Clinical Trials Directory

Trials / Completed

CompletedNCT00103194

Lapatinib Ditosylate in Treating Patients With a Rising PSA Indicating Recurrent Prostate Cancer

Phase II Trial of GW572016 in Patients With Recurrent Prostate Cancer as Evident by a Rising PSA

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

Summary

This phase II trial studies how well lapatinib ditosylate works in treating patients with a rising prostate-specific antigen (PSA), a protein made by the prostate gland, indicating that prostate cancer has come back after previous treatment. Lapatinib ditosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and may delay or prevent the progression of prostate cancer.

Detailed description

PRIMARY OBJECTIVES: I. To evaluate the percentage of patients with hormone sensitive prostate cancer who experience \> 50% decline in serum PSA during treatment with GW572016 (lapatinib ditosylate). SECONDARY OBJECTIVES: I. To evaluate the duration of PSA decline. II. To characterize the change in PSA slope with GW572016. III. To characterize the safety and tolerability of GW572016 in this patient population. IV. To estimate the time to progression (TTP) and progression-free survival at 2 years (from start of therapy). V. To evaluate the correlation of epidermal growth factor receptor (EGFR) expression/signaling (from available prostate biopsy specimens or prostatectomy blocks) and its relationship to change in PSA in patients treated with GW572016. OUTLINE: Patients receive lapatinib ditosylate orally (PO) daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 3 months if patient is \< 2 years from study entry, every 6 months if patient is 2-5 years from study entry, or every year if patient is 5-10 years from study entry for 10 years.

Conditions

Interventions

TypeNameDescription
DRUGlapatinib ditosylateGiven PO
OTHERlaboratory biomarker analysisCorrelative studies

Timeline

Start date
2005-09-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2005-02-08
Last updated
2014-09-30
Results posted
2012-04-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00103194. Inclusion in this directory is not an endorsement.