ConductScience.org, home

Trial · NCT01209598

PD0332991 (Palbociclib) in Patients With Advanced or Metastatic Liposarcoma

NCT01209598, Phase 2, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2017-11-06

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. PD0332991 (Palbociclib) in Patients With Advanced or Metastatic Liposarcoma. Trials, record NCT01209598. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01209598

On this page

Trial

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

Title
PD0332991 (Palbociclib) in Patients With Advanced or Metastatic Liposarcoma
NCT number
NCT01209598
Status
Completed
Phases
Phase 2
Enrollment
90 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Sarcoma, Liposarcoma
Interventions
Palbociclib 200mg, Palbociclib 125mg
First posted
2010-09-27
Last updated
2017-11-06
Results first posted
2017-11-06

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryProgression Free Survival at 12 Weeks12 weeksPFS, defined as RECIST 1.1 (CR + PR + SD) when treated with Palbociclib
SecondaryBest Response2 years
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYProgression Free Survival at 12 Weeks12 weekspercentage of particpantsMEDIAN
SECONDARYBest Response2 yearsParticipantsCOUNT_OF_PARTICIPANTS

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Progression Free Survival at 12 WeeksPalbociclib 200mg6695% Confidence Interval 51 to 100percentage of particpants
Progression Free Survival at 12 WeeksPalbociclib 125mg57.295% Confidence Interval 42.4 to 68.8percentage of particpants
Best ResponsePalbociclib 200mgPartial Response1Participants
Best ResponsePalbociclib 125mgPartial Response0Participants
Best ResponsePalbociclib 200mgComplete Response0Participants
Best ResponsePalbociclib 125mgComplete Response1Participants
Best ResponsePalbociclib 200mgStable Disease5Participants
Best ResponsePalbociclib 125mgStable Disease8Participants
Best ResponsePalbociclib 200mgProgression of Disease23Participants
Best ResponsePalbociclib 125mgProgression of Disease50Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPalbociclib 200mg30
Overall StudySTARTEDPalbociclib 125mg60
Overall StudyCOMPLETEDPalbociclib 200mg29
Overall StudyCOMPLETEDPalbociclib 125mg60
Overall StudyNOT COMPLETEDPalbociclib 200mg1
Overall StudyNOT COMPLETEDPalbociclib 125mg0

Adverse events66

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnorexiaMetabolism and nutrition disordersPalbociclib 200mg230
otherAnorexiaMetabolism and nutrition disordersPalbociclib 125mg060
otherDizzinessNervous system disordersPalbociclib 200mg230
otherDizzinessNervous system disordersPalbociclib 125mg060
otherDyspneaRespiratory, thoracic and mediastinal disordersPalbociclib 200mg230
otherDyspneaRespiratory, thoracic and mediastinal disordersPalbociclib 125mg060
otherEdema limbsGeneral disordersPalbociclib 200mg230
otherEdema limbsGeneral disordersPalbociclib 125mg060
otherEpistaxisRespiratory, thoracic and mediastinal disordersPalbociclib 200mg230
otherEpistaxisRespiratory, thoracic and mediastinal disordersPalbociclib 125mg060

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPalbociclib 200mg
Total, all-cause mortalityPalbociclib 125mg
Total, other adverse eventsPalbociclib 200mg3030
Total, other adverse eventsPalbociclib 125mg6060
Total, serious adverse eventsPalbociclib 200mg2430
Total, serious adverse eventsPalbociclib 125mg5560

Papers3

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
23569312DERIVEDPubMed
27124835DERIVEDPubMed
32641862DERIVEDPubMed

Grants0

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.

None in this release.

Trial comparisons1

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

Comparison
Palbociclib 200mg vs Palbociclib 125mg: serious adverse events

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/NCT01209598

GET https://conductscience.org/api/trials/v1/NCT01209598/events?page=2