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NCT00602667 · OUTCOME

Erlotinib Apparent Volume of Central Compartment

Risk-Adapted Therapy for Young Children With Embryonal Brain Tumors, Choroid Plexus Carcinoma, High Grade Glioma or Ependymoma · Source last updated 2026-05-19

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEDIAN
Unit
L/m^2
Interval / dispersion
Full Range
Time frame
Pre-dose, 1, 2, 4, 8, and 24 hours post-dose

What was measured

Erlotinib plasma concentration-time data are collected on day 1 of maintenance cycle B2. Individual estimates of erlotinib apparent volume of central compartment are obtained using post hoc analysis.

Analysis population: Eligible patients who received oral erlotinib during maintenance therapy cycle B2 and had samples collected for PK analysis.

Groups in this outcome

Low-Risk Group

Patients with gross total resection (GTR)/no evidence of metastatic disease (M0) medulloblastoma, nodular desmoplastic histology, or high grade glioma

Intermediate-Risk Group

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

High-Risk Group

Patients with central nervous system (CNS) metastatic disease

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Low-Risk Group10
Intermediate-Risk Group11
High-Risk Group3

Reported measurements

Source class 1
Values in L/m^2 · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
Low-Risk Group72.9Not reported39.5233.7Not reported
Intermediate-Risk Group61.7Not reported41.3119.0Not reported
High-Risk Group104.8Not reported47.6109.9Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        39.5
        upper Limit
        233.7
        value
        72.9
      2. group Id
        OG001
        lower Limit
        41.3
        upper Limit
        119.0
        value
        61.7
      3. group Id
        OG002
        lower Limit
        47.6
        upper Limit
        109.9
        value
        104.8
denoms
  1. counts
    1. group Id
      OG000
      value
      10
    2. group Id
      OG001
      value
      11
    3. group Id
      OG002
      value
      3
    units
    Participants
description
Erlotinib plasma concentration-time data are collected on day 1 of maintenance cycle B2. Individual estimates of erlotinib apparent volume of central compartment are obtained using post hoc analysis.
dispersion Type
Full Range
groups
  1. 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
  2. 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
  3. description
    Patients with central nervous system (CNS) metastatic disease
    id
    OG002
    title
    High-Risk Group
param Type
MEDIAN
population Description
Eligible patients who received oral erlotinib during maintenance therapy cycle B2 and had samples collected for PK analysis.
reporting Status
POSTED
time Frame
Pre-dose, 1, 2, 4, 8, and 24 hours post-dose
title
Erlotinib Apparent Volume of Central Compartment
type
SECONDARY
unit Of Measure
L/m^2

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice