201. Osteonecrosis of the jaw related to non-antiresorptive medications: a systematic review
- Author
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Nikolaos Tsoukalas, Jean-Jacques Body, Winston Tan, Joel B. Epstein, Kivanc Bektas-Kayhan, Cesar A. Migliorati, Rajesh V. Lalla, Giuseppina Campisi, Emmanouil Vardas, Dimitra Galiti, Ourania Nicolatou-Galitis, Erofili Papadopoulou, Maria Kouri, Sharon Elad, Nicolatou-Galitis, Ourania, Kouri, Maria, Papadopoulou, Erofili, Vardas, Emmanouil, Galiti, Dimitra, Epstein, Joel B, Elad, Sharon, Campisi, Giuseppina, Tsoukalas, Nikolao, Bektas-Kayhan, Kivanc, Tan, Winston, Body, Jean-Jacque, Migliorati, Cesar, and Lalla, Rajesh V
- Subjects
Adult ,Male ,Oncology ,BRAF inhibitor ,medicine.medical_specialty ,mTOR inhibitors ,Immune checkpoint inhibitors ,Inhibitors of angiogenesi ,Tyrosine kinase inhibitor ,Bone resorption ,Immune checkpoint inhibitor ,Delayed diagnosis ,Cytotoxic chemotherapy ,03 medical and health sciences ,0302 clinical medicine ,Prostate ,Internal medicine ,medicine ,Humans ,030212 general & internal medicine ,Stage (cooking) ,Aged ,Bone Density Conservation Agents ,Diphosphonates ,Osteonecrosis of the jaw ,business.industry ,Osteonecrosis ,Cancer ,Middle Aged ,medicine.disease ,medicine.anatomical_structure ,Jaw ,030220 oncology & carcinogenesis ,Bisphosphonate-Associated Osteonecrosis of the Jaw ,Female ,business - Abstract
The reporting of osteonecrosis of the jaw (ONJ) related to anticancer agents without known antiresorptive properties (non-antiresorptives), such as antiangiogenics, tyrosine kinase inhibitors, mammalian target of rapamycin inhibitors, immune checkpoint inhibitors, and cytotoxic chemotherapy is increasing. To review characteristics of ONJ in cancer patients receiving non-antiresorptives. A systematic review of the literature between 2009 and 2017 was conducted by the Bone Study Group of MASCC/ISOO. Of 6249 articles reviewed and from personal communication, 42 ONJ cases related to non-antiresorptives were identified. No gender predilection was noted. Median age was 60 years and ONJ stage 2 was most common, with predilection for posterior mandible. Exposed bone, pain, and infection were common at diagnosis. In comparison to bone targeting agents (BTAs), radiology, histology, and management were similar, with medication often discontinued. Delayed diagnosis (median 8 weeks) was noted. Important differences included earlier time to ONJ onset (median 20 weeks), absence of trigger event (40%), and greater likelihood of healing and shorter healing time (median 8 weeks) as compared to BTA-related ONJ. Gastrointestinal cancers predominated, followed by renal cell carcinomas compared to breast, followed by prostate cancers in BTA-related ONJ, reflecting different medications. Data about non-antiresorptive-related ONJ is sparse. This type of ONJ may have better prognosis compared to the BTA-related ONJ, suggested by greater likelihood of healing and shorter healing time. However, the delay in diagnosis highlights the need for more education. This is the first attempt to characterize ONJ associated with different non-antiresorptives, including BRAF and immune checkpoint inhibitors.
- Published
- 2018