Prostate Cancer
Conditions
Keywords
adenocarcinoma of the prostate, stage IV prostate cancer, recurrent prostate cancer
Brief summary
RATIONALE: Drugs used in chemotherapy, such as docetaxel and prednisone, 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. It is not yet known which schedule of docetaxel and prednisone is more effective in treating prostate cancer. PURPOSE: This randomized phase III trial is studying two different schedules of docetaxel and prednisone to compare how well they work in treating patients with metastatic prostate cancer.
Detailed description
OBJECTIVES: Primary * Compare the time to treatment failure in patients with hormone-refractory metastatic prostate cancer treated with two different schedules of docetaxel in combination with prednisone. Secondary * Compare overall survival of patients treated with these regimens. * Compare the response rate in patients treated with these regimens. * Compare the safety of these regimens in these patients. * Compare the quality of life of patients treated with these regimens. * Compare the need for epoetin beta in patients treated with these regimens. * Determine the effect of epoetin beta on hemoglobin response rate, transfusion rate, and quality of life of patients treated with these regimens. OUTLINE: This is a randomized, controlled, multicenter study. Patients are stratified according to participating center and WHO performance status (0-1 vs 2). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive docetaxel IV over 1 hour on days 1 and 15 and oral prednisone once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive docetaxel IV over 1 hour on day 1 and prednisone once daily on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients who experience anemia (hemoglobin \< 11 g/dL) receive epoetin beta subcutaneously once weekly during chemotherapy. Quality of life is assessed at baseline, every 6 weeks during study treatment, at completion of study treatment, and then every 2 months thereafter. After completion of study treatment, patients are followed every 2 months. PROJECTED ACCRUAL: A total of 360 patients (180 per treatment arm) will be accrued for this study within 4 years.
Interventions
DRUGdocetaxel
Given in 3- or 4- week courses
DRUGprednisone
Given in 3- or 4- week courses
Sponsors
Tampere University
Study design
Allocation
RANDOMIZED
Primary purpose
TREATMENT
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed adenocarcinoma of the prostate * Metastatic disease by imaging or clinical examination * Hormone-refractory disease, defined as prostate-specific antigen (PSA) level \> 10 µg/L AND rising between 2 sequential measurements * Testosterone within castration levels by orchiectomy or medical castration comprising luteinizing hormone-releasing hormone (LHRH) analogues PATIENT CHARACTERISTICS: Age * Over 18 Performance status * WHO 0-2 Life expectancy * Not specified Hematopoietic * Neutrophil count ≥ 1,500/mm\^3 * Hemoglobin ≥ 11.0 g/dL * Platelet count ≥ 100,000/mm\^3 Hepatic * ALT and AST ≤ 2.5 times upper limit of normal (ULN) * Bilirubin normal * Alkaline phosphatase ≤ 6 times ULN (unless due to the presence of extensive bone disease) * No serious liver disease Renal * Creatinine ≤ 1.5 times ULN Cardiovascular * No ischemic or thromboembolic cardiac disease * No myocardial infarction within the past 12 months * No other serious cardiac disease Pulmonary * No pulmonary emboli Immunologic * No active infection * No autoimmune disease, including any of the following: * Lupus * Scleroderma * Rheumatoid polyarthritis Other * No active peptic ulcer * No unstable diabetes mellitus * No contraindication to corticosteroids * No other malignant disease within the past 5 years except basalioma * No functional iron deficiency (i.e., transferrin saturation \< 20%) that cannot be treated with iron supplementation * No other serious illness or medical condition PRIOR CONCURRENT THERAPY: Biologic therapy * More than 2 months since prior recombinant human epoetin alfa or any other erythropoiesis-stimulating drug Chemotherapy * At least 3 weeks since prior estramustine Endocrine therapy * See Disease Characteristics * At least 3 weeks since prior antiandrogen treatment * Concurrent chemical castration with LHRH allowed provided patient has begun treatment prior to study entry * No initiation of chemical castration therapy during study treatment Radiotherapy * No prior radiotherapy to \> 25% of bone marrow * No prior radioisotope therapy * Concurrent local palliative radiotherapy for pain allowed Surgery * See Disease Characteristics * At least 4 weeks since prior surgery Other * No other prior cytostatic treatment * Concurrent bisphosphonates allowed provided patient has begun treatment prior to study entry * No initiation of bisphosphonates during study treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to treatment failure (TTF) | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life every 6 weeks until TTF | — |
| Safety | — |
| Overall survival | — |
| Response rate | — |
| Use of epoetin beta | — |
Countries
Finland, Ireland, Sweden
Outcome results
None listed