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NCT00026312 · OUTCOME

Incidence of Toxicities Assessed Using Common Terminology Criteria for Adverse Events Version 4.0

Isotretinoin With or Without Dinutuximab, Aldesleukin, and Sargramostim Following Stem Cell Transplant in Treating Patients With Neuroblastoma · Source last updated 2026-03-05

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

Measure
NUMBER
Unit
Proportion
Interval / dispersion
95% Confidence Interval
Time frame
From enrollment to follow-up

What was measured

Proportion of patients experiencing at least one Grade 3 or higher toxicity.

Analysis population: Eligible patients enrolled prior to halting of randomization.

Groups in this outcome

Regimen A

Randomized to Regimen A - RA Only

Regimen B

Patients that received RA + Immunotherapy before halting of randomization

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

Analysis denominator · Participants

GroupSource count
Regimen A112
Regimen B141

Reported measurements

Source class 1
Values in Proportion · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Regimen A0.64Not reported0.550.73Not reported
Regimen B0.94Not reported0.900.98Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        0.55
        upper Limit
        0.73
        value
        0.64
      2. group Id
        OG001
        lower Limit
        0.90
        upper Limit
        0.98
        value
        0.94
denoms
  1. counts
    1. group Id
      OG000
      value
      112
    2. group Id
      OG001
      value
      141
    units
    Participants
description
Proportion of patients experiencing at least one Grade 3 or higher toxicity.
dispersion Type
95% Confidence Interval
groups
  1. description
    Randomized to Regimen A - RA Only
    id
    OG000
    title
    Regimen A
  2. description
    Patients that received RA + Immunotherapy before halting of randomization
    id
    OG001
    title
    Regimen B
param Type
NUMBER
population Description
Eligible patients enrolled prior to halting of randomization.
reporting Status
POSTED
time Frame
From enrollment to follow-up
title
Incidence of Toxicities Assessed Using Common Terminology Criteria for Adverse Events Version 4.0
type
SECONDARY
unit Of Measure
Proportion

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

Preserved source evidence · Not medical advice