Zoledronate or Observation in Maintaining Bone Mineral Density in Patients Who Are Undergoing Surgery to Remove Both Ovaries
Hereditary Breast and Ovarian Cancer Syndrome, Osteoporosis, Ovarian Carcinoma
About this trial
This is an interventional supportive care trial for Hereditary Breast and Ovarian Cancer Syndrome
Eligibility Criteria
Inclusion Criteria: Patients who have elected to undergo, or who have undergone (within 8 weeks) a surgical procedure that results (at minimum) in the absence of both ovaries Patients enrolled in the screening arm of GOG-0199 who decide to undergo surgery are potentially eligible for GOG-0215 Baseline bone mass density (BMD) T-Score ? -1.5 (no more than 1.5 standard deviation below the mean value for young adults) on both the total lumbar spine (L1-L4 region, not individual bones) and bilateral hip Patients who had/have at least 1 intact ovary at the time of surgery are eligible No prior distant metastatic malignant disease within the past 5 years Patients treated for stage M1 (any T, any N) diagnosis in the past 5 years are ineligible Patients who achieved a complete response after treatment for rM0 (any T, any N) within the past 5 years are eligible Premenopausal* Last menstrual cycle occurred < 12 months prior to study enrollment GOG performance status 0-2 Creatinine clearance > 60 mL/min No clinical or radiological evidence of existing fracture of the lumbar spine or bilateral hip No history of hip of spine fracture with low-intensity trauma or not associated with trauma No uncontrolled seizure disorder associated with falls No diseases that influence bone metabolism, including any of the following: Paget?s disease Osteogenesis imperfecta Uncontrolled thyroid or parathyroid dysfunction within 12 months prior to study entry No other nonmalignant systemic disease, including any of the following: Uncontrolled infection Uncontrolled type 2 diabetes mellitus Cardiovascular, renal, hepatic, or lung disease that would prevent prolonged follow-up History of thrombosis or thromboembolism allowed No known HIV positivity No known hypersensitivity to zoledronate or other bisphosphonates No psychiatric, psychological, or other conditions that prevent fully informed consent No other active malignancy except nonmelanoma skin cancer No history of any medical condition that places the patient at risk for donating blood for research purposes (e.g., chronic infectious diseases, sever anemia, or hemophilia) Not pregnant Negative pregnancy test No current active dental problems, including any of the following: Infection of the teeth or jawbone (maxilla or mandible) Dental or fixture trauma Current or prior diagnosis of osteonecrosis of the jaw Exposed bone in the mouth Slow healing after dental procedures No recent (within 6 weeks) or planned dental or jaw surgery (e.g., extraction or implants) No prior treatment for osteoporosis No adjuvant radiotherapy within the past 31 days No chemotherapy within the past 30 days No prior surgery to the hip or spine No prior systemic sodium fluoride for > 3 months during the past 2 years No more than 30 days use in the past 12 months and no concurrent tamoxifen, raloxifene, or any other selective estrogen-receptor modulator (SERM) More than 12 months since prior and no concurrent endocrine therapy Insulin and/or oral antidiabetic medications allowed Thyroid hormone replacement allowed More than 12 months since prior and no concurrent estrogen or hormone replacement therapy (estrogen plus progesterone or estrogen alone) Prior or concurrent oral contraceptives allowed Systemic (oral) hormone replacement therapy following surgery not allowed Vaginal (non-systemic) estrogen allowed More than 12 months since prior and no concurrent oral or IV bisphosphonate More than 12 months since prior and no concurrent anabolic steroids or growth hormone More than 12 months since prior and no concurrent systemic corticosteroids Concurrent short term corticosteroid therapy (to prevent/treat chemotherapy-induced nausea/vomiting) allowed More than 6 months since prior and no concurrent Tibolone More than 2 weeks since prior and no concurrent drugs known to affect the skeleton (e.g., calcitonin, mithramycin, or gallium nitrate) No concurrent chemotherapy or radiotherapy No concurrent aromatase inhibitors Concurrent enrollment on protocol GOG-0199 allowed
Sites / Locations
- Mayo Clinic in Arizona
- Banner University Medical Center - Tucson
- University of Arizona Cancer Center-North Campus
- Providence Saint Joseph Medical Center/Disney Family Cancer Center
- City of Hope Comprehensive Cancer Center
- Kaiser Permanente Los Angeles Medical Center
- Cedars Sinai Medical Center
- UC Irvine Health/Chao Family Comprehensive Cancer Center
- Stanford Cancer Institute Palo Alto
- University of California Davis Comprehensive Cancer Center
- University of California San Diego
- Colorado Gynecologic Oncology Group
- Boulder Community Hospital
- Penrose-Saint Francis Healthcare
- SCL Health Saint Joseph Hospital
- Rose Medical Center
- North Colorado Medical Center
- McKee Medical Center
- North Suburban Medical Center
- SCL Health Lutheran Medical Center
- Hartford Hospital
- The Hospital of Central Connecticut
- Yale University
- Beebe Medical Center
- Christiana Care Health System-Christiana Hospital
- MedStar Washington Hospital Center
- Holy Cross Hospital
- Jupiter Medical Center
- UF Cancer Center at Orlando Health
- Tripler Army Medical Center
- University of Illinois
- NorthShore University HealthSystem-Evanston Hospital
- Carle Cancer Center
- Northwestern Medicine Central DuPage Hospital
- Indiana University/Melvin and Bren Simon Cancer Center
- Saint Vincent Hospital and Health Care Center
- Memorial Hospital of South Bend
- University of Iowa/Holden Comprehensive Cancer Center
- Menorah Medical Center
- Saint Luke's South Hospital
- Baptist Health Lexington
- Norton Hospital Pavilion and Medical Campus
- MedStar Franklin Square Medical Center/Weinberg Cancer Institute
- Union Hospital of Cecil County
- West Michigan Cancer Center
- William Beaumont Hospital-Royal Oak
- University of Minnesota/Masonic Cancer Center
- Mayo Clinic
- Truman Medical Center
- Saint Luke's Hospital of Kansas City
- North Kansas City Hospital
- Heartland Hematology and Oncology Associates Incorporated
- Research Medical Center
- Saint Luke's East - Lee's Summit
- Heartland Regional Medical Center
- Mercy Hospital Saint Louis
- Saint Louis-Cape Girardeau CCOP
- Mercy Hospital Springfield
- CoxHealth South Hospital
- Sunrise Hospital and Medical Center
- Center of Hope at Renown Medical Center
- Cooper Hospital University Medical Center
- Virtua Memorial
- University of New Mexico Cancer Center
- Northwell Health/Center for Advanced Medicine
- North Shore University Hospital
- Long Island Jewish Medical Center
- Laura and Isaac Perlmutter Cancer Center at NYU Langone
- Mount Sinai Hospital
- Cone Health Cancer Center at Alamance Regional
- Novant Health Presbyterian Medical Center
- FirstHealth of the Carolinas-Moore Regional Hospital
- University of Cincinnati/Barrett Cancer Center
- Good Samaritan Hospital - Cincinnati
- Case Western Reserve University
- Ohio State University Comprehensive Cancer Center
- Riverside Methodist Hospital
- Mount Carmel Health Center West
- UH Seidman Cancer Center at Lake Health Mentor Campus
- University of Oklahoma Health Sciences Center
- Oklahoma Cancer Specialists and Research Institute-Tulsa
- Oregon Health and Science University
- Main Line Health NCORP
- Women and Infants Hospital
- Avera Cancer Institute
- Chattanooga's Program in Women's Oncology
- Meharry Medical College
- Vanderbilt University/Ingram Cancer Center
- The Don and Sybil Harrington Cancer Center
- University of Vermont Medical Center
- University of Virginia Cancer Center
- Virginia Commonwealth University/Massey Cancer Center
- Carilion Clinic Gynecological Oncology
- Saint Vincent Hospital Cancer Center Green Bay
- Aurora West Allis Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Arm I (zoledroic acid)
Arm II (clinical observation)
Beginning 60-90 days after surgery, patients receive zoledronate IV over 15 minutes once in months 3, 9, and 15.
Patients are observed for 18 months after surgery.