Horak Peter, Klink Barbara, Heining Christoph, Gröschel Stefan, Hutter Barbara, Fröhlich Martina, Uhrig Sebastian, Hübschmann Daniel, Schlesner Matthias, Eils Roland, Richter Daniela, Pfütze Katrin, Geörg Christina, Meißburger Bettina, Wolf Stephan, Schulz Angela, Penzel Roland, Herpel Esther, Kirchner Martina, Lier Amelie, Endris Volker, Singer Stephan, Schirmacher Peter, Weichert Wilko, Stenzinger Albrecht, Schlenk Richard F, Schröck Evelin, Brors Benedikt, von Kalle Christof, Glimm Hanno, Fröhling Stefan
Department of Translational Oncology, National Center for Tumor Diseases (NCT) Heidelberg, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Section for Personalized Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Int J Cancer. 2017 Sep 1;141(5):877-886. doi: 10.1002/ijc.30828. Epub 2017 Jun 21.
Precision oncology implies the ability to predict which patients will likely respond to specific cancer therapies based on increasingly accurate, high-resolution molecular diagnostics as well as the functional and mechanistic understanding of individual tumors. While molecular stratification of patients can be achieved through different means, a promising approach is next-generation sequencing of tumor DNA and RNA, which can reveal genomic alterations that have immediate clinical implications. Furthermore, certain genetic alterations are shared across multiple histologic entities, raising the fundamental question of whether tumors should be treated by molecular profile and not tissue of origin. We here describe MASTER (Molecularly Aided Stratification for Tumor Eradication Research), a clinically applicable platform for prospective, biology-driven stratification of younger adults with advanced-stage cancer across all histologies and patients with rare tumors. We illustrate how a standardized workflow for selection and consenting of patients, sample processing, whole-exome/genome and RNA sequencing, bioinformatic analysis, rigorous validation of potentially actionable findings, and data evaluation by a dedicated molecular tumor board enables categorization of patients into different intervention baskets and formulation of evidence-based recommendations for clinical management. Critical next steps will be to increase the number of patients that can be offered comprehensive molecular analysis through collaborations and partnering, to explore ways in which additional technologies can aid in patient stratification and individualization of treatment, to stimulate clinically guided exploratory research projects, and to gradually move away from assessing the therapeutic activity of targeted interventions on a case-by-case basis toward controlled clinical trials of genomics-guided treatments.
精准肿瘤学意味着能够基于日益精确的高分辨率分子诊断以及对个体肿瘤的功能和机制理解,预测哪些患者可能对特定的癌症治疗产生反应。虽然可以通过不同方式实现患者的分子分层,但一种很有前景的方法是对肿瘤DNA和RNA进行下一代测序,这可以揭示具有直接临床意义的基因组改变。此外,某些基因改变在多个组织学实体中都有出现,这就引出了一个基本问题,即肿瘤是否应该根据分子特征而非起源组织来进行治疗。我们在此描述MASTER(用于肿瘤根除研究的分子辅助分层),这是一个临床适用的平台,用于对所有组织学类型的晚期癌症年轻成人患者和罕见肿瘤患者进行前瞻性、生物学驱动的分层。我们阐述了一个标准化的工作流程,该流程包括患者的选择和同意、样本处理、全外显子组/基因组和RNA测序、生物信息学分析、对潜在可采取行动的发现进行严格验证,以及由专门的分子肿瘤委员会进行数据评估,从而能够将患者分类到不同的干预类别中,并为临床管理制定基于证据的建议。关键的下一步将是通过合作与伙伴关系增加能够接受全面分子分析的患者数量,探索其他技术可以帮助患者分层和治疗个体化的方式,推动临床指导的探索性研究项目,并逐步从逐案评估靶向干预的治疗活性转向基因组学指导治疗的对照临床试验。