Stage III Bladder Urothelial Carcinoma AJCC v6 and v7 Clinical Trial
Official title:
Phase II Trial of Gemcitabine-Eribulin (GE) in Cisplatin Ineligible Patients With Advanced or Unresectable Urothelial Carcinoma of the Bladder
This phase II trial studies how well gemcitabine hydrochloride and eribulin mesylate work in treating patients with bladder cancer that has spread to other places in the body or cannot be removed by surgery. Drugs used in chemotherapy, such as gemcitabine hydrochloride and eribulin mesylate, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
PRIMARY OBJECTIVES:
I. To estimate the objective response rate of gemcitabine (gemcitabine
hydrochloride)-eribulin (eribulin mesylate) (GE) when given to cisplatin ineligible patients
with advanced or unresectable urothelial carcinoma who have not received any prior
chemotherapy for the advanced disease.
SECONDARY OBJECTIVES:
I. To estimate the median progression-free survival (PFS). II. To summarize the toxicity
profile (using Common Terminology Criteria for Adverse Events [CTCAE] version [v] 4 criteria)
of the GE regimen in these patients.
OUTLINE:
Patients receive gemcitabine hydrochloride intravenously (IV) over 30 minutes on days 1 and 8
and eribulin mesylate IV over 2-5 minutes on days 1 and 8. Courses repeat every 21 days in
the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 3 months for up to 36
months.
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Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
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