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TIL(肿瘤浸润淋巴细胞)治疗:这一突破性肿瘤治疗方法的临床方面与未来发展

英文原题:Tumor-infiltrating lymphocyte therapy: Clinical aspects and future developments in this breakthrough cancer treatment.

查看英文原题

Tumor-infiltrating lymphocyte therapy: Clinical aspects and future developments in this breakthrough cancer treatment.

PubMed 2023/05/11(内容时间) Bioessays Q1 · IF 3.3(JCR 2025)

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中文摘要

TIL(肿瘤浸润淋巴细胞)疗法是一种利用从癌症组织中采集的自体 TIL 来治疗难治性或晚期实体癌的有前景的方法。尽管癌症具有异质性,TIL 疗法仍有可能产生积极的治疗反应,包括完全缓解。经过数十年对淋巴细胞功能、培养/扩增方法、治疗方案以及多项临床试验的研究,TIL 疗法终于达到了可以正式获批用于临床的阶段。TIL 疗法有望作为标准干预措施,在抗癌治疗选择中占据独特地位。为了成功将 TIL 疗法引入临床环境,需要扩大治疗适应证,并建立癌症组织采样和制备的最佳方案及相关临床试验。此外,关于下一代 TIL 疗法的研究已经开始,获批后的真实世界数据将促进并支持进一步的研究。

展开英文摘要原文

Tumor-infiltrating lymphocyte (TIL) therapy is a promising approach for treating refractory or advanced solid cancers by using autologous TILs harvested from cancer tissues. Despite the heterogeneity of cancer, TIL therapy can potentially produce a positive therapeutic response, including complete remission. After decades of research on lymphocyte functions, culture/expansion methods, therapeutic protocols, and multiple clinical trials, TIL therapy has finally reached a stage where it can be formally approved for clinical use.

TIL therapy is expected to hold a unique position among anti-cancer therapeutic options as a standard intervention. To successfully introduce TIL therapy into clinical settings, there is a need to expand therapeutic indications and set up the best protocols for cancer tissue sampling and manufacturing, and related clinical trials.

Moreover, studies on next-generation TIL therapy have already begun, and post-approval real-world data will promote and support further research.

论文信息

作者
Lee H、Kim K、Chung J、Hossain M、Lee HJ
第一作者单位
Department of Pathology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.South Korea
通讯作者单位
Research and Development Center, NeogenTC corp., Seoul, Republic of Korea.South Korea
期刊
BioEssays : news and reviews in molecular, cellular and developmental biology2023 Jul
原文标识
PubMed 37166068 · DOI 10.1002/bies.202200204