Clinical trial · Interventional
Estramustine, Docetaxel, and Carboplatin in Treating Patients With Prostate Cancer That Has Not Responded to Hormone Therapy
A Phase I Study of Estramustine, Taxotere and Carboplatin (ETP) in Patients With Horomone Refractory Prostate Cancer
NCT00005627CI-TRIAL-00011398completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of estramustine, docetaxel, and carboplatin in treating patients who have prostate cancer that has not responded to hormonal therapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| carboplatin | Drug | Carboplatin | ALIAS |
| docetaxel | Drug | Docetaxel | ALIAS |
| estramustine phosphate sodium | Drug | Estramustine | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
- Maximum age
- 85 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS:
* Histologically confirmed adenocarcinoma of the prostate
* Disease progression following androgen ablation therapy (hormonal or surgical) by either:
* Increase in the product of bidimensional diameters of 1 or more radiographically documented sites of measurable disease OR
* Two consecutive increases in PSA documented over a previous reference value
* First increase in PSA should occur a minimum of 1 week from the reference value and be confirmed
* First PSA value is less than the previous value, then patient is eligible provided next PSA is greater than the second PSA
* Testosterone levels documented in the castrate range (i.e., less than 30 ng/mL)
PATIENT CHARACTERISTICS:
Age:
* 18 to 85
Performance status:
* CALGB 0-2
Life expectancy:
* Not specified
Hematopoietic:
* WBC at least 3,000/mm3
* Platelet count at least 100,000/mm3
Hepatic:
* Bilirubin normal
* SGOT no greater than 2.5 times upper limit of normal (ULN) if alkaline phosphatase normal OR
* Alkaline phosphatase no greater than 4 times ULN if SGOT normal OR
* SGOT no greater than 1.5 times ULN and alkaline phosphatase no greater than 2.5 times ULN
Renal:
* Creatinine no greater than 2.0 mg/dL
Cardiovascular:
* No myocardial infarction within past year
* No significant change in anginal pattern within past 6 months
* No New York Heart Association class II-IV heart disease
* No deep venous thrombosis within past year
Other:
* No significant peripheral neuropathy
PRIOR CONCURRENT THERAPY:
Biologic therapy:
* Not specified
Chemotherapy:
* Prior chemotherapy allowed except taxanes or platinum derivatives
Endocrine therapy:
* See Disease Characteristics
* At least 4 weeks since prior antiandrogens
Radiotherapy:
* At least 4 weeks since prior radiotherapy
Surgery:
* See Disease CharacteristicsReferences
Publications (1)
- RESULTOh WK, Hagmann E, Manola J, George DJ, Gilligan TD, Jacobson JO, Smith MR, Kaufman DS, Kantoff PW. A phase I study of estramustine, weekly docetaxel, and carboplatin chemotherapy in patients with hormone-refractory prostate cancer. Clin Cancer Res. 2005 Jan 1;11(1):284-9. PMID 15671557