Efficacy and Safety of Abemaciclib in Combination With Endocrine Therapy for HR+/HER2- Advanced or Metastatic Breast Cancer: A 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, particularly the hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-) subtype, remains a major global health concern. Abemaciclib, a CDK4/6 inhibitor, has shown promising results in treating advanced cases. This study comprehensively assesses the efficacy and safety of abemaciclib in combination with endocrine therapy for HR+/HER2- advanced or metastatic breast cancer.

Methods: Following PRISMA guidelines, a systematic review and meta-analysis was conducted. A thorough literature search was conducted on PubMed, EMBASE, Cochrane Library, and ClinicalTrials.gov til December 2023. Inclusion criteria encompassed randomized controlled trials and retrospective cohort studies reporting on abemaciclib in approved doses, either as monotherapy or in combination. Outcome assessments included progression-free survival (PFS), overall response rate (ORR), side effects/adverse effects (SE/AE), and overall survival (OS). Quality assessment utilized Cochrane's revised risk of bias tool and Newcastle-Ottawa scale.

Results: Pooled results of 22 studies involving 14,010 patients revealed that abemaciclib significantly improved PFS (hazard ratio=0.53; 95% CI: 0.48-0.59; P=0.00; I2=0%), ORR (risk ratio=2.31; 95% CI: 1.93-2.75; P=0.00; I2=0%), and OS (risk ratio=0.76 (95% CI: 0.65-0.87; P=0.001; I2=0%). However, abemaciclib increased the risk of adverse events in the fulvestrant and nonsteroidal aromatase inhibitor (NSAI) combinations, respectively.

Conclusions: Abemaciclib, particularly in combination with fulvestrant, emerges as an effective therapeutic option for HR+/HER2- advanced or metastatic breast cancer, improving PFS and OS. The higher toxicity profile warrants cautious use, especially in treatment-naive patients.

Abemaciclib 联合内分泌疗法治疗 HR+/HER2- 晚期或转移性乳腺癌的有效性和安全性:系统综述与元分析》。
目的:乳腺癌,尤其是激素受体阳性(HR+)和人表皮生长因子受体 2 阴性(HER2-)亚型乳腺癌,仍然是全球关注的主要健康问题。CDK4/6抑制剂Abemaciclib在治疗晚期病例方面取得了可喜的成果。本研究全面评估了阿柏西尼联合内分泌疗法治疗HR+/HER2-晚期或转移性乳腺癌的疗效和安全性:按照PRISMA指南,进行了系统性回顾和荟萃分析。在PubMed、EMBASE、Cochrane Library和ClinicalTrials.gov上进行了全面的文献检索,直至2023年12月。纳入标准包括随机对照试验和回顾性队列研究,这些研究报告了阿柏西尼在批准剂量下作为单药或联合用药的情况。结果评估包括无进展生存期(PFS)、总反应率(ORR)、副作用/不良反应(SE/AE)和总生存期(OS)。质量评估采用 Cochrane 的修订版偏倚风险工具和纽卡斯尔-渥太华量表:涉及14010名患者的22项研究的汇总结果显示,阿柏西尼能显著改善PFS(危险比=0.53;95% CI:0.48-0.59;P=0.00;I2=0%)、ORR(风险比=2.31;95% CI:1.93-2.75;P=0.00;I2=0%)和OS(风险比=0.76(95% CI:0.65-0.87;P=0.001;I2=0%)。然而,在氟维司群和非甾体芳香化酶抑制剂(NSAI)组合中,阿贝昔单抗分别增加了不良事件的风险:结论:阿培莫司利(尤其是与氟维司群联用)是治疗HR+/HER2-晚期或转移性乳腺癌的有效选择,可改善PFS和OS。较高的毒性需要谨慎使用,尤其是对未接受治疗的患者。
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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