Evidence map›Paper›PMID 40259519›Full record

ArticleClinical and translational science2025

Phenoconversion of CYP3A4, CYP2C19 and CYP2D6 in Pediatrics, Adolescents and Young Adults With Lymphoma: Rationale and Design of the PEGASUS Study.

Rachel Conyers, Tayla Stenta, Andrew A Somogyi, Carl Kirkpatrick, Andreas Halman, Sophie Wang, Claire Moore, Dhrita Khatri, Elizabeth Williams, Roxanne Dyas and 4 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06383338 (A Prospective Feasibility Study Investigating PhEnoconversion of CYP3A4, CYP2C19 and CYP2D6 Genotype in Paediatric and Adolescent and Young Adult patientS With an acUte diagnosiS of Hodgkin or Non-Hodgkin Lymphoma.), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT06383338 phase1recruitingnot on this map

A Prospective Feasibility Study Investigating PhEnoconversion of CYP3A4, CYP2C19 and CYP2D6 Genotype in Paediatric and Adolescent and Young Adult patientS With an acUte diagnosiS of Hodgkin or Non-Hodgkin Lymphoma.

TypeinterventionalSponsorMurdoch Childrens Research InstituteRan2025 to 2026Enrolled10ConditionsHodgkin Lymphoma, Non Hodgkin LymphomaArmsOmeprazole, Dextromethorphan
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Rachel ConyersCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0002-2344-1365
Tayla StentaCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0003-4794-030X
Andrew A SomogyiSchool of Biomedicine, University of Adelaide, Adelaide, Australia.ORCID 0000-0003-4779-0380
Carl KirkpatrickFaculty of Pharmacy and Pharmaceutical Sciences, Monash University, Parkville, Australia.ORCID 0000-0002-5715-1534
Andreas HalmanCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0001-5248-4121
Sophie WangCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0009-0000-0169-644X
Claire MooreCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0001-7253-7913
Dhrita KhatriCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0009-0004-3096-6022
Elizabeth WilliamsCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0009-0003-7692-2837
Roxanne DyasCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0009-0005-1826-2257
Tim SpelmanDepartment of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.ORCID 0000-0001-9204-3216
David A ElliottCancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0003-1052-7407
Amanda GweeDepartment of Paediatrics, The University of Melbourne, Parkville, Australia.ORCID 0000-0003-4016-8986
Marliese AlexanderSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0001-5782-7912

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phenoconversion is the discrepancy between genotype-predicted phenotype and clinical phenotype, due to nongenetic factors. In oncology patients, the impact of phenoconversion on drug selection, efficacy, toxicity, and treatment outcomes is unknown. This study will assess acceptability and feasibility of investigating phenoconversion using probe medications in a pediatric and adolescent and young adult (AYA) oncology population. This prospective, single-arm, single-blind, nonrandomized feasibility study, will enroll individuals aged 6-25 years with a new diagnosis of Hodgkin Lymphoma or Non-Hodgkin Lymphoma. Genotyping will be performed at baseline using whole genome sequencing or targeted panel testing. Longitudinal phenotyping will be conducted throughout the cancer treatment using exogenous oral enzyme-specific probes, specifically subtherapeutic dextromethorphan (CYP2D6) and omeprazole (CYP2C19, CYP3A4) for enzyme activity assessment. The primary outcome measure will be the proportion of patients who consent to the study and successfully complete baseline and at least two longitudinal time points with valid probe drug metabolic ratio measurements. Secondary outcomes include classification of clinical phenotypes based on probe drug metabolic ratios, probe drug safety, barriers to consent, acceptability of pharmacogenomic and phenoconversion testing, longitudinal genotype/phenotype concordance, inflammatory profiles, and patient and disease factors influencing phenoconversion. The trial has received ethics approval (2023/ETH1954) and is registered at ClinicalTrials.gov (NCT06383338). Findings will be disseminated through peer-reviewed publications and professional conferences, providing critical insights to advance the understanding of phenoconversion in oncology from pediatrics to adults. These results will help shape future research and drive the implementation of more personalized precision medicine strategies for all people with cancer.

Indexed as

Cytochrome P-450 CYP2C19Cytochrome P-450 CYP2D6Cytochrome P-450 CYP3AHodgkin DiseaseLymphomaAdolescentAdultChildDextromethorphanFeasibility StudiesFemaleGenotypeHumansMaleOmeprazolePhenotypeCYP2C19 protein, humanCYP3A4 protein, humanCytochrome P-450 CYP2C19Cytochrome P-450 CYP2D6Cytochrome P-450 CYP3ADextromethorphanOmeprazoleAustraliaoncologypharmacogenomic implementationpharmacogenomicsPhenoconversion

Identifiers

PMID40259519
PMCPMC12011636

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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.