Literature DB >> 28597939

Precision oncology based on omics data: The NCT Heidelberg experience.

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.
© 2017 UICC.

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


  40 in total

Review 1.  Taking Systems Medicine to Heart.

Authors:  Kalliopi Trachana; Rhishikesh Bargaje; Gustavo Glusman; Nathan D Price; Sui Huang; Leroy E Hood
Journal:  Circ Res       Date:  2018-04-27       Impact factor: 17.367

Review 2.  Clinical applications of (epi)genetics in gastroenteropancreatic neuroendocrine neoplasms: Moving towards liquid biopsies.

Authors:  Gitta Boons; Timon Vandamme; Marc Peeters; Guy Van Camp; Ken Op de Beeck
Journal:  Rev Endocr Metab Disord       Date:  2019-09       Impact factor: 6.514

Review 3.  Histopathological, immunohistochemical, genetic and molecular markers of neuroendocrine neoplasms.

Authors:  Georgios Kyriakopoulos; Vasiliki Mavroeidi; Eleftherios Chatzellis; Gregory A Kaltsas; Krystallenia I Alexandraki
Journal:  Ann Transl Med       Date:  2018-06

4.  Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors.

Authors:  Michael W Ronellenfitsch; Patrick N Harter; Martina Kirchner; Christoph Heining; Barbara Hutter; Laura Gieldon; Jens Schittenhelm; Martin U Schuhmann; Marcos Tatagiba; Gerhard Marquardt; Marlies Wagner; Volker Endris; Christian H Brandts; Victor-Felix Mautner; Evelin Schröck; Wilko Weichert; Benedikt Brors; Andreas von Deimling; Michel Mittelbronn; Joachim P Steinbach; David E Reuss; Hanno Glimm; Albrecht Stenzinger; Stefan Fröhling
Journal:  J Clin Invest       Date:  2020-05-01       Impact factor: 14.808

5.  Identification and characterization of a BRAF fusion oncoprotein with retained autoinhibitory domains.

Authors:  Hanno Glimm; Stefan Fröhling; Tilman Brummer; Florian Weinberg; Ricarda Griffin; Martina Fröhlich; Christoph Heining; Sandra Braun; Corinna Spohr; Mary Iconomou; Viola Hollek; Michael Röring; Peter Horak; Simon Kreutzfeldt; Gregor Warsow; Barbara Hutter; Sebastian Uhrig; Olaf Neumann; David Reuss; Dieter Henrik Heiland; Christof von Kalle; Wilko Weichert; Albrecht Stenzinger; Benedikt Brors
Journal:  Oncogene       Date:  2019-09-26       Impact factor: 9.867

Review 6.  [Personalized oncology].

Authors:  C Heining; P Horak; S Gröschel; H Glimm; S Fröhling
Journal:  Radiologe       Date:  2017-10       Impact factor: 0.635

7.  Response to Cabozantinib Following Acquired Entrectinib Resistance in a Patient With ETV6-NTRK3 Fusion-Positive Carcinoma Harboring the NTRK3 G623R Solvent-Front Mutation.

Authors:  Dorothea Hanf; Christoph Heining; Karin Laaber; Heiner Nebelung; Sebastian Uhrig; Barbara Hutter; Arne Jahn; Daniela Richter; Daniela Aust; Friederike Herbst; Stefan Fröhling; Hanno Glimm; Gunnar Folprecht
Journal:  JCO Precis Oncol       Date:  2021-04-22

8.  Knowledge bases and software support for variant interpretation in precision oncology.

Authors:  Florian Borchert; Andreas Mock; Aurelie Tomczak; Jonas Hügel; Samer Alkarkoukly; Alexander Knurr; Anna-Lena Volckmar; Albrecht Stenzinger; Peter Schirmacher; Jürgen Debus; Dirk Jäger; Thomas Longerich; Stefan Fröhling; Roland Eils; Nina Bougatf; Ulrich Sax; Matthieu-P Schapranow
Journal:  Brief Bioinform       Date:  2021-11-05       Impact factor: 11.622

9.  Deconvolution of sarcoma methylomes reveals varying degrees of immune cell infiltrates with association to genomic aberrations.

Authors:  Malte Simon; Sadaf S Mughal; Peter Horak; Sebastian Uhrig; Jonas Buchloh; Bogac Aybey; Albrecht Stenzinger; Hanno Glimm; Stefan Fröhling; Benedikt Brors; Charles D Imbusch
Journal:  J Transl Med       Date:  2021-05-12       Impact factor: 8.440

10.  EGFR and PI3K Pathway Activities Might Guide Drug Repurposing in HPV-Negative Head and Neck Cancers.

Authors:  Andreas Mock; Michaela Plath; Julius Moratin; Maria Johanna Tapken; Dirk Jäger; Jürgen Krauss; Stefan Fröhling; Jochen Hess; Karim Zaoui
Journal:  Front Oncol       Date:  2021-06-11       Impact factor: 6.244

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