Meng Yuan, Wang Xuerui, Yang Jie, Zhu Meiying, Yu Minghui, Li Longhui, Liang Yangyueying, Kong Fanming
Department of Oncology, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Anshanxi Road, Nankai District, Tianjin, 300193, China.
National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin, China.
Discov Oncol. 2024 Aug 1;15(1):327. doi: 10.1007/s12672-024-01171-1.
Small cell lung cancer (SCLC) is an extremely aggressive cancer with a relatively low median survival rate after diagnosis. Treatment options such as chemotherapy or combination immunotherapy have shown clinical benefits, but resistance and relapse can occur. Antibody-drug conjugates (ADCs), as a novel class of biopharmaceutical compounds, have broad application prospects in the treatment of SCLC. ADCs consist of monoclonal antibodies that specifically target cancer cells and are attached to cytotoxic drugs, allowing for targeted killing of cancer cells while sparing healthy tissues. Current clinical studies focus on Delta-like protein 3 (DLL3), CD56, Trophoblast cell surface antigen 2 (Trop-2), B7-H3, and SEZ6. Although toxicities exceeding expectations have been observed with Rova-T, drugs targeting TROP-2 (Sacituzumab Govitecan), B7-H3 (DS-7300), and SEZ6 (ABBV-011) have shown exciting clinical benefits. In this review, we collect the latest clinical evidence to describe the therapeutic efficacy and safety of ADCs in SCLC and discuss prospects and challenges.
小细胞肺癌(SCLC)是一种极具侵袭性的癌症,诊断后的中位生存率相对较低。化疗或联合免疫疗法等治疗方案已显示出临床益处,但仍可能出现耐药和复发情况。抗体药物偶联物(ADC)作为一类新型生物制药化合物,在SCLC治疗中具有广阔的应用前景。ADC由特异性靶向癌细胞的单克隆抗体与细胞毒性药物连接而成,可在保护健康组织的同时实现对癌细胞的靶向杀伤。目前的临床研究集中在Delta样蛋白3(DLL3)、CD56、滋养层细胞表面抗原2(Trop-2)、B7-H3和SEZ6上。尽管Rova-T出现了超出预期的毒性,但靶向TROP-2(戈沙妥珠单抗)、B7-H3(DS-7300)和SEZ6(ABBV-011)的药物已显示出令人振奋的临床益处。在本综述中,我们收集了最新的临床证据,以描述ADC在SCLC中的治疗效果和安全性,并探讨前景与挑战。