Recruiting | Phase II
A Phase II Randomized Trial of Olaparib (NSC-747856) Administered Concurrently with Radiotherapy versus Radiotherapy Alone for Inflammatory Breast Cancer
To determine if adding the drug olaparib to the usual radiation therapy for inflammatory breast cancer will decrease the risk of cancer returning.
- Olaparib (Lynparza®)
- Radiation Therapy
- Lab Biomarker Analysis
- ARM I: Olaparib 25mg BID + Standard Radiation Therapy
- ARM II: Radiation Therapy Alone
Patients will be followed every 3 months from start of study for the first 3 years, and then every 6 months until 8 years from start of study.
Key Participation Requirements:
Male or female
19 years and older
Breast cancer patients who have had surgery and whose cancer is diagnosed as inflammatory.
All ER/PR/Her2 statuses are accepted
Patients must have completed chemotherapy before mastectomy, as well as the mastectomy, itself. They may or may not have had chemotherapy after surgery.
Must be registered to the study at least 3 weeks, but no more than 12 weeks after mastectomy.
Patients must sign an approved informed consent and authorization permitting release of personal health information.
Methodist Health System Trial Code:
For more information, visit the U.S. National Library of Medicine clinical trial database.