曲妥珠单抗德鲁司坦治疗转移性HER2+和HER2-low乳腺癌的安全性和有效性:临床试验的最新系统回顾和元分析》。

IF 1.6 4区 医学 Q4 ONCOLOGY American Journal of Clinical Oncology-Cancer Clinical Trials Pub Date : 2024-11-01 Epub Date: 2024-07-02 DOI:10.1097/COC.0000000000001126
Zaheer Qureshi, Faryal Altaf, Abdur Jamil, Rimsha Siddique, Eeshal Fatima
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引用次数: 0

摘要

研究目的曲妥珠单抗德鲁司坦(T-DXd)是一种新型抗体药物共轭物(ADC),有望治疗转移性HER2+和HER2-low乳腺癌。这项最新的系统综述和荟萃分析整合了最新的临床试验数据,旨在评估T-DXd在这一患者群体中的安全性和有效性:我们遵循了系统综述和荟萃分析首选报告项目(PRISMA)指南。截至 2024 年 1 月,我们在 PubMed、Scopus 和 Web of Science 上进行了全面检索,重点关注评估 T-DXd 疗效和安全性的临床试验。资格标准基于 PICOS 框架,所选研究均经过严格的质量评估和数据提取。主要结果为无进展生存期(PFS)、总生存期(OS)和不良事件发生率。对数据进行了随机效应荟萃分析:共有7项研究符合纳入标准,涉及2201名患者。汇总分析显示,T-DXd能显著改善PFS(OR=0.37,95% CI:0.27-0.52),表明其在延缓疾病进展方面疗效显著。然而,治疗与贫血(OR=2.10,95% CI:1.36-3.25)、疲劳(OR=1.56,95% CI:1.21-2.02)、恶心(OR=6.42,95% CI:4.37-9.42)、呕吐(OR=6.21,95% CI:3.14-12.25)、便秘(OR=2.26,95% CI:1.53-3.34),尤其是与药物相关的间质性肺病(OR=10.89,95% CI:3.81-31.12)。疗效结果显示出显著的异质性,通过敏感性分析解决了这一问题:T-DXd在治疗转移性HER2+和HER2-low乳腺癌方面疗效显著,为晚期患者提供了有价值的治疗选择。然而,治疗过程中会出现明显的不良反应,包括ILD风险升高。这些发现强调了谨慎选择患者、监测和管理策略以降低风险的必要性。未来的研究应侧重于优化治疗方案和探索提高安全性的方法。
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Safety and Efficacy of Trastuzumab Deruxtecan for Metastatic HER2+ and HER2-low Breast Cancer: An Updated Systematic Review and Meta-Analysis of Clinical Trials.

Objectives: Trastuzumab deruxtecan (T-DXd) is a novel antibody-drug conjugate (ADC) promising in treating metastatic HER2+ and HER2-low breast cancer. This updated systematic review and meta-analysis, integrating data from the latest clinical trials, aimed to evaluate the safety and efficacy of T-DXd in this patient population.

Methods: We adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. A comprehensive search was conducted across PubMed, Scopus, and Web of Science up to January 2024, focusing on clinical trials that assessed T-DXd's efficacy and safety. Eligibility criteria were based on the PICOS framework, and selected studies underwent rigorous quality assessment and data extraction. The primary outcomes were progression-free survival (PFS), overall survival (OS), and the incidence of adverse events. A random-effects meta-analysis was performed to synthesize the data.

Results: Seven studies involving 2,201 patients met the inclusion criteria. The pooled analysis revealed that T-DXd significantly improved PFS (OR=0.37, 95% CI: 0.27-0.52), indicating a robust efficacy in slowing disease progression. However, treatment was associated with an increased risk of anemia (OR=2.10, 95% CI: 1.36-3.25), fatigue (OR=1.56, 95% CI: 1.21-2.02), nausea (OR=6.42, 95% CI: 4.37-9.42), vomiting (OR=6.21, 95% CI: 3.14-12.25), constipation (OR=2.26, 95% CI: 1.53-3.34), and notably, drug-related interstitial lung disease (OR=10.89, 95% CI: 3.81-31.12). The efficacy outcomes demonstrated significant heterogeneity, which was addressed through sensitivity analysis.

Conclusions: T-DXd shows significant efficacy in treating metastatic HER2+ and HER2-low breast cancer, offering a valuable therapeutic option for patients with advanced disease. However, the treatment is associated with notable adverse events, including a heightened risk of ILD. These findings underscore the need for careful patient selection, monitoring, and management strategies to mitigate risks. Future research should focus on optimizing treatment protocols and exploring methods to enhance safety profiles.

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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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