DLL3: an emerging target in small cell lung cancer

被引:0
作者
Dwight H. Owen
Michael J. Giffin
Julie M. Bailis
Marie-Anne Damiette Smit
David P. Carbone
Kai He
机构
[1] The Ohio State University Comprehensive Cancer Center,Division of Medical Oncology, Department of Internal Medicine
[2] Amgen Inc.,Oncology Research
[3] Amgen Inc.,Oncology Research
[4] Amgen Inc.,Translational Medicine
来源
Journal of Hematology & Oncology | / 12卷
关键词
Antibody-drug conjugate (ADC); Bispecific T cell engager (BiTE®) antibody construct; Chimeric antigen receptor (CAR) T cell therapy; Delta-like ligand 3 (DLL3); Immuno-oncology therapy; Neuroendocrine; Small cell lung cancer (SCLC); Targeted therapy;
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摘要
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.
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