Incidence of antibody-drug conjugate-related hepatotoxicity in breast cancer: a systematic review and meta-analysis.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Therapeutic Advances in Drug Safety Pub Date : 2024-12-18 eCollection Date: 2024-01-01 DOI:10.1177/20420986241304680
Ping Yang, Hengheng Zhang, Jinming Li, Zitao Li, Zhen Liu, Miaozhou Wang, Fuxing Zhao, Jiuda Zhao, GuoShuang Shen, Yi Zhao
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Abstract

Background: Antibody-drug conjugates (ADCs), as a new type of targeted drug, have been widely used in breast cancer patients in recent years. However, while achieving better efficacy, its hepatotoxicity should not be ignored.

Objectives: To clarify the incidence of hepatotoxicity associated with ADCs and compare the incidence of hepatotoxicity of ADCs with different drugs.

Design: We performed a systematic review and meta-analysis to summarize the clinical trials and combined the data using meta-analysis.

Methods: We searched the PubMed, Embase, and Web of Science databases up to March 12, 2023. The primary outcome was the incidence of ADC-related hepatotoxicity in breast cancer patients. The data were merged using Stata 17.0 software.

Results: ADCs caused a high incidence of all grades of hepatotoxicity. Sacituzumab govitecan caused the highest incidence of all grades of alanine aminotransferase (ALT) elevation at 25.30% (95% confidence interval (CI): 19.29-31.82). Trastuzumab deruxtecan caused the highest incidence of all grades of aspartate aminotransferase (AST) elevation. The highest incidence of AST elevation was 31.89% (95% CI: 18.56-46.85). Conversely, trastuzumab emtansine caused the highest incidence of grade ⩾3 AST and ALT elevation (incidence rates were 3.95% (95% CI: 2.39-5.85) and 3.42% (95% CI: 1.95-5.24), respectively).

Conclusion: Hepatotoxicity is an adverse reaction that cannot be ignored when ADCs are used for treating breast cancer. Moreover, clinicians should pay more attention to the assessment of patients' liver function and monitoring of liver indices, particularly ALT and AST, when using ADCs.

乳腺癌中抗体-药物结合物相关肝毒性的发生率:一项系统回顾和荟萃分析。
背景:抗体-药物偶联物(Antibody-drug conjugates, adc)作为一种新型靶向药物,近年来在乳腺癌患者中得到了广泛的应用。然而,在取得较好疗效的同时,其肝毒性也不容忽视。目的:明确adc的肝毒性发生率,比较不同药物对adc的肝毒性发生率。设计:我们进行了系统回顾和荟萃分析来总结临床试验,并使用荟萃分析合并数据。方法:我们检索了PubMed、Embase和Web of Science数据库,截止日期为2023年3月12日。主要终点是乳腺癌患者中adc相关肝毒性的发生率。数据合并采用Stata 17.0软件。结果:adc引起各级别肝毒性发生率高。Sacituzumab govitecan导致所有级别丙氨酸转氨酶(ALT)升高的发生率最高,为25.30%(95%可信区间(CI): 19.29-31.82)。曲妥珠单抗德鲁西替康导致所有级别的天冬氨酸转氨酶(AST)升高的发生率最高。AST升高的最高发生率为31.89% (95% CI: 18.56 ~ 46.85)。相反,曲妥珠单抗emtansine引起了大于或小于3级AST和ALT升高的最高发生率(发生率分别为3.95% (95% CI: 2.39-5.85)和3.42% (95% CI: 1.95-5.24))。结论:肝毒性是adc治疗乳腺癌不可忽视的不良反应。此外,临床医生在使用adc时应更加重视患者肝功能的评估和肝脏指标的监测,特别是ALT和AST。
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
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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