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

被引:0
作者
Conyers, Rachel [1 ,2 ,3 ]
Stenta, Tayla [1 ]
Somogyi, Andrew A. [4 ]
Kirkpatrick, Carl [5 ]
Halman, Andreas [1 ]
Wang, Sophie [1 ,2 ,6 ]
Moore, Claire [1 ,2 ]
Khatri, Dhrita [1 ]
Williams, Elizabeth [1 ]
Dyas, Roxanne [1 ]
Spelman, Tim [7 ,8 ]
Elliott, David A. [1 ,2 ,9 ]
Gwee, Amanda [2 ,10 ,11 ]
Alexander, Marliese [8 ]
机构
[1] Murdoch Childrens Res Inst, Canc Therapies Grp, Parkville, Australia
[2] Univ Melbourne, Dept Paediat, Parkville, Australia
[3] Royal Childrens Hosp, Childrens Canc Ctr, Parkville, Australia
[4] Univ Adelaide, Sch Biomed, Adelaide, Australia
[5] Monash Univ, Fac Pharm & Pharmaceut Sci, Parkville, Australia
[6] Peter MacCallum Canc Ctr, Dept Pharm, Melbourne, Vic, Australia
[7] Peter MacCallum Canc Ctr, Dept Hlth Serv Res, Melbourne, Vic, Australia
[8] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
[9] Novo Nordisk Fdn, Ctr Stem Cell Med, ReNEW, Parkville, Australia
[10] Royal Childrens Hosp, Infect Dis Unit, Parkville, Australia
[11] Murdoch Childrens Res Inst, Antimicrobials Grp, Parkville, Australia
来源
CTS-CLINICAL AND TRANSLATIONAL SCIENCE | 2025年 / 18卷 / 04期
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Australia; oncology; pharmacogenomic implementation; pharmacogenomics; Phenoconversion; GENEVA COCKTAIL; IN-VIVO; CYTOCHROME-P450; DEXTROMETHORPHAN; DISPOSITION; INHIBITION; ENZYMES; URINE;
D O I
10.1111/cts.70209
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 (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.
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页数:13
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