Chawla Sant P, Pang Skyler S, Jain Darshit, Jeffrey Samantha, Chawla Neal S, Song Paul Y, Hall Frederick L, Gordon Erlinda M
Sarcoma Oncology Center/Cancer Center of Southern California, Santa Monica, CA 90403, USA.
Aveni Foundation, Santa Monica, CA 90403, USA.
Cancers (Basel). 2025 Mar 27;17(7):1125. doi: 10.3390/cancers17071125.
: The heterogeneity of sarcomas and resulting distinct sub-type specific characteristics, their high recurrence rates, and tendency for distant metastasis, continue to present significant challenges to providing optimal treatments. : To provide a comprehensive review of current literature and clinical trials in gene and cell therapies for sarcomas. : A comprehensive literature search was conducted utilizing the following databases: PubMed, Medline, Google Scholar and clinicaltrials.gov. Search terms included "gene therapy", "cell therapy", "NK cell therapy, "CAR-T therapy", "virotherapy", "sarcoma", "gene therapy", and "solid tumors". Additional sources were identified through manual searching for references of relevant studies. No language restrictions were set. The NCT number, study status, condition, and phase were noted for clinical trials. : There are only three gene and cell therapies for sarcomas that have been approved by a federal regulatory agency. Rexin-G: the first tumor-targeted gene therapy vector designed to target all advanced solid malignancies, including chemo-refractory osteosarcomas and soft tissue sarcomas, was approved by the Philippine FDA in 2007. Gendicine was the first oncolytic virus approved for intratumoral delivery in China in 2003. Afami-cel, an innovative chimeric antigen receptor (CAR) T cell therapy, was approved for synovial sarcoma in the United States in 2024. Other promising therapies are discussed in the text. : The future of gene and cell therapy for sarcomas holds great promise, as research moves to late-stage clinical development. The integration of gene and cell therapies into standard sarcoma treatment protocols has the potential to significantly improve the quality of life and outcomes for patients with this rare and challenging group of cancers.
肉瘤的异质性以及由此产生的不同亚型的特定特征、高复发率和远处转移倾向,继续给提供最佳治疗带来重大挑战。
为全面综述肉瘤基因和细胞治疗的当前文献及临床试验。
PubMed、Medline、谷歌学术和clinicaltrials.gov。检索词包括“基因治疗”“细胞治疗”“自然杀伤细胞治疗”“嵌合抗原受体T细胞疗法”“病毒疗法”“肉瘤”“基因治疗”和“实体瘤”。通过手动搜索相关研究的参考文献确定了其他来源。未设置语言限制。记录了临床试验的NCT编号、研究状态、疾病和阶段。
目前只有三种用于肉瘤的基因和细胞疗法已获得联邦监管机构的批准。Rexin - G:首个旨在靶向所有晚期实体恶性肿瘤(包括化疗难治性骨肉瘤和软组织肉瘤)的肿瘤靶向基因治疗载体,于2007年获得菲律宾食品药品监督管理局批准。2003年,中国首个批准用于瘤内注射的溶瘤病毒安柯瑞。2024年,创新嵌合抗原受体(CAR)T细胞疗法afami - cel在美国被批准用于滑膜肉瘤。文中还讨论了其他有前景的疗法。
随着研究进入后期临床开发阶段,肉瘤基因和细胞治疗的未来前景广阔。将基因和细胞疗法整合到标准肉瘤治疗方案中,有可能显著提高这类罕见且具有挑战性的癌症患者的生活质量和治疗效果。