Efficacy of Sacituzumab Govitecan in Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer: A Comprehensive Systematic Review and Meta-analysis.

IF 1.6 4区 医学 Q4 ONCOLOGY
Zaheer Qureshi, Abdur Jamil, Eeshal Fatima, Faryal Altaf, Rimsha Siddique
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引用次数: 0

Abstract

Objectives: Breast cancer is the most diagnosed cancer in women, with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) being the predominant subtype. Sacituzumab govitecan (SG), a novel antibody-drug conjugate, has emerged as a promising treatment for metastatic HR+/HER2- breast cancer. This systematic review and meta-analysis aimed to evaluate its efficacy and safety.

Methods: Adhering to "Preferred Reporting Items for Systematic Reviews and Meta-Analyses" guidelines, a comprehensive search was conducted in PubMed, Scopus, and Cochrane databases up to December 2023. We included clinical trials and observational studies evaluating SG in patients with HR+/HER2- advanced breast cancer. The primary outcome was progression-free survival (PFS). In contrast, the secondary outcomes included overall survival, objective response rate, clinical benefit rate, duration of response (DOR), and adverse event profiles. Review Manager (Version 5.4) was used for the statistical analysis.

Results: Nine studies met the inclusion criteria for systematic review; 2 were suitable for meta-analysis. The pooled analysis showed a hazard ratio of 0.53 (95% CI: 0.34-0.83; P = 0.005; I2 = 86%) for PFSl and a hazard ratio of 0.63 (95% CI: 0.36-1.11; P = 0.11; I2 = 92%) for overall survival. The pooled analysis of the duration of response showed significant results with a standard mean difference = 0.22 (95% CI: 0.03-0.42; P = 0.02; I2 = 61%).

Conclusion: SG demonstrates significant benefit in PFS and duration of response in patients of HR+/HER2- advanced breast cancer.

萨妥珠单抗戈维替康对激素受体阳性/人类表皮生长因子受体 2 阴性晚期乳腺癌的疗效:全面系统综述与 Meta 分析》。
目的:乳腺癌是女性确诊率最高的癌症,其中激素受体阳性/人表皮生长因子受体2阴性(HR+/HER2-)是最主要的亚型。萨妥珠单抗-戈维替康(SG)是一种新型抗体-药物共轭物,已成为治疗转移性HR+/HER2-乳腺癌的一种很有前景的方法。本系统综述和荟萃分析旨在评估其疗效和安全性:根据 "系统综述和荟萃分析首选报告项目 "指南,我们在 PubMed、Scopus 和 Cochrane 数据库中进行了全面检索,检索期截至 2023 年 12 月。我们纳入了对 HR+/HER2- 晚期乳腺癌患者进行 SG 评估的临床试验和观察性研究。主要结果为无进展生存期(PFS)。而次要结果包括总生存期、客观反应率、临床获益率、反应持续时间(DOR)和不良事件概况。统计分析使用的是 Review Manager(5.4 版):9项研究符合系统综述的纳入标准;2项适合进行荟萃分析。汇总分析显示,PFSl 的危险比为 0.53 (95% CI: 0.34-0.83; P= 0.005; I2 = 86%),总生存期的危险比为 0.63 (95% CI: 0.36-1.11; P= 0.11; I2 = 92%)。对反应持续时间的汇总分析结果显示,标准平均差=0.22(95% CI:0.03-0.42;P=0.02;I2=61%):SG对HR+/HER2-晚期乳腺癌患者的PFS和反应持续时间有明显益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
130
审稿时长
4-8 weeks
期刊介绍: ​​​​​​​American Journal of Clinical Oncology is a multidisciplinary journal for cancer surgeons, radiation oncologists, medical oncologists, GYN oncologists, and pediatric oncologists. The emphasis of AJCO is on combined modality multidisciplinary loco-regional management of cancer. The journal also gives emphasis to translational research, outcome studies, and cost utility analyses, and includes opinion pieces and review articles. The editorial board includes a large number of distinguished surgeons, radiation oncologists, medical oncologists, GYN oncologists, pediatric oncologists, and others who are internationally recognized for expertise in their fields.
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