De Mel Sanjay, Lee Ainsley Ryan, Tan Joelle Hwee Inn, Tan Rachel Zi Yi, Poon Li Mei, Chan Esther, Lee Joanne, Chee Yen Lin, Lakshminarasappa Satish R, Jaynes Patrick William, Jeyasekharan Anand D
Department of Haematology-Oncology, National University Cancer Institute, Singapore, National University Health System, Singapore, Singapore.
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Front Oncol. 2024 Jan 29;14:1307839. doi: 10.3389/fonc.2024.1307839. eCollection 2024.
Deregulation of the DNA damage response (DDR) plays a critical role in the pathogenesis and progression of many cancers. The dependency of certain cancers on DDR pathways has enabled exploitation of such through synthetically lethal relationships e.g., Poly ADP-Ribose Polymerase (PARP) inhibitors for BRCA deficient ovarian cancers. Though lagging behind that of solid cancers, DDR inhibitors (DDRi) are being clinically developed for haematological cancers. Furthermore, a high proliferative index characterize many such cancers, suggesting a rationale for combinatorial strategies targeting DDR and replicative stress. In this review, we summarize pre-clinical and clinical data on DDR inhibition in haematological malignancies and highlight distinct haematological cancer subtypes with activity of DDR agents as single agents or in combination with chemotherapeutics and targeted agents. We aim to provide a framework to guide the design of future clinical trials involving haematological cancers for this important class of drugs.
DNA损伤反应(DDR)失调在许多癌症的发病机制和进展中起着关键作用。某些癌症对DDR通路的依赖性使得通过合成致死关系来利用这一点成为可能,例如,聚ADP-核糖聚合酶(PARP)抑制剂用于治疗BRCA缺陷型卵巢癌。尽管血液系统癌症的DDR抑制剂(DDRi)的研发落后于实体癌,但目前正在进行临床开发。此外,许多此类癌症具有高增殖指数,这为针对DDR和复制应激的联合策略提供了理论依据。在这篇综述中,我们总结了血液系统恶性肿瘤中DDR抑制的临床前和临床数据,并强调了DDR药物作为单一药物或与化疗药物和靶向药物联合使用时具有活性的不同血液系统癌症亚型。我们旨在提供一个框架,以指导未来涉及血液系统癌症的此类重要药物的临床试验设计。