In this revision of the position paper, medication-related osteonecrosis of the jaw (MRONJ) was chosen as the name, because of the number of causative agents for ONJ has increased. These drugs include angiogenesis inhibitors, tyrosine kinase inhibitors, and mTOR inhibitors, which have recently been increasingly used as main anticancer drugs. However, most ONJs in anticancer drug treatment are used in combination with antiresorptive agents (ARA), and the greatest risk of developing the disease remains the administration of ARA, bisphosphonates and denosumab (Dmab). For cancer bone metastases, not only anticancer drugs but also high doses ARA are administered from an early stage of metastasis detection, which is the standard treatment for preventing pathological fractures. Fracture prevention is because fractures not only lead to a decrease in quality of life, but also worsen the prognosis of life. Therefore, in principle, the ARA that was started will not be interrupted during cancer treatment. 
 Another bone problem in cancer treatment is cancer treatment-related bone loss (CTIBL) which occurs almost with adjuvant therapy to prevent recurrence of the cancer. Breast cancer and prostate cancer, for which hormonal therapy is particularly effective, have an increased risk of CTIBL, requiring long-term administration of low doses ARA in combination with cancer treatment. 
 In this way, the risk of MRONJ in cancer patients is thought to be increasing. At MRONJ, it is important to maintain good oral hygiene for prevention, and it is recommended to visit the dentist regularly before and after starting anticancer drug treatment. The higher the dose of ARA and the longer the administration period, the greater the risk of ONJ, but the combination drug and oral conditions are also greatly affected. So medical, dental and phalmacological collaboration is essential.
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