免疫疗法
药品
封锁
限制
抗药性
聚合酶
医学
聚ADP核糖聚合酶
免疫检查点
药理学
癌症研究
生物
计算生物学
免疫系统
DNA
免疫学
内科学
遗传学
受体
工程类
机械工程
作者
Melissa Pham,Natalie Ngoi,Guang Peng,David S.P. Tan,Timothy A. Yap
标识
DOI:10.1016/j.trecan.2021.05.004
摘要
The efficacy of poly(ADP-ribose) polymerase inhibitors (PARPi) is restricted by inevitable drug resistance, while their use in combination with chemotherapy and targeted agents is commonly associated with dose-limiting toxicities. Immune checkpoint blockade (ICB) has demonstrated durable responses in different solid tumors and is well-established across multiple cancers. Despite this, single agent activity is limited to a minority of patients and drug resistance remains an issue. Building on the monotherapy success of both drug classes, combining PARPi with ICB may be a safe and well-tolerated strategy with the potential to improve survival outcomes. In this review, we present the preclinical, translational, and clinical data supporting the combination of DNA damage response (DDR) and ICB as well as consider important questions to be addressed with future research.
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