<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(3)</volume><submitter>Ghasemi DR</submitter><pubmed_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 n</pubmed_abstract><journal>Cancers</journal><pagination>679</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8833659</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Current Landscape of Targeted Clinical Trials in Non-WNT/Non-SHH Medulloblastoma.</pubmed_title><pmcid>PMC8833659</pmcid><pubmed_authors>Fleischhack G</pubmed_authors><pubmed_authors>Pajtler KW</pubmed_authors><pubmed_authors>Ghasemi DR</pubmed_authors><pubmed_authors>Milde T</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Current Landscape of Targeted Clinical Trials in Non-WNT/Non-SHH Medulloblastoma.</name><description>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 n</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-04T07:55:05.949Z</modification><creation>2025-02-19T05:04:43.922Z</creation></dates><accession>S-EPMC8833659</accession><cross_references><pubmed>35158947</pubmed><doi>10.3390/cancers14030679</doi></cross_references></HashMap>