Overview

Docetaxel in Treating Patients With Relapsed Prostate Cancer

Status:
Terminated
Trial end date:
2009-07-01
Target enrollment:
0
Participant gender:
Male
Summary
RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well docetaxel works in treating patients with relapsed prostate cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
OHSU Knight Cancer Institute
Collaborator:
National Cancer Institute (NCI)
Treatments:
Docetaxel
Criteria
Criteria for Patient eligibility

Inclusion criteria

1. Histologically confirmed adenocarcinoma of the prostate.

2. Prior primary therapy for prostate cancer, including radical prostatectomy, external
beam radiation therapy, or brachytherapy.

3. Serum PSA > 0.2 ng/dL following 8 months of androgen deprivation therapy or a nadir
PSA >0.2 ng/dL and at least 1 subsequent PSA values at the same or higher level, if
prior to 8 months.

4. Serum testosterone < 50 ng/ml.

5. No evidence of metastases on bone scan.

6. No evidence of metastases on CT scan of the abdomen and pelvis.

7. ECOG performance status < 2.

8. Laboratory criteria for entry: absolute neutrophil count ≥ 1.2 K/cu mm, platelets ≥
100 K/cu mm, serum bilirubin ≤ upper limit of normal (ULN), SGOT and SGPT ≤ 1.5 times
institutional ULN if alkaline phosphatase ≤ ULN, alkaline phosphatase ≤ 5 times ULN if
SGOT and SGPT are ≤ ULN, a serum creatinine ≤ 2 times institutional ULN.

9. Signed informed consent.

Exclusion Criteria

1. A second active malignancy during the last 5 years, except adequately treated
non-melanoma skin cancer.

2. Life expectancy < 3 months.

3. Grade 2 or higher peripheral neuropathy.

4. Prior investigational agent within the past 28 days.

5. Less than a 10% decrease (or continued rise) in PSA in response to initial
androgen-deprivation therapy.

6. More than 12 months since initiation of androgen-deprivation therapy.

7. Prior docetaxel chemotherapy.

8. Patients recently (within 28 days) started on corticosteroids, with the exception of
inhaled and topical steroids. Patients on stable doses of systemic corticosteroids
will be eligible.