Literature DB >> 29733704

Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?

Kathryn A Phillips1, Patricia A Deverka2, Gillian W Hooker3, Michael P Douglas4.   

Abstract

Genetic testing and spending on that testing have grown rapidly since the mapping of the human genome in 2003. However, it is not widely known how many tests there are, how they are used, and how they are paid for. Little evidence from large data sets about their use has emerged. We shed light on the issue of genetic testing by providing an overview of the testing landscape. We examined test availability and spending for the full spectrum of genetic tests, using unique data sources on test availability and commercial payer spending for privately insured populations, focusing particularly on tests measuring multiple genes in the period 2014-17. We found that there were approximately 75,000 genetic tests on the market, with about ten new tests entering the market daily. Prenatal tests accounted for the highest percentage of spending on genetic tests, and spending on hereditary cancer tests accounted for the second-highest. Our results provide insights for those interested in assessing genetic testing markets, test usage, and health policy implications, including current debates over the most appropriate regulatory and payer coverage mechanisms.

Entities:  

Keywords:  Genetic Testing; Health Economics; Market

Mesh:

Year:  2018        PMID: 29733704      PMCID: PMC5987210          DOI: 10.1377/hlthaff.2017.1427

Source DB:  PubMed          Journal:  Health Aff (Millwood)        ISSN: 0278-2715            Impact factor:   6.301


  11 in total

1.  Use of BRCA Mutation Test in the U.S., 2004-2014.

Authors:  Fangjian Guo; Jacqueline M Hirth; Yu-Li Lin; Gwyn Richardson; Lyuba Levine; Abbey B Berenson; Yong-Fang Kuo
Journal:  Am J Prev Med       Date:  2017-03-22       Impact factor: 5.043

2.  National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.

Authors:  Christopher P Childers; Kimberly K Childers; Melinda Maggard-Gibbons; James Macinko
Journal:  J Clin Oncol       Date:  2017-08-18       Impact factor: 44.544

3.  Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice.

Authors:  Latrice G Landry; Nadya Ali; David R Williams; Heidi L Rehm; Vence L Bonham
Journal:  Health Aff (Millwood)       Date:  2018-05       Impact factor: 6.301

4.  Genomic sequencing: assessing the health care system, policy, and big-data implications.

Authors:  Kathryn A Phillips; Julia R Trosman; Robin K Kelley; Mark J Pletcher; Michael P Douglas; Christine B Weldon
Journal:  Health Aff (Millwood)       Date:  2014-07       Impact factor: 6.301

5.  Growth of molecular diagnostics and genetic testing in the USA, 2008-2011: analysis and implications.

Authors:  Jeanne De Sa; Brantley Carlson; Nadine Caputo; Deneen Vojta; Lewis Sandy; Simon Stevens
Journal:  Per Med       Date:  2013-11       Impact factor: 2.512

6.  Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning?

Authors:  Kathryn A Phillips
Journal:  JAMA       Date:  2018-06-19       Impact factor: 56.272

7.  Utilization of genetic tests: analysis of gene-specific billing in Medicare claims data.

Authors:  Julie A Lynch; Brygida Berse; W David Dotson; Muin J Khoury; Nicole Coomer; John Kautter
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

8.  Creating a data resource: what will it take to build a medical information commons?

Authors:  Patricia A Deverka; Mary A Majumder; Angela G Villanueva; Margaret Anderson; Annette C Bakker; Jessica Bardill; Eric Boerwinkle; Tania Bubela; Barbara J Evans; Nanibaa' A Garrison; Richard A Gibbs; Robert Gentleman; David Glazer; Melissa M Goldstein; Hank Greely; Crane Harris; Bartha M Knoppers; Barbara A Koenig; Isaac S Kohane; Salvatore La Rosa; John Mattison; Christopher J O'Donnell; Arti K Rai; Heidi L Rehm; Laura L Rodriguez; Robert Shelton; Tania Simoncelli; Sharon F Terry; Michael S Watson; John Wilbanks; Robert Cook-Deegan; Amy L McGuire
Journal:  Genome Med       Date:  2017-09-22       Impact factor: 11.117

9.  Payer decision making for next-generation sequencing-based genetic tests: insights from cell-free DNA prenatal screening.

Authors:  Andrew P Dervan; Patricia A Deverka; Julia R Trosman; Christine B Weldon; Michael P Douglas; Kathryn A Phillips
Journal:  Genet Med       Date:  2016-09-22       Impact factor: 8.822

10.  Trends in utilization and costs of BRCA testing among women aged 18-64 years in the United States, 2003-2014.

Authors:  Zhuo Chen; Katherine Kolor; Scott D Grosse; Juan L Rodriguez; Julie A Lynch; Ridgely Fisk Green; W David Dotson; M Scott Bowen; Muin J Khoury
Journal:  Genet Med       Date:  2017-09-21       Impact factor: 8.822

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  38 in total

Review 1.  Precision Medicine: From Science To Value.

Authors:  Geoffrey S Ginsburg; Kathryn A Phillips
Journal:  Health Aff (Millwood)       Date:  2018-05       Impact factor: 6.301

2.  FHIR Lab Reports: using SMART on FHIR and CDS Hooks to increase the clinical utility of pharmacogenomic laboratory test results.

Authors:  Michael Watkins; Karen Eilbeck
Journal:  AMIA Jt Summits Transl Sci Proc       Date:  2020-05-30

3.  Defining and Achieving Health Equity in Genomic Medicine.

Authors:  Sonya Jooma; Michael J Hahn; Lucia A Hindorff; Vence L Bonham
Journal:  Ethn Dis       Date:  2019-02-21       Impact factor: 1.847

4.  A framework for youth-friendly genetic counseling.

Authors:  Mary-Anne Young; Kate Thompson; Jeremy Lewin; Lucy Holland
Journal:  J Community Genet       Date:  2019-11-05

5.  Clinical Genetic Screening in Adult Patients with Kidney Disease.

Authors:  Enrico Cocchi; Jordan Gabriela Nestor; Ali G Gharavi
Journal:  Clin J Am Soc Nephrol       Date:  2020-07-09       Impact factor: 8.237

6.  Ranking evidence in substance use and addiction.

Authors:  Hudson Reddon; Thomas Kerr; M-J Milloy
Journal:  Int J Drug Policy       Date:  2020-07-06

7.  Methods for Moving the Evaluation of Precision Medicine Into Practice and Policy.

Authors:  Kathryn A Phillips
Journal:  Value Health       Date:  2020-04-17       Impact factor: 5.725

Review 8.  Use of Real-World Evidence in US Payer Coverage Decision-Making for Next-Generation Sequencing-Based Tests: Challenges, Opportunities, and Potential Solutions.

Authors:  Patricia A Deverka; Michael P Douglas; Kathryn A Phillips
Journal:  Value Health       Date:  2020-03-26       Impact factor: 5.725

9.  Insights From a Temporal Assessment of Increases in US Private Payer Coverage of Tumor Sequencing From 2015 to 2019.

Authors:  Julia R Trosman; Michael P Douglas; Su-Ying Liang; Christine B Weldon; Allison W Kurian; Robin K Kelley; Kathryn A Phillips
Journal:  Value Health       Date:  2020-03-19       Impact factor: 5.725

Review 10.  Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines.

Authors:  William S Bush; Jessica N Cooke Bailey; Mark F Beno; Dana C Crawford
Journal:  Public Health Genomics       Date:  2019-08-27       Impact factor: 2.000

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