Determinants of Mercaptopurine Toxicity in Paediatric Acute Lymphoblastic Leukemia Maintenance Therapy
- Registration Number
- NCT03920813
- Lead Sponsor
- Shandong University
- Brief Summary
The present study was conducted to assess the population pharmacokinetics of 6-mercaptopurine (6-MP) in Pediatric Acute Lymphoblastic Leukemia (ALL) and genetic polymorphisms
- Detailed Description
The investigators' purpose was to identify genetic factors and metabolite concentrations associated with both hematological toxicity in patients with ALL maintained on 6-MP in Chinese.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 500
- Patients have been diagnosed with Acute Lymphoblastic Leukemia
- Childhood patients who were undergoing chemotherapy or continuous follow-up after completion of chemotherapy
- Patients received the phase of maintenance therapy that included oral 6-MP (>4 weeks) and completion of ≥ 6 months according to the CCLG (Chinese Children's Leukemia Group) protocol-ALL 2015
- Patients with high-risk ALL (presence of higher-risk features: MRD ≥ 1% at 46 day, or age < 6 month and white blood cell (WBC) count ≥ 300×109/L with translocations t(9;22) (q34;q11) [BCR-ABL], t(4;11) (q21;q23) [AF4/MLL], t(1;19) (q23;p13) [E2A-PBX1] or other MLL-rearrangements) were removed
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Antitumor drugs Mercaptopurine Mercaptopurine administered at standard dose for children with hematological neoplasms.
- Primary Outcome Measures
Name Time Method Red blood cells (RBC) concentration of 6-mercaptopurine (6-MP) at second day after oral administration To detect of RBC 6-MP metabolite concentrations and evaluate the association of metabolite concentrations and side effects
Genetic polymorphisms in Chinese patients with ALL at second day after oral administration To detect the frequencies of genetic polymorphisms of Chinese patients receiving 6-MP for treatment of ALL
- Secondary Outcome Measures
Name Time Method