Bisphosphonates (BPs) are potent inhibitors of bone resorption currently used in the treatment of osteoporosis, hypercalcemia of malignancy, multiple myeloma, and bone metastases associated with, breast, prostate, and lung cancer. In 2003, Marx reported 36 patients receiving intravenous BPs who developed unusual lesions of exposed bone in the jaws. Thirty five of these patients were concurrently receiving chemotherapy for cancer. Subsequently, Ruggiero et al. reported 63 patients with similar lesions of the jaws. In their series, 56 patients were under treatment for various malignancies and 7 patients were receiving therapy for osteoporosis. Intravenous BPs had been administered to all patients. Many, but not all patients had dental extractions or surgical manipulation prior to the development of osteonecrosis (ON). While it appears likely that an association of ON with BP therapy exists, scientifically-based studies are critical in order to define the pathogenesis and natural history of this condition. Although BPs is currently utilized in the treatment of a limited number of conditions, the potential for these drugs to be used in many other applications is vast. It is therefore critical to future patient care to identify risk factors and candidate markers for the development of jaw ON. This proposal will describe a case controlled, cross-sectional as well as a prospective longitudinal pilot study of a well defined group of breast cancer patients being treated with chemotherapy. The case controlled study will evaluate patients who present with ON. Age and ethnically matched patients without ON from the prospective study will be compared to affected patients in order to identify local and systemic abnormalities that are associated with this condition. The prospective study will examine two groups of 200 breast cancer patients on maintenance chemotherapy, with one group receiving BPs for the treatment of skeletal related events secondary to bone metastases. We will examine a number of risk factors including oral hygiene, the presence of dental disease, early radiographic findings, bone turnover, coagulopathies, depression of serum angiogenesis factors, and alteration of blood cells or serum chemistry to determine if we can predict which patients will develop this condition. The findings will be used to define the natural history, risk factors, and candidate markers for the development of jaw osteonecrosis and allow future development of rational prevention and treatment regimens. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DE017164-01A1
Application #
7145967
Study Section
Special Emphasis Panel (ZDE1-PZ (48))
Program Officer
Shum, Lillian
Project Start
2006-09-01
Project End
2008-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
1
Fiscal Year
2006
Total Cost
$241,500
Indirect Cost
Name
Columbia University (N.Y.)
Department
Dentistry
Type
Schools of Dentistry
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Marolt, Darja; Cozin, Matthew; Vunjak-Novakovic, Gordana et al. (2012) Effects of pamidronate on human alveolar osteoblasts in vitro. J Oral Maxillofac Surg 70:1081-92
Cozin, Matthew; Pinker, Bradley M; Solemani, Kimberley et al. (2011) Novel therapy to reverse the cellular effects of bisphosphonates on primary human oral fibroblasts. J Oral Maxillofac Surg 69:2564-78
Landesberg, Regina; Woo, Victoria; Cremers, Serge et al. (2011) Potential pathophysiological mechanisms in osteonecrosis of the jaw. Ann N Y Acad Sci 1218:62-79