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作 者:Raffaella Franca Giulia Zudeh Sofia Pagarin Marco Rabusin Marianna Lucafò Gabriele Stocco Giuliana Decorti
机构地区:[1]Department of Medical,Surgical and Health Sciences,University of Trieste,Trieste 34127,Italy [2]PhD Course in Reproductive and Developmental Sciences,University of Trieste,Trieste 34127,Italy [3]Department of Life Sciences,University of Trieste,Trieste 34127,Italy [4]Institute for Maternal and Child Health I.R.C.C.S.Burlo Garofolo,Trieste 34127,Italy [5]Experimental and Clinical Pharmacology Unit,Centro di riferimento oncologico,I.R.C.C.S.,Aviano 33081,Italy.
出 处:《Cancer Drug Resistance》2019年第2期256-270,共15页癌症耐药(英文)
基 金:This project is supported by the Italian Ministry of Health(Progetto Ricerca Corrente 5/2012).
摘 要:Polychemotherapeutic protocols for the treatment of pediatric acute lymphoblastic leukemia(ALL)always include thiopurines.Specific approaches vary in terms of drugs,dosages and combinations.Such therapeutic schemes,including risk-adapted intensity,have been extremely successful for children with ALL who have reached an outstanding 5-year survival of greater than 90%in developed countries.Innovative drugs such as the proteasome inhibitor bortezomib and the bi-specific T cell engager blinatumomab are available to further improve therapeutic outcomes.Nevertheless,daily oral thiopurines remain the backbone maintenance or continuation therapy.Pharmacogenetics allows the personalization of thiopurine therapy in pediatric ALL and clinical guidelines to tailor therapy on the basis of genetic variants in TPMT and NUDT15 genes are already available.Other genes of interest,such as ITPA and PACSIN2,have been implicated in interindividual variability in thiopurines efficacy and adverse effects and need additional research to be implemented in clinical protocols.In this review we will discuss current literature and clinical guidelines available to implement pharmacogenetics for tailoring therapy with thiopurines in pediatric ALL.
关 键 词:THIOPURINES acute lymphoblastic leukemia therapy personalization thiopurine methyltransferase NUDT15 PACSIN2 inosine triphosphate pyrophosphatase pharmacogenetics clinical implementation
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