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Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database
Background Medication-related osteonecrosis of the jaw is a serious adverse event associated with bone-modifying agents, such as injectable bisphosphonate (zoledronic acid) and the anti-receptor activator of nuclear factor-κB ligand antibody (denosumab). Objective This study aims to evaluate and com...
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Published in: | Drugs - Real World Outcomes 2022-12, Vol.9 (4), p.659-665 |
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creator | Hasegawa, Shiori Ikesue, Hiroaki Satake, Riko Inoue, Misaki Yoshida, Yu Tanaka, Mizuki Matsumoto, Kiyoka Wakabayashi, Wataru Oura, Keita Muroi, Nobuyuki Hashida, Tohru Iguchi, Kazuhiro Nakamura, Mitsuhiro |
description | Background
Medication-related osteonecrosis of the jaw is a serious adverse event associated with bone-modifying agents, such as injectable bisphosphonate (zoledronic acid) and the anti-receptor activator of nuclear factor-κB ligand antibody (denosumab).
Objective
This study aims to evaluate and compare the time-to-onset profile for medication-related osteonecrosis of the jaw associated with denosumab between treatment-naïve (naïve group) and pre-treatment with zoledronic acid (post-zoledronic acid group) patients using the Japanese Adverse Drug Event Report database.
Methods
Medication-related osteonecrosis of the jaw was defined according to the
Medical Dictionary for Regulatory Activities
. The medication-related osteonecrosis of the jaw onset profiles were evaluated using the Weibull shape parameter and the log-rank test.
Results
The Japanese Adverse Drug Event Report database contains 632,409 reports published between April 2004 and March 2020. In the time-to-onset analysis, after extracting the combinations with complete information for the treatment start date and the medication-related osteonecrosis of the jaw onset date, 272 reports of the naïve group and 86 reports of the post-zoledronic acid group were analyzed. The median onset in the naïve and post-zoledronic acid groups was 487.0 (25–75%: 274.0–690.8) and 305.5 (25–75%: 158.3–508.5) days, respectively. Medication-related osteonecrosis of the jaw occurred earlier in the post-zoledronic acid group than in the naïve group, and the log-rank test demonstrated a significant difference in their time transitions (
p
< 0.0001).
Conclusions
The results indicated a risk of medication-related osteonecrosis of the jaw in naïve and post-zoledronic acid groups and a shorter onset time in the latter than in the former. Thus, healthcare professionals should take the early risk of medication-related osteonecrosis of the jaw into account when switching patients from zoledronic acid to denosumab treatment. |
doi_str_mv | 10.1007/s40801-022-00324-4 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9712889</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A728466428</galeid><sourcerecordid>A728466428</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-2a32fa482721147f6458434285ff0a2adf8abb14d9364874a6f6b868207a9f543</originalsourceid><addsrcrecordid>eNp9UsFuEzEUXCEQrUp_gJMlLuXg4vU6a5sDUpSEQlURVNILF8u7-zYx2rVT25sqX8VH9MdwmqhVEUI-PMuemffGnix7m5PznBD-ITAiSI4JpZiQgjLMXmTHNJcCSy7Ey4e9xHk-YkfZaQimIozxggnGX2dHxUgWBZPiOLufhwjOQu1dMAG5FsUVoEt9hyZ6CNCgaoumYF0Yel0hY9HCg4492Ii_6fvfG0DaNui7B_x4ge5MXKGfroPGO2tqNK5Ngy68G9bhIxqjhekBR4fnNkBEP-LQbNFNMHZ5aL3WFgKgcbMBn-rUD0s02-yEr2HtfERnl-Pp7Po9muqoKx3gTfaq1V2A00M9yW4-zxaTL_hqfvF1Mr7CNWMiYqoL2momKKd5znhbspFgBaNi1LZEU920QldVzhpZlExwpsu2rEQpKOFatiNWnGSf9rrroeqhqdNIXndq7U2v_VY5bdTzG2tWauk2SvKcCiGTwNlBwLvbAUJUvQk1dF1y7IagaCklJ1SWRYK--wv6yw3eJnuKckYlEaLMn1BL3YEytnWpb70TVWNOBSvLZC-hzv-BSquB3tTp81uTzp8R6J6wS0Xw0D56zInapU_t06dS-tRD-tTudYo9KSSwXYJ_mvg_rD95CttY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2742908861</pqid></control><display><type>article</type><title>Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database</title><source>PubMed (Medline)</source><source>ABI/INFORM Global</source><source>Springer Nature - SpringerLink Journals - Fully Open Access </source><source>Publicly Available Content (ProQuest)</source><source>Alma/SFX Local Collection</source><creator>Hasegawa, Shiori ; Ikesue, Hiroaki ; Satake, Riko ; Inoue, Misaki ; Yoshida, Yu ; Tanaka, Mizuki ; Matsumoto, Kiyoka ; Wakabayashi, Wataru ; Oura, Keita ; Muroi, Nobuyuki ; Hashida, Tohru ; Iguchi, Kazuhiro ; Nakamura, Mitsuhiro</creator><creatorcontrib>Hasegawa, Shiori ; Ikesue, Hiroaki ; Satake, Riko ; Inoue, Misaki ; Yoshida, Yu ; Tanaka, Mizuki ; Matsumoto, Kiyoka ; Wakabayashi, Wataru ; Oura, Keita ; Muroi, Nobuyuki ; Hashida, Tohru ; Iguchi, Kazuhiro ; Nakamura, Mitsuhiro</creatorcontrib><description>Background
Medication-related osteonecrosis of the jaw is a serious adverse event associated with bone-modifying agents, such as injectable bisphosphonate (zoledronic acid) and the anti-receptor activator of nuclear factor-κB ligand antibody (denosumab).
Objective
This study aims to evaluate and compare the time-to-onset profile for medication-related osteonecrosis of the jaw associated with denosumab between treatment-naïve (naïve group) and pre-treatment with zoledronic acid (post-zoledronic acid group) patients using the Japanese Adverse Drug Event Report database.
Methods
Medication-related osteonecrosis of the jaw was defined according to the
Medical Dictionary for Regulatory Activities
. The medication-related osteonecrosis of the jaw onset profiles were evaluated using the Weibull shape parameter and the log-rank test.
Results
The Japanese Adverse Drug Event Report database contains 632,409 reports published between April 2004 and March 2020. In the time-to-onset analysis, after extracting the combinations with complete information for the treatment start date and the medication-related osteonecrosis of the jaw onset date, 272 reports of the naïve group and 86 reports of the post-zoledronic acid group were analyzed. The median onset in the naïve and post-zoledronic acid groups was 487.0 (25–75%: 274.0–690.8) and 305.5 (25–75%: 158.3–508.5) days, respectively. Medication-related osteonecrosis of the jaw occurred earlier in the post-zoledronic acid group than in the naïve group, and the log-rank test demonstrated a significant difference in their time transitions (
p
< 0.0001).
Conclusions
The results indicated a risk of medication-related osteonecrosis of the jaw in naïve and post-zoledronic acid groups and a shorter onset time in the latter than in the former. Thus, healthcare professionals should take the early risk of medication-related osteonecrosis of the jaw into account when switching patients from zoledronic acid to denosumab treatment.</description><identifier>ISSN: 2199-1154</identifier><identifier>EISSN: 2198-9788</identifier><identifier>DOI: 10.1007/s40801-022-00324-4</identifier><identifier>PMID: 35933498</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Acids ; Brand names ; Cancer ; Drug dosages ; Fractures ; Internal Medicine ; Ligands ; Medical personnel ; Medicine ; Medicine & Public Health ; Metastasis ; Monoclonal antibodies ; Multiple myeloma ; Necrosis ; Original ; Original Research Article ; Osteoporosis ; Pharmacology/Toxicology ; Pharmacotherapy ; Quality of life ; Statistical analysis</subject><ispartof>Drugs - Real World Outcomes, 2022-12, Vol.9 (4), p.659-665</ispartof><rights>The Author(s) 2022</rights><rights>COPYRIGHT 2022 Springer</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-2a32fa482721147f6458434285ff0a2adf8abb14d9364874a6f6b868207a9f543</citedby><cites>FETCH-LOGICAL-c448t-2a32fa482721147f6458434285ff0a2adf8abb14d9364874a6f6b868207a9f543</cites><orcidid>0000-0002-5062-5522</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2742908861/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2742908861?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,11668,25732,27903,27904,36039,36991,44342,44569,53770,53772,74642,74873</link.rule.ids></links><search><creatorcontrib>Hasegawa, Shiori</creatorcontrib><creatorcontrib>Ikesue, Hiroaki</creatorcontrib><creatorcontrib>Satake, Riko</creatorcontrib><creatorcontrib>Inoue, Misaki</creatorcontrib><creatorcontrib>Yoshida, Yu</creatorcontrib><creatorcontrib>Tanaka, Mizuki</creatorcontrib><creatorcontrib>Matsumoto, Kiyoka</creatorcontrib><creatorcontrib>Wakabayashi, Wataru</creatorcontrib><creatorcontrib>Oura, Keita</creatorcontrib><creatorcontrib>Muroi, Nobuyuki</creatorcontrib><creatorcontrib>Hashida, Tohru</creatorcontrib><creatorcontrib>Iguchi, Kazuhiro</creatorcontrib><creatorcontrib>Nakamura, Mitsuhiro</creatorcontrib><title>Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database</title><title>Drugs - Real World Outcomes</title><addtitle>Drugs - Real World Outcomes</addtitle><description>Background
Medication-related osteonecrosis of the jaw is a serious adverse event associated with bone-modifying agents, such as injectable bisphosphonate (zoledronic acid) and the anti-receptor activator of nuclear factor-κB ligand antibody (denosumab).
Objective
This study aims to evaluate and compare the time-to-onset profile for medication-related osteonecrosis of the jaw associated with denosumab between treatment-naïve (naïve group) and pre-treatment with zoledronic acid (post-zoledronic acid group) patients using the Japanese Adverse Drug Event Report database.
Methods
Medication-related osteonecrosis of the jaw was defined according to the
Medical Dictionary for Regulatory Activities
. The medication-related osteonecrosis of the jaw onset profiles were evaluated using the Weibull shape parameter and the log-rank test.
Results
The Japanese Adverse Drug Event Report database contains 632,409 reports published between April 2004 and March 2020. In the time-to-onset analysis, after extracting the combinations with complete information for the treatment start date and the medication-related osteonecrosis of the jaw onset date, 272 reports of the naïve group and 86 reports of the post-zoledronic acid group were analyzed. The median onset in the naïve and post-zoledronic acid groups was 487.0 (25–75%: 274.0–690.8) and 305.5 (25–75%: 158.3–508.5) days, respectively. Medication-related osteonecrosis of the jaw occurred earlier in the post-zoledronic acid group than in the naïve group, and the log-rank test demonstrated a significant difference in their time transitions (
p
< 0.0001).
Conclusions
The results indicated a risk of medication-related osteonecrosis of the jaw in naïve and post-zoledronic acid groups and a shorter onset time in the latter than in the former. Thus, healthcare professionals should take the early risk of medication-related osteonecrosis of the jaw into account when switching patients from zoledronic acid to denosumab treatment.</description><subject>Acids</subject><subject>Brand names</subject><subject>Cancer</subject><subject>Drug dosages</subject><subject>Fractures</subject><subject>Internal Medicine</subject><subject>Ligands</subject><subject>Medical personnel</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Multiple myeloma</subject><subject>Necrosis</subject><subject>Original</subject><subject>Original Research Article</subject><subject>Osteoporosis</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacotherapy</subject><subject>Quality of life</subject><subject>Statistical analysis</subject><issn>2199-1154</issn><issn>2198-9788</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><sourceid>PIMPY</sourceid><recordid>eNp9UsFuEzEUXCEQrUp_gJMlLuXg4vU6a5sDUpSEQlURVNILF8u7-zYx2rVT25sqX8VH9MdwmqhVEUI-PMuemffGnix7m5PznBD-ITAiSI4JpZiQgjLMXmTHNJcCSy7Ey4e9xHk-YkfZaQimIozxggnGX2dHxUgWBZPiOLufhwjOQu1dMAG5FsUVoEt9hyZ6CNCgaoumYF0Yel0hY9HCg4492Ii_6fvfG0DaNui7B_x4ge5MXKGfroPGO2tqNK5Ngy68G9bhIxqjhekBR4fnNkBEP-LQbNFNMHZ5aL3WFgKgcbMBn-rUD0s02-yEr2HtfERnl-Pp7Po9muqoKx3gTfaq1V2A00M9yW4-zxaTL_hqfvF1Mr7CNWMiYqoL2momKKd5znhbspFgBaNi1LZEU920QldVzhpZlExwpsu2rEQpKOFatiNWnGSf9rrroeqhqdNIXndq7U2v_VY5bdTzG2tWauk2SvKcCiGTwNlBwLvbAUJUvQk1dF1y7IagaCklJ1SWRYK--wv6yw3eJnuKckYlEaLMn1BL3YEytnWpb70TVWNOBSvLZC-hzv-BSquB3tTp81uTzp8R6J6wS0Xw0D56zInapU_t06dS-tRD-tTudYo9KSSwXYJ_mvg_rD95CttY</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Hasegawa, Shiori</creator><creator>Ikesue, Hiroaki</creator><creator>Satake, Riko</creator><creator>Inoue, Misaki</creator><creator>Yoshida, Yu</creator><creator>Tanaka, Mizuki</creator><creator>Matsumoto, Kiyoka</creator><creator>Wakabayashi, Wataru</creator><creator>Oura, Keita</creator><creator>Muroi, Nobuyuki</creator><creator>Hashida, Tohru</creator><creator>Iguchi, Kazuhiro</creator><creator>Nakamura, Mitsuhiro</creator><general>Springer International Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88C</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>KB0</scope><scope>L.-</scope><scope>M0C</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5062-5522</orcidid></search><sort><creationdate>20221201</creationdate><title>Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database</title><author>Hasegawa, Shiori ; Ikesue, Hiroaki ; Satake, Riko ; Inoue, Misaki ; Yoshida, Yu ; Tanaka, Mizuki ; Matsumoto, Kiyoka ; Wakabayashi, Wataru ; Oura, Keita ; Muroi, Nobuyuki ; Hashida, Tohru ; Iguchi, Kazuhiro ; Nakamura, Mitsuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-2a32fa482721147f6458434285ff0a2adf8abb14d9364874a6f6b868207a9f543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acids</topic><topic>Brand names</topic><topic>Cancer</topic><topic>Drug dosages</topic><topic>Fractures</topic><topic>Internal Medicine</topic><topic>Ligands</topic><topic>Medical personnel</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastasis</topic><topic>Monoclonal antibodies</topic><topic>Multiple myeloma</topic><topic>Necrosis</topic><topic>Original</topic><topic>Original Research Article</topic><topic>Osteoporosis</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacotherapy</topic><topic>Quality of life</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hasegawa, Shiori</creatorcontrib><creatorcontrib>Ikesue, Hiroaki</creatorcontrib><creatorcontrib>Satake, Riko</creatorcontrib><creatorcontrib>Inoue, Misaki</creatorcontrib><creatorcontrib>Yoshida, Yu</creatorcontrib><creatorcontrib>Tanaka, Mizuki</creatorcontrib><creatorcontrib>Matsumoto, Kiyoka</creatorcontrib><creatorcontrib>Wakabayashi, Wataru</creatorcontrib><creatorcontrib>Oura, Keita</creatorcontrib><creatorcontrib>Muroi, Nobuyuki</creatorcontrib><creatorcontrib>Hashida, Tohru</creatorcontrib><creatorcontrib>Iguchi, Kazuhiro</creatorcontrib><creatorcontrib>Nakamura, Mitsuhiro</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Source</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health & Medical Collection (ProQuest Medical & Health Databases)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Global (Alumni Edition)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Public Health Database (ProQuest Medical & Health Databases)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest Business Premium Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ABI/INFORM Global</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Drugs - Real World Outcomes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hasegawa, Shiori</au><au>Ikesue, Hiroaki</au><au>Satake, Riko</au><au>Inoue, Misaki</au><au>Yoshida, Yu</au><au>Tanaka, Mizuki</au><au>Matsumoto, Kiyoka</au><au>Wakabayashi, Wataru</au><au>Oura, Keita</au><au>Muroi, Nobuyuki</au><au>Hashida, Tohru</au><au>Iguchi, Kazuhiro</au><au>Nakamura, Mitsuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database</atitle><jtitle>Drugs - Real World Outcomes</jtitle><stitle>Drugs - Real World Outcomes</stitle><date>2022-12-01</date><risdate>2022</risdate><volume>9</volume><issue>4</issue><spage>659</spage><epage>665</epage><pages>659-665</pages><issn>2199-1154</issn><eissn>2198-9788</eissn><abstract>Background
Medication-related osteonecrosis of the jaw is a serious adverse event associated with bone-modifying agents, such as injectable bisphosphonate (zoledronic acid) and the anti-receptor activator of nuclear factor-κB ligand antibody (denosumab).
Objective
This study aims to evaluate and compare the time-to-onset profile for medication-related osteonecrosis of the jaw associated with denosumab between treatment-naïve (naïve group) and pre-treatment with zoledronic acid (post-zoledronic acid group) patients using the Japanese Adverse Drug Event Report database.
Methods
Medication-related osteonecrosis of the jaw was defined according to the
Medical Dictionary for Regulatory Activities
. The medication-related osteonecrosis of the jaw onset profiles were evaluated using the Weibull shape parameter and the log-rank test.
Results
The Japanese Adverse Drug Event Report database contains 632,409 reports published between April 2004 and March 2020. In the time-to-onset analysis, after extracting the combinations with complete information for the treatment start date and the medication-related osteonecrosis of the jaw onset date, 272 reports of the naïve group and 86 reports of the post-zoledronic acid group were analyzed. The median onset in the naïve and post-zoledronic acid groups was 487.0 (25–75%: 274.0–690.8) and 305.5 (25–75%: 158.3–508.5) days, respectively. Medication-related osteonecrosis of the jaw occurred earlier in the post-zoledronic acid group than in the naïve group, and the log-rank test demonstrated a significant difference in their time transitions (
p
< 0.0001).
Conclusions
The results indicated a risk of medication-related osteonecrosis of the jaw in naïve and post-zoledronic acid groups and a shorter onset time in the latter than in the former. Thus, healthcare professionals should take the early risk of medication-related osteonecrosis of the jaw into account when switching patients from zoledronic acid to denosumab treatment.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>35933498</pmid><doi>10.1007/s40801-022-00324-4</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5062-5522</orcidid><oa>free_for_read</oa></addata></record> |
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source | PubMed (Medline); ABI/INFORM Global; Springer Nature - SpringerLink Journals - Fully Open Access ; Publicly Available Content (ProQuest); Alma/SFX Local Collection |
subjects | Acids Brand names Cancer Drug dosages Fractures Internal Medicine Ligands Medical personnel Medicine Medicine & Public Health Metastasis Monoclonal antibodies Multiple myeloma Necrosis Original Original Research Article Osteoporosis Pharmacology/Toxicology Pharmacotherapy Quality of life Statistical analysis |
title | Osteonecrosis of the Jaw Caused by Denosumab in Treatment-Naïve and Pre-Treatment with Zoledronic Acid Groups: A Time-to-Onset Study Using the Japanese Adverse Drug Event Report (JADER) Database |
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