Clinical Trials Directory

Trials / Completed

CompletedNCT00843167

Broccoli Sprout Extract in Treating Women Who Have Had a Mammogram and Breast Biopsy

Sulforaphane: A Dietary Histone Deacetylase (HDAC) Inhibitor in Ductal Carcinoma in Situ (DCIS)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
54 (actual)
Sponsor
OHSU Knight Cancer Institute · Academic / Other
Sex
Female
Age
21 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Broccoli sprout extract supplements may slow the growth of tumor cells or abnormal cells and may be an effective treatment for ductal carcinoma in situ and/or atypical ductal hyperplasia. PURPOSE: This randomized phase II trial is studying how well broccoli sprout extract works in treating women with a diagnosis of breast cancer, ductal carcinoma in situ and/or atypical ductal hyperplasia.

Detailed description

OBJECTIVES: * To determine the correlation between supplemental sulforaphane (broccoli sprout extract) dose and concentrations of sulforaphane and its metabolites in blood and urine samples from women positive for cancer, ductal carcinoma in situ and/or atypical ductal hyperplasia. * To determine the effect of this supplement on biomarkers of prognosis in these patients. * To determine the effect of this supplement on HDAC inhibition in peripheral blood cell and normal and cancerous breast tissue samples from these patients. OUTLINE: Patients are randomized to 1 of 2 treatment arms. * Sulforaphane Supplement: Patients receive oral broccoli sprout extract supplementation three times daily for 2-8 weeks in the absence of unacceptable toxicity. * Placebo: Patients receive oral placebo supplementation three times daily for 2-8 weeks in the absence of unacceptable toxicity. Blood and urine samples are collected at baseline and after completion of study treatment for laboratory biomarker studies. Patients scheduled to undergo surgery (mastectomy or lumpectomy) also undergo breast tissue sample collection at baseline and at the time of surgery. Samples are analyzed for sulforaphane metabolism (isothiocyanate levels), HDAC activity (acetylated histone expression), cell proliferation (Ki-67 index by IHC), and apoptosis (TUNEL assay). Patients complete questionnaires at baseline and periodically during study about their dietary history, family history, cruciferous vegetable intake, adverse events, and dietary and medication changes. After completion of study therapy, patients are followed at/around 30 days.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTbroccoli sprout extractGiven orally
OTHERplaceboGiven orally

Timeline

Start date
2009-08-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2009-02-13
Last updated
2017-04-27
Results posted
2015-02-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00843167. Inclusion in this directory is not an endorsement.