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Spots Global Cancer Trial Database for Lapatinib in Treating Patients With Recurrent or Metastatic Prostate Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Lapatinib in Treating Patients With Recurrent or Metastatic Prostate Cancer

Official Title: A Phase 2 Study of GW572016 in Hormone Naive Recurrent or Metastatic Hormone Sensitive Prostate Cancer

Study ID: NCT00095667

Study Description

Brief Summary: Lapatinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Phase II trial to study the effectiveness of lapatinib in treating patients who have recurrent or metastatic prostate cancer.

Detailed Description: PRIMARY OBJECTIVES: I. To determine the antitumor activity of GW572016 in hormone naïve, recurrent and/or metastatic hormone sensitive prostate cancer using PSA response rate. SECONDARY OBJECTIVES: I. To estimate objective tumor response in patients with measurable disease. II. To determine the duration of PSA response, rate and duration of stable disease, progression-free, median and overall survival rates of GW572016 in recurrent and/or metastatic prostate cancer. III. To document the safety and tolerability of GW572016 in these patient populations. TERTIARY OBJECTIVES: I. To investigate if differences in baseline levels of EGFR and/or erbB2 expression, and receptor phosphorylation status in tumor specimens predict outcome to therapy. II. To investigate if the inhibitory effects of GW572016 on EGFR and/or erbB2 pathway activation in tumor specimens correlates with clinical outcome. OUTLINE: This is a nonrandomized, open-label, multicenter study. Patients receive oral lapatinib once daily on days 1-28. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression. Patients are followed for survival. PROJECTED ACCRUAL: A total of 21-41 patients will be accrued for this study within 11.7 months.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Princess Margaret Hospital Phase 2 Consortium, Toronto, Ontario, Canada

Contact Details

Name: John Trachtenberg

Affiliation: Princess Margaret Hospital Phase 2 Consortium

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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