Gemcitabine With Or Without Oxaliplatin in Treating Patients With Locally Advanced or Metastatic Bladder Cancer

Institut du Cancer de Montpellier - Val d'Aurelle

Status and phase: Completed; Phase 2

Conditions: Bladder Cancer

Treatments: Drug: gemcitabine hydrochloride; Drug: oxaliplatin

Study type: Interventional

Funder types: Other

Identifiers

NCT00627432

LILLY-CLCC-VESUNFIT

RECF0368

SANOFI-AVENTIS-CLCC-VESUNFIT

CDR0000574179

CLCC-VESUNFIT

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

PURPOSE: This randomized phase II trial is studying how well giving gemcitabine together with oxaliplatin works compared to gemcitabine alone in treating patients with locally advanced or metastatic bladder cancer.

Full description

OBJECTIVES:

Primary

• Determine the objective response rate in patients with advanced urothelial cancer treated with gemcitabine hydrochloride with vs without oxaliplatin.

Secondary

• Determine the tolerance of these regimens in these patients.
• Determine the overall survival and progression-free survival of patients treated with these regimens.
• Determine the quality of life of patients treated with these regimens.
• Determine the duration of response in patients treated with these regimens.

OUTLINE: This is a multicenter study. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive gemcitabine hydrochloride IV over 120 minutes on days 1, 8, and 15.
• Arm II: Patients receive gemcitabine IV over 100 minutes on days 1 and 15 and oxaliplatin IV over 120 minutes on days 2 and 16.

Treatment in both arms repeats every 4 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3 months.

Enrollment: 44 patients

Sex: All

Ages: 18 to 120 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed urothelial carcinoma, or transitional cell carcinoma of the bladder or upper urinary tract

  • Locally advanced disease (T4b) or metastatic disease (N2, N3, or M1)

• Unable to receive cisplatin-based chemotherapy due to creatinine clearance 30-60 mL/min or performance status 2

• At least 1 unidimensionally measurable lesion according to RECIST criteria

• No nonmeasurable lesions only, including any of the following:

  • Ascites
  • Pleural or pericardial effusion
  • Bone metastases
  • Lymphangitis

• No symptomatic cerebral metastases unless they have been stabilized

PATIENT CHARACTERISTICS:

• See Disease Characteristics

• Performance status 0-2

• ANC ≥ 1,500/mm³

• Platelet count ≥ 100,000/mm³

• Alkaline phosphatase ≤ 2 times normal (unless bone metastases are present)

• Transaminases ≤ 2 times normal (5 times normal if hepatic metastases present)

• Bilirubin ≤ 1.5 times normal

• Not pregnant or nursing

• Fertile patients must use effective contraception during and for at least 6 months after completion of treatment

• No prior malignancy within the past 5 years except carcinoma in situ of the cervix or basal cell skin cancer

• No peripheral neuropathy ≥ grade 2

• No uncontrolled infection

• No other medical conditions that could interfere with evaluating tolerability, including any of the following:

  • Congestive heart failure
  • Angina pectoris that cannot be stabilized with medication
  • Myocardial infarction within the past 12 months
  • Serious thromboembolic disease

• No psychologic, social, or geographic reason that would make follow-up impossible

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No prior chemotherapy for advanced disease
• More than 4 weeks since prior radiotherapy to a target measurable lesion

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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44 participants in 2 patient groups

Gemcitabine,

Active Comparator group

Description:

•Arm I: Patients receive gemcitabine hydrochloride IV over 120 minutes on days 1, 8, and 15.

Treatment:

Drug: gemcitabine hydrochloride

Gemcitabine, Oxaliplatine

Experimental group

Description:

•Arm II: Patients receive gemcitabine IV over 100 minutes on days 1 and 15 and oxaliplatin IV over 120 minutes on days 2 and 16.

Treatment:

Drug: oxaliplatin

Drug: gemcitabine hydrochloride