Evidence map›Paper›PMID 40579854›Full record

Trial reportClinical pharmacology and therapeutics2025

Impact of First-of-Its-Kind Patient-Facing Pharmacogenetics Tool on Dosing Decisions and Treatment Outcomes.

Youngwoo Cho, Sami Elahi, Matthew M Jack, John Campbell, Emily Smith, Randall W Knoebel, David George, Larry House, Kiang-Teck J Yeo, Theodore Karrison and 6 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04541381 (The PhOCus Trial), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04541381 nasuspendednot on this map

The PhOCus Trial: Implementation of Pharmacogenomic Testing in Oncology Care

TypeinterventionalSponsorUniversity of ChicagoRan2022 to 2028Enrolled860ConditionsGastrointestinal Cancer, Head and Neck Cancer, Dihydropyrimidine Dehydrogenase Deficiency, UGT1A1 Gene MutationArmsAvailability of clinical decision support based on pharmacogenomic results.
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Youngwoo ChoCommittee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, Illinois, USA.
Sami ElahiCenter for Personalized Therapeutics, University of Chicago, Chicago, Illinois, USA.ORCID 0009-0008-8890-6523
Matthew M JackCenter for Personalized Therapeutics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0003-1248-8851
John CampbellCenter for Personalized Therapeutics, University of Chicago, Chicago, Illinois, USA.ORCID 0009-0004-2102-1932
Emily SmithCenter for Personalized Therapeutics, University of Chicago, Chicago, Illinois, USA.
Randall W KnoebelCenter for Personalized Therapeutics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-0166-4955
David GeorgeDepartment of Pathology, University of Chicago Medical Center and Biological Sciences, Chicago, Illinois, USA.
Larry HouseDepartment of Pathology, University of Chicago Medical Center and Biological Sciences, Chicago, Illinois, USA.ORCID 0000-0003-2066-9855
Kiang-Teck J YeoCommittee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-4708-8420
Theodore KarrisonDepartment of Public Health Sciences, University of Chicago, Chicago, Illinois, USA.
Samuel L VolchenboumCenter for Research Informatics, University of Chicago, Chicago, Illinois, USA.
David O MeltzerDepartment of Medicine, University of Chicago Medical Center and Biological Sciences, Chicago, Illinois, USA.
Russell Z SzmulewitzCommittee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, Illinois, USA.
Everett E VokesDepartment of Medicine, University of Chicago Medical Center and Biological Sciences, Chicago, Illinois, USA.
Mark J RatainCommittee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-0938-4392
Peter H O'DonnellCommittee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0003-2650-0049

Funding

CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
Pharmacogenomics to Catalyze Decision Support in Oncology CareR01HG012273 · NHGRI · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell · 2023 to 2026
$3.5M
NHGRI NIH HHS R01 HG012273NIGMS NIH HHS T32 GM007019
6 · The paper itself

Abstract

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.

Indexed as

NeoplasmsPatient PortalsPharmacogeneticsAdultAgedFemaleHumansMaleMiddle AgedPatient ParticipationPharmacogenomic TestingPrecision MedicineProspective StudiesTreatment Outcome

Identifiers

PMID40579854
PMCPMC12439013

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.