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Trial · NCT00066469

Cyclophosphamide, Rituximab, and Either Prednisone or Methylprednisolone in Treating Patients With Lymphoproliferative Disease After Solid Organ Transplantation

NCT00066469, Phase 2, Completed, Children's Oncology Group; results first posted 2014-01-17

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Cyclophosphamide, Rituximab, and Either Prednisone or Methylprednisolone in Treating Patients With Lymphoproliferative Disease After Solid Organ Transplantation. Trials, record NCT00066469. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00066469

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Cyclophosphamide, Rituximab, and Either Prednisone or Methylprednisolone in Treating Patients With Lymphoproliferative Disease After Solid Organ Transplantation
NCT number
NCT00066469
Status
Completed
Phases
Phase 2
Enrollment
55 participants, actual
Lead sponsor
Children's Oncology Group
Conditions
Lymphoproliferative Disorder
Interventions
rituximab, cyclophosphamide, methylprednisolone, prednisone
First posted
2003-08-07
Last updated
2019-08-06
Results first posted
2014-01-17

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEvent-free Survival2 yearsAlive in continuous complete remission with functioning original allograft. The Event Free Survival (EFS) will be estimated by the Kaplan-Meier method.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEvent-free Survival2 yearsOne patient out of the 55 patients enrolled was ineligible for study and therefore was excluded from analysis.percentage of participants analyzedNUMBER

Results by group1

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Event-free SurvivalCyclophosphamide, Prednisone, Rituximab7195% Confidence Interval 57 to 82percentage of participants analyzed

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCyclophosphamide, Prednisone, Rituximab55
Overall StudyCOMPLETEDCyclophosphamide, Prednisone, Rituximab39
Overall StudyNOT COMPLETEDCyclophosphamide, Prednisone, Rituximab16

Adverse events69

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnemiaBlood and lymphatic system disordersCyclophosphamide, Prednisone, Rituximab3543
otherBlood and lymphatic system disorders - Other, specifyBlood and lymphatic system disordersCyclophosphamide, Prednisone, Rituximab1541
otherFebrile neutropeniaBlood and lymphatic system disordersCyclophosphamide, Prednisone, Rituximab125412
otherSinus tachycardiaCardiac disordersCyclophosphamide, Prednisone, Rituximab1541
otherAbdominal distensionGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab1541
otherAbdominal painGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab2542
otherGastrointestinal disorders - Other, specifyGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab1541
otherLower gastrointestinal hemorrhageGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab1541
otherMucositis oralGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab1541
otherNauseaGastrointestinal disordersCyclophosphamide, Prednisone, Rituximab1541

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCyclophosphamide, Prednisone, Rituximab
Total, other adverse eventsCyclophosphamide, Prednisone, Rituximab3854
Total, serious adverse eventsCyclophosphamide, Prednisone, Rituximab254

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
22883417RESULT

Source PubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
U10CA098543Children's Oncology Group Chair's GrantADAMSON, PETER C.CHILDREN'S HOSP OF PHILADELPHIANATIONAL CANCER INSTITUTE2003 to 2013

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00066469

GET https://conductscience.org/api/trials/v1/NCT00066469/events?page=2