Clinical trial · Interventional
Docetaxel and Gemcitabine in Hormonal Refractory Metastatic Prostate Cancer
A Phase I/II Study With Docetaxel and Gemcitabine in Hormonal Refractory Metastatic Prostate Cancer
NCT00115635CI-TRIAL-00000899completedPhase 1 / Phase 2ClinicalTrials.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)
The aim of the study is to determine the optimal dose of the combination of docetaxel and gemcitabine in patients with hormone refractory prostate cancer, and evaluate this dose with respect to efficacy and toxicity in a phase II trial.
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 (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| docetaxel | Drug | Docetaxel | ALIAS |
| gemcitabine | Drug | Gemcitabine | ALIAS |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Prostate-specific antigen (PSA) response
Secondary outcomes (3)
- measure
- Clinical response
- measure
- Time to PSA progression
- measure
- Toxicity
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
- Maximum age
- 95 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically verified adenocarcinoma of the prostate. * Hormone refractory prostate cancer (HRPC) defined as progression during previous anti-hormone treatment. Patients must have been off previous anti-androgen therapy for more than 4 weeks. * Stage IV disease (verified by imaging or clinical examination). * PSA \> 10 microgram/l. * PSA progression defined as a \> 25% increase between two independent measurements performed with a 1-month interval or more after discontinuation of anti-androgen treatment. * Castrate level of testosterone (\< 50 ng). * No previous oestrogen or steroid as metastatic prostate cancer treatment. * Satisfactory hepatic function in the form of total bilirubin ≤ UNL (upper normal limit), ASAT/ALAT ≤ 2.5 x UNL, alkaline phosphatase ≤ 5 x UNL. * Satisfactory renal function, defined as serum creatinine ≤ 1.5 x UNL. * Satisfactory haematologic function defined as ANC \>1.5 x 10\^9/l, leucocytes \>3.0 x 10\^9/l, thrombocytes ≥ 100 x 10\^9/l, haemoglobin \> 7 mmol/l * ECOG performance status ≤ 2. * Life expectancy \> 3 months. * Patient must be able to adhere to protocol requirements. * Written informed consent. * \> 18 years of age. Exclusion Criteria: * Previous prostate cancer treatment with oestrogens or steroid hormones. * Previous chemotherapy. * Previous treatment with systemic radioactive isotopes. * Bisphosphonate treatment (concomitant). * Radiation therapy covering more than 25% of the bone marrow producing area. * Other serious coincidental and/or concomitant medical condition. * Symptomatic cerebral metastases. * Other previous or current malignant disease, excluding \*adequately treated and cured planocellular skin carcinoma; or \*other cancer assessed to carry minimal risk of recurrence. * ECOG performance status \> 2.
References
Publications (0)
Data not yet available
No reference posted for this study.