TARGET: A Randomized, Noninferiority Trial of a Pretest, Patient-Driven Genetic Education Webtool Versus Genetic Counseling for Prostate Cancer Germline Testing

Author:

Loeb Stacy1234ORCID,Keith Scott W.5ORCID,Cheng Heather H.67ORCID,Leader Amy E.8ORCID,Gross Laura910,Sanchez Nolasco Tatiana124ORCID,Byrne Nataliya124,Hartman Rebecca5,Brown Lauren H.7,Pieczonka Christopher Michael11ORCID,Gomella Leonard G.12,Kelly William Kevin8ORCID,Lallas Costas D.12,Handley Nathan813ORCID,Mille Patrick Johnston8ORCID,Mark James Ryan12ORCID,Brown Gordon Andrew14,Chopra Sameer14,McClellan Alexandra10ORCID,Wise David R.3ORCID,Hollifield Lucas3,Giri Veda N.915ORCID

Affiliation:

1. Department of Urology, NYU Langone Health, New York, NY

2. Department of Population Health, NYU Langone Health, New York, NY

3. Perlmutter Cancer Center, NYU Langone Health, New York, NY

4. Department of Surgery/Urology, Manhattan Veterans Affairs, New York, NY

5. Division of Biostatistics and Bioinformatics, Department of Pharmacology, Physiology and Cancer Biology, Thomas Jefferson University, Philadelphia, PA

6. Division of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA

7. Fred Hutchinson Cancer Center, Seattle, WA

8. Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA

9. Yale Cancer Center, New Haven, CT

10. Yale New Haven Health, New Haven, CT

11. Associated Medical Professionals of NY, Syracuse, NY

12. Department of Urology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA

13. Department of Integrative Medicine and Nutritional Sciences, Thomas Jefferson University, Philadelphia, PA

14. New Jersey Urology, Summit Health, Voorhees, NJ

15. Department of Medicine, Yale School of Medicine, New Haven, CT

Abstract

PURPOSE Germline genetic testing (GT) is important for prostate cancer (PCA) management, clinical trial eligibility, and hereditary cancer risk. However, GT is underutilized and there is a shortage of genetic counselors. To address these gaps, a patient-driven, pretest genetic education webtool was designed and studied compared with traditional genetic counseling (GC) to inform strategies for expanding access to genetic services. METHODS Technology-enhanced acceleration of germline evaluation for therapy (TARGET) was a multicenter, noninferiority, randomized trial (ClinicalTrials.gov identifier: NCT04447703 ) comparing a nine-module patient-driven genetic education webtool versus pretest GC. Participants completed surveys measuring decisional conflict, satisfaction, and attitudes toward GT at baseline, after pretest education/counseling, and after GT result disclosure. The primary end point was noninferiority in reducing decisional conflict between webtool and GC using the validated Decisional Conflict Scale. Mixed-effects regression modeling was used to compare decisional conflict between groups. Participants opting for GT received a 51-gene panel, with results delivered to participants and their providers. RESULTS The analytic data set includes primary outcome data from 315 participants (GC [n = 162] and webtool [n = 153]). Mean difference in decisional conflict score changes between groups was –0.04 (one-sided 95% CI, –∞ to 2.54; P = .01), suggesting the patient-driven webtool was noninferior to GC. Overall, 145 (89.5%) GC and 120 (78.4%) in the webtool arm underwent GT, with pathogenic variants in 15.8% (8.7% in PCA genes). Satisfaction did not differ significantly between arms; knowledge of cancer genetics was higher but attitudes toward GT were less favorable in the webtool arm. CONCLUSION The results of the TARGET study support the use of patient-driven digital webtools for expanding access to pretest genetic education for PCA GT. Further studies to optimize patient experience and evaluate them in diverse patient populations are warranted.

Publisher

American Society of Clinical Oncology (ASCO)

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