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OpenTrials
Completed

NCT Number: NCT00586898

Rapid Hormonal Cycling as Treatment for Patients With Prostate Cancer: The Men's Cycle

Objective: To determine the response to rapid hormonal cycling in patients with non-castrate prostate cancer.

Completed

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

Memorial Sloan Kettering Cancer Center

New York, 10065, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

-Patients residing in the following clinical states wit! be considered: A. Rising PSA: Patients with a history of localized disease who have undergone definitive radiation or surgery. These patients must demonstrate progression of disease biochemically as outlined below. Patients in this group may not have radiographically evident disease.

B. Non-castrate metastatic: Patients must present with radiographic evidence of metastatic disease at the time of diagnosis or after treatment for localized disease. These patients must show newly detected disease or progressing disease in bone or in soft tissue. Biochemical progression is defined as: minimum no. of determinations: 3 Interval: >2 weeks Minimal Baseline PSA value (ng/ml): 2 Minimal % increase in range of values: 50%

  • Diagnosis of prostate adenocarcinoma histologically confirmed at MSKCC.
  • Patient must have level of serum testosterone above the lower limit of normal.
  • Karnofskcy performance status (KPS) >_70%.
  • Patients must have adequate organ function as defined by the following laboratory criteria:
  • WBC >_3500/mm3, platelet count >_100,000/mm3.
  • Bilirubin <2.0 mg/dl or SGOT <3.0 X the upper limit of normal.
  • Creatinine <_1.6 mg/dl or creatinine clearance >_60 cc/min.
  • Prior hormonal therapy is allowed as:
  • Neoadjuvant treatment prior to radiation therapy or radical prostatectomy, provided that the total duration of exposure does not exceed 10 months.
  • One cycle of intermittent therapy up to a maximum exposure of 10 months.
  • Patients must be at least 18 years of age.
  • Patients must have signed an informed consent document stating that they understand the investigational nature of the proposed treatment

Exclusion criteria

  • Clinically significant cardiac disease (New York Heart Association Class III/IV),or severe debilitating puhnonary disease.
  • Uncontrolled serious active infection.
  • Anticipated survival of less than 3 months.
  • Active CNS or epiduraltumor
  • Inability or unwillingness to comply with the treatment protocol, follow-up, or research tests.

Treatment and study plan

GnRH

Drug

leuprolide and goserelin are gonadotropin-releasing hormone analogues

Other names: LUPRON, ZOLADEX

Ketoconazole

Drug

An imidazole antifungal agent. reduces adrenal and testicular androgen production in men

Other names: Nizoral

bicalutamide

Drug

A pure nonsteroidal antiandrogen

Other names: Casodex

Testosterone transdermal gel

Drug

an androgenic anabolic steroid

Other names: Androgel

Estrogen transdermal patch

Drug

Estradiol is the primary and most potent estrogen

Other names: CLIMARA

Primary outcomes

  1. Response

    Time frame: 6 months

    Complete Response: Normalization of the PSA (< or = to 4.0 for patients with castrate metastatic disease, or < 0.5 for patients with a rising PSA) that is maintained on 3 successive evaluations a minimum of 2 weeks apart. Partial Response: Decrease in PSA value by > or = to 50% from baseline value (without normalization) for 3 successive evaluations a minimum of 2 weeks apart. Stabilization: Patients who do not meet the criteria for PR or PROG for at least 90 days will be considered stable.

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Registry information

Important dates

Study start
2001
Primary completion
2009
Study completion
2009
First posted
Jan 7, 2008
Registry last updated
Mar 25, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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