Randomized Phase III Trial of Leukine® vs Neupogen® in Patients Receiving Cisplatin & Gemcitabine for Urothelial Cancer

Stopped early · Phase 3

Conditions studied: Bladder Cancer

In brief

The main objective of this study is to compare the effectiveness of Leukine \& Neupogen to decrease the incidence of grade 3 \& 4 neutropenia in the treatment of patients receiving cisplatin \& gemcitabine for urothelial (bladder) cancer. All patients will receive chemotherapy with cisplatin plus gemcitabine in six 21-day cycles. Patients will also receive either Leukine (Arm A) or Neupogen (Arm B). Patient Population: 100 patients will be enrolled (n=100) in this study. Patients cannot have undergone previous chemotherapy. Approximately 50 patients will be enrolled into each treatment arm. Test Product, Dose, Mode of Administration: All patients will receive chemotherapy treatment with cisplatin (70 mg/kg) on Day 1 and gemcitabine (1000 mg/m2) on Days 1, 8, \& 15 of each 21-day cycle. Patients will be randomized to receive either Leukine (250 µg/m2) or Neupogen (5 µg/kg) injected under the skin on Days 2-6, 9-13, \& 16-20 of each cycle. Duration of Treatment: Patients will receive a maximum of six 21-day cycles of treatment. The overall trial, including follow-up, is expected to be 3 years in duration.

Key facts

Study ID

NCT00237575

Run by

University of Kentucky

People needed

100

Starts

2005-11-01

Expected to finish

2006-03-01

Last updated by the study team

2012-05-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Biopsy-proven, regionally advanced (T4b, N2, N3), or metastatic (M1) urothelial cancer of the bladder, ureter, or renal pelvis
• A minimum of one target lesion according to the RECIST criteria (Appendix D). Note: Bone metastases, leptomeningeal disease, ascites, pleural or pericardial effusions, lymphangitic spread or cystic lesions are not acceptable as target lesions.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 (Appendix B).
• Age >/=18 years or the age of majority in the state of the participating institution.
• Women of childbearing potential must have a negative pregnancy test and must be willing to consent to using effective contraception while on treatment and for a reasonable period thereafter. Post menopausal women must have been amenorrheic for at least 12 months to be considered of non-childbearing potential.
• An expected survival of at least four months.
• Adequate organ and marrow function as defined as follows:
• leukocytes >/=3,000/µl,
• absolute neutrophil count >/=1,500/µl,
• hemoglobin >/=8.0g/dl,
• platelets >/=100,000/µl,
• total bilirubin and serum creatinine must be < 1.5 mg/dl
• liver transaminases (SGOT and/or SGPT) may be up to 2.5 x institutional ULN if alkaline phosphatase is </=ULN, or
• alkaline phosphatase may be up to 4 x ULN if transaminases are </=ULN.
• Patients who have undergone previous radiation therapy or surgery may be enrolled into the study but such treatment must have been completed 4 or more weeks prior to entry to the study and the patient must have recovered. Further, patients who have undergone radiotherapy may not have received radiation to > 25% of the bone marrow. Previous intravesicular immunotherapy and chemotherapy are allowed.
• Ability to understand and the willingness to sign a written informed consent document.

You may not qualify if…

• Undergone previous systemic chemotherapy.
• Major surgery <4 weeks prior to study treatment start, or lack of complete recovery from major surgery.
• Participation in any investigational drug study within 4 weeks preceding treatment start.
• History of uncontrolled seizures, central nervous system disorders or psychiatric disability judged by the Investigator to be significant enough to preclude informed consent or interfering with compliance for oral drug intake.
• Previous history of cancer unless treatment was curative and completed >/=5 years prior to entry onto study, or unless diagnosed as one of the following: in situ carcinoma (any location), basal cell carcinoma, or non-metastatic squamous cell carcinoma of the skin.
• Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled or untreated cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant women are excluded from this study because of the teratogenic potential of cisplatin and gemcitabine. Lactating women are also excluded. (Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.)
• Peripheral neuropathy >/= grade 2.

Where it is running

• University of Louisville — Louisville, Kentucky, United States
• University of Nebraska — Omaha, Nebraska, United States
• New York Medical College — Hawthorne, New York, United States
• Montefiore Medical Center — The Bronx, New York, United States

Full record on ClinicalTrials.gov

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