Effect of NUDT15 on incidence of neutropenia in children with acute lymphoblastic leukemia

Abstract Background 6‐Mercaptopurine (6‐ MP ) is considered the backbone of therapy in the maintenance phase of acute lymphoblastic leukemia ( ALL ). Gene polymorphisms involved in thiopurine degradation are predictors of toxicity in patients treated with 6‐ MP . We investigated the effects of nucleoside diphosphate linked moiety X (nudix) type motif 15 ( NUDT 15 ) polymorphism NUDT 15c.415C>T on neutropenia incidence, dose adjustment for 6‐ MP , and survival rates in Thai children with ALL . Methods Children diagnosed with ALL who received 6‐ MP in the maintenance phase of treatment, in 2005–2016, were retrospectively enrolled. Results The subjects consisted of 102 patients (median age, 5.2 years; 58 boys). On genetic testing 78, 22, and two patients were normal ( CC ), heterozygous ( CT ), and homozygous ( TT ), respectively. The incidence of neutropenia at 3 months was significantly higher in the CT / TT than CC polymorphism groups ( OR , 12; 95% CI : 3.781–38.085, P < 0.001). The mean dose of 6‐ MP at 3, 6, and 12 months was significantly lower in the CT / TT versus the CC group ( P < 0.001). The 5 year overall survival ( OS ) rate for CC was 80.4%, and for CT / TT , 95.5% ( P = 0.34). The 5 year event‐free survival ( EFS ) for CC and CT / TT was 75.1% and 85.7%, respectively ( P = 0.17). After adjusted risk classification, no significant differences were observed for OS or EFS between the CC and CT / TT groups. Conclusion Patients harboring the CT / TT polymorphism of NUDT 15 had a significantly higher incidence of neutropenia during the first 3 months of maintenance, resulting in significantly lower doses of 6‐ MP .