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CompletedNCT00003323Updated Jul 4, 2016

Hormone Therapy in Treating Patients With Prostate Cancer

A Phase 2 interventional study of finasteride and flutamide in Prostate Cancer and Sexual Dysfunction and Infertility, sponsored by Alliance for Clinical Trials in Oncology. Completed at 43 sites in United States. Open to male participants. Per ClinicalTrials.gov, last updated 2016-07-04.

Sponsored by Alliance for Clinical Trials in Oncology · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
101
Allocation
Non-randomized
Sex
Male
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Study summary

RATIONALE: Male hormones can stimulate the growth of prostate cancer cells. Hormone therapy using flutamide and finasteride may fight prostate cancer by reducing the production of male hormones.

PURPOSE: Phase II trial to study the effectiveness of flutamide and finasteride in treating prostate cancer patients with high PSA levels who were previously treated with radiation therapy or radical prostatectomy.

Read the detailed description

OBJECTIVES:

  • Determine the efficacy of finasteride and flutamide in suppressing prostate specific antigen (PSA) levels in patients with elevated PSA after definitive radiation therapy or radical prostatectomy for prostate cancer.
  • Assess sexual function and other quality of life issues during this therapy.
  • Estimate the response to flutamide withdrawal in this group of patients who have not had a major reduction in circulating testosterone levels.
  • Measure the response rate to further hormonal manipulation with combined androgen blockade after the failure of this therapy.
  • Obtain data that may predict more aggressive disease.

OUTLINE: This is a multicenter study.

Patients receive finasteride and flutamide by mouth three times a day. Patients experiencing recurrence or a greater than 4 nu/mL (above 50%) increase in PSA level will discontinue flutamide treatments. Otherwise, patients continue therapy in the absence of unacceptable toxicity or disease progression.

Quality of life is assessed prior to therapy and at 3 and 6 months.

Patients are followed every 3 months for one year and every 6 months thereafter.

PROJECTED ACCRUAL: This study will accrue 100 patients over 2 years.

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Conditions studied

  • Prostate Cancer
  • Sexual Dysfunction and Infertility

Keywords

  • adenocarcinoma of the prostate
  • recurrent prostate cancer
  • sexual dysfunction and infertility
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In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 101 is above the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Alliance for Clinical Trials in Oncology is the lead sponsor of 499 studies on the registry; 27 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 6 (100%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
No

Eligibility criteria

  1. Histologic Documentation: Previous histologic evidence of adenocarcinoma of the prostate.
  2. Prior Treatment:

    2.1 Definitive Local Therapy: Patients must have had a previous attempt at definitive therapy, which is defined as a previous radical prostatectomy or radiation therapy with at least 5500 cGy to the prostate.

    1. Patients may have had both radiation therapy to the prostate and surgical resection, given as definitive therapy, provided they began the radiation therapy within 3 months of their prostatectomy. Also, brachytherapy alone and combinations of brachytherapy and external beam radiation therapy are also allowed, if given as a single therapy, and not given for a rising PSA after the previous therapy.
    2. The previous treatment must have occurred at least 6 months, but no more than 10 years, prior to registration.

    2.2 Previous Hormonal Therapy or Other Treatments: Patients may have had no more than 6 months of hormonal therapy with their other treatment, and must have been off all hormones used for the treatment of prostate cancer including Megace for at least 12 months.

    1. No therapy within 2 years with finasteride or other 5 alpha-reductase inhibitors.
    2. No previous chemotherapy for this malignancy.
    3. No orchiectomy.
    4. No corticosteroids in excess of standard replacement doses for adrenal failure.
  3. Elevated PSA Criteria:

    3.1 Patients must a PSA level between 1 ng/ml and 10 ng/ml, with a rise of at least 1 ng/ml above the nadir produced by definitive therapy. The PSA level must be repeated at least once, one month later to confirm the rise of 1 ng/ml above nadir.

    3.2 After the second PSA has been drawn to confirm the rise, one additional PSA should be drawn as close to the start of therapy as possible. Therefore, a total of three PSAs must be drawn prior to the start of therapy. Only the last two need to be drawn at the same lab (ie, the second confirmatory PSA and the PSA drawn just prior to the start of the trial). The nadir PSA and the initial PSA suggesting a rise can be drawn at outside laboratories. The combination of the nadir PSA and the two PSAs showing a rise of 1.0 ng/ml are used for determining eligibility. The two elevated PSAs must be at least one month apart.

  4. No clear evidence of local recurrence on the digital rectal exam.
  5. No metastatic disease on the CT or bone scan.
  6. Performance status 0-2
  7. Required initial laboratory data

    1. SGOT and/or SGPT ≤2 x upper limits of normal
    2. Creatinine ≤2 x upper limits of normal
    3. Bilirubin ≤2 x upper limits of normal
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Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
101 participants (actual)

Study arms

  • Experimental
    Hormone Therapy

    Treatment of prostate cancer pts post radiation or surgery with potency sparing hormones

    Drug: finasteride · Drug: flutamide · Other: quality-of-life assessment

Interventions

  • Drugfinasteride

    5 mg/d PO

  • Drugflutamide

    250 mg PO tid

  • Otherquality-of-life assessment

    Assessment survey administered at baseline, and 3 \& 6 months post initiation of treatment

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What researchers measure

Primary outcomes

  1. PSA levels

    Time frame: 1 year post treatment

Secondary outcomes

  1. QOL issues associated with treatment protocol

    Time frame: 3 & 6 months

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Study locations

43 sites
  • Veterans Affairs Medical Center - Birmingham
    Birmingham, Alabama 35233-1996, United States
  • University of California San Diego Cancer Center
    La Jolla, California 92093-0658, United States
  • Veterans Affairs Medical Center - San Francisco
    San Francisco, California 94121, United States
  • UCSF Cancer Center and Cancer Research Institute
    San Francisco, California 94143-0128, United States
  • CCOP - Christiana Care Health Services
    Wilmington, Delaware 19899, United States
  • Walter Reed Army Medical Center
    Washington, District of Columbia 20307-5000, United States
  • CCOP - Mount Sinai Medical Center
    Miami Beach, Florida 33140, United States
  • Veterans Affairs Medical Center - Chicago (Westside Hospital)
    Chicago, Illinois 60612, United States
  • University of Chicago Cancer Research Center
    Chicago, Illinois 60637-1470, United States
  • Holden Comprehensive Cancer Center at The University of Iowa
    Iowa City, Iowa 52242-1009, United States
  • Veterans Affairs Medical Center - Togus
    Togus, Maine 04330, United States
  • Marlene & Stewart Greenebaum Cancer Center, University of Maryland
    Baltimore, Maryland 21201, United States
  • Dana-Farber Cancer Institute
    Boston, Massachusetts 02115, United States
  • University of Massachusetts Memorial Medical Center
    Worcester, Massachusetts 01655, United States
  • Veterans Affairs Medical Center - Minneapolis
    Minneapolis, Minnesota 55417, United States
  • Veterans Affairs Medical Center - Columbia (Truman Memorial)
    Columbia, Missouri 65201, United States
  • Ellis Fischel Cancer Center - Columbia
    Columbia, Missouri 65203, United States
  • Barnes-Jewish Hospital
    Saint Louis, Missouri 63110, United States
  • Washington University Siteman Cancer Center
    Saint Louis, Missouri 63110, United States
  • University of Nebraska Medical Center
    Omaha, Nebraska 68198-3330, United States
  • CCOP - Southern Nevada Cancer Research Foundation
    Las Vegas, Nevada 89106, United States
  • Norris Cotton Cancer Center
    Lebanon, New Hampshire 03756-0002, United States
  • Veterans Affairs Medical Center - Buffalo
    Buffalo, New York 14215, United States
  • Roswell Park Cancer Institute
    Buffalo, New York 14263-0001, United States
  • CCOP - North Shore University Hospital
    Manhasset, New York 11030, United States
  • Schneider Children's Hospital at North Shore
    Manhasset, New York 11030, United States
  • Memorial Sloan-Kettering Cancer Center
    New York, New York 10021, United States
  • New York Presbyterian Hospital - Cornell Campus
    New York, New York 10021, United States
  • Mount Sinai Medical Center, NY
    New York, New York 10029, United States
  • State University of New York - Upstate Medical University
    Syracuse, New York 13210, United States
  • Veterans Affairs Medical Center - Syracuse
    Syracuse, New York 13210, United States
  • CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C.
    Syracuse, New York 13217, United States
  • Lineberger Comprehensive Cancer Center, UNC
    Chapel Hill, North Carolina 27599-7295, United States
  • Veterans Affairs Medical Center - Durham
    Durham, North Carolina 27705, United States
  • Duke Comprehensive Cancer Center
    Durham, North Carolina 27710, United States
  • CCOP - Southeast Cancer Control Consortium
    Winston-Salem, North Carolina 27104-4241, United States
  • Comprehensive Cancer Center at Wake Forest University
    Winston-Salem, North Carolina 27157-1082, United States
  • Rhode Island Hospital
    Providence, Rhode Island 02903, United States
  • University of Tennessee, Memphis Cancer Center
    Memphis, Tennessee 38103, United States
  • Veterans Affairs Medical Center - Memphis
    Memphis, Tennessee 38104, United States
  • Veterans Affairs Medical Center - White River Junction
    White River Junction, Vermont 05009, United States
  • Veterans Affairs Medical Center - Richmond
    Richmond, Virginia 23249, United States
  • MBCCOP - Massey Cancer Center
    Richmond, Virginia 23298-0037, United States
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References and documents

Publications

  • Picus J, Halabi S, Small E, et al.: Long term efficacy of peripheral androgen blockade on prostate cancer: CALGB 9782. [Abstract] J Clin Oncol 24 (Suppl 18): A-4573, 2006.
  • Picus J, Halabi S, Small E, et al.: Efficacy of peripheral androgen blockade on prostate cancer: results of CALGB 9782. [Abstract] J Clin Oncol 22 (Suppl 14): A-4559, 396s, 2004.
  • Picus J, Halabi S, Hussain A, et al.: Efficacy of peripheral androgen blockade on prostate cancer: initial results of CALGB 9782. [Abstract] Proceedings of the American Society of Clinical Oncology 21: A-727, 2002.
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 4, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00003323
Lead sponsor
Alliance for Clinical Trials in Oncology
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Aug 13, 2003
Start date
May 1998
Primary completion
May 2002
Completion
Mar 2010
Last update
Jul 4, 2016

Study contacts

Joel Picus, MD
study chair · Washington University Siteman Cancer Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.

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