Dolkar Tsering, Gates Christopher, Hao Zhonglin, Munker Reinhold
Hospital Medicine, University of Kentucky, Lexington, Kentucky, USA.
Hematology - Oncology, University of Kentucky, Lexington, Kentucky, USA.
J Immunother Cancer. 2025 Jan 6;13(1):e009667. doi: 10.1136/jitc-2024-009667.
Small cell lung cancer (SCLC) is an aggressive form of neuroendocrine neoplasm known for its striking initial response to treatment, followed by fast relapse and refractoriness in response to additional lines of therapy. New advances in immunotherapy are paving the way for more effective treatment strategies and have promising results with early clinical trial data. While SCLC rarely harbors actionable mutations, the receptor DLL3 is extensively present in SCLC, making it a potential target for immunotherapy. Three emerging therapeutic options include bispecific T cell engagers targeting DLL3, chimeric antigen receptor T cells (CAR-T cells), and antibody-drug conjugates. Several phase II and phase III clinical trials for bispecific T cell engagers show promise. Additionally, the first CAR-T cell trials in humans for SCLC are currently underway.
小细胞肺癌(SCLC)是一种侵袭性神经内分泌肿瘤,以其对治疗的显著初始反应而闻名,随后会迅速复发并对后续治疗产生耐药性。免疫疗法的新进展为更有效的治疗策略铺平了道路,早期临床试验数据显示出了有前景的结果。虽然SCLC很少携带可操作的突变,但受体DLL3在SCLC中广泛存在,使其成为免疫疗法的潜在靶点。三种新兴的治疗选择包括靶向DLL3的双特异性T细胞衔接器、嵌合抗原受体T细胞(CAR-T细胞)和抗体药物偶联物。双特异性T细胞衔接器的几项II期和III期临床试验显示出了前景。此外,目前正在进行针对SCLC的首例人体CAR-T细胞试验。