复发性和难治性尤文氏肉瘤I/II期试验:来自欧洲-尤文氏联盟的当前观点。

IF 5.6 2区 医学 Q1 ONCOLOGY
JCO precision oncology Pub Date : 2025-09-01 Epub Date: 2025-09-19 DOI:10.1200/PO-25-00377
Antonio Juan Ribelles, Arthur Felix, Nuria Benavent, Josep Escrivá-Fernández, Mehdi Brahmi, Nathalie Gaspar, Susanne A Gatz, Thomas Grünewald, Christina Linder-Stragliotto, Emanuela Palmerini, Pan Pantziarka, Sandra Strauss, Didier Surdez, Pablo Berlanga, Martin G McCabe
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引用次数: 0

摘要

目的:对过去11年复发/难治性(R/R)尤文氏肉瘤(EwS)的I/II期临床试验进行最新分析。方法:对2014年至2024年三个数据库(WHO、美国国家医学图书馆和欧洲临床试验数据库)和/或PubMed/ASCO/欧洲肿瘤医学学会网站上发表的R/R EwS的I/II期试验进行系统评价。搜索标准包括EwS或骨肉瘤和i期或ii期。入选资格和数据提取由三名审稿人独立完成,优先考虑具有EwS指定数据的试验。试验按治疗干预进行分类,包括靶向治疗、免疫治疗、化疗和联合治疗。结果:108项试验符合纳入标准,主要是学术(70%)和多中心(81.5%),有重要的美国和欧洲合作。试验设计主要是单组试验,近年来多组试验有所增加,并且越来越关注儿科人群。试验方式强调酪氨酸激酶、多聚adp核糖聚合酶、EWSR1::FLI1和细胞周期抑制剂的靶向治疗。以单克隆抗体和CAR-T细胞为主要药物的免疫治疗也在研究中。在2019冠状病毒病大流行期间,2020年开展的试验数量显著减少。在可评估的数据中,疾病控制率平均为44%,缓解率为8%。结论:本文综述了R/R EwS治疗方向的发展,重点是靶向治疗和免疫治疗。尽管与大流行相关的延迟,但在探索新靶点方面的试验取得了进展,包括EWSR1::FLI1致癌融合和DNA修复途径。这些发现强调了全球正在努力解决EwS治疗中关键的未满足需求,为未来的试验设计提供了基础,特别是在所有年龄段的国际随机ii期试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent and Refractory Ewing Sarcoma Phase I/II Trials: Current Perspective From the Euro-Ewing Consortium.

Purpose: Updated analysis of phase I/II trials in recurrent/refractory (R/R) Ewing sarcoma (EwS) over the past 11 years.

Methods: A systematic review was performed to identify phase I/II trials for R/R EwS in three databases (WHO, US National Library of Medicine, and European Clinical Trials Database) and/or published in PubMed/ASCO/European Society for Medical Oncology websites from 2014 to 2024. The search criteria included EwS OR bone sarcoma OR sarcoma AND Phase-I OR Phase-II. Eligibility and data extraction were performed independently by three reviewers, with priority given to trials with EwS specified data. Trials were categorized by therapeutic intervention, including targeted therapies, immunotherapy, chemotherapy, and combined therapies.

Results: One hundred eight trials met inclusion criteria, predominantly academic (70%) and multicenter (81.5%), with significant US and European collaboration. Trial designs were mainly single-arm, with an increase in multiarm trials in the recent years and increased focus on the pediatric population. Trial modalities emphasized targeted therapies with tyrosine kinase, poly-ADP ribose polymerase, EWSR1::FLI1, and cell cycle inhibitors. Immunotherapy with monoclonal antibodies and CAR-T cells as primary agents is also under investigation. The COVID-19 pandemic coincided with a marked reduction in trial initiation in 2020. Among evaluable data, disease control rates averaged 44% and response rates 8%.

Conclusion: This review highlights evolving therapeutic directions in R/R EwS, with increased emphasis on targeted therapies and immunotherapies. Despite pandemic-related delays, trials have progressed in exploring novel targets, including EWSR1::FLI1 oncogenic fusion and DNA repair pathways. These findings underscore ongoing global efforts to address critical unmet needs in EwS treatment, offering a foundation for future trial designs, especially international, randomized phase-II trials across all age ranges.

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CiteScore
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