montreal, PQ, Canada
关键词
Breast cancer; Metastatic; Locally advanced; Network meta-analysis; Triple negative breast cancer; overall survival; IXABEPILONE PLUS CAPECITABINE; RANDOMIZED PHASE-II; OPEN-LABEL; PRETREATED PATIENTS; MESYLATE; ANTHRACYCLINE; PACLITAXEL; WOMEN; MULTICENTER; GEMCITABINE;
D O I
10.1186/s12885-021-08446-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Eribulin mesylate (ERI; Halaven (R)) is a microtubule inhibitor approved in the United States for metastatic breast cancer patients with at least two prior chemotherapy regimens for metastatic breast cancer, and in the European Union in locally advanced breast cancer or metastatic breast cancer patients who progressed after at least one chemotherapy for advanced disease. This network meta-analysis compared the efficacy and safety of ERI versus other chemotherapies in this setting. Methods Systematic searches conducted in MEDLINE, Embase, and the Cochrane Central Register of Clinical Trials identified randomized controlled trials of locally advanced breast cancer/metastatic breast cancer chemotherapies in second- or later-line settings. Efficacy assessment included pre-specified subgroup analysis of breast cancer subtypes. Included studies were assessed for quality using the Centre for Reviews and Dissemination tool. Bayesian network meta-analysis estimated primary outcomes of overall survival and progression-free survival using fixed-effect models. Comparators included: capecitabine (CAP), gemcitabine (GEM), ixabepilone (IXA), utidelone (UTI), treatment by physician's choice (TPC), and vinorelbine (VIN). Results The network meta-analysis included seven trials. Results showed that second- or later-line patients treated with ERI had statistically longer overall survival versus TPC (hazard ratio [HR]: 0.81; credible interval [CrI]: 0.66-0.99) or GEM+VIN (0.62; 0.42-0.90) and statistically longer progression-free survival versus TPC (0.76; 0.64-0.90), but statistically shorter progression-free survival versus CAP+IXA (1.40; 1.17-1.67) and CAP+UTI (1.61; 1.23-2.12). In triple negative breast cancer, ERI had statistically longer overall survival versus CAP (0.70; 0.54-0.90); no statistical differences in progression-free survival were observed in triple negative breast cancer. Conclusions This network meta-analysis suggests that ERI may provide an overall survival benefit in the overall locally advanced breast cancer/metastatic breast cancer populations and triple negative breast cancer subgroup compared to standard treatments. These findings support the use of ERI in second- or later-line treatment of patients with locally advanced breast cancer/metastatic breast cancer.
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页数:15
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