Precision oncology based on omics data: the NCT Heidelberg experience

Gespeichert in:

Veröffentlicht in:	International journal of cancer 141(2017), 5, Seite 877-886
Personen und Körperschaften:	Horak, Peter (VerfasserIn), Heining, Christoph (VerfasserIn), Gröschel, Stefan (VerfasserIn), Hutter, Barbara (VerfasserIn), Fröhlich, Martina (VerfasserIn), Hübschmann, Daniel (VerfasserIn), Schlesner, Matthias (VerfasserIn), Eils, Roland (VerfasserIn), Richter, Daniela (VerfasserIn), Pfütze, Katrin (VerfasserIn), Geörg, Christina (VerfasserIn), Meissburger, Bettina (VerfasserIn), Wolf, Stephan (VerfasserIn), Penzel, Roland (VerfasserIn), Herpel, Esther (VerfasserIn), Kirchner, Martina (VerfasserIn), Lier, Amelie (VerfasserIn), Endris, Volker (VerfasserIn), Singer, Stephan (VerfasserIn), Schirmacher, Peter (VerfasserIn), Stenzinger, Albrecht (VerfasserIn), Schlenk, Richard Friedrich (VerfasserIn), Brors, Benedikt (VerfasserIn), Kalle, Christof von (VerfasserIn), Glimm, Hanno (VerfasserIn), Fröhling, Stefan (VerfasserIn)
Titel:	Precision oncology based on omics data: the NCT Heidelberg experience/ Peter Horak, Barbara Klink, Christoph Heining, Stefan Gröschel, Barbara Hutter, Martina Fröhlich, Sebastian Uhrig, Daniel Hübschmann, Matthias Schlesner, Roland Eils, Daniela Richter, Katrin Pfütze, Christina Geörg, Bettina Meißburger, Stephan Wolf, Angela Schulz, Roland Penzel, Esther Herpel, Martina Kirchner, Amelie Lier, Volker Endris, Stephan Singer, Peter Schirmacher, Wilko Weichert, Albrecht Stenzinger, Richard F. Schlenk, Evelin Schröck, Benedikt Brors, Christof von Kalle, Hanno Glimm, Stefan Fröhling
Format:	E-Book-Kapitel
Sprache:	Englisch
veröffentlicht:	09 June 2017
Gesamtaufnahme:	: International journal of cancer, 141(2017), 5, Seite 877-886 , volume:141
Schlagwörter:	clinical trial design next-generation sequencing personalized medicine precision oncology whole-exome sequencing
Quelle:	Verbunddaten SWB Lizenzfreie Online-Ressourcen

Details
Zusammenfassung:	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.
Beschreibung:	Gesehen am 04.09.2018
Umfang:	10
ISSN:	1097-0215
DOI:	10.1002/ijc.30828