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DLL3:小细胞肺癌的一个新兴靶点。

DLL3: an emerging target in small cell lung cancer.

机构信息

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

Oncology Research, Amgen Inc., Thousand Oaks, CA, USA.

出版信息

J Hematol Oncol. 2019 Jun 18;12(1):61. doi: 10.1186/s13045-019-0745-2.

Abstract

Small cell lung cancer (SCLC) accounts for approximately 15% of all lung cancers. Despite high rates of response to first-line chemotherapy and radiotherapy, patients with extensive-stage disease eventually relapse, and very few patients survive more than 5 years from diagnosis. Treatment options for recurrent or refractory disease are limited, and the treatments that do exist are associated with significant treatment-related toxicities. Delta-like ligand 3 (DLL3) is an inhibitory Notch ligand that is highly expressed in SCLC and other neuroendocrine tumors but minimally expressed in normal tissues. It is therefore being explored as a potential therapeutic target in SCLC. Here, we review the preclinical and clinical evidence for targeting DLL3 in SCLC and discuss several DLL3-specific therapies being developed for the treatment of SCLC: the antibody-drug conjugate rovalpituzumab tesirine, the bispecific T cell engager immuno-oncology therapy AMG 757, and the chimeric antigen receptor T cell therapy AMG 119.

摘要

小细胞肺癌(SCLC)约占所有肺癌的 15%。尽管广泛期疾病患者对一线化疗和放疗有很高的反应率,但最终仍会复发,从诊断到存活超过 5 年的患者非常少。复发性或难治性疾病的治疗选择有限,而且现有的治疗方法与显著的治疗相关毒性相关。Delta-like 配体 3(DLL3)是一种抑制性 Notch 配体,在 SCLC 和其他神经内分泌肿瘤中高度表达,但在正常组织中表达很少。因此,它被作为 SCLC 的潜在治疗靶点进行探索。在这里,我们回顾了靶向 SCLC 中 DLL3 的临床前和临床证据,并讨论了几种正在开发用于治疗 SCLC 的 DLL3 特异性疗法:抗体药物偶联物 rovalpituzumab tesirine、双特异性 T 细胞衔接免疫肿瘤学疗法 AMG 757 以及嵌合抗原受体 T 细胞疗法 AMG 119。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4f8/6582566/420caa39ec2d/13045_2019_745_Fig1_HTML.jpg

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