{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"0.26","upperLimit":"3.12","value":"0.64"},{"groupId":"OG001","lowerLimit":"0.22","upperLimit":"3.22","value":"0.64"},{"groupId":"OG002","lowerLimit":"0.20","upperLimit":"1.79","value":"0.55"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"34"},{"groupId":"OG001","value":"80"},{"groupId":"OG002","value":"34"}],"units":"Participants"}],"description":"Methotrexate plasma concentration-time data are collected after the start of methotrexate infusion in induction cycle 4. Population parameters and inter-subject variability are estimated. Individual estimates of methotrexate concentration at 42 hours post-dose are obtained using post hoc analysis.","dispersionType":"Full Range","groups":[{"description":"Patients with gross total resection (GTR)/no evidence of metastatic disease (M0) medulloblastoma, nodular desmoplastic histology, or high grade glioma","id":"OG000","title":"Low-Risk Group"},{"description":"Patients with no evidence of metastatic disease (M0) medulloblastoma or nodular desmoplastic histology with less than a gross total resection (GTR), other histologic diagnoses with no metastatic disease","id":"OG001","title":"Intermediate-Risk Group"},{"description":"Patients with central nervous system (CNS) metastatic disease","id":"OG002","title":"High-Risk Group"}],"paramType":"MEDIAN","populationDescription":"Eligible patients who received methotrexate during induction cycle 4 and had samples collected for PK analysis.","reportingStatus":"POSTED","timeFrame":"42 hours from start of MTX","title":"Methotrexate Concentration at 42 Hours Post-dose in Induction Cycle 4","type":"SECONDARY","unitOfMeasure":"µmol/L"}