免疫放化疗联合治疗对肝胆胰肿瘤免疫微环境影响的临床研究。

IF 8.3
Jun-Jie Cheng, Qiu-Yi Zheng, Yi-Lan Huang, Yi-Xing Chen, Shi-Suo Du
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引用次数: 0

摘要

肝胆癌和胰腺癌(hbpc)仍然是最具侵袭性和致命性的恶性肿瘤之一,对其治疗提出了艰巨的挑战。手术切除仍然是早期乙肝病毒携带者根治性治疗的基石;然而,晚期病例往往需要多学科的系统方法,包括放疗和免疫治疗。近年来,放疗技术的创新促进了杀瘤剂量的精确和靶向递送,最大限度地减少了对周围正常组织的损伤,扩大了放疗在治疗HBPCs中的应用。此外,放射治疗对肿瘤免疫微环境(TIME)的复杂影响正日益被了解。放射治疗与免疫治疗的协同作用,在局部和全身范围内诱导强大和持续的抗肿瘤免疫反应,是当前研究的一个有前途和日益重要的途径。本综述首先描述了hbpc中TIME的异质性,并讨论了放疗如何在各种条件下刺激或抑制TIME。它还强调了最近在放射治疗与免疫治疗相结合的临床前和临床进展,这些进展在提高局部控制率和诱导全身抗肿瘤反应方面显示出潜力。这种新兴的模式需要持续的研究,以充分实现其在HBPC管理中的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical aspect of combined immunotherapy and radiotherapy effect on tumor immune microenvironment in hepatobiliary and pancreatic cancers.

Hepatobiliary and pancreatic cancers (HBPCs) remain among the most aggressive nature and lethal malignancies, presenting formidable challenges in their treatment. Surgical resection remains the cornerstone of curative treatment for early-stage HBPCs; however, advanced cases often necessitate a multidisciplinary systematic approach incorporating radiotherapy and immunotherapy. In recent years, innovations in radiotherapy technology have facilitated the precise and targeted delivery of tumoricidal doses, minimizing damage to surrounding normal tissue and expanding the application of radiotherapy in treating HBPCs. Moreover, the intricate impact of radiotherapy on the tumor immune microenvironment (TIME) is being increasingly understood. Synergizing radiotherapy with immunotherapy to induce a robust and sustained antitumor immune response, both locally at the irradiated site and systemically throughout the body, represents a promising and increasingly critical avenue of current research. This review begins by delineating the heterogeneity of the TIME in HBPCs and discusses how radiotherapy can either stimulate or suppress the TIME under various conditions. It also highlights recent preclinical and clinical advances in combining radiotherapy with immunotherapy, which have shown potential in improving local control rates and inducing systemic antitumor responses. This emerging paradigm warrants sustained research to fully realize its therapeutic potential in HBPC management.

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