As the only national nonprofit advocacy organization focused on hereditary breast and ovarian cancer, FORCE has a strong commitment to promoting research.
Study identifier: NCT01445418
Full study details on clinicaltrials.gov
Name of PARP Inhibitor used in study:
Patients 18 years of age or older who have a family history of cancer or who have a BRCA1 or BRCA2 mutation.
Patients must have breast and/or epithelial ovarian cancer, primary peritoneal cancer, and/or fallopian tube cancer histologically or cytologically confirmed at the NCI that is metastatic or unresectable and for which standard curative measures do not exist or are no longer effective. All patients in cohort 1 must have measurable and/or evaluable disease.
Patients in the expansion cohort 2 must have safely biopsible disease as determine by an interventional radiologist and must agree to the first mandatory biopsy (the other two biopsies optional).
Breast cancer patients with locally advanced, unresectable disease must have been previously treated with standard therapy.
There is no limit on number of prior therapy.
Patients must be at least 6 months from their last platinum exposure.
Type of study:
Phase I study
Patients receive treatment in 21-day cycles as follows: AZD2281 by mouth twice a day every day; carboplatin thorough a vein on day 8 of each cycle. Treatment may continue until it is no longer beneficial.
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
Contact: Laura D.Otten, R.N., B.S.N., O.C.N.
Medical Oncology Referral Coordinator 301-451-1228
1-866-611-6310 (Toll Free) email@example.com