NUDT15 Pharmacogenetics in Acute Lymphoblastic Leukemia: Synthesizing Progress for Personalized Thiopurine Therapy.

IF 4.4 Q1 Medicine
Isfahan Shah Lubis, Kusnandar Anggadiredja, Aluicia Anita Artarini, Nur Melani Sari, Nur Suryawan, Zulfan Zazuli
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引用次数: 0

Abstract

The management of acute lymphoblastic leukemia (ALL), the most common pediatric malignancy, critically relies on thiopurine therapy, such as 6-mercaptopurine (6-MP), during the maintenance phase. However, significant inter-individual response variety and high risk of myelosuppression often disrupt therapy efficacy. Pharmacogenetics offer crucial strategies to personalized therapy. While thiopurine methyltransferase (TPMT) was initially the primary focus, the discovery of nudix hydrolase 15 (NUDT15) appears as a more comprehensive determinant of thiopurine intolerance. This review aims to consolidate and critically evaluate the advancement achieved in unraveling the biological mechanism and clinical significance of NUDT15 pharmacogenetics in thiopurine therapy. Foundational studies showed the vital role of NUDT15 in the detoxification of active thiopurines, with common genetic variants (for instance, p. Arg139Cys) significantly disrupting its activity, leading to the accumulation of toxic metabolites. Observational studies consistently associated NUDT15 variants with severe myelosuppression, notably in Asian populations. Recent randomized controlled trials (RCTs) confirmed that NUDT15 genotype-guided dosing effectively reduces thiopurine-induced toxicity without interfering with the therapeutic outcome. Despite these advancements, challenges remain present, including the incomplete characterization of rare variants, limited data in the diverse Asian populations, and the need for standardized integration with metabolite monitoring. In conclusion, NUDT15 pharmacogenetics is essential for improving patient safety and thiopurine dosage optimization in the treatment of ALL. For thiopurine tailored medicine to be widely and fairly implemented, future research should focus on increasing genetic data across different populations, improving the dose adjustment algorithm, and harmonizing therapeutic guidelines.

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急性淋巴细胞白血病的药物遗传学:个体化硫嘌呤治疗的合成进展。
急性淋巴细胞白血病(ALL)是最常见的儿科恶性肿瘤,其治疗在维持期严重依赖硫嘌呤治疗,如6-巯基嘌呤(6-MP)。然而,显著的个体间反应差异和骨髓抑制的高风险经常破坏治疗效果。药物遗传学为个性化治疗提供了重要的策略。虽然硫嘌呤甲基转移酶(TPMT)最初是主要的焦点,但nudix水解酶15 (NUDT15)的发现似乎是硫嘌呤不耐受的更全面的决定因素。本文旨在巩固和批判性评价在揭示NUDT15药物遗传学在硫嘌呤治疗中的生物学机制和临床意义方面取得的进展。基础研究表明NUDT15在活性硫嘌呤解毒中的重要作用,常见的遗传变异(例如,p. Arg139Cys)显着破坏其活性,导致有毒代谢物的积累。观察性研究一致将NUDT15变异与严重的骨髓抑制联系起来,特别是在亚洲人群中。最近的随机对照试验(rct)证实,NUDT15基因型引导给药可有效降低硫嘌呤诱导的毒性,而不会干扰治疗结果。尽管取得了这些进展,但挑战仍然存在,包括罕见变异的不完整特征,亚洲不同人群的数据有限,以及需要与代谢物监测标准化整合。总之,NUDT15药物遗传学对于提高ALL患者安全性和优化硫嘌呤剂量至关重要。为了使硫嘌呤定制药物得到广泛和公平的实施,未来的研究应侧重于增加不同人群的遗传数据,改进剂量调整算法,并协调治疗指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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0.00%
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