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Osteonecrosis of the Jaw in Patients Receiving Bone-Targeted Therapies: An Overview--Part I
Abstract:
Urologic patients receiving bone-targeted therapies are at risk of developing osteonecrosis of the jaw (ONJ). ONJ has historically been associated with bisphosphonate therapy. More recently, RANK-Ligand inhibitors (denosumab) have also been used to reduce the risk of skeletal-related events in patients who have advanced cancers with bone metastases. More than 65% of men with metastatic prostate cancer and nearly 75% of women with metastatic breast cancer are affected by bone metastases. The literature has described ONJ associated with bisphosphonate therapy as bisphosphonate-related osteonecrosis of the jaw (BRONJ). However, with evidence also linking the use of RANK-Ligand inhibitors with osteonecrosis of the jaw, we advocate use of the term "anti-bone resorption therapy-related osteonecrosis of the jaw" (ABRT-ONJ). The term "medication-related osteonecrosis of the jaw" (MRONJ) is now becoming more widespread. There is not a universally accepted definition of ABRT-ONJ, which may have hindered recognition and reporting of the condition. In Part I of this article, a review of current knowledge around the etiology of ABRT-ONJ and incidence data are provided. In Part II, we provide an audit of ONJ in a nurse consultant-led bone support clinic. In the article, we refer to zoledronic acid because this is the bisphosphonate of choice for use in men with prostate cancer in the United Kingdom.
Insights
Patients on bone-targeted therapies face osteonecrosis of the jaw (ONJ) risk. This review advocates for the term anti-bone resorption therapy-related osteonecrosis of the jaw (ABRT-ONJ) to encompass newer treatments.
Area of Science:
- Oncology
- Pharmacology
- Oral Surgery
Background:
- Bone-targeted therapies, including bisphosphonates and RANK-Ligand inhibitors, are crucial for managing bone metastases in cancer patients.
- Osteonecrosis of the jaw (ONJ) is a recognized complication associated with these therapies, historically linked to bisphosphonates (BRONJ).
- The emergence of other bone-modifying agents necessitates a broader terminology to accurately reflect the causative medications.
Purpose of the Study:
- To review the current understanding of the etiology and incidence of anti-bone resorption therapy-related osteonecrosis of the jaw (ABRT-ONJ).
- To propose and advocate for the adoption of the term ABRT-ONJ to encompass ONJ associated with various bone-targeted therapies.
- To present an audit of ONJ cases managed in a specialized bone support clinic.
Main Methods:
- Literature review of existing knowledge on ABRT-ONJ etiology and incidence.
- Discussion of the evolution of terminology from BRONJ to ABRT-ONJ and the emerging term MRONJ.
- Audit of ONJ cases within a nurse consultant-led bone support clinic, referencing zoledronic acid use in prostate cancer patients.
Main Results:
- Bone metastases affect a significant proportion of patients with advanced prostate and breast cancers.
- Existing literature primarily describes bisphosphonate-related ONJ (BRONJ), but RANK-Ligand inhibitors also contribute to ONJ.
- A lack of a universally accepted definition for ABRT-ONJ may impede its recognition and reporting.
Conclusions:
- The term anti-bone resorption therapy-related osteonecrosis of the jaw (ABRT-ONJ) is proposed to encompass ONJ linked to all bone-modifying agents.
- Standardizing terminology is crucial for improving the recognition, reporting, and management of ONJ.
- Further research and clinical audits are needed to fully understand the incidence and risk factors associated with ABRT-ONJ across different therapeutic agents.
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