Cyproterone Acetate in Treating Patients With Newly Diagnosed Stage III or Stage IV Prostate Cancer

NCT ID: NCT00363285

Last Updated: 2013-08-26

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 900 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-01-31

Brief Summary

RATIONALE: Androgens can cause the growth of prostate cancer cells. Hormone therapy, such as cyproterone acetate may stop the adrenal glands from making androgens. Sometimes the tumor may not need treatment until it progresses. In this case, observation may be sufficient. It is not yet known whether giving cyproterone acetate continuously is more effective than giving cyproterone acetate after tumor progression in treating prostate cancer.

PURPOSE: This randomized phase III trial is studying cyproterone acetate to compare how well it works when given continuously or after tumor progression in treating patients with newly diagnosed stage III or stage IV prostate cancer.

Detailed Description

OBJECTIVES:

Primary

• Compare time to loss of androgen dependence, based on serum prostate-specific antigen failure, in patients with newly diagnosed stage III or IV prostate cancer treated with intermittent vs continuous androgen suppression comprising cyproterone acetate.
• Compare time to treatment failure (subjective or objective progression) in patients treated with these regimens.
• Compare quality of life of patients treated with these regimens.
• Compare survival of patients treated with these regimens.

Secondary

• Compare the side effects in patients treated with these regimens.
• Determine the first and total therapy-free intervals in patients treated with intermittent cyproterone acetate.

OUTLINE: This is a randomized, multicenter study.

All patients receive cyproterone acetate daily for 16 weeks. Patients also receive monthly injections of luteinizing hormone-releasing hormone (LHRH) agonist beginning in week 2 and continuing for 14 weeks. Patients with a prostate-specific antigen (PSA) level of ≤ 4 ng/mL and who are asymptomatic at 14 weeks are randomized to 1 of 2 treatment arms.

• Arm I (continuous maximum-androgen blockade): Patients receive cyproterone acetate daily and monthly LHRH agonist depot injections in the absence of disease progression or unacceptable toxicity. Patients may also undergo orchidectomy.

Quality of life is assessed every 6 months for 2 years and then annually thereafter.

• Arm II (intermittent treatment): Patients are observed after randomization. Treatment with daily cyproterone acetate resumes if symptoms demand hormone treatment and patient has any PSA level OR if patient is asymptomatic and has a PSA level ≥ 20 ng/mL. Treatment continues in the absence of disease progression or unacceptable toxicity. If after 9 months of treatment, a PSA level of ≤ 4 ng/mL is not achieved or the patient remains symptomatic, treatment is discontinued.

Quality of life is assessed every 6 months and when therapy is restarted.

Pain and performance status are assessed at each visit in both treatment arms.

After completion of study therapy, patients are followed periodically.

PROJECTED ACCRUAL: A total of 900 patients will be accrued for this study.

Conditions

Prostate Cancer

Keywords

adenocarcinoma of the prostate; stage III prostate cancer; stage IV prostate cancer

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT

Interventions

gonadotrophin releasing hormone

Intervention Type: BIOLOGICAL

cyproterone acetate

Intervention Type: DRUG

quality-of-life assessment

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma of the prostate

• T3 -T4, M0-M1 (stage III or IV disease)
• Prostate-specific antigen level ≥ 4 ng/mL and ≤ 100 ng/mL

PATIENT CHARACTERISTICS:

• Performance status 0-2
• Normal liver function
• No other neoplasia (except skin, excluding melanoma)
• No expected difficulties of follow-up related to psychiatric disorders, marked senility, or too large a distance between patient's home and investigator's center
• No severe chronic disease

PRIOR CONCURRENT THERAPY:

• No prior hormonal therapy or chemotherapy
• No prior surgery (radical prostatectomy), except transurethral resection, for M0 patients
• No prior radiotherapy to the primary tumor for M0 patients

• Maximum Eligible Age: 79 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

St. Bartholomew's Hospital

OTHER

Sponsor Role: lead

Principal Investigators

R. T. Oliver, MD

Role: STUDY_CHAIR

St. Bartholomew's Hospital

Locations

Saint Bartholomew's Hospital

London, England, United Kingdom

Site Status: RECRUITING

Scarborough General Hospital

Scarborough, England, United Kingdom

Site Status: RECRUITING

Countries

United Kingdom

Facility Contacts

R. T. Oliver, MD

Role: primary

Simon Hawkyard, MD

Role: primary

Other Identifiers

SEUG-9901

Identifier Type: -

Identifier Source: secondary_id

BARTS-SEUK-9901

Identifier Type: -

Identifier Source: secondary_id

MREC-04/5/006

Identifier Type: -

Identifier Source: secondary_id

BARTS-P/02/203

Identifier Type: -

Identifier Source: secondary_id

EU-20630

Identifier Type: -

Identifier Source: secondary_id

CDR0000495321

Identifier Type: -

Identifier Source: org_study_id