Papers

Peer-reviewed Open access
Dec, 2015

Incidence and Risk Factors of Osteonecrosis of the Jaw in Advanced Cancer Patients after Treatment with Zoledronic Acid or Denosumab: A Retrospective Cohort Study

BIOLOGICAL & PHARMACEUTICAL BULLETIN
  • Makoto Kajizono
  • ,
  • Hikaru Sada
  • ,
  • Yuhko Sugiura
  • ,
  • Yoshihiko Soga
  • ,
  • Yoshihisa Kitamura
  • ,
  • Junji Matsuoka
  • ,
  • Toshiaki Sendo

Volume
38
Number
12
First page
1850
Last page
1855
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1248/bpb.b15-00385
Publisher
PHARMACEUTICAL SOC JAPAN

Zoledronic acid and denosumab are two antiresorptive drugs currently in use for treating osteoporosis. They have different mechanisms of action, but both have been shown to delay the onset of skeletal-related events in patients with advanced cancer. However, medication-related osteonecrosis of the jaw (MRONJ) has been reported in cancer patients treated with zoledronic acid or denosumab. We studied 155 patients with several types of advanced cancer who were treated with zoledronic acid or denosumab in our hospital during the period from April 2010 through March 2013. Thirteen of these 155 patients (8.4%) developed MRONJ. MRONJ development was significantly associated with the number of zoledronic acid or denosumab infusions (p<0.001) and the duration of zoledronic acid or denosumab therapy (p<0.001). Logistic regression analysis showed that diabetes [odds ratio (OR)=6.699, 95% confidence interval (CI), 1.435-31.277, p=0.016], anemia [OR=14.559, 95% CI, 2.161-98.069, p=0.006], and pus discharge [OR=6.491, 95% CI, 1.514-27.835, p=0.012] significantly increased the risk of developing MRONJ. However, the risk of MRONJ was significantly lower [OR=0.137, 95% CI, 0.020-0.944, p=0.043] when patients received periodical dentistry maintenance. Diabetes, anemia, and pus discharge may also play roles in its development. These findings suggest that the active inclusion of dentistry maintenance in bisphosphonate or denosumab treatment of cancer patients can reduce MRONJ development.

Link information
DOI
https://doi.org/10.1248/bpb.b15-00385
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26632176
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000365694800004&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84948708780&origin=inward Open access
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84948708780&origin=inward
ID information
  • DOI : 10.1248/bpb.b15-00385
  • ISSN : 0918-6158
  • eISSN : 1347-5215
  • Pubmed ID : 26632176
  • SCOPUS ID : 84948708780
  • Web of Science ID : WOS:000365694800004

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