Kieran Mark W
Pediatric Medical Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Neuro Oncol. 2014 Aug;16(8):1037-47. doi: 10.1093/neuonc/nou109. Epub 2014 Jun 20.
Novel treatment options, including targeted therapies, are needed for patients with medulloblastoma (MB), especially for those with high-risk or recurrent/relapsed disease. Four major molecular subgroups of MB have been identified, one of which is characterized by activation of the sonic hedgehog (SHH) pathway. Preclinical data suggest that inhibitors of the hedgehog (Hh) pathway could become valuable treatment options for patients with this subgroup of MB. Indeed, agents targeting the positive regulator of the pathway, smoothened (SMO), have demonstrated efficacy in a subset of patients with SHH MB. However, because of resistance and the presence of mutations downstream of SMO, not all patients with SHH MB respond to SMO inhibitors. The development of agents that target these resistance mechanisms and the potential for their combination with traditional chemotherapy and SHH inhibitors will be discussed. Due to its extensive molecular heterogeneity, the future of MB treatment is in personalized therapy, which may lead to improved efficacy and reduced toxicity. This will include the development of clinically available tests that can efficiently discern the SHH subgroup. The preliminary use of these tests in clinical trials is also discussed herein.
髓母细胞瘤(MB)患者需要新的治疗选择,包括靶向治疗,尤其是对于那些患有高危或复发/难治性疾病的患者。已确定MB的四个主要分子亚组,其中一个亚组的特征是音猬因子(SHH)信号通路激活。临床前数据表明,刺猬因子(Hh)信号通路抑制剂可能成为该亚组MB患者有价值的治疗选择。事实上,靶向该信号通路正向调节因子 smoothened(SMO)的药物已在一部分SHH MB患者中显示出疗效。然而,由于耐药性以及SMO下游存在突变,并非所有SHH MB患者都对SMO抑制剂有反应。将讨论针对这些耐药机制的药物研发以及它们与传统化疗和SHH抑制剂联合使用的可能性。由于其广泛的分子异质性,MB治疗的未来在于个性化治疗,这可能会提高疗效并降低毒性。这将包括开发能够有效识别SHH亚组的临床可用检测方法。本文还讨论了这些检测方法在临床试验中的初步应用。