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Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases

PURPOSE: This study aimed to evaluate the association between clinical characteristics and development of medication-related osteonecrosis of the jaw (MRONJ) in patients who underwent dental examinations before the initiation of treatment with denosumab or zoledronic acid, which are bone-modifying a...

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Autores principales: Ikesue, Hiroaki, Mouri, Moe, Tomita, Hideaki, Hirabatake, Masaki, Ikemura, Mai, Muroi, Nobuyuki, Yamamoto, Shinsuke, Takenobu, Toshihiko, Tomii, Keisuke, Kawakita, Mutsushi, Katoh, Hironori, Ishikawa, Takayuki, Yasui, Hisateru, Hashida, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236436/
https://www.ncbi.nlm.nih.gov/pubmed/33527228
http://dx.doi.org/10.1007/s00520-021-06018-x
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author Ikesue, Hiroaki
Mouri, Moe
Tomita, Hideaki
Hirabatake, Masaki
Ikemura, Mai
Muroi, Nobuyuki
Yamamoto, Shinsuke
Takenobu, Toshihiko
Tomii, Keisuke
Kawakita, Mutsushi
Katoh, Hironori
Ishikawa, Takayuki
Yasui, Hisateru
Hashida, Tohru
author_facet Ikesue, Hiroaki
Mouri, Moe
Tomita, Hideaki
Hirabatake, Masaki
Ikemura, Mai
Muroi, Nobuyuki
Yamamoto, Shinsuke
Takenobu, Toshihiko
Tomii, Keisuke
Kawakita, Mutsushi
Katoh, Hironori
Ishikawa, Takayuki
Yasui, Hisateru
Hashida, Tohru
author_sort Ikesue, Hiroaki
collection PubMed
description PURPOSE: This study aimed to evaluate the association between clinical characteristics and development of medication-related osteonecrosis of the jaw (MRONJ) in patients who underwent dental examinations before the initiation of treatment with denosumab or zoledronic acid, which are bone-modifying agents (BMAs), for bone metastases. Additionally, the clinical outcomes of patients who developed MRONJ were evaluated along with the time to resolution of MRONJ. METHODS: The medical charts of patients with cancer who received denosumab or zoledronic acid for bone metastases between January 2012 and September 2016 were retrospectively reviewed. Patients were excluded if they did not undergo a dental examination at baseline. RESULTS: Among the 374 included patients, 34 (9.1%) developed MRONJ. The incidence of MRONJ was significantly higher in the denosumab group than in the zoledronic acid (27/215 [12.6%] vs 7/159 [4.4%], P = 0.006) group. Multivariate Cox proportional hazards regression analysis revealed that denosumab treatment, older age, and tooth extraction before and after starting BMA treatments were significantly associated with developing MRONJ. The time to resolution of MRONJ was significantly shorter for patients who received denosumab (median 26.8 months) than for those who received zoledronic acid (median not reached; P = 0.024). CONCLUSION: The results of this study suggest that treatment with denosumab, age > 65 years, and tooth extraction before and after starting BMA treatments are significantly associated with developing MRONJ in patients undergoing treatment for bone metastases. However, MRONJ caused by denosumab resolves faster than that caused by zoledronic acid.
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spelling pubmed-82364362021-07-09 Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases Ikesue, Hiroaki Mouri, Moe Tomita, Hideaki Hirabatake, Masaki Ikemura, Mai Muroi, Nobuyuki Yamamoto, Shinsuke Takenobu, Toshihiko Tomii, Keisuke Kawakita, Mutsushi Katoh, Hironori Ishikawa, Takayuki Yasui, Hisateru Hashida, Tohru Support Care Cancer Original Article PURPOSE: This study aimed to evaluate the association between clinical characteristics and development of medication-related osteonecrosis of the jaw (MRONJ) in patients who underwent dental examinations before the initiation of treatment with denosumab or zoledronic acid, which are bone-modifying agents (BMAs), for bone metastases. Additionally, the clinical outcomes of patients who developed MRONJ were evaluated along with the time to resolution of MRONJ. METHODS: The medical charts of patients with cancer who received denosumab or zoledronic acid for bone metastases between January 2012 and September 2016 were retrospectively reviewed. Patients were excluded if they did not undergo a dental examination at baseline. RESULTS: Among the 374 included patients, 34 (9.1%) developed MRONJ. The incidence of MRONJ was significantly higher in the denosumab group than in the zoledronic acid (27/215 [12.6%] vs 7/159 [4.4%], P = 0.006) group. Multivariate Cox proportional hazards regression analysis revealed that denosumab treatment, older age, and tooth extraction before and after starting BMA treatments were significantly associated with developing MRONJ. The time to resolution of MRONJ was significantly shorter for patients who received denosumab (median 26.8 months) than for those who received zoledronic acid (median not reached; P = 0.024). CONCLUSION: The results of this study suggest that treatment with denosumab, age > 65 years, and tooth extraction before and after starting BMA treatments are significantly associated with developing MRONJ in patients undergoing treatment for bone metastases. However, MRONJ caused by denosumab resolves faster than that caused by zoledronic acid. Springer Berlin Heidelberg 2021-02-01 2021 /pmc/articles/PMC8236436/ /pubmed/33527228 http://dx.doi.org/10.1007/s00520-021-06018-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Ikesue, Hiroaki
Mouri, Moe
Tomita, Hideaki
Hirabatake, Masaki
Ikemura, Mai
Muroi, Nobuyuki
Yamamoto, Shinsuke
Takenobu, Toshihiko
Tomii, Keisuke
Kawakita, Mutsushi
Katoh, Hironori
Ishikawa, Takayuki
Yasui, Hisateru
Hashida, Tohru
Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title_full Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title_fullStr Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title_full_unstemmed Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title_short Associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
title_sort associated characteristics and treatment outcomes of medication-related osteonecrosis of the jaw in patients receiving denosumab or zoledronic acid for bone metastases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236436/
https://www.ncbi.nlm.nih.gov/pubmed/33527228
http://dx.doi.org/10.1007/s00520-021-06018-x
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