Literature DB >> 29045504

Molecular Tumor Boards: current practice and future needs.

D L van der Velden1, C M L van Herpen2, H W M van Laarhoven3, E F Smit4, H J M Groen5, S M Willems6, P M Nederlof7, M H G Langenberg8, E Cuppen9, S Sleijfer10, N Steeghs11, E E Voest1.   

Abstract

BACKGROUND: Due to rapid technical advances, steeply declining sequencing costs, and the ever-increasing number of targeted therapies, it can be expected that extensive tumor sequencing such as whole-exome and whole-genome sequencing will soon be applied in standard care. Clinicians will thus be confronted with increasingly complex genetic information and multiple test-platforms to choose from. General medical training, meanwhile, can hardly keep up with the pace of innovation. Consequently, there is a rapidly growing gap between clinical knowledge and genetic potential in cancer care. Multidisciplinary Molecular Tumor Boards (MTBs) have been suggested as a means to address this disparity, but shared experiences are scarce in literature and no quality requirements or guidelines have been published to date.
METHODS: Based on literature review, a survey among hospitals in The Netherlands, and our own experience with the establishment of a nationally operating MTB, this article evaluates current knowledge and unmet needs and lays out a strategy for successful MTB implementation.
RESULTS: Having access to an MTB can improve and increase the application of genetics-guided cancer care. In our survey, however, <50% of hospitals and only 5% of nonacademic hospitals had access to an MTB. In addition, current MTBs vary widely in terms of composition, tasks, tools, and workflow. This may not only lead to variation in quality of care but also hinders data sharing and thus creation of an effective learning community.
CONCLUSIONS: This article acknowledges a leading role for MTBs to govern (extensive) tumor sequencing into daily practice and proposes three basic necessities for successful MTB implementation: (i) global harmonization in cancer sequencing practices and procedures, (ii) minimal member and operational requirements, and (iii) an appropriate unsolicited findings policy. Meeting these prerequisites would not only optimize MTB functioning but also improve general interpretation and application of genomics-guided cancer care.
© The Author 2017. Published by Oxford University Press on behalf of the European Society for Medical Oncology. [br]All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Molecular Tumor Board; genetics-guided cancer care; targeted therapy; whole-genome sequencing (WGS)

Mesh:

Year:  2017        PMID: 29045504     DOI: 10.1093/annonc/mdx528

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  43 in total

1.  Clinical Impact of Plasma and Tissue Next-Generation Sequencing in Advanced Non-Small Cell Lung Cancer: A Real-World Experience.

Authors:  Laura Bonanno; Alberto Pavan; Alessandra Ferro; Lorenzo Calvetti; Stefano Frega; Giulia Pasello; Giuseppe Aprile; Valentina Guarneri; PierFranco Conte
Journal:  Oncologist       Date:  2020-07-07

Review 2.  Tumor mutational burden in non-small cell lung cancer-the pathologist's point of view.

Authors:  Frédérique Penault-Llorca; Nina Radosevic-Robin
Journal:  Transl Lung Cancer Res       Date:  2018-12

3.  From Somatic Variants Toward Precision Oncology: An Investigation of Reporting Practice for Next-Generation Sequencing-Based Circulating Tumor DNA Analysis.

Authors:  Rongxue Peng; Rui Zhang; Martin P Horan; Li Zhou; Sze Yee Chai; Nalishia Pillay; Kwang Hong Tay; Tony Badrick; Jinming Li
Journal:  Oncologist       Date:  2019-08-30

4.  From Somatic Variants Toward Precision Oncology: An Investigation of Reporting Practice for Next-Generation Sequencing-Based Circulating Tumor DNA Analysis.

Authors:  Rongxue Peng; Rui Zhang; Martin P Horan; Li Zhou; Sze Yee Chai; Nalishia Pillay; Kwang Hong Tay; Tony Badrick; Jinming Li
Journal:  Oncologist       Date:  2019-08-30

5.  A Canadian guideline on the use of next-generation sequencing in oncology.

Authors:  S Yip; A Christofides; S Banerji; M R Downes; I Izevbaye; B Lo; A MacMillan; J McCuaig; T Stockley; G M Yousef; A Spatz
Journal:  Curr Oncol       Date:  2019-04-01       Impact factor: 3.677

6.  Healthcare professionals' perspectives on implementation of universal tumor DNA testing in ovarian cancer patients: multidisciplinary focus groups.

Authors:  Margreet G E M Ausems; Joanne A de Hullu; Vera M Witjes; Jozé C C Braspenning; Nicoline Hoogerbrugge; Yvonne H C M Smolders; Dorien M A Hermkens; Marian J E Mourits; Marjolijn J L Ligtenberg
Journal:  Fam Cancer       Date:  2022-05-16       Impact factor: 2.375

Review 7.  Genetic Predisposition to Myelodysplastic Syndrome in Clinical Practice.

Authors:  Kristen E Schratz; Amy E DeZern
Journal:  Hematol Oncol Clin North Am       Date:  2020-01-06       Impact factor: 3.722

8.  Assessing the utility and attitudes toward molecular testing in neuro-oncology: a survey of the Society for Neuro-Oncology members.

Authors:  Shannon Fortin Ensign; Maya Hrachova; Susan Chang; Maciej M Mrugala
Journal:  Neurooncol Pract       Date:  2021-02-17

9.  Criteria-based curation of a therapy-focused compendium to support treatment recommendations in precision oncology.

Authors:  Frank P Lin; Subotheni Thavaneswaran; John P Grady; Mandy Ballinger; Maya Kansara; Samantha R Oakes; Jayesh Desai; Chee Khoon Lee; John Simes; David M Thomas
Journal:  NPJ Precis Oncol       Date:  2021-06-23

10.  Postgraduate training in Cancer Genetics-a cross-specialty survey exploring experience of clinicians in Ireland.

Authors:  Jana K McHugh; Gozie Offiah; Sean Daly; Nazmy El Beltagi; Michael Kevin Barry; Seamus O'Reilly; Terri P McVeigh
Journal:  Ir J Med Sci       Date:  2021-06-30       Impact factor: 2.089

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