Prostate Cancer Clinical Trial
Docetaxel, Radiation Therapy, and Prednisone in Treating Patients Who Have Undergone Surgery For Prostate Cancer
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. Radiation therapy uses high-energy x-rays to kill tumor cells. Docetaxel may make tumor cells more sensitive to radiation therapy. Giving docetaxel together with radiation therapy and prednisone after surgery may kill any tumor cells that remain after surgery.
PURPOSE: This phase II trial is studying how well giving docetaxel together with radiation therapy and prednisone works in treating patients who have undergone surgery for prostate cancer.
Full Description
OBJECTIVES:
Primary
Determine the rate of prostate-specific antigen (PSA) decline and the number of patients reaching a PSA nadir of zero after treatment with chemoradiotherapy comprising docetaxel and external-beam radiotherapy followed by docetaxel and prednisone in patients with hormone-naive prostate cancer who have a persistent or rising PSA after radical prostatectomy.
Secondary
Determine the tolerability of this regimen in these patients.
Determine the progression-free survival, based on PSA progression, of these patients.
Determine the overall survival of patients treated with chemoradiotherapy for rising PSA after radical prostatectomy.
Determine if the velocity of subsequent PSA failure impacts survival of these patients.
Tertiary
Document subsequent therapy for patients whose previous treatment has failed and if there is a response to that therapy.
Quaternary: To collect data on a contemporary cohort to those on study that received radiation alone. We will match cancer and patient characteristics to determine if the variable of chemotherapy has any impact on outcomes.
OUTLINE: Patients receive docetaxel IV over 1 hour on days 1, 8, 15, 22, 29, 36, and 43 and undergo external-beam radiotherapy on days 1-5, 8-12, 15-19, 22-26, 29-33, 36-40, and 43-47.
Beginning within 6 weeks after completion of chemoradiotherapy, patients receive docetaxel IV over 1 hour on day 1 and oral prednisone twice daily on days 1-21. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed at 1 month, every 4 months for 2 years, and then every 6 months for 3 years.
PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed prostate cancer
Prostate-specific antigen (PSA) level > 0.2 ng/mL after radical prostatectomy performed ≥ 6 weeks ago
No lymph node-positive prostate cancer
No documented metastatic disease
CT scan of the abdomen and pelvis negative (within the past 6 months)
No bone pain OR negative bone scan (within the past 6 months)
ECOG performance status 0-2
Absolute neutrophil count ≥ 1,500/mm³
Platelet count ≥ 100,000/mm³
Hemoglobin ≥ 9 g/dL
Bilirubin normal
ALT and AST ≤ 1.5 times upper limit of normal
Alkaline phosphatase normal
Fertile patients must use effective contraception
No peripheral neuropathy > grade 1
No other malignancy within the last 5 years that could affect the diagnosis or assessment of prostate cancer
No serious illness with a life expectancy of < 5 years
No concurrent medical, psychological, or social circumstance that would preclude study compliance
No history of severe hypersensitivity reaction to docetaxel or other drugs formulated with polysorbate 80
Exclusion Criteria:
No prior orchiectomy
No prior chemotherapy regimen for this disease
No prior pelvic radiotherapy
No pre- or postoperative androgen manipulation, such as luteinizing hormone-releasing hormone agonists, antiandrogens (flutamide, bicalutamide, or nilutamide), or finasteride
Preoperative androgen manipulation for a duration of ≤ 3 months allowed
No prior immunotherapy
No prior strontium chloride Sr 89, samarium Sm 153 lexidronam pentasodium, or other systemic radioisotopes
No concurrent filgrastim (G-CSF) or sargramostim (GM-CSF)
No concurrent herbal or alternative regimens including, but not limited to, any of the following:
Saw palmetto
PC-SPES
Shark cartilage
No other concurrent investigational agents
No other concurrent chemotherapy, immunotherapy, or hormonal therapy (except for replacement steroids)
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There is 1 Location for this study
San Antonio Texas, 78229, United States
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