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