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肉瘤细胞治疗:现状与未来方向

英文原题:Cell therapy in sarcoma: current landscape and future directions.

PubMed 2026/01/12(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

研究概要

肉瘤是起源于间充质的罕见恶性肿瘤,具有显著的生物学与临床异质性。

中文摘要

肉瘤是一类罕见的间充质来源恶性肿瘤,生物学和临床异质性显著。许多亚型对免疫检查点抑制剂等标准全身治疗敏感性有限。细胞疗法已成为有前景策略;例如,靶向滑膜肉瘤癌睾抗原MAGE-A4的基因工程T细胞受体T(TCR-T)疗法显示持久临床应答,并促成afamitresgene autoleucel于2024年获美国FDA批准。这是lifileucel治疗黑色素瘤后第二个获批用于实体瘤的细胞疗法,彰显细胞治疗在肉瘤中的潜力。本综述介绍肉瘤细胞疗法的现状和不断增长的潜力,包括TCR-T、CAR-T(CAR-T)细胞、TIL(肿瘤浸润淋巴细胞)、自然杀伤(NK)细胞和间充质基质细胞。然而,这些疗法的广泛应用受限于缺乏肉瘤特异性、可靶向的免疫原性表位,肿瘤内时空异质性,以及严重免疫抑制性肿瘤微环境;后者阻碍效应细胞归巢、扩增和持久性。细胞疗法有望纳入肉瘤精准医疗,但成功实施需要审慎评估临床可行性、操作流程和成本效益,以优化患者结局。

展开英文摘要原文

Sarcomas are rare malignancies of mesenchymal origin, characterized by significant biological and clinical heterogeneity. Many subtypes demonstrate limited sensitivity to standard systemic treatments, including immune checkpoint inhibitors. Cell therapy has emerged as a promising strategy, with the potential of durable clinical responses seen with genetically-engineered T-cell receptor T-cell therapies (TCR-T) such as those targeting the cancer-testis antigen MAGE-A4 in synovial sarcoma, leading to the US Food and Drug Administration approval of afamitresgene autoleucel in 2024. This constituted only the second approval of a cell therapy in a solid tumor following lifileucel in melanoma and demonstrated the potential of cell therapies in sarcomas. This review provides the current landscape and growing potential of cell therapies in sarcomas, including TCR-T, chimeric antigen receptor-T cells, tumor-infiltrating lymphocytes, natural killer (NK) cells, and mesenchymal stromal cells. However, the broader application of these therapies is hindered by the lack of targetable sarcoma-restricted immunogenic epitopes, spatiotemporal intratumoral heterogeneity, and a profoundly immunosuppressive tumor microenvironment that impedes effector-cell trafficking, expansion and persistence. While cell therapies hold promise for integration into precision medicine approaches for sarcomas, their successful implementation will require careful evaluation of clinical feasibility, logistical considerations and cost-effectiveness to optimize patient outcomes.

论文信息

作者
Sahin TK、Germetaki T、Guven DC、Akin S、Dizdar O、Thistlethwaite F、Connolly EA、Lim KHJ
第一作者单位
Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.Turkey
通讯作者单位
Advanced Immunotherapy and Cell Therapy Team, Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, England, UK jon.lim@manchester.ac.uk.United Kingdom
文献类型
综述
期刊
Journal for immunotherapy of cancer2026 Jan 12
原文标识
PubMed 41526168 · DOI 10.1136/jitc-2025-013396