Prados Michael D, Byron Sara A, Tran Nhan L, Phillips Joanna J, Molinaro Annette M, Ligon Keith L, Wen Patrick Y, Kuhn John G, Mellinghoff Ingo K, de Groot John F, Colman Howard, Cloughesy Timothy F, Chang Susan M, Ryken Timothy C, Tembe Waibhav D, Kiefer Jeffrey A, Berens Michael E, Craig David W, Carpten John D, Trent Jeffrey M
University of California San Francisco, San Francisco, California (M.D.P, J.J.P., A.M.M., S.M.C.); Translational Genomics Research Institute, Phoenix, Arizona (S.A.B., N.L.T., W.D.T., J.A.K., M.E.B., D.W.C., J.D.C., J.M.T.); Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts (K.L.L., P.Y.W.); University of Texas Health Science Center, San Antonio, Texas (J.G.K.); Memorial Sloan-Kettering Cancer Center, New York, New York (I.K.M.); The University of Texas M.D. Anderson Cancer Center, Houston, Texas (J.F.d.G.); University of Utah Huntsman Cancer Institute, Salt Lake City, Utah (H.C.); University of California Los Angeles, Los Angeles, California (T.F.C.); Iowa Spine and Brain Institute, Waterloo, Iowa (T.C.R.).
Neuro Oncol. 2015 Aug;17(8):1051-63. doi: 10.1093/neuonc/nov031. Epub 2015 May 1.
Integrated sequencing strategies have provided a broader understanding of the genomic landscape and molecular classifications of multiple cancer types and have identified various therapeutic opportunities across cancer subsets. Despite pivotal advances in the characterization of genomic alterations in glioblastoma, targeted agents have shown minimal efficacy in clinical trials to date, and patient survival remains poor. In this review, we highlight potential reasons why targeting single alterations has yielded limited clinical efficacy in glioblastoma, focusing on issues of tumor heterogeneity and pharmacokinetic failure. We outline strategies to address these challenges in applying precision medicine to glioblastoma and the rationale for applying targeted combination therapy approaches that match genomic alterations with compounds accessible to the central nervous system.
综合测序策略使人们对多种癌症类型的基因组格局和分子分类有了更广泛的了解,并在不同癌症亚群中发现了各种治疗机会。尽管胶质母细胞瘤基因组改变的特征取得了关键进展,但靶向药物在迄今为止的临床试验中显示出的疗效甚微,患者生存率仍然很低。在本综述中,我们强调了针对单一改变在胶质母细胞瘤中临床疗效有限的潜在原因,重点关注肿瘤异质性和药代动力学失败问题。我们概述了在胶质母细胞瘤中应用精准医学应对这些挑战的策略,以及应用将基因组改变与中枢神经系统可及化合物相匹配的靶向联合治疗方法的基本原理。