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淋巴瘤患儿、青少年及青年中CYP3A4、CYP2C19和CYP2D6的表型转换:PEGASUS研究的原理与设计

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

作者信息

Conyers Rachel, Stenta Tayla, Somogyi Andrew A, Kirkpatrick Carl, Halman Andreas, Wang Sophie, Moore Claire, Khatri Dhrita, Williams Elizabeth, Dyas Roxanne, Spelman Tim, Elliott David A, Gwee Amanda, Alexander Marliese

机构信息

Cancer Therapies Group, Murdoch Children's Research Institute, Parkville, Australia.

Department of Paediatrics, The University of Melbourne, Parkville, Australia.

出版信息

Clin Transl Sci. 2025 Apr;18(4):e70209. doi: 10.1111/cts.70209.

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.

摘要

表型转换是指由于非遗传因素导致的基因型预测表型与临床表型之间的差异。在肿瘤患者中,表型转换对药物选择、疗效、毒性和治疗结果的影响尚不清楚。本研究将评估在儿科、青少年和青年成人(AYA)肿瘤患者群体中使用探针药物研究表型转换的可接受性和可行性。这项前瞻性、单臂、单盲、非随机的可行性研究将纳入6至25岁新诊断为霍奇金淋巴瘤或非霍奇金淋巴瘤的个体。在基线时将使用全基因组测序或靶向基因检测进行基因分型。在整个癌症治疗过程中,将使用外源性口服酶特异性探针进行纵向表型分析,具体为使用亚治疗剂量的右美沙芬(CYP2D6)和奥美拉唑(CYP2C19、CYP3A4)评估酶活性。主要结局指标将是同意参与研究并成功完成基线以及至少两个纵向时间点且有有效探针药物代谢率测量值的患者比例。次要结局包括基于探针药物代谢率的临床表型分类、探针药物安全性、同意参与的障碍、药物基因组学和表型转换检测的可接受性、纵向基因型/表型一致性、炎症谱以及影响表型转换的患者和疾病因素。该试验已获得伦理批准(2023/ETH1954),并在ClinicalTrials.gov上注册(NCT06383338)。研究结果将通过同行评审出版物和专业会议进行传播,为增进从儿科到成人肿瘤学中表型转换的理解提供关键见解。这些结果将有助于塑造未来的研究,并推动为所有癌症患者实施更个性化的精准医学策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6928/12011636/1b68f8991b79/CTS-18-e70209-g001.jpg

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