Phase 2
N=27
Chemotherapy, Hormone Therapy, and Radiation Therapy in Treating Patients With Locally Advanced Prostate Cancer
Prostate Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00016913 ↗Enrolled (actual)
27
Serious AEs
0.0%
Results posted
Jan 2016
Primary outcome: Primary: Toxicity — 2; 0 Events
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- carboplatin (Drug); estramustine (Drug); paclitaxel (Drug); radiation therapy (Radiation); leuprolide or goserelin acetate (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Male
- Sponsor
- Alliance for Clinical Trials in Oncology
- Primary completion
- Jul 2007
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Toxicity |
2; 0 | — |
| SECONDARY Time to Prostate-specific Antigen Failure |
17.1; 12.1 | — |
| SECONDARY Progression-free Survival (PFS) |
12.1 | — |
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Androgens can stimulate the growth of prostate cancer cells. Drugs such as goserelin or leuprolide may stop the adrenal glands from producing androgens. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining chemotherapy, hormone therapy, and radiation therapy may kill more tumor cells.
PURPOSE: This phase II trial is studying giving chemotherapy together with hormone therapy and radiation therapy in treating patients with locally advanced prostate cancer.
Eligibility Criteria
DISEASE CHARACTERISTICS:
- Histologically confirmed adenocarcinoma of the prostate with one of the following prognostic factors:
- Tx N0, baseline prostate specific antigen (PSA) greater than 20 ng/mL, and Gleason score at least 7
- T3b-4 N0, any baseline PSA, and any Gleason score
- No pelvic lymph node disease requiring pelvic radiotherapy
- No metastatic disease by bone scan, CT scan, or MRI
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- ECOG 0-2
Life expectancy:
- Not specified
Hematopoietic:
- Granulocyte count at least 1,500/mm^3
- Platelet count at least 100,000/mm^3
Hepatic:
- Bilirubin no greater than 1.5 times upper limit of normal (ULN)
- SGOT no greater than 1.5 times ULN
Renal:
- Creatinine no greater than 1.5 times ULN
Cardiovascular:
- No significant cardiovascular disease
- No New York Heart Association class III or IV congestive heart failure
- No active angina pectoris
- No myocardial infarction within the past 6 months
- No history of hemorrhagic or thrombotic cerebral vascular accident
- No deep vein thrombosis within the past 6 months
Pulmonary:
- No pulmonary embolism within the past 6 months
Other:
- Fertile patients must use effective contraception
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- No prior immunotherapy for prostate cancer
- No concurrent routine filgrastim (G-CSF) or sargramostim (GM-CSF)
Chemotherapy:
- No prior chemotherapy for prostate cancer
- No other concurrent anticancer chemotherapy
Endocrine therapy:
- No more than 6 weeks of prior androgen deprivation therapy
- No other concurrent anticancer hormonal therapy except steroids for adrenal failure and/or hormones for nondisease-related conditions (e.g., insulin for diabetes)
Radiotherapy:
- See Disease Characteristics
- No prior radiotherapy for prostate cancer
- No other concurrent anticancer radiotherapy
Surgery:
- At least 4 weeks since prior major surgery
Other:
- No prior alternative therapy (e.g., PC-SPES) for prostate cancer
- No concurrent alternative medicine (e.g., PC-SPES or saw palmetto) or large quantities of vitamins
- No other concurrent anticancer therapy
Data sourced from ClinicalTrials.gov (NCT00016913). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.