新诊断高级别胶质瘤成人患者的新辅助临床试验:系统回顾。

Tiffany M Juarez, Jaya M Gill, Boris R Minev, Akanksha Sharma, Santosh Kesari
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引用次数: 0

摘要

背景:高级别胶质瘤是一种毁灭性癌症,标准的手术切除和放化疗仍无法治愈。辐射虽然对肿瘤有益,但会降低淋巴细胞数量,削弱免疫激活,并招募抑制性髓系细胞,损害免疫反应。接受放射治疗的肿瘤环境会经历长期的免疫抑制,从而降低免疫治疗的效果并导致复发。对新诊断患者进行放疗前治疗的调查可以确定活性药物,评估免疫疗法的影响,并在没有辐射引起的混杂因素的情况下进行多组学分析。本文献综述旨在描述针对新诊断高级别胶质瘤成人患者的手术后、放疗前临床试验的可行性、安全性和结果:方法:我们对报道新诊断高级别胶质瘤患者在放疗前接受手术后治疗的临床试验结果的英文文献进行了系统性综述。在PubMed上进行了搜索,同时还考虑了研究和综述文章中引用的参考文献:结果:从 1991 年到 2024 年,共发现了 52 项临床试验:结果:从 1991 年到 2024 年,共发现 52 项临床试验:3 项 I 期、38 项 II 期、4 项 III 期和 7 项未知期。其中9项为随机试验,24项为多中心试验,21项研究了含替莫唑胺的治疗方案,12项主要针对无法手术的肿瘤,共涉及2737名患者:结论:放疗前新辅助治疗研究是可行的,而且可以发现活性药物。结论:放疗前新辅助治疗研究是可行的,而且可以发现有活性的药物。在个性化医疗时代,脑穿刺药物、靶向治疗和免疫肿瘤学的发展尤为重要。在免疫系统和肿瘤微环境保持不变的情况下,对新确诊的高级别胶质瘤进行放疗前治疗研究是快速确定活性和非活性方案的可行方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neoadjuvant clinical trials in adults with newly diagnosed high-grade glioma: A systematic review.

Background: High-grade gliomas are devastating cancers that remain incurable with standard surgical resection and radiochemotherapy. Although beneficial against neoplasms, radiation lowers lymphocyte counts, weakens immune activation, and recruits suppressive myeloid cells impairing immune responses. Tumor environments treated with radiation experience long-term immunosuppression, reducing immunotherapy effectiveness and contributing to recurrence. Investigating pre-radiation treatments in newly diagnosed patients could identify active agents, assess immunotherapy impact, and enable multiomic analyses without radiation-induced confounding factors. This literature review was conducted to describe the feasibility, safety, and outcomes of postsurgical, pre-radiation clinical trials for adults with newly diagnosed high-grade glioma.

Methods: A systematic review was performed of the English-language literature reporting results of clinical trials for adults with newly diagnosed high-grade glioma administered postsurgical treatment prior to radiation therapy. A search was conducted in PubMed and references cited in research and review articles were also considered.

Results: From 1991 to 2024, 52 clinical trials were identified: 3 phase I, 38 phase II, 4 phase III, and 7 of unknown phase. Nine trials were randomized, 24 were multicenter trials, 21 investigated temozolomide-containing regimens, and 12 focused on inoperable tumors, involving a total of 2737 patients.

Conclusion: Pre-radiation neoadjuvant studies are feasible and may identify active drugs. This is particularly relevant in the era of personalized medicine with brain-penetrant drugs, targeted therapy, and immuno-oncology advancements. Investigating pre-radiation treatments in newly diagnosed high-grade glioma is a viable approach to rapidly identify active and inactive regimens while the immune system and tumor microenvironment remain intact.

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