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腹膜癌病腹腔内免疫治疗:当前治疗选择与展望

英文原题:Peritoneal carcinomatosis with intraperitoneal immunotherapy: current treatment options and perspectives.

查看英文原题

Peritoneal carcinomatosis with intraperitoneal immunotherapy: current treatment options and perspectives.

PubMed 2022/09/19(内容时间) Expert Rev Gastroenterol Hepatol Q2 · IF 3.3(JCR 2025)

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中文摘要

引言:腹膜癌病(PC)是一种晚期恶性肿瘤,对常规全身化疗不敏感。PC治疗通常以姑息为主,而非根治。细胞减灭术和腹腔热灌注化疗的疗效有限。不过,腹膜可通过募集并促进T淋巴细胞增殖形成有效免疫;腹膜独特的免疫环境为PC腹腔内免疫治疗提供了理论依据。综述范围:作者从PubMed和Medline检索PC腹腔内免疫治疗相关文献,介绍腹膜免疫微环境和腹腔内免疫治疗的相关知识,涵盖免疫刺激剂、放射免疫治疗、catumaxomab、癌症疫苗、嵌合抗原受体(CAR)T细胞和免疫检查点抑制剂。专家观点:PC预后较差,但腹腔是一个独特的免疫区室,富含能够产生有效免疫应答的免疫细胞。腹腔内免疫治疗可能成为PC患者一种有前景的治疗策略。

展开英文摘要原文

INTRODUCTION: Peritoneal carcinomatosis (PC) is an advanced malignancy that is not sensitive to systemic conventional chemotherapy. Treatment options for PC are usually palliative rather than curative. Cytoreductive surgery and hyperthermic intraperitoneal (IP) chemotherapy are associated with limited efficacy in patients with PC.

However, the peritoneum can produce effective immunity by inducing T-lymphocyte recruitment and proliferation, and the unique immune environment of the peritoneum provides the rationale for IP immunotherapy in PC. AREAS COVERED: The authors retrieved relevant documents of IP immunotherapy for PC from PubMed and Medline.

This review elaborates on the knowledge of the peritoneal immune microenvironment and IP immunotherapy for PC covering immune stimulators, radioimmunotherapy, catumaxomab, cancer vaccines, chimeric antigen receptor (CAR)-T cells, and immune checkpoint inhibitors. EXPERT OPINION: The prognosis of PC is poor.

However, the peritoneal cavity is a unique immune compartment with abundant immune cells which can produce effective immunity. IP immunotherapy may be a promising strategy in patients with PC.

论文信息

作者
Wei GX、Du Y、Zhou YW、Li LJ、Qiu M
单位
Department of Colorectal Cancer Center, West China Hospital of Sichuan University, Chengdu, China.China
文献类型
综述
期刊
Expert review of gastroenterology & hepatology2022 Sep
原文标识
PubMed 36107723 · DOI 10.1080/17474124.2022.2125866