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Combined Administration of Bisphosphonates, Chemotherapeutic Agents, and/or Targeted Drugs Increases the Risk for Stage 3 Medication‐Related Osteonecrosis of the Jaw: A 4‐Year Retrospective Study
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Objectives. Patients with stage 3 medication‐related osteonecrosis of the jaw (MRONJ) suffer from severe complications. Chemotherapeutic agents and targeted drugs are considered to be associated with the development of MRONJ. However, little is known regarding the association of those agents with stage 3 MRONJ. The purpose of this study is to analyze the comprehensive medication history of patients with advanced‐stage MRONJ (stage 2 and stage 3) and evaluate the possible risk factors for stage 3 MRONJ. Patients and Methods. Sixty patients with advanced‐stage MRONJ were involved in this retrospective study. Patients with developmental maxillofacial anomalies, previous radiation in the head and neck areas, and jaw bone tumors were excluded from the study. All patients were divided into two groups by their MRONJ stage (stage 2 or stage 3). Demographic and clinical characteristics, comprehensive medication data (bisphosphonates, chemotherapeutic agents, targeted drugs, and immunosuppressive agents), and results of serological biomarkers were recorded and compared between two groups. Univariate and multivariate logistic regressions were performed by SPSS 25.0 for evaluating risk factors of stage 3 MRONJ. Results. Our results indicate that chemotherapy (adjusted OR = 3.43; 95% CI: 1.03 to 11.38), targeted drugs (adjusted OR = 3.69; 95% CI: 1.06 to 12.80), and maxillary lesions (adjusted OR = 4.26; 95% CI: 1.19 to 15.23) increase the risk of stage 3 MRONJ. Conclusion. The outcome of this study justifies that chemotherapeutic agents and targeted drugs are probably risk factors for stage 3 MRONJ. In addition, the osteonecrosis in maxilla is more easily to develop into stage 3 MRONJ. Intense clinical observation is recommended in MRONJ patients with maxillary osteonecrosis and in those who concurrently administered bisphosphonates, chemotherapeutic agents, and/or targeted drugs. This trial is registered with ChiCTR2000032428.
Title: Combined Administration of Bisphosphonates, Chemotherapeutic Agents, and/or Targeted Drugs Increases the Risk for Stage 3 Medication‐Related Osteonecrosis of the Jaw: A 4‐Year Retrospective Study
Description:
Objectives.
Patients with stage 3 medication‐related osteonecrosis of the jaw (MRONJ) suffer from severe complications.
Chemotherapeutic agents and targeted drugs are considered to be associated with the development of MRONJ.
However, little is known regarding the association of those agents with stage 3 MRONJ.
The purpose of this study is to analyze the comprehensive medication history of patients with advanced‐stage MRONJ (stage 2 and stage 3) and evaluate the possible risk factors for stage 3 MRONJ.
Patients and Methods.
Sixty patients with advanced‐stage MRONJ were involved in this retrospective study.
Patients with developmental maxillofacial anomalies, previous radiation in the head and neck areas, and jaw bone tumors were excluded from the study.
All patients were divided into two groups by their MRONJ stage (stage 2 or stage 3).
Demographic and clinical characteristics, comprehensive medication data (bisphosphonates, chemotherapeutic agents, targeted drugs, and immunosuppressive agents), and results of serological biomarkers were recorded and compared between two groups.
Univariate and multivariate logistic regressions were performed by SPSS 25.
0 for evaluating risk factors of stage 3 MRONJ.
Results.
Our results indicate that chemotherapy (adjusted OR = 3.
43; 95% CI: 1.
03 to 11.
38), targeted drugs (adjusted OR = 3.
69; 95% CI: 1.
06 to 12.
80), and maxillary lesions (adjusted OR = 4.
26; 95% CI: 1.
19 to 15.
23) increase the risk of stage 3 MRONJ.
Conclusion.
The outcome of this study justifies that chemotherapeutic agents and targeted drugs are probably risk factors for stage 3 MRONJ.
In addition, the osteonecrosis in maxilla is more easily to develop into stage 3 MRONJ.
Intense clinical observation is recommended in MRONJ patients with maxillary osteonecrosis and in those who concurrently administered bisphosphonates, chemotherapeutic agents, and/or targeted drugs.
This trial is registered with ChiCTR2000032428.
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