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Barriers to clinical adoption of nextgeneration sequencing: A policy Delphi panel's solutions

  • Donna A. Messner
  • , Pei Koay
  • , Jennifer Al Naber
  • , Robert Cook-Deegan
  • , Mary Majumder
  • , Gail Javitt
  • , Rachel Dvoskin
  • , Juli Bollinger
  • , Margaret Curnutte
  • , Amy L. McGuire

Research output: Contribution to journalArticlepeer-review

Abstract

Aim: Identify solutions to the most important policy barriers to the clinical adoption of next-generation sequencing. Materials & methods: Four-round modified policy Delphi with a multistakeholder panel of 48 experts. The panel deliberated policy solutions to (previously reported) challenges deemed most important to address. Results: The group advocated using consensus panels to promote consistency in payer policies and to standardize test reporting, and favored making genomic data-sharing a condition of regulatory clearance, certification, or accreditation processes. They were split on the role of US FDA. Conclusion: Panelists found common ground on solutions for health plan coverage policy consistency, data-sharing, and standardizing reporting, but were sharply divided on the role of the FDA in mitigating risks to patients.

Original languageEnglish (US)
Pages (from-to)339-354
Number of pages16
JournalPersonalized Medicine
Volume14
Issue number4
DOIs
StatePublished - Jul 2017

Keywords

  • Clinical data reporting
  • Clinical genomics
  • Coverage and reimbursement
  • Intellectual property
  • Next-generation sequencing
  • Personalized medicine
  • Policy
  • Regulation

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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