Molecular Therapies Research Unit, Vall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Barcelona, Spain; Universitat Autònoma de Barcelona, Barcelona, Spain.
Oncologist. 2013;18(11):1180-8. doi: 10.1634/theoncologist.2013-0135. Epub 2013 Oct 17.
Advances in diagnostics and targeted therapies during the past decade have changed how oncology is viewed. "Stratified medicine" has emerged from the accumulated evidence garnered from matching targeted therapies with tumor molecular aberrations. Concomitantly, current knowledge derived from large-scale, massively parallel sequencing technologies and global research initiatives such as the international 1000 Genomes Project, the Cancer Genome Atlas, the International Cancer Genome Consortium, and publicly available catalogs such as the Catalogue of Somatic Mutations in Cancer and Genomics of Drug Sensitivity in Cancer have illuminated the utility of understanding the molecular basis of cancer through genome analysis. In addition, multiple collaborative efforts are widening the possibility of universally personalizing cancer care. Although several key challenges of personalized cancer medicine (PCM) need to be addressed, some pilot studies are transforming the way we analyze tumor tissue molecular aberrations, design clinical trials, and measure treatment efficacy. Taken together, these pilot studies are paving the way for clinical trials that are designed to empirically test the concept of PCM. In this paper, we describe lessons learned from the first pilot initiatives of PCM and how this knowledge is being used to design novel clinical trials.
在过去的十年中,诊断和靶向治疗的进展改变了人们对肿瘤学的看法。“分层医学”是从将靶向治疗与肿瘤分子异常相匹配的累积证据中发展而来的。同时,当前从大规模平行测序技术和全球研究计划(如国际 1000 基因组计划、癌症基因组图谱、国际癌症基因组联盟以及公开可用的目录,如癌症体细胞突变目录和癌症药物敏感性基因组学)中获得的知识阐明了通过基因组分析了解癌症分子基础的实用性。此外,多项合作努力拓宽了普遍实现癌症个体化治疗的可能性。尽管个性化癌症医学(PCM)仍存在几个关键挑战需要解决,但一些试点研究正在改变我们分析肿瘤组织分子异常、设计临床试验和衡量治疗效果的方式。总之,这些试点研究正在为旨在实证检验 PCM 概念的临床试验铺平道路。在本文中,我们描述了从 PCM 的第一个试点计划中吸取的经验教训,以及如何利用这些知识来设计新的临床试验。