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Trial · NCT00544778

Combination Chemotherapy and Dexrazoxane Followed by Surgery and Radiation Therapy in Treating Patients With Advanced Soft Tissue Sarcoma or Recurrent Bone Sarcoma

NCT00544778, Phase 2, Terminated, City of Hope Medical Center; results first posted 2014-08-28

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Combination Chemotherapy and Dexrazoxane Followed by Surgery and Radiation Therapy in Treating Patients With Advanced Soft Tissue Sarcoma or Recurrent Bone Sarcoma. Trials, record NCT00544778. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00544778

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Trial

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

Title
Combination Chemotherapy and Dexrazoxane Followed by Surgery and Radiation Therapy in Treating Patients With Advanced Soft Tissue Sarcoma or Recurrent Bone Sarcoma
NCT number
NCT00544778
Status
Terminated
Phases
Phase 2
Enrollment
7 participants, actual
Lead sponsor
City of Hope Medical Center
Conditions
Sarcoma
Interventions
filgrastim, dexrazoxane hydrochloride, doxorubicin hydrochloride, ifosfamide, irinotecan hydrochloride, protein expression analysis, immunoenzyme technique, adjuvant therapy, conventional surgery, neoadjuvant therapy, radiation therapy
First posted
2007-10-16
Last updated
2014-08-28
Results first posted
2014-08-28
Limitations and caveats
The study was terminated…protocol objectives not met. It was closed prematurely due to withdrawal of support by the sponsor. Subjects have been followed, but there is not enough data generated to continue following the subjects.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryResponse RateFirst disease evaluation one month after the start of treatment and every 3 months there after, up to 2 years.Response rate defined as the proportion of subjects with confirmed partial or complete response as defined by the RECIST criteria.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYResponse RateFirst disease evaluation one month after the start of treatment and every 3 months there after, up to 2 years.percentage of patients respondingNUMBER

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Response RateArm 10percentage of patients responding

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDArm 17
Overall StudyCOMPLETEDArm 17
Overall StudyNOT COMPLETEDArm 10

Adverse events69

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherFebrile neutropeniaBlood and lymphatic system disordersArm 1475
otherHemoglobin decreasedBlood and lymphatic system disordersArm 16721
otherPacked red blood cell transfusionBlood and lymphatic system disordersArm 1375
otherSinus tachycardiaCardiac disordersArm 1375
otherVision blurredEye disordersArm 1171
otherAbdominal painGastrointestinal disordersArm 1474
otherConstipationGastrointestinal disordersArm 1476
otherDiarrheaGastrointestinal disordersArm 1374
otherDyspepsiaGastrointestinal disordersArm 1475
otherEsophagitisGastrointestinal disordersArm 1171

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityArm 1
Total, other adverse eventsArm 167
Total, serious adverse eventsArm 107

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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
P30CA033572Cancer Center Support GrantCARPTEN, JOHN D.BECKMAN RESEARCH INSTITUTE/CITY OF HOPENATIONAL CANCER INSTITUTE1985 to 2025

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/NCT00544778

GET https://conductscience.org/api/trials/v1/NCT00544778/events?page=2