Transitional Cell Carcinoma of the Bladder Clinical Trial
Official title:
Phase II Study of Oral Suberoylanilide Hydroxamic Acid (SAHA) in Recurrent or Metastatic Transitional Cell Carcinoma of the Urothelium
Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. This phase II trial is studying how well vorinostat works in treating patients with locally recurrent or metastatic cancer of the urothelium.
PRIMARY OBJECTIVES:
I. To determine response rate measured by RECIST criteria for SAHA in patients with
recurrent or metastatic transitional cell carcinoma of the urothelium.
SECONDARY OBJECTIVES:
I. To determine the time to progression and overall survival for SAHA in patients with
recurrent or metastatic transitional cell carcinoma of the urothelium.
II. To provide data on safety and toxicity of SAHA in patients with recurrent or metastatic
transitional cell carcinoma of the urothelium.
III. To obtain preliminary data on molecular correlates in tissue, oral mucosa and blood to
determine feasibility and clinical efficacy.
OUTLINE: This is a multicenter study.
Patients receive oral vorinostat (SAHA) twice daily on days 1-21. Courses repeat every 21
days in the absence of disease progression or unacceptable toxicity.
Patients undergo blood and buccal mucosa collection and tumor biopsies (if accessible) at
baseline and periodically during study for correlative studies. Samples are examined by gene
expression profiling and immunohistochemistry.
After completion of study treatment, patients are followed for up to 26 weeks.
PROJECTED ACCRUAL: A total of 37 patients will be accrued for this study.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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