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小细胞肺癌DLL3靶向治疗的进展:挑战、机遇与未来方向。

Advances in DLL3-targeted therapies for small cell lung cancer: challenges, opportunities, and future directions.

作者信息

Ding Jianhua, Yeong Chaihong

机构信息

Taylor's University, Subang Jaya, Selangor, Malaysia.

出版信息

Front Oncol. 2024 Dec 5;14:1504139. doi: 10.3389/fonc.2024.1504139. eCollection 2024.

Abstract

Small cell lung cancer (SCLC) remains one of the most aggressive and challenging malignancies to treat, with limited therapeutic options and poor outcomes. Recent advances in understanding SCLC biology have identified Delta-like ligand 3 (DLL3) as a promising target for novel therapies. This review explores the evolving landscape of DLL3-targeted therapies in SCLC, examining their mechanistic basis, preclinical promise, and clinical development. We discuss various therapeutic modalities, including antibody-drug conjugates (ADCs), bispecific T-cell engagers (BiTEs), chimeric antigen receptor T-cell (CAR-T) therapies, and emerging approaches such as near-infrared photoimmunotherapy (NIR-PIT) and radiopharmaceutical therapy (RPT). The review highlights the challenges encountered in translating these promising approaches into clinical practice, including the setbacks faced by early DLL3-targeted therapies like Rovalpituzumab Tesirine (Rova-T). We also explore potential strategies to overcome these obstacles, emphasizing the need for a more nuanced understanding of DLL3 biology and its role in SCLC pathogenesis. The integration of cutting-edge technologies and interdisciplinary collaboration is proposed as a path forward to optimize DLL3-targeted therapies and improve outcomes for SCLC patients. This comprehensive overview provides insights into the current state and future directions of DLL3-targeted therapies, underscoring their potential to revolutionize SCLC treatment paradigms.

摘要

小细胞肺癌(SCLC)仍然是最难治疗且最具挑战性的恶性肿瘤之一,治疗选择有限且预后较差。近年来,对SCLC生物学的深入了解已将Delta样配体3(DLL3)确定为新型疗法的一个有前景的靶点。本综述探讨了SCLC中针对DLL3疗法的不断演变的格局,研究了其作用机制、临床前前景和临床开发情况。我们讨论了各种治疗方式,包括抗体药物偶联物(ADCs)、双特异性T细胞衔接器(BiTEs)、嵌合抗原受体T细胞(CAR-T)疗法,以及近红外光免疫疗法(NIR-PIT)和放射性药物疗法(RPT)等新兴方法。该综述强调了将这些有前景的方法转化为临床实践中所遇到的挑战,包括早期针对DLL3的疗法如罗伐单抗替西瑞(Rova-T)所面临的挫折。我们还探讨了克服这些障碍的潜在策略,强调需要更细致地了解DLL3生物学及其在SCLC发病机制中的作用。提出整合前沿技术和跨学科合作是优化针对DLL3疗法并改善SCLC患者预后的前进方向。这一全面概述深入了解了针对DLL3疗法的当前状况和未来方向,突显了它们有可能彻底改变SCLC治疗模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/11655346/07d6eccc36f5/fonc-14-1504139-g001.jpg

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