Survey-based perspectives and reported barriers to DPYD testing among U.S. oncologists
7 affiliations
- 1Department of Health Outcomes and Biomedical Informatics, University of Florida
- 2Department of Biostatistics, University of Florida
- 3Departments of Pathology and Translational Pathology, Moffitt Cancer Center
- 4MedStar Health
- 5Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, University of Florida
- 6Department of Laboratory Medicine and Pathology, University of Minnesota
- 7Division of Translational Medicine and Human Genetics, University of Pennsylvania Perelman School of Medicine
Abstract
Background: Patients with cancer with deleterious DPYD variants are at significantly increased risk for severe toxicity with standard fluoropyrimidine doses. Prior to recent guidelines recommending it, the uptake of pre-treatment DPYD testing in the United States has been low. We aimed to explore oncologists’ perceptions and barriers to DPYD testing adoption on a national level.
Materials and methods: Survey invitations were sent to U.S. oncologists listed in the American Medical Association (AMA) Masterfile in April and May 2025. The surveys assessed physician knowledge, attitudes, and perceptions of DPYD testing in clinics caring for patients with cancer in the United States. Descriptive statistics were used to evaluate survey responses.
Results: Of 5,525 physicians invited to participate, 47 oncologists completed the survey (response rate: 0.85%). The majority (85%) indicated that DPYD testing could help them manage patients; however, only 34% reported routinely performing DPYD testing. Most physicians (77%) agreed that adequate resources were available to order DPYD testing. When directly asked, 36% indicated that limited laboratory access was a barrier. In open-ended responses, respondents identified insurance reimbursement concerns (21%) and prolonged turnaround time (19%) as additional barriers. Forty-three percent reported needing assistance interpreting results and applying them to drug selection and dosing. Webinars (25.5%) and self-paced online modules (21%) were the most preferred educational modalities.
Conclusion: Most respondents indicated that DPYD testing could help manage patients, yet concerns persist. While regulatory guidance is evolving, these preliminary findings from a small sample highlight the need for future research to characterize implementation barriers and inform policy development.
Implications for practice: Our findings highlight gaps in implementation that can inform targeted strategies to improve the integration of DPYD testing into oncology practice, with the potential to enhance patient safety and reduce fluoropyrimidine-related toxicity.
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BibTeX
@article{tohme2026surveybased,
title = {{Survey-based perspectives and reported barriers to DPYD testing among U.S. oncologists}},
author = {Sara Tohme and Ramzi G. Salloum and Jacqueline De La Cruz and Qing Lu and Kejin Dong and J. Kevin Hicks and D. Max Smith and David DeRemer and Pawel Mroz and Sony Tuteja and Larisa H. Cavallari},
journal = {Frontiers in Oncology},
year = {2026},
month = oct,
doi = {10.3389/fonc.2026.1903512},
url = {https://www.frontiersin.org/articles/10.3389/fonc.2026.1903512/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Survey-based perspectives and reported barriers to DPYD testing among U.S. oncologists
AU - Sara Tohme
AU - Ramzi G. Salloum
AU - Jacqueline De La Cruz
AU - Qing Lu
AU - Kejin Dong
AU - J. Kevin Hicks
AU - D. Max Smith
AU - David DeRemer
AU - Pawel Mroz
AU - Sony Tuteja
AU - Larisa H. Cavallari
PY - 2026
DA - 2026/10/13
JO - Frontiers in Oncology
DO - 10.3389/fonc.2026.1903512
UR - https://www.frontiersin.org/articles/10.3389/fonc.2026.1903512/full
AB - Background: Patients with cancer with deleterious DPYD variants are at significantly increased risk for severe toxicity with standard fluoropyrimidine doses. Prior to recent guidelines recommending it, the uptake of pre-treatment DPYD testing in the United States has been low. We aimed to explore oncologists’ perceptions and barriers to DPYD testing adoption on a national level. Materials and methods: Survey invitations were sent to U.S. oncologists listed in the American Medical Association (AMA) Masterfile in April and May 2025. The surveys assessed physician knowledge, attitudes, and perceptions of DPYD testing in clinics caring for patients with cancer in the United States. Descriptive statistics were used to evaluate survey responses. Results: Of 5,525 physicians invited to participate, 47 oncologists completed the survey (response rate: 0.85%). The majority (85%) indicated that DPYD testing could help them manage patients; however, only 34% reported routinely performing DPYD testing. Most physicians (77%) agreed that adequate resources were available to order DPYD testing. When directly asked, 36% indicated that limited laboratory access was a barrier. In open-ended responses, respondents identified insurance reimbursement concerns (21%) and prolonged turnaround time (19%) as additional barriers. Forty-three percent reported needing assistance interpreting results and applying them to drug selection and dosing. Webinars (25.5%) and self-paced online modules (21%) were the most preferred educational modalities. Conclusion: Most respondents indicated that DPYD testing could help manage patients, yet concerns persist. While regulatory guidance is evolving, these preliminary findings from a small sample highlight the need for future research to characterize implementation barriers and inform policy development. Implications for practice: Our findings highlight gaps in implementation that can inform targeted strategies to improve the integration of DPYD testing into oncology practice, with the potential to enhance patient safety and reduce fluoropyrimidine-related toxicity.
SN - 2234-943X
ER -