Phase II Study of Docetaxel for Clinically Asymptomatic High Risk Prostate Cancer Patients

NCT ID: NCT00714376

Last Updated: 2012-10-31

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-05-31
• Study Completion Date: 2008-07-31

Brief Summary

The purpose of this study is to assess the response to Taxotere (docetaxel) chemotherapy given as a primary treatment to patients with early and rapid PSA rising after prostatectomy for high risk disease.

Detailed Description

Patients with high-risk prostate cancer have a high probability of PSA failure after radical prostatectomy. However, more than half of these patients will remain free of PSA recurrence for more than 10 years. To the contrary, patients with early PSA recurrence and a doubling time less than 10 months have a mortality rate approaching 50% at 10 years despite hormone therapy. Although androgen deprivation therapy (ADT) remains the standard treatment for patients with early and rapidly rising PSA after prostatectomy, this treatment is not curative on the long term for most patients. The recent demonstration of activity of Taxotere (docetaxel) in a high proportion of patients with advanced metastatic disease has stimulated a great interest in it use at an earlier stage of the disease. Recent studies performed in animal models of prostate cancer suggested that the response rate of prostate cancer cells to docetaxel-induced cell death was significantly enhanced by androgen stimulation in AR-positive, androgen-dependent prostate cancer cells (i.e. before ADT). Therefore, this protocol proposes to assess the response rate to primary Taxotere chemotherapy in patients with early and rapid PSA rising after prostatectomy for high risk disease.

Conditions

Prostate Cancer

Keywords

Prostate cancer; High-risk prostate cancer; Radical prostatectomy; Early rising PSA; Taxotere; Docetaxel

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Docetaxel

Docetaxel (Taxotere) 75 mg/m² IV every 3 weeks for 8 cycles.

Group Type: EXPERIMENTAL

Docetaxel

Intervention Type: DRUG

75 mg/m2 iv every 3 weeks for 8 cycles

Interventions

Docetaxel

75 mg/m2 iv every 3 weeks for 8 cycles

Intervention Type: DRUG

Other Intervention Names

Taxotere

Eligibility Criteria

Inclusion Criteria

1. Diagnosis of prostate adenocarcinoma on a radical prostatectomy.

2. Prior radical prostatectomy within less than 2 years from the time of first PSA rise.

3. Demonstration of biochemical recurrence based on a PSA detectable >0.03 less than 24 months after radical prostatectomy and confirmed on 2 additional tests.

4. PSA doubling time over three values must be <= 9 months for PSA >=0.4 and PSA <=10. If PSA is >10, there is no need for PSA doubling time.

5. Karnofsky performance status (KPS) >=70%

6. Adequate organ function as defined by hemogram with haemoglobin >8.0, platelet >100 000, white blood cell >3,500, creatinine clearance >=60 cc/min and normal liver function tests.

7. Neoadjuvant hormone therapy prior to radical prostatectomy is allowed provided that the total duration of therapy did not exceed 6 months.

8. Subjects must have signed an informed consent document stating that they understand the investigational or nature of the proposed treatment.

9. Subjects must be willing and able to comply with scheduled visits, treatment plans, laboratory tests and other procedures.

Exclusion Criteria

1. Clinical significant cardiac disease (New York Heart Association Class III/IV), or severe debilitating pulmonary disease.

2. Uncontrolled serious active infection.

3. Anticipated duration of life less than 2 years.

4. Less than 5-year history of successful treatment for other cancers or concurrent active non prostate cancer other than non melanoma dermatologic tumors and non-muscle invasive bladder tumors.

5. Peripheral neuropathy >=2 grade 2

6. Concurrent experimental treatment or involvement in other clinical trials involving drugs.

7. Other severe acute or chronic medical conditions including psychiatric diseases or significant laboratory abnormality requiring further investigation that may cause undue risk for the subject's safety.

8. Subjects who participated in another clinical study/received investigational product within 30 days of screening for this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

CHU de Quebec-Universite Laval

OTHER

Sponsor Role: lead

Responsible Party

Yves Fradet

Urologist-Oncologist

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Yves Fradet, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Quebec (CHUQ)

Pierre Ouellet, MD

Role: PRINCIPAL_INVESTIGATOR

CHU de Quebec-Universite Laval

Locations

Centre de recherche clinique et evaluative en oncologie, L'Hôtel-Dieu de Québec-CHUQ

Québec, Quebec, Canada

Countries

Canada

Other Identifiers

Project 5.2.08.02

Identifier Type: -

Identifier Source: org_study_id