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Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab
OBJECTIVES: While risk factors of bisphosphonate (BP) associated osteonecrosis of the jaw have been properly analyzed, studies focusing on risk factors associated with denosumab (DNO) are sparse. The purpose of this study was to identify risk factors influencing the onset of medication-related osteo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898220/ https://www.ncbi.nlm.nih.gov/pubmed/34812959 http://dx.doi.org/10.1007/s00784-021-04261-4 |
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author | Wick, Alexander Bankosegger, Philipp Otto, Sven Hohlweg-Majert, Bettina Steiner, Timm Probst, Florian Ristow, Oliver Pautke, Christoph |
author_facet | Wick, Alexander Bankosegger, Philipp Otto, Sven Hohlweg-Majert, Bettina Steiner, Timm Probst, Florian Ristow, Oliver Pautke, Christoph |
author_sort | Wick, Alexander |
collection | PubMed |
description | OBJECTIVES: While risk factors of bisphosphonate (BP) associated osteonecrosis of the jaw have been properly analyzed, studies focusing on risk factors associated with denosumab (DNO) are sparse. The purpose of this study was to identify risk factors influencing the onset of medication-related osteonecrosis of the jaw (MRONJ) in patients receiving antiresorptive treatment (ART) with DNO by comparing patients suffering from MRONJ and patients without MRONJ. Multiple variables were evaluated including the impact of a previous BP intake. MATERIALS AND METHODS: A retrospective single-center cohort study with patients receiving DNO was conducted. One-hundred twenty-eight patients were included and divided into three groups: I (control, n = 40) receiving DNO with absence of MRONJ; group II (Test 1, n = 46), receiving DNO with presence of MRONJ; and group III (Test 2, n = 42) sequentially receiving BP and DNO with presence of MRONJ. Patients’ medical history, focusing on the identification of MRONJ risk factors, was collected and evaluated. Parameters were sex, age, smoking habit, alcohol consumption, underlying disease (cancer type, osteoporosis), internal diseases, additional chemo/hormonal therapy, oral inflammation, and trauma. RESULTS: The following risk factors were identified to increase MRONJ onset significantly in patients treated with DNO: chemo/hormonal therapy (p = 0.02), DNO dosage (p < 0.01), breast cancer (p = 0.03), intake of corticosteroids (p = 0.04), hypertension (p = 0.02), diabetes mellitus (p = 0.04), periodontal disease (p = 0.03), apical ostitis (p = 0.02), and denture use (p = 0.02). A medication switch did not affect MRONJ development (p = 0.86). CONCLUSIONS: Malignant diseases, additional chemotherapy, DNO dosage, and oral inflammations as well as diabetes mellitus and hypertension influence MRONJ onset in patients treated with DNO significantly. CLINICAL RELEVANCE: Patients receiving ART with DNO featuring aforementioned risk factors have a higher risk of MRONJ onset. These patients need a sound and regular prophylaxis in order to prevent the onset of MRONJ under DNO treatment. |
format | Online Article Text |
id | pubmed-8898220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-88982202022-03-08 Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab Wick, Alexander Bankosegger, Philipp Otto, Sven Hohlweg-Majert, Bettina Steiner, Timm Probst, Florian Ristow, Oliver Pautke, Christoph Clin Oral Investig Original Article OBJECTIVES: While risk factors of bisphosphonate (BP) associated osteonecrosis of the jaw have been properly analyzed, studies focusing on risk factors associated with denosumab (DNO) are sparse. The purpose of this study was to identify risk factors influencing the onset of medication-related osteonecrosis of the jaw (MRONJ) in patients receiving antiresorptive treatment (ART) with DNO by comparing patients suffering from MRONJ and patients without MRONJ. Multiple variables were evaluated including the impact of a previous BP intake. MATERIALS AND METHODS: A retrospective single-center cohort study with patients receiving DNO was conducted. One-hundred twenty-eight patients were included and divided into three groups: I (control, n = 40) receiving DNO with absence of MRONJ; group II (Test 1, n = 46), receiving DNO with presence of MRONJ; and group III (Test 2, n = 42) sequentially receiving BP and DNO with presence of MRONJ. Patients’ medical history, focusing on the identification of MRONJ risk factors, was collected and evaluated. Parameters were sex, age, smoking habit, alcohol consumption, underlying disease (cancer type, osteoporosis), internal diseases, additional chemo/hormonal therapy, oral inflammation, and trauma. RESULTS: The following risk factors were identified to increase MRONJ onset significantly in patients treated with DNO: chemo/hormonal therapy (p = 0.02), DNO dosage (p < 0.01), breast cancer (p = 0.03), intake of corticosteroids (p = 0.04), hypertension (p = 0.02), diabetes mellitus (p = 0.04), periodontal disease (p = 0.03), apical ostitis (p = 0.02), and denture use (p = 0.02). A medication switch did not affect MRONJ development (p = 0.86). CONCLUSIONS: Malignant diseases, additional chemotherapy, DNO dosage, and oral inflammations as well as diabetes mellitus and hypertension influence MRONJ onset in patients treated with DNO significantly. CLINICAL RELEVANCE: Patients receiving ART with DNO featuring aforementioned risk factors have a higher risk of MRONJ onset. These patients need a sound and regular prophylaxis in order to prevent the onset of MRONJ under DNO treatment. Springer Berlin Heidelberg 2021-11-23 2022 /pmc/articles/PMC8898220/ /pubmed/34812959 http://dx.doi.org/10.1007/s00784-021-04261-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Wick, Alexander Bankosegger, Philipp Otto, Sven Hohlweg-Majert, Bettina Steiner, Timm Probst, Florian Ristow, Oliver Pautke, Christoph Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title | Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title_full | Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title_fullStr | Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title_full_unstemmed | Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title_short | Risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
title_sort | risk factors associated with onset of medication-related osteonecrosis of the jaw in patients treated with denosumab |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898220/ https://www.ncbi.nlm.nih.gov/pubmed/34812959 http://dx.doi.org/10.1007/s00784-021-04261-4 |
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