Clinical Trials Directory

Trials / Completed

CompletedNCT00025220

Thalidomide in Treating Patients With Recurrent or Persistent Cancer of the Uterus

A Phase II Evaluation of Thalidomide (NSC #66847) in the Treatment of Recurrent or Persistent Leiomyosarcoma of the Uterus

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Phase II trial to study the effectiveness of thalidomide in treating patients who have recurrent or persistent cancer of the uterus. Thalidomide may stop the growth of cancer by stopping blood flow to the tumor.

Detailed description

PRIMARY OBJECTIVES: I. Determine the antitumor cytostatic activity of thalidomide, as measured by the probability of progression-free survival (PFS) for at least 6 months, in patients with recurrent or persistent uterine leiomyosarcoma. II. Determine the nature and degree of the toxicity of this drug in these patients. III. Determine the partial and complete response rates in patients treated with this drug. IV. Determine the duration of PFS and overall survival of patients treated with this drug. V. Determine the effect of this drug on initial performance status in these patients. VI. Determine the effects of this drug at 4 weeks on endogenous angiogenesis factors (vascular endothelial growth factor and basic fibroblast growth factor) in plasma and urine of these patients. VII. Assess the association of endogenous angiogenesis factors with clinical outcome (PFS) in patients treated with this drug. OUTLINE: This is a multicenter study. Patients receive oral thalidomide once daily on days 1-28. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

Conditions

Interventions

TypeNameDescription
DRUGThalidomideGiven PO
OTHERLaboratory Biomarker AnalysisCorrelative studies

Timeline

Start date
2001-09-01
Primary completion
2003-04-01
Completion
2008-07-01
First posted
2003-01-27
Last updated
2019-07-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00025220. Inclusion in this directory is not an endorsement.