A Retrospective Study Evaluating Frequency and Risk Factors of Osteonecrosis of the Jaw in 576 Cancer Patients Receiving Intravenous Bisphosphonates
Overview
Authors
Affiliations
Objective: To evaluate the frequency, risk factors, and clinical presentation of bisphosphonate (BP)-related osteonecrosis of the jaw (BRONJ).
Study Design: We performed a retrospective analysis of 576 patients with cancer treated with intravenous pamidronate and/or zoledronate between January, 2003 and December, 2007 at the University of Minnesota Masonic Cancer Center and Park Nicollet Institute.
Results: Eighteen of 576 identified patients (3.1%) developed BRONJ including 8 of 190 patients (4.2%) with breast cancer, 6 of 83 patients (7.2%) with multiple myeloma, 2 of 84 patients (2.4%) with prostate cancer, 1 of 76 patients (1.3%) with lung cancer, 1 of 52 patients (1.9%) with renal cell carcinoma, and in none of the 73 patients with other malignancies. Ten patients (59%) developed BRONJ after tooth extraction, whereas 7 (41%) developed it spontaneously (missing data for 1 patient). The mean number of BP infusions (38.1 ± 19.06 infusions vs. 10.5 ± 12.81 infusions; P<0.001) and duration of BP treatment (44.3 ± 24.34 mo vs. 14.6 ± 18.09 mo; P<0.001) were significantly higher in patients with BRONJ compared with patients without BRONJ. Multivariate Cox proportional hazards regression analysis showed that diabetes [hazard ratio (HR)=3.40; 95% confidence interval (CI), 1.14-10.11; P=0.028], hypothyroidism (HR=3.59; 95% CI, 1.31-9.83; P=0.013), smoking (HR=3.44; 95% CI, 1.28-9.26; P=0.015), and higher number of zoledronate infusions (HR=1.07; 95% CI, 1.03-1.11; P=0.001) significantly increased the risk of developing BRONJ.
Conclusions: Increased cumulative doses and long-term BP treatment are the most important risk factors for BRONJ development. Type of BP, diabetes, hypothyroidism, smoking, and prior dental extractions may play a role in BRONJ development.
Hanna R, Miron I, Dalvi S, Arany P, Bensadoun R, Benedicenti S Pharmaceuticals (Basel). 2024; 17(8).
PMID: 39204116 PMC: 11357434. DOI: 10.3390/ph17081011.
Ferreira S, Amaral J, Pacheco J, Salazar F, Monteiro L J Clin Med. 2024; 13(9).
PMID: 38731207 PMC: 11084472. DOI: 10.3390/jcm13092679.
Hadad H, Matheus H, Pai S, Souza F, Guastaldi F Arch Oral Biol. 2023; 159():105875.
PMID: 38160519 PMC: 11729500. DOI: 10.1016/j.archoralbio.2023.105875.
Bittrich M, Hetterich R, Solimando A, Krebs M, Loda S, Danhof S Clin Exp Med. 2023; 23(8):5215-5226.
PMID: 37805620 PMC: 10725344. DOI: 10.1007/s10238-023-01100-6.
Bracchi P, Zecca E, Brunelli C, Miceli R, Tine G, Maniezzo M Cancer Med. 2023; 12(17):18317-18326.
PMID: 37559413 PMC: 10523953. DOI: 10.1002/cam4.6429.