Kathryn Phillips, PhD

Kathryn A. Phillips, PhD

Professor of Health Services Research and Health Economics, Department of Clinical Pharmacy, School of Pharmacy; Director/Founder, Center for Translational and Policy Research on Personalized Medicine (TRANSPERS), UCSF

Cancer Center Program Membership

Cancer Control

[email protected]

Phone: (415) 502-8271 (voice)

Box 0613, UCSF
San Francisco, CA 94143-0613

UCSF Profiles

Research Summary

My research focuses on the value of new technologies, with a specific emphasis on the application of genetics to cancer care and control and other conditions (“precision medicine"). In 2008, I founded the UCSF Center for Translational and Policy Research on Personalized Medicine (TRANSPERS), which focuses on how personalized/precision medicine can most effectively and efficiently be adopted into health care delivery and health policies. I have had continuous funding from the NIH as Principal Investigator for over 25 years and have published over 150 peer-reviewed articles in the leading journals in health policy. A focus is cross-disciplinary/cross-sector research as exemplified by my advisory role to many government and industry organizations.

My work in cancer screening spans almost my entire academic career, with early work on predictors of mammography screening followed by work on colorectal cancer screening. I now work on policy issues relevant to hereditary cancer risk assessment testing and tumor profiling using sequencing technologies (funded by NCI and others). I work closely with the UCSF HDFCCC as a long-time member of the Population Sciences/Cancer Control Program and previously was the designated leader for comparative effectiveness research. I have presented at multiple IOM, NCI, and other meetings focused on cancer and have published in leading cancer journals. My work has been funded by several cancer organizations, including R01s and a Program Project Grant (P01) funded by NCI.

Research Funding

  • July 8, 2021 - April 30, 2026 - BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENING , Principal Investigator . Sponsor: NIH, Sponsor Award ID: R01HG011792
  • July 1, 2018 - June 30, 2021 - Coverage, Price, and Reimbursement for Multigene Tests for Cancer and Related Conditions , Principal Investigator . Sponsor: NIH, Sponsor Award ID: R01CA221870
  • February 15, 2013 - January 31, 2019 - Risk-Benefit Trade-Offs for Whole Genome Sequencing , Principal Investigator . Sponsor: NIH, Sponsor Award ID: R01HG007063
  • September 16, 2008 - August 31, 2013 - Personalized Medicine for Colorectal and Breast Cancer , Principal Investigator . Sponsor: NIH, Sponsor Award ID: P01CA130818

Education

University of Texas, Austin, BA, 1978, Psychology
Kennedy School of Government, Harvard Univ., Cambridge, MA, MPA, 1986, Policy Analysis
University of California, Berkeley, PhD, 1991, Health Services Research
Center for AIDS Prevention Studies, Univ. of CA San Francisco, Postdoc, 1993, Health Services Research

Honors & Awards

  • 1996
    Article published in New England Journal of Medicine contributed to FDA decision to approve the first home collection HIV test
  • 2009
    Grollman Lecture (honorary), University of Maryland School of Pharmacy
  • 2010
    NHGRI Director's Lecture, National Human Genome Research Institute (NHGRI)
  • 2013
    Accelerated Promotion due to sustained productivity, UCSF
  • 2016
    Promotion to Full Professor Step 7 requiring “international prominence” and university review, UCSF
  • 2016
    Rockefeller Center Bellagio Residency Award for Global Scholars, Rockefeller Foundation
  • 2017
    Nominated, National Academy of Medicine
  • 2017
    Honorary Lectureship, Program for Personalized and Genomic Medicine Seminar, University of Maryland
  • 2018
    Honorary Lectureship, Opportunities and Challenges for Moving New Genomic Technologies into Clinical Care and Health Policies, University of British Columbia & BC Cancer Agency
  • 2019, 2020
    Dean’s Apple Award for Outstanding Teaching (multiple), University of California, San Francisco

Selected Publications

  1. Weldon CB, Trosman JR, Liang SY, Douglas MP, Scheuner MT, Kurian A, Schaa KL, Roscow B, Erwin D, Phillips KA. Genetic counselors' experience with reimbursement and patient out-of-pocket cost for multi-cancer gene panel testing for hereditary cancer syndromes. J Genet Couns. 2022 12; 31(6):1394-1403.  View on PubMed
  2. Deverka PA, Douglas MP, Phillips KA. Multicancer Screening Tests: Anticipating And Addressing Considerations For Payer Coverage And Patient Access. Health Aff (Millwood). 2022 03; 41(3):383-389.  View on PubMed
  3. Arias JJ, Lin GA, Tyler AM, Douglas MP, Phillips KA. Geriatricians' Perspectives on the Multiple Dimensions of Utility of Genetic Testing for Alzheimer's Disease: A Qualitative Study. J Alzheimers Dis. 2022; 90(3):1011-1019.  View on PubMed
  4. Phillips KA, Trosman JR, Douglas MP, Gelb BD, Ferket BS, Hindorff LA, Slavotinek AM, Berg JS, Russell HV, Devine B, Greve V, Smith HS. US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER). Genet Med. 2022 01; 24(1):238-244.  View on PubMed
  5. Douglas MP, Lin GA, Trosman JR, Phillips KA. Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants. J Community Genet. 2022 Feb; 13(1):75-80.  View on PubMed
  6. Lin GA, Trosman JR, Douglas MP, Weldon CB, Scheuner MT, Kurian A, Phillips KA. Influence of payer coverage and out-of-pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings. J Genet Couns. 2022 02; 31(1):130-139.  View on PubMed
  7. Scheuner MT, Douglas MP, Sales P, Ackerman SL, Phillips KA. Laboratory business models and practices: implications for availability and access to germline genetic testing. Genet Med. 2021 09; 23(9):1681-1688.  View on PubMed
  8. Phillips KA, Douglas MP, Wordsworth S, Buchanan J, Marshall DA. Availability and funding of clinical genomic sequencing globally. BMJ Glob Health. 2021 02; 6(2).  View on PubMed
  9. Arias JJ, Tyler AM, Douglas MP, Phillips KA. Private payer coverage policies for ApoE-e4 genetic testing. Genet Med. 2021 04; 23(4):614-620.  View on PubMed
  10. Phillips KA, Douglas MP, Marshall DA. Expanding Use of Clinical Genome Sequencing and the Need for More Data on Implementation. JAMA. 2020 11 24; 324(20):2029-2030.  View on PubMed
  11. Douglas MP, Gray SW, Phillips KA. Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019. J Natl Compr Canc Netw. 2020 07; 18(7):866-872.  View on PubMed
  12. Phillips KA. Methods for Moving the Evaluation of Precision Medicine Into Practice and Policy. Value Health. 2020 05; 23(5):527-528.  View on PubMed
  13. Marshall DA, Grazziotin LR, Regier DA, Wordsworth S, Buchanan J, Phillips K, Ijzerman M. Addressing Challenges of Economic Evaluation in Precision Medicine Using Dynamic Simulation Modeling. Value Health. 2020 05; 23(5):566-573.  View on PubMed
  14. Deverka PA, Douglas MP, Phillips KA. Use of Real-World Evidence in US Payer Coverage Decision-Making for Next-Generation Sequencing-Based Tests: Challenges, Opportunities, and Potential Solutions. Value Health. 2020 05; 23(5):540-550.  View on PubMed
  15. Mackay ZP, Dukhovny D, Phillips KA, Beggs AH, Green RC, Parad RB, Christensen KD, BabySeq Project Team. Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing. Value Health. 2020 05; 23(5):559-565.  View on PubMed
  16. Trosman JR, Douglas MP, Liang SY, Weldon CB, Kurian AW, Kelley RK, Phillips KA. Insights From a Temporal Assessment of Increases in US Private Payer Coverage of Tumor Sequencing From 2015 to 2019. Value Health. 2020 05; 23(5):551-558.  View on PubMed
  17. Phillips KA, Marshall DA, Kurian AW. Can precision medicine help achieve the goal of reducing care when the risks exceed the benefits? Per Med. 2019 09; 16(5):365-367.  View on PubMed
  18. Trosman JR, Weldon CB, Slavotinek A, Norton ME, Douglas MP, Phillips KA. Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS). Genet Med. 2020 02; 22(2):283-291.  View on PubMed
  19. Phillips KA, Trosman JR, Douglas MP. Emergence of Hybrid Models of Genetic Testing Beyond Direct-to-Consumer or Traditional Labs. JAMA. 2019 06 25; 321(24):2403-2404.  View on PubMed
  20. Zakinova A, Long-Boyle JR, French D, Croci R, Wilson L, Phillips KA, Kroetz DL, Shin J, Tamraz B. A Practical First Step Using Needs Assessment and a Survey Approach to Implementing a Clinical Pharmacogenomics Consult Service. J Am Coll Clin Pharm. 2019 Jun; 2(3):214-221.  View on PubMed

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