Bone turnover markers can predict healing time in medication-related osteonecrosis of the jaw

Support Care Cancer. 2021 Dec;29(12):7895-7902. doi: 10.1007/s00520-021-06361-z. Epub 2021 Jun 30.

Abstract

Objectives: Medication-related osteonecrosis of the jaw (MRONJ) is a severe and difficult-to-treat adverse event of bone-modifying agents. Therefore predictive strategies determining patients at risk for a prolonged healing duration are needed to optimize treatment. Thus, the present study evaluates whether or not bone turnover markers can be used to predict the healing duration in MRONJ patients.

Materials and methods: The present study is a retrospective data analysis of patients suffering from MRONJ and positive histology for Actinomyces spp., who were identified at the General Hospital Vienna from 2014 to 2018. During the first visit, the patients' demographics and levels of bone formation parameters were compiled. Healing times were analysed by Cox regression in dependence on these factors.

Results: A total of 52 patients were identified who fulfilled the inclusion criteria. The indication for bone-modifying agents was breast cancer (n = 21), prostate cancer (n = 14), multiple myeloma (n = 6) and other malignant diseases (n = 11). In 43 (82.7%) of our patients, we were able to document complete mucosal healing. Furthermore, patients who responded faster to therapy showed higher levels of C-telopeptide (P < 0.05), osteocalcin (P < 0.05) and bone-specific alkaline phosphatase (P < 0.05), but lower levels of 1.25-dihydroxyvitamin D (P < 0.05) than slower responding patients. No correlation was found regarding parathyroid hormone or calcitonin levels. Interestingly, patients who had a slower response were less likely to report dental procedures, but more likely to report a history of chemotherapy.

Conclusion: CTX and osteocalcin levels may be used for predicting healing duration for MRONJ.

Keywords: Actinomycosis; Medication-related osteonecrosis of the jaw; Personalized medicine; Prediction of healing duration.

MeSH terms

  • Bisphosphonate-Associated Osteonecrosis of the Jaw*
  • Bone Remodeling
  • Diphosphonates
  • Humans
  • Male
  • Multiple Myeloma*
  • Retrospective Studies

Substances

  • Diphosphonates