Influence of prostate cancer status on the prevalence of medication-related osteonecrosis of the jaw

被引:2
|
作者
Yasui, Takazumi [1 ,2 ]
Kimura, Moemi [1 ,2 ]
Nagamine, Hiroki [1 ]
Yajima, Shosuke [3 ]
Karube, Takeshi [2 ]
Sato, Hitoshi [4 ]
Asoda, Seiji [2 ]
Hara, Satoshi [5 ]
Onizawa, Katsuhiro [1 ]
机构
[1] Kawasaki Municipal Kawasaki Hosp, Dept Dent & Oral Surg, Kawasaki, Kanagawa, Japan
[2] Keio Univ, Sch Med, Dept Dent & Oral Surg, Tokyo, Japan
[3] Kawasaki Municipal Ida Hosp, Dept Dent & Oral Surg, Kawasaki, Kanagawa, Japan
[4] Showa Univ, Sch Dent, Dept Oral & Maxillofacial Surg, Div Oral Oncol, Tokyo, Japan
[5] Kawasaki Municipal Kawasaki Hosp, Dept Urol, Kawasaki, Kanagawa, Japan
关键词
BISPHOSPHONATE-INDUCED OSTEONECROSIS; INCREASED SURVIVAL; ZOLEDRONIC ACID; RISK-FACTORS; DENOSUMAB; PHASE; MITOXANTRONE; CABAZITAXEL; PREDNISONE; THERAPY;
D O I
10.1016/j.oooo.2020.12.018
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective. The aim of this study was to evaluate the risk of osteonecrosis of the jaw (ONJ) in patients with prostate cancer, particularly the relationship between prostate cancer progression and ONJ development. Study Design. This single-center, retrospective, observational study included 113 patients who received zoledronic acid or denosumab for prostate cancer with bone metastasis between January 2012 and March 2020. The risk of ONJ was evaluated regarding age; antiresorptive drugs; duration of antiresorptive treatment; prostate cancer status, including castration-resistant prostate cancer (CRPC) and prostate-specific antigen level; chemotherapy; radium-223 treatment; corticosteroid treatment; diabetes mellitus; and dental extractions. Results. Overall, 28 patients had ONJ; 10 patients received zoledronic acid and 18 patients received denosumab. Multiple logistic regression analysis demonstrated that CRPC (odds ratio = 6.01; 95% confidence interval, 1.76-20.05; P = .004) and dental extractions (odds ratio = 12.40; 95% confidence interval, 3.42-44.70; P < .001) were significantly associated with ONJ. In addition, antiresorptive treatment lasting more than 1 year partially mediated between CRPC and development of ONJ. Conclusion. CRPC and dental extraction are risk factors for developing ONJ, and antiresorptive treatment lasting more than 1 year is a partial mediator between CRPC and ONJ.
引用
收藏
页码:312 / 318
页数:7
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