Forte Marta, d'Amati Antonio, Limongelli Luisa, Corsalini Massimo, Favia Gianfranco, Ingravallo Giuseppe, Barile Giuseppe, Capodiferro Saverio
Department of Interdisciplinary Medicine, University of Bari, Piazza Giulio Cesare, 11, 70124 Bari, Italy.
Unit of Anatomical Pathology, Department of Precision and Regenerative Medicine and Ionian Area, University of Bari, Piazza Giulio Cesare, 11, 70124 Bari, Italy.
Healthcare (Basel). 2024 Feb 10;12(4):457. doi: 10.3390/healthcare12040457.
Medication-related osteonecrosis of the jaws is the most frequent complication in patients treated or in therapy with antiresorptive/antiangiogenetic drugs. The list of medications possibly related to MRONJ onset is constantly growing; we aimed to report on a third-generation epidermal growth factor receptor tyrosine kinase inhibitor (Osimertinib) as possibly responsible for bilateral maxillary necrosis onset in the herein-described case.
In June 2023, an oncologic patient with two different maxillary bone exposures was referred to our attention. His medical history revealed a two-year Denosumab regimen along with Osimertinib, the latter not suspended before teeth extractions. The clinicians performed a sequestrum removal and bone debridement after three cycles of antibiotic therapy.
Histologic examinations confirmed the clinical diagnosis of MRONJ excluding a metastatic occurrence, while complete mucosal healing was achieved after 15 days.
The patient suspended Denosumab for more than six months before teeth extraction for MRONJ prevention; hence, failure to discontinue Osimertinib led us to consider it a possible etiological factor. From a literature analysis, only one case has already been published reporting a possible Osimertinib-related occurrence of MRONJ in lung cancer patients. Our case is a further report that could be intended as an alert both for oncologists and dentists to share decisions about the oral management of such patients together, also informing them about this possible risk. Also, this report could trigger in the scientific community the necessity to evaluate further guidelines for similar doubtful cases in which the drug interaction, the mono-suspension, and the possible removable prosthesis-related additional trauma should be considered causes or con-causes.
颌骨药物相关性骨坏死是接受抗吸收/抗血管生成药物治疗或正在接受该类药物治疗的患者中最常见的并发症。可能与颌骨药物相关性骨坏死发病相关的药物清单在不断增加;我们旨在报告一例第三代表皮生长因子受体酪氨酸激酶抑制剂(奥希替尼)可能导致双侧上颌骨坏死发病的病例。
2023年6月,一名有两处不同上颌骨暴露的肿瘤患者引起了我们的注意。他的病史显示曾接受为期两年的地诺单抗治疗以及奥希替尼治疗,后者在拔牙前未停用。临床医生在三个周期的抗生素治疗后进行了死骨清除和骨清创术。
组织学检查证实了颌骨药物相关性骨坏死的临床诊断,排除了转移的可能性,15天后黏膜完全愈合。
患者在拔牙前停用了地诺单抗超过六个月以预防颌骨药物相关性骨坏死;因此,未停用奥希替尼使我们认为它是一个可能的病因。通过文献分析,仅已发表过一例报告,称肺癌患者中可能出现与奥希替尼相关的颌骨药物相关性骨坏死。我们的病例是进一步的报告,可作为警示,提醒肿瘤学家和牙医共同就此类患者的口腔管理做出决策,同时告知他们这种可能的风险。此外,本报告可能促使科学界有必要评估针对类似可疑病例的进一步指南,其中药物相互作用、单一停药以及可能与可摘义齿相关的额外创伤应被视为病因或共同病因。