Patient perspectives on testing for clonal hematopoiesis of indeterminate potential

Author:

Sella Tal123,Fell Geoffrey G.4,Miller Peter G.35ORCID,Gibson Christopher J.13,Rosenberg Shoshana M.6,Snow Craig1,Stover Daniel G.7ORCID,Ruddy Kathryn J.8ORCID,Peppercorn Jeffrey M.39,Schapira Lidia10,Borges Virginia F.11,Come Steven E.312,Warner Ellen13,Frank Elizabeth12,Neuberg Donna S.4,Ebert Benjamin L.1314ORCID,Partridge Ann H.123

Affiliation:

1. 1Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

2. 2Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA

3. 3Harvard Medical School, Harvard University, Boston, MA

4. 4Data Science, Dana-Farber Cancer Institute, Boston, MA

5. 5Center for Cancer Research and Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA

6. 6Department of Population Health Sciences, Weill Cornell Medicine, New York, NY

7. 7Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH

8. 8Department of Oncology, Mayo Clinic, Rochester, MN

9. 9Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA

10. 10Department of Medicine, Stanford University, Stanford, CA

11. 11Division of Medical Oncology, University of Colorado Comprehensive Cancer Center, Aurora, CO

12. 12Division of Oncology, Beth Israel Deaconess Medical Center, Boston, MA

13. 13Division of Medical Oncology, Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

14. 14Howard Hughes Medical Institute, Boston, MA

Abstract

Abstract Clonal hematopoiesis of indeterminate potential (CHIP), an emerging biomarker for personalized risk-directed interventions, is increased in cancer survivors. However, little is known about patient preferences for CHIP testing. We surveyed participants in a prospective cohort study of young women with breast cancer (BC). The emailed survey included an introduction to CHIP and a vignette eliciting participants’ preferences for CHIP testing, considering sequentially: population-based 10-year risk of BC recurrence, hematologic malignancy, and heart disease; increased CHIP-associated risks; current CHIP management; dedicated CHIP clinic; and hypothetical CHIP treatment. Preference changes were evaluated using the McNemar test. The survey response rate was 82.2% (528/642). Median age at time of survey was 46 years and median time from diagnosis was 108 months. Only 5.9% had prior knowledge of CHIP. After vignette presentation, most survivors (87.1%) recommended CHIP testing for the vignette patient. Presented next with CHIP-independent, population-based risks, 11.1% shifted their preference from testing to not testing. After receiving information about CHIP-associated risks, an additional 10.1% shifted their preference to testing. Preference for testing increased if vignette patient was offered a CHIP clinic or hypothetical CHIP treatment, with 7.2% and 14.1% switching preferences toward testing, respectively. Finally, 75.8% of participants desired CHIP testing for themselves. Among participants, 28.2% reported that learning about CHIP caused at least moderate anxiety. Most young survivors favored CHIP testing, with preferences influenced by risk presentation and potential management strategies. Our findings highlight the importance of risk communication and psychosocial support when considering biomarkers for future risk in cancer survivors. This trial has been registered at www.clinicaltrials.gov as #NCT01468246.

Publisher

American Society of Hematology

Subject

Hematology

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