Thompson Eric M, Ashley David, Landi Daniel
Department of Neurosurgery, Duke University, Durham, NC, USA.
Preston Robert Tisch Brain Tumor Center, Duke University, Durham, NC, USA.
Transl Pediatr. 2020 Apr;9(2):157-162. doi: 10.21037/tp.2020.03.03.
Medulloblastoma is a heterogeneous disease with at least four distinct molecular subgroups: wingless (WNT), sonic hedgehog (SHH), Group 3, and Group 4. Recently there has been considerable progress defining the molecular drivers and prognostic factors of each subgroup. However, this information has only rarely been used to stratify risk or impact treatment. The purpose of this work is to provide an update on current clinical trials that provide molecularly stratified treatment paradigms. A search was conducted on ClinicalTrials.gov using the following search terms: "medulloblastoma and subgroup", "medulloblastoma and SHH", "medulloblastoma and WNT", and "medulloblastoma and Non-WNT/Non-SHH". This search resulted in nine distinct clinical trials, five for newly diagnosed medulloblastoma and four for recurrent medulloblastoma. Four trials for newly diagnosed medulloblastoma had a component of craniospinal irradiation reduction for patients with WNT medulloblastoma. Molecularly stratified trials for recurrent medulloblastoma largely focus on SHH. As these trials are ongoing, there are limited data available. A trial in which newly-diagnosed WNT patients received modest chemotherapy without radiation has been closed to accrual due to several early failures. Phase II trials evaluating vismodegib for SHH medulloblastoma in children and adults have been disappointing. In conclusion, although there is an expanding array of clinical trials which incorporate molecular data in prescribing treatment for newly-diagnosed and recurrent medulloblastoma, treatments for these diseases are fairly uniform, with craniospinal radiation dose being the main variable. As the drivers of the distinct subgroups and their associated prognoses are better elucidated, future clinical trials and novel targeted agents are needed to improve outcomes and reduce toxicity where feasible.
髓母细胞瘤是一种异质性疾病,至少有四个不同的分子亚组:无翅型(WNT)、音猬因子(SHH)、3组和4组。最近,在确定每个亚组的分子驱动因素和预后因素方面取得了相当大的进展。然而,这些信息很少被用于风险分层或影响治疗。这项工作的目的是提供有关当前提供分子分层治疗模式的临床试验的最新情况。在ClinicalTrials.gov上使用以下搜索词进行了搜索:“髓母细胞瘤和亚组”、“髓母细胞瘤和SHH”、“髓母细胞瘤和WNT”以及“髓母细胞瘤和非WNT/非SHH”。该搜索产生了九项不同的临床试验,五项针对新诊断的髓母细胞瘤,四项针对复发性髓母细胞瘤。四项针对新诊断的髓母细胞瘤的试验对WNT髓母细胞瘤患者有减少全脑脊髓照射的组成部分。复发性髓母细胞瘤的分子分层试验主要集中在SHH。由于这些试验正在进行中,可用数据有限。一项新诊断的WNT患者接受适度化疗而不进行放疗的试验,由于早期出现几次失败而停止入组。评估维莫德吉用于儿童和成人SHH髓母细胞瘤的II期试验令人失望。总之,尽管有越来越多的临床试验在为新诊断和复发性髓母细胞瘤开处方时纳入了分子数据,但这些疾病的治疗相当统一,全脑脊髓放射剂量是主要变量。随着不同亚组的驱动因素及其相关预后得到更好的阐明,未来需要进行临床试验和新型靶向药物,以在可行的情况下改善治疗效果并降低毒性。