Impact of First‐of‐Its‐Kind Patient‐Facing Pharmacogenetics Tool on Dosing Decisions and Treatment Outcomes
Germline pharmacogenetics (PGx) is increasingly used to tailor medication selection/dosing. However, existing systems primarily communicate PGx results to providers, limiting direct patient engagement. To address this, we developed YourPGx Oncology, an innovative patient-facing portal that delivers multi-gene PGx results (CYP2D6, UGT1A1, DPYD) through 33 unique, patient-friendly summaries. The utility of this tool was prospectively evaluated in an oncology population, where these pharmacogenes impact high-stakes treatments. Patients enrolled in the PhOCus study (NCT04541381) participated in single-session evaluations of the tool in-person or via videoconference, with a pharmacist available for questions and administering pre- and post-surveys that assessed educational impact. Each patient viewed their own previously obtained PGx results. Of 190 eligible patients, 70 responded to solicitations via email, phone, and in-person, of whom 51 (73%) completed an observed session and completed surveys. Patients spent a median of 13.4 minutes (range 8.1-21.0) navigating YourPGx Oncology. After portal interaction, patients' ability to identify individual efficacy and safety estimates for chemotherapies and pain medications significantly improved, with the proportion accurately recognizing PGx-informed drug efficacy likelihoods rising from 32% to 72% (Odds Ratio [OR] = 5.8 for the shift from discordant to concordant efficacy knowledge, P < 0.001), and PGx-related toxicity recognition increasing from 31% to 57% (OR = 3.2, P = 0.01). Our findings show that a customized patient-facing PGx results portal enhances patient understanding of individual medication efficacy and toxicity likelihoods, highlighting the potential key role of direct-to-patient PGx tools to facilitate optimized treatment-informed care and promote genetically guided shared decision-making.
Authors
- Kiang-Teck J Yeo (ORCID: https://orcid.org/0000-0002-4708-8420)
- Peter H. O’Donnell (ORCID: https://orcid.org/0000-0003-2650-0049)
- Samuel L. Volchenboum (ORCID: https://orcid.org/0000-0001-9863-851X)
- Theodore Karrison
- John Campbell
- David O. Meltzer (ORCID: https://orcid.org/0000-0003-2790-7393)
- Matthew Jack (ORCID: https://orcid.org/0000-0003-1248-8851)
- Larry House (ORCID: https://orcid.org/0000-0003-2066-9855)
- Everett E. Vokes (ORCID: https://orcid.org/0000-0002-8645-8068)
- Randall W. Knoebel (ORCID: https://orcid.org/0000-0002-0166-4955)
- Mark J. Ratain (ORCID: https://orcid.org/0000-0002-0938-4392)
- Russell Z. Szmulewitz (ORCID: https://orcid.org/0000-0002-1444-3617)
- Emily Smith (ORCID: https://orcid.org/0000-0002-1916-0843)
- Youngwoo Cho (ORCID: https://orcid.org/0000-0002-1902-0381)
- David L. George
- Sami Elahi
Institutions
- Chicago Department of Public Health (US)
- University of Chicago (US)
- University of Chicago Medical Center (US)
Publication Details
- Journal
- Clinical Pharmacology & Therapeutics
- Published
- 2025-06-27
- DOI
- https://doi.org/10.1002/cpt.3747
- Primary Topic
- Pharmacogenetics and Drug Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institutes of Health