Adenocarcinoma of the Prostate, Hormone-resistant Prostate Cancer, Recurrent Prostate Cancer, Stage IV Prostate Cancer
Conditions
Brief summary
This randomized pilot phase I trial studies the side effects of dietary fat levels and abiraterone acetate uptake in patients with metastatic hormone-resistant prostate cancer. Abiraterone acetate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Eating a low or high fat diet may increase the uptake of abiraterone acetate.
Detailed description
PRIMARY OBJECTIVES: I. To assess the dietary effects of a low fat and high fat diet at a low abiraterone acetate dose (250 mg) on drug levels compared to standard dose administered in a fasting condition. SECONDARY OBJECTIVES: I. To potentially guide decisions in the future to use low dose abiraterone in a fed state and decrease overall cost. II. To evaluate the potential relationship between esterase activity and abiraterone metabolism in an exploratory analysis. III. To determine the feasibility of using patient-collected dried blood spot (DBS) samples for pharmacokinetic monitoring. OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM I: Patients receive standard dose abiraterone acetate orally (PO) once daily (QD) (held on days 2, 3, 9, and 10), and low-dose abiraterone acetate PO QD on days 3 and 10. Patients eat a low fat breakfast on day 3 and a high fat breakfast on day 10. ARM II: Patients receive abiraterone acetate as in Arm I. Patients eat a high fat breakfast on day 3, and a low fat breakfast on day 10.
Interventions
DRUGabiraterone acetate
Given PO
DIETARY_SUPPLEMENTdietary intervention
Receive low fat breakfast
OTHERpharmacological study
Correlative studies
OTHERquestionnaire administration
Ancillary studies
OTHERlaboratory biomarker analysis
Correlative studies
Sponsors
National Cancer Institute (NCI)
OHSU Knight Cancer Institute
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically confirmed adenocarcinoma of the prostate * About to initiate or currently being treated with abiraterone acetate 1000 mg orally once daily * Clinically able to receive abiraterone acetate in the opinion of the investigator in accordance with standard prescribing practices * Ability to consume a low fat and high fat diet * Expected duration of continuous abiraterone therapy \> 8 weeks * Signed and dated informed consent
Exclusion criteria
* Patients taking medications that strongly inhibit or induce cytochrome P450 (CYP)3A4 within 28 days prior to the start of the study will be excluded
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Area under the curve (AUC)0-24 measurement | Up to 24 hours (day 1) | The cross-over difference (log\[AUC0-24(low fat)\] - log\[AUC0-24(high fat)\]) of each patient will be computed and graphically illustrated. The cross-over difference will be estimated and reported with 95% confidence interval. Hills-Armitage approach will be used to adjust for the period effect for the estimation. In addition, a bioequivalence range will be computed for the log(AUC0-24\[1000 mg with fasting food\]), allowing for 20% differences in each side. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Accuracy of patient-collected DBS sampling technique | Day 3 | The first three patients enrolled will have duplicate venous blood samples obtained in clinic 2 hours post-dose for in vivo confirmation of the DBS methodology. |
| Patient adherence to pre-defined sampling schedule | Up to day 14 | Patients will document the date/time of drug administration and the date/time of sample collection using a drug and DBS sample diary. Deviations greater than 10% of the shorter of the two time intervals surrounding the pre-defined time point will be considered non-adherent. Adherence rates will be compared for different time points. |
| Patient satisfaction of DBS method, measured using the Patient Questionnaire of DBS Sampling Method | Day 14 | Paired t-test will be conducted to compare the DBC (or transformed DBC) for the evaluation of carry-over effect. |
Countries
United States
Outcome results
None listed