Association of NUDT15 *3 and FPGS 2572C>T Variants with the Risk of Early Hematologic Toxicity During 6-MP and Low-Dose Methotrexate-Based Maintenance Therapy in Indian Patients with Acute Lymphoblastic Leukemia.

Genetic variants influencing the pharmacokinetics and/or pharmacodynamics of the chemotherapeutic drugs used in Acute Lymphoblastic Leukemia (ALL) therapy often contribute to the occurrence of treatment related toxicity (TRT). In this study, we explored the association of candidate genetic variants with early hematological TRT (grade 3-4) occurring within the first 100 days of low-dose methotrexate and 6-mercaptopurine based maintenance therapy (n= 73). Fourteen variants in the following candidate genes were genotyped using allele discrimination assay by real-time PCR:ABCB1,DHFR,GGH,FPGS,MTHFR,RFC1,SLCO1B1,TPMT, andNUDT15. Methotrexate polyglutamate (MTXPG3-5) levels in red blood cells were measured by LC-MS/MS. Early hematological TRT (grade 3-4) was seen in 54.9% of patients. TheNUDT15c.415T allele was associated with early TRT occurrence [HR: 3.04 (95% CI: 1.5-6.1);p= 0.007]. Sensitivity of early TRT prediction improved (from 30.7% to 89.7%) by consideringFPGSvariant (rs1544105'T') carrier status along withNUDT15c.415T allele [HR = 2.7 (1.5-4.7,p= 0.008)]. None of the considered genetic variants were associated with MTXPG3-5 levels, which in turn were not associated with early TRT.NUDT15c.415T allele carrier status could be used as a stratifying marker for Indian ALL patients to distinguish patients at high or low risk of developing early hematological TRT.