Comparative efficacy and safety of eribulin versus paclitaxel in breast cancer: a systematic review and meta-analysis

被引:0
作者
Zhang, Jialin [1 ]
Su, Jingyang [2 ]
Ni, Cui [1 ]
Lu, Jinhua [1 ]
机构
[1] Zhejiang Chinese Med Univ, Dept Oncol, Hangzhou TCM Hosp, Hangzhou Hosp Tradit Chinese Med, 453 Tiyuchang Rd, Hangzhou 310007, Peoples R China
[2] Zhejiang Chinese Med Univ, Dept Gen Internal Med, Tongde Hosp, Tongde Hosp Zhejiang Prov, Hangzhou, Peoples R China
关键词
Breast cancer; eribulin; paclitaxel; neutropenia; neuropathy; PHASE-II; JAPANESE PATIENTS; CHEMOTHERAPY; WOMEN; MESYLATE; MULTICENTER; MONOTHERAPY; METASTASIS; NEUROPATHY; THERAPY;
D O I
10.1080/14796694.2024.2431479
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: We conducted a meta-analysis of published randomized controlled trials to compare the effectiveness and safety of eribulin versus paclitaxel for patients with breast cancer. Methods: We systematically searched multiple databases including Cochrane, PubMed, Medline, and Embase. The primary outcomes analyzed were overall survival (OS), complete response (CR), partial response (PR), stable disease (SD), and adverse events (AEs). These outcomes were evaluated using RevMan5.3 software. Results: A total of 5 studies were included in the analysis. Compared to paclitaxel plus other chemotherapy drugs, eribulin plus other chemotherapy drugs not only extended the overall survival of patients but also improved the disease control rate (DCR) [risk ratio (RR) 0.98, (95% confidence intervals (CI): 0.70, 1.38), p=0.92]. Hematological system diseases [RR 1.18 (95% CI: 1.07, 1.31), p=0.002] were the most frequently observed adverse event with eribulin, while paclitaxel was more likely to cause nervous system lesion [RR 0.66 (95% CI: 0.54, 0.80), p<0.0001]. Conclusion: Compared with paclitaxel plus other chemotherapy drugs, eribulin plus other chemotherapy drugs can also prolong the PFS and OS of BC patients. Our recommendation is to use eribulin plus other chemotherapy drugs to treat advanced BC and to continuously monitor and manage the drug-related adverse events.
引用
收藏
页码:3507 / 3517
页数:11
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