A working group report from the 2024 NCI/GCSC endometrial cancer clinical trials planning meeting: refining the approach to endometrial cancer in the immunotherapy era

Casey M Cosgrove, Dmitriy Zamarin, Jose R Conejo-Garcia, Kari E Hacker, Roberto Vargas, Panagiotis A Konstantinopoulos, Haider S Mahdi, Stephanie Gaillard, Stephanie Markovina, Elise C Kohn, Sarah F Adams
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Abstract

Endometrial cancer (EC) is now the leading cause of gynecologic cancer death in the United States. Recognizing the urgent need to improve outcomes for patients diagnosed with EC, The National Cancer Institute (NCI) Gynecologic Cancer Steering Committee (GCSC) convened a Clinical Trials Planning Meeting (CTPM) on January 8th and 9th 2024, “Refining the Approach to Endometrial Cancer in the Immunotherapy Era.” Multi-disciplinary experts were charged with addressing critical challenges, to optimize treatment of EC in the new immunotherapy landscape. As part of the CTPM working groups were assembled to address several important aspects of clinical trial design. Working Group 1 (WG1) focused on translational science and was tasked with reviewing the scientific literature for data on validated discriminants of response to immunotherapy to inform trial concept development by the therapy-focused groups. The WG established that molecular subtyping of EC is now the standard approach for classifying endometrial tumors. Molecular subtyping for both prognostic and predictive applications should be considered when assessing biomarkers as well as therapeutic targets. Additionally, strategies to improve immune response like incorporation of radiation as well as therapy sequencing considerations should continue to be explored. A major key observation from WG1 was lack of validated discriminants for immunotherapy response beyond mismatch repair status and tumor mutational burden and exploration of additional discriminants of response and resistance will be critical with the increasing use of immunotherapy in EC.
来自2024年NCI/GCSC子宫内膜癌临床试验计划会议的工作组报告:在免疫治疗时代改进子宫内膜癌的方法
子宫内膜癌(EC)现在是美国妇科癌症死亡的主要原因。认识到迫切需要改善诊断为EC的患者的预后,美国国家癌症研究所(NCI)妇科癌症指导委员会(GCSC)于2024年1月8日和9日召开了临床试验计划会议(CTPM),“在免疫治疗时代改进子宫内膜癌的方法”。多学科专家负责解决关键挑战,在新的免疫治疗领域优化EC的治疗。作为CTPM的一部分,工作组被召集来处理临床试验设计的几个重要方面。工作组1 (WG1)侧重于转化科学,其任务是审查科学文献中关于免疫治疗反应的有效鉴别数据,为治疗小组制定试验概念提供信息。工作组确定EC的分子分型现在是子宫内膜肿瘤分类的标准方法。在评估生物标志物和治疗靶点时,应考虑预后和预测应用的分子分型。此外,应继续探索改善免疫反应的策略,如结合放疗以及治疗顺序考虑。WG1的一个主要关键观察结果是,除了错配修复状态和肿瘤突变负担之外,缺乏有效的免疫治疗反应判别因素,随着免疫治疗在EC中的应用越来越多,探索其他反应和耐药性判别因素将是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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