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非WNT/非SHH型髓母细胞瘤靶向临床试验的现状

The Current Landscape of Targeted Clinical Trials in Non-WNT/Non-SHH Medulloblastoma.

作者信息

Ghasemi David R, Fleischhack Gudrun, Milde Till, Pajtler Kristian W

机构信息

Hopp Children's Cancer Center Heidelberg (KiTZ), 69120 Heidelberg, Germany.

Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Consortium for Translational Cancer Research (DKTK), 69120 Heidelberg, Germany.

出版信息

Cancers (Basel). 2022 Jan 28;14(3):679. doi: 10.3390/cancers14030679.

Abstract

Medulloblastoma is an embryonal pediatric brain tumor and can be divided into at least four molecularly defined groups. The category non-WNT/non-SHH medulloblastoma summarizes medulloblastoma groups 3 and 4 and is characterized by considerable genetic and clinical heterogeneity. New therapeutic strategies are needed to increase survival rates and to reduce treatment-related toxicity. We performed a noncomprehensive targeted review of the current clinical trial landscape and literature to summarize innovative treatment options for non-WNT/non-SHH medulloblastoma. A multitude of new drugs is currently evaluated in trials for which non-WNT/non-SHH patients are eligible, for instance immunotherapy, kinase inhibitors, and drugs targeting the epigenome. However, the majority of these trials is not restricted to medulloblastoma and lacks molecular classification. Whereas many new molecular targets have been identified in the last decade, which are currently tested in clinical trials, several challenges remain on the way to reach a new therapeutic strategy for non-WNT/non-SHH medulloblastoma. These include the severe lack of faithful preclinical models and predictive biomarkers, the question on how to stratify patients for clinical trials, and the relative lack of studies that recruit large, homogeneous patient collectives. Innovative trial designs and international collaboration will be a key to eventually overcome these obstacles.

摘要

髓母细胞瘤是一种儿童胚胎性脑肿瘤,可至少分为四个分子定义的组。非WNT/非SHH髓母细胞瘤类别汇总了第3组和第4组髓母细胞瘤,其特征是具有相当大的遗传和临床异质性。需要新的治疗策略来提高生存率并降低治疗相关毒性。我们对当前的临床试验情况和文献进行了非全面的靶向综述,以总结非WNT/非SHH髓母细胞瘤的创新治疗选择。目前有多种新药正在进行试验评估,非WNT/非SHH患者符合条件,例如免疫疗法、激酶抑制剂和靶向表观基因组的药物。然而,这些试验大多数并不局限于髓母细胞瘤,且缺乏分子分类。尽管在过去十年中已经确定了许多新的分子靶点,目前正在临床试验中进行测试,但在为非WNT/非SHH髓母细胞瘤制定新的治疗策略的道路上仍存在一些挑战。这些挑战包括严重缺乏可靠的临床前模型和预测性生物标志物、如何为临床试验对患者进行分层的问题,以及相对缺乏招募大型、同质患者群体的研究。创新的试验设计和国际合作将是最终克服这些障碍的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1c/8833659/f18cc6c29e73/cancers-14-00679-g001.jpg

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