Memorial Sloan Kettering Cancer Center
New York, 10065, United States
NCT Number: NCT00586898
Objective: To determine the response to rapid hormonal cycling in patients with non-castrate prostate cancer.
Looking for future studies?
Notify Me18 year and older
Male
Interventional
Phase 2
New York, 10065, United States
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%
Exclusion criteria
leuprolide and goserelin are gonadotropin-releasing hormone analogues
Other names: LUPRON, ZOLADEX
An imidazole antifungal agent. reduces adrenal and testicular androgen production in men
Other names: Nizoral
A pure nonsteroidal antiandrogen
Other names: Casodex
an androgenic anabolic steroid
Other names: Androgel
Estradiol is the primary and most potent estrogen
Other names: CLIMARA
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.
Memorial Sloan Kettering Cancer Center
Other
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.
Published trials that share one or more normalized conditions with this study.
NCT00579423
Cancer, Neoplasms
New York, United States
View Trial DetailsNCT06192758
Cancer, Chromosome 2q32-Q33 Deletion Syndrome
Chicago, Illinois, United States
View Trial DetailsNCT07424547
Adnexal Diseases, Advanced Metastatic Cancer
Plantation, Florida, United States
View Trial DetailsNCT00026689
Brain, Breast
Bethesda, Maryland, United States
View Trial Details