Ketoconazole, Hydrocortisone and Dutasteride in Asymptomatic Hormone Refractory Prostate Cancer (KHAD)
This study has been completed.
Sponsor:
Beth Israel Deaconess Medical Center
Collaborators:
Massachusetts General Hospital
Dana-Farber Cancer Institute
Sunnybrook Health Sciences Centre
Oregon Health and Science University
M.D. Anderson Cancer Center
Sidney Kimmel Comprehensive Cancer Center
Information provided by (Responsible Party):
Steven Balk, MD, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier:
NCT00673127
First received: May 5, 2008
Last updated: December 27, 2012
Last verified: December 2012
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Purpose
The combination of ketaconazole and hydrocortisone is commonly used for the treatment of prostate cancer. The purpose of this study is to determine if the addition of a drug called dutasteride to this approved combination will make the combination more effective in treating prostate cancer.
| Condition | Intervention | Phase |
|---|---|---|
|
Prostate Cancer |
Drug: Ketaconazole Drug: Hydrocortisone Drug: Dutasteride |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase II Trial of Ketoconazole, Hydrocortisone and Dutasteride in Asymptomatic Hormone Refractory Prostate Cancer |
Resource links provided by NLM:
Drug Information available for:
Hydrocortisone acetate
Hydrocortisone
Hydrocortisone sodium succinate
Hydrocortisone cypionate
Hydrocortisone butyrate
Hydrocortisone valerate
Ketoconazole
Hydrocortisone probutate
Dutasteride
U.S. FDA Resources
Further study details as provided by Dana-Farber Cancer Institute:
Primary Outcome Measures:
- To evaluate the efficacy of high dose ketoconazole and hydrocortisone in combination with dutasteride (KHAD) in the treatment of hormone refractory prostate cancer. [ Time Frame: TBD ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- To evaluate the toxicity of the combination in hormone refractory prostate cancer. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
- To evaluate the time to progression on KHAD. [ Time Frame: TBD ] [ Designated as safety issue: No ]
- Correlate levels of androgens and metabolites with response. [ Time Frame: TBD ] [ Designated as safety issue: No ]
| Enrollment: | 57 |
| Study Start Date: | February 2005 |
| Study Completion Date: | December 2012 |
| Primary Completion Date: | February 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: KHAD
KHAD
|
Drug: Ketaconazole
200mg orally three times a day on an empty stomach.
Drug: Hydrocortisone
30mg in the morning and 10mg in the evening. Pills should be taken with food or milk.
Drug: Dutasteride
0.5mg orally once a day on an empty stomach or after eating a meal.
|
Detailed Description:
- Participants will be seen by the study physician every four weeks and have a short physical examination, blood tests and be asked to provide information about their condition. Every three months they will undergo a bone scan. If the CT scan that was obtained before the participant started the study shows evidence of cancer, they will be asked to repeat this test every three months.
- Ketaconazole will be taken orally three times a day on an empty stomach. Hydrocortisone will be taken orally in the morning and at night. Dutasteride will be taken orally once a day.
- Participants may remain on study drug until there is evidence of disease progression.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Histologically documented evidence of prostate cancer (needle biopsy or prostatectomy). In the abscence of histologically documented evidence of prostate cancer, the diagnosis must be based on elevated serum PSA and metastatic lesions on bone scan.
- Progressive HRPC defined as a PSA increase over baseline of >25% or 5ng/ml or new lesions on bone/CT scan after conventional androgen deprivation and antiandrogen withdrawal. Evidence of metastatic disease based on positive CT or bone scan is not required.
- PSA of greater than or equal to 2ng/ml and serum total testosterone less than or equal to 50ng/ml
- Prior chemotherapy is permitted if discontinued > 4 weeks prior to starting therapy
- Prior therapy with estrogens is permitted but must have been discontinued > 4 weeks prior to registration
- ECOG Performance Status 0-2
- Adequate renal function, hepatic function, and bone marrow function as outlined in protocol
- ECG showing a normal QT interval
Exclusion Criteria:
- Prior therapy with ketoconazole or corticosteroids for HRPC
- Major surgery or radiation therapy within 4 weeks
- Strontium-89 or samarium-153 therapy within 4 weeks
- Thromboembolism in past 6 months
- Patients who are taking drugs that may further prolong QT intervals and present a known risk for Torsades de Pointes.
- Concomitant use of drugs known to be narrow therapeutic index CTP3A4
- Drugs that are sensitive CYP3A4 substrates
- Alcohol or drug dependence currently or in the last 6 months
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00673127
Locations
| United States, Maryland | |
| Sidney Kimmel Comprehensive Cancer Center at John Hopkins University | |
| Baltimore, Maryland, United States | |
| United States, Massachusetts | |
| Beth Israel Deaconess Medical Center | |
| Boston, Massachusetts, United States, 02115 | |
| Dana-Farber Cancer Institute | |
| Boston, Massachusetts, United States, 02115 | |
| Massachusetts General Hospital | |
| Boston, Massachusetts, United States, 02214 | |
| United States, Oregon | |
| Oregon Health and Science University | |
| Portland, Oregon, United States | |
| United States, Texas | |
| MD Anderson Cancer Center | |
| Houston, Texas, United States | |
| Canada | |
| Sunnybrook and Women's College Health Sciences Center | |
| Toronto, Canada | |
Sponsors and Collaborators
Beth Israel Deaconess Medical Center
Massachusetts General Hospital
Dana-Farber Cancer Institute
Sunnybrook Health Sciences Centre
Oregon Health and Science University
M.D. Anderson Cancer Center
Sidney Kimmel Comprehensive Cancer Center
Investigators
| Principal Investigator: | Steven Balk, MD | Beth Israel Deaconess Medical Center |
More Information
No publications provided
| Responsible Party: | Steven Balk, MD, Principle Investigator, Dana-Farber Cancer Institute |
| ClinicalTrials.gov Identifier: | NCT00673127 History of Changes |
| Other Study ID Numbers: | 04-414 |
| Study First Received: | May 5, 2008 |
| Last Updated: | December 27, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Dana-Farber Cancer Institute:
|
hormone refractory KHAD ketoconazole dutasteride hydrocortisone |
Additional relevant MeSH terms:
|
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site Neoplasms Genital Diseases, Male Prostatic Diseases Hormones Cortisol succinate Hydrocortisone acetate Hydrocortisone 17-butyrate 21-propionate Hydrocortisone Hydrocortisone-17-butyrate Ketoconazole |
Dutasteride Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions Anti-Inflammatory Agents Therapeutic Uses Dermatologic Agents 14-alpha Demethylase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Antifungal Agents Anti-Infective Agents 5-alpha Reductase Inhibitors |
ClinicalTrials.gov processed this record on May 22, 2013