Department of Internal Medicine, Advocate Lutheran General Hospital, 1775 Dempster Street, Park Ridge, IL, 60068, USA.
BMC Pharmacol Toxicol. 2023 Mar 6;24(1):15. doi: 10.1186/s40360-023-00657-y.
Osteonecrosis of the jaw (ONJ) is a rare but serious adverse drug reaction (ADR) commonly associated with bisphosphonate and denosumab therapy. Prior research utilized an online, public FDA Adverse Event Reporting System (FAERS) Database to explore this ADR. This data identified and described several novel medications associated with ONJ. Our study aims to build upon the prior findings, reporting trends of medication induced ONJ over time and identifying newly described medications.
We searched the FAERS database for all reported cases of medication related osteonecrosis of the jaw (MRONJ) from 2010 to 2021. Cases lacking patient age or gender were excluded. Only adults (18 +) and reports from Healthcare Professions were included. Duplicate cases were removed. The top 20 medications were identified and described for April 2010-December 2014 and April 2015-January 2021.
Nineteen thousand six hundred sixty-eight cases of ONJ were reported to the FAERS database from 2010-2021. 8,908 cases met inclusion criteria. 3,132 cases were from 2010-2014 and 5,776 cases from 2015-2021. Within the cases from 2010-2014, 64.7% were female and 35.3% were male, and the average age was 66.1 ± 11.1 years. Between 2015-2021, 64.3% were female and 35.7% were male, and the average age was 69.2 ± 11.5 years. Review of the 2010-2014 data identified several medications and drug classes associated with ONJ not previously described. They include lenalidomide, corticosteroids (prednisolone and dexamethasone), docetaxel and paclitaxel, letrozole, methotrexate, imatinib, and teriparatide. Novel drugs and classes described between 2015-2021 include palbociclib, pomalidomide, radium 223, nivolumab, and cabozantinib.
While stricter inclusion criteria and removal of duplicate cases led to fewer overall identified cases of MRONJ when compared to prior research, our data represents a more reliable analysis of MRONJ reports to the FAERS database. Denosumab was the most frequently reported medication associated with ONJ. While unable to imply incidence rates from our data due to the nature of the FAERS database, our findings provide further description of the various medications associated with ONJ and elucidate patient demographics associated with the ADR. Additionally, our study identifies cases of several newly described drugs and drug classes that have not been previously described in literature.
颌骨坏死(ONJ)是一种罕见但严重的药物不良反应(ADR),通常与双膦酸盐和地舒单抗治疗有关。先前的研究利用在线公共 FDA 不良事件报告系统(FAERS)数据库来探索这种 ADR。该数据确定并描述了几种与 ONJ 相关的新型药物。我们的研究旨在在前人的研究基础上进一步报告药物诱导的 ONJ 随时间的趋势,并确定新描述的药物。
我们从 2010 年至 2021 年在 FAERS 数据库中搜索所有与药物相关的颌骨坏死(MRONJ)报告。排除缺乏患者年龄或性别的病例。仅包括成年人(18 岁+)和医疗保健专业人员的报告。删除重复病例。对 2010 年 4 月至 2014 年 12 月和 2015 年 1 月至 2021 年 1 月期间的前 20 种药物进行了识别和描述。
2010 年至 2021 年期间,FAERS 数据库共报告了 19668 例 ONJ 病例。8908 例符合纳入标准。2010-2014 年有 3132 例,2015-2021 年有 5776 例。在 2010-2014 年的病例中,64.7%为女性,35.3%为男性,平均年龄为 66.1±11.1 岁。2015-2021 年期间,64.3%为女性,35.7%为男性,平均年龄为 69.2±11.5 岁。对 2010-2014 年的数据进行审查,发现了一些先前未描述的与 ONJ 相关的药物和药物类别。它们包括来那度胺、皮质类固醇(泼尼松龙和地塞米松)、多西他赛和紫杉醇、来曲唑、甲氨蝶呤、伊马替尼和特立帕肽。2015-2021 年期间描述的新型药物和类别包括帕博西尼、泊马度胺、镭 223、纳武单抗和卡博替尼。
虽然更严格的纳入标准和重复病例的删除导致与先前的研究相比,总体识别出的 MRONJ 病例较少,但我们的数据代表了对 FAERS 数据库中 MRONJ 报告的更可靠分析。地舒单抗是最常报告与 ONJ 相关的药物。由于 FAERS 数据库的性质,我们无法从我们的数据中推断出发病率,但我们的研究结果提供了对与 ONJ 相关的各种药物的进一步描述,并阐明了与 ADR 相关的患者特征。此外,我们的研究还发现了一些以前未在文献中描述的新描述的药物和药物类别。