Division of Thoracic Tumor Multimodality Treatment, Cancer Center, and Laboratory of Clinical Cell Therapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Division of Thoracic Tumor Multimodality Treatment, Cancer Center, and Laboratory of Clinical Cell Therapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Department of Radiation Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Cancer Lett. 2023 Jul 1;565:216239. doi: 10.1016/j.canlet.2023.216239. Epub 2023 May 19.
Progress in the treatment of small cell lung cancer (SCLC) has been modest over the past decades until the advent of immune checkpoint inhibitors, which have redefined the standard first-line treatment for extensive-stage SCLC (ES-SCLC). However, despite the positive results of several clinical trials, the limited survival benefit achieved suggests that the priming and sustaining of immunotherapeutic efficacy are poor and further investigation is urgently needed. In this review, we aim to summarize the potential mechanisms underlying the limited efficacy of immunotherapy and intrinsic resistance in ES-SCLC, including impaired antigen presentation and limited T cell infiltration. Moreover, to tackle the current dilemma, given the synergistic effects of radiotherapy on immunotherapy, especially the unique advantages of low-dose radiotherapy (LDRT), such as less immunosuppression and lower radiation toxicity, we propose radiotherapy as a booster to enhance the immunotherapeutic efficacy by overcoming the poor priming effect. Recent clinical trials, including ours, have also focused on adding radiotherapy, including LDRT, to first-line treatment of ES-SCLC. Additionally, we also suggest combination strategies to sustain the immunostimulatory effect of radiotherapy, as well as the cancer-immunity cycle, and further improve survival outcomes.
在过去的几十年中,小细胞肺癌 (SCLC) 的治疗进展一直较为缓慢,直到免疫检查点抑制剂的出现,这重新定义了广泛期小细胞肺癌 (ES-SCLC) 的标准一线治疗。然而,尽管多项临床试验取得了积极的结果,但所获得的有限生存获益表明,免疫治疗的激发和维持效果不佳,迫切需要进一步研究。在这篇综述中,我们旨在总结 ES-SCLC 中免疫治疗和内在耐药性的疗效有限的潜在机制,包括抗原呈递受损和 T 细胞浸润有限。此外,为了解决当前的困境,鉴于放疗对免疫治疗的协同作用,特别是低剂量放疗 (LDRT) 的独特优势,如免疫抑制作用较弱且放射毒性较低,我们提出放疗作为增强剂,通过克服激发作用差的问题来提高免疫治疗效果。最近的临床试验,包括我们的临床试验,也专注于将放疗(包括 LDRT)添加到 ES-SCLC 的一线治疗中。此外,我们还提出了联合策略,以维持放疗的免疫刺激作用以及癌症免疫循环,从而进一步提高生存结果。