Skip to content
← Full study record

NCT00653068 · OUTCOME

Non-hematological Toxicity Associated With Chemotherapy: Grade 3 or Higher During Protocol Therapy

Combination Chemotherapy, Radiation Therapy, and an Autologous Peripheral Blood Stem Cell Transplant in Treating Young Patients With Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System · Source last updated 2024-04-23

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

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
During protocol therapy up to 1 year after enrollment.

What was measured

Number of Participants with Nonhematological Toxicity Associated With Chemotherapy: Grade 3 or Higher During Protocol Therapy.

Analysis population: 68 eligible patients were evaluable

Groups in this outcome

All Patients

Experimental

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

Analysis denominator · Participants

GroupSource count
All Patients68

Reported measurements

Acidosis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Acute kidney injury
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Apnea
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Adult respiratory distress syndrome
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Aspiration
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients3Not reportedNot reportedNot reportedNot reported
Atelectasis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Catheter related infection
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Central nervous system necrosis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Dehydration
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Diarrhea
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Dissmeminated intravascular coagulation (DIC)
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Enterocolitis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Febrile neutropenia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients6Not reportedNot reportedNot reportedNot reported
Hearing impairment
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Hematuria
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Hydrocephalus
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Hypernatremia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Hypoalbuminemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Hypocalcemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients3Not reportedNot reportedNot reportedNot reported
Hypoglycemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Hypokalemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients9Not reportedNot reportedNot reportedNot reported
Hyponatremia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Hypophosphatemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Hypotension
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients4Not reportedNot reportedNot reportedNot reported
Hypoxia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients6Not reportedNot reportedNot reportedNot reported
Increased Alanine aminotransferase
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients5Not reportedNot reportedNot reportedNot reported
Increased Aspartate aminotransferase
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients4Not reportedNot reportedNot reportedNot reported
Increased Lipase
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Intracranial hemorrhage
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
ntraoperative venous injury
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Laryngospasm
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Left ventricular systolic dysfunction
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Lung infection
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients3Not reportedNot reportedNot reportedNot reported
Multi-organ failure
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Mucositis oral
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients3Not reportedNot reportedNot reportedNot reported
Poisoning and procedural complications
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Other gastrointestinal disorders
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Other infection
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients7Not reportedNot reportedNot reportedNot reported
Pneumonitis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Productive cough
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Pulmonary edema
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Recurrent laryngeal nerve palsy
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Renal calculi
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Respiratory failure
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients3Not reportedNot reportedNot reportedNot reported
Seizure
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Sepsis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients6Not reportedNot reportedNot reportedNot reported
Sinus tachycardia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Stridor
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients2Not reportedNot reportedNot reportedNot reported
Upper respiratory infection
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Vascular access complication
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Voice alteration
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Vomiting
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Weight loss
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
All Patients1Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Acidosis
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Acute kidney injury
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        2
    title
    Apnea
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Adult respiratory distress syndrome
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        3
    title
    Aspiration
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Atelectasis
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        2
    title
    Catheter related infection
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Central nervous system necrosis
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Dehydration
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Diarrhea
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Dissmeminated intravascular coagulation (DIC)
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        1
    title
    Enterocolitis
denoms
  1. counts
    1. group Id
      OG000
      value
      68
    units
    Participants
description
Number of Participants with Nonhematological Toxicity Associated With Chemotherapy: Grade 3 or Higher During Protocol Therapy.
groups
  1. description
    Experimental
    id
    OG000
    title
    All Patients
param Type
COUNT_OF_PARTICIPANTS
population Description
68 eligible patients were evaluable
reporting Status
POSTED
time Frame
During protocol therapy up to 1 year after enrollment.
title
Non-hematological Toxicity Associated With Chemotherapy: Grade 3 or Higher During Protocol Therapy
type
SECONDARY
unit Of Measure
Participants

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

Preserved source evidence · Not medical advice