| Literature DB >> 28597939 |
Peter Horak1,2, Barbara Klink3,4, Christoph Heining1,2, Stefan Gröschel1,2,5,6,7, Barbara Hutter8, Martina Fröhlich8, Sebastian Uhrig8, Daniel Hübschmann9,10, Matthias Schlesner9, Roland Eils9,11, Daniela Richter1, Katrin Pfütze1,12, Christina Geörg1,12, Bettina Meißburger1,12, Stephan Wolf13, Angela Schulz13, Roland Penzel14, Esther Herpel14, Martina Kirchner14, Amelie Lier14, Volker Endris14, Stephan Singer14, Peter Schirmacher7,14, Wilko Weichert15,16, Albrecht Stenzinger7,14, Richard F Schlenk17, Evelin Schröck3,4, Benedikt Brors7,8, Christof von Kalle1,2,7,12, Hanno Glimm1,2,7, Stefan Fröhling1,2,7.
Abstract
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.Entities:
Keywords: clinical trial design; next-generation sequencing; personalized medicine; precision oncology; whole-exome sequencing
Mesh:
Year: 2017 PMID: 28597939 DOI: 10.1002/ijc.30828
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396