Denosumab-associated jaw bone necrosis in cancer patients: retrospective descriptive case series study.

IF 2 Q2 DENTISTRY, ORAL SURGERY & MEDICINE Maxillofacial Plastic and Reconstructive Surgery Pub Date : 2023-06-30 DOI:10.1186/s40902-023-00391-9
Ji-Yeon Kang, Sang-Yup Kim, Jae-Seok Lim, Jwa-Young Kim, Ga-Youn Jin, Yeon-Jung Lee, Eun-Young Lee
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引用次数: 1

Abstract

Background: Denosumab (DMB) is a bone antiresorptive agent used to treat osteoporosis or metastatic cancer of the bones. However, denosumab-associated osteonecrosis of the jaw (DRONJ) has become a common complication in cancer patients. The prevalence of osteonecrosis of the jaw (ONJ) in cancer patients is estimated to be similar for both bisphosphonate-related cases (1.1 to 1.4%) and denosumab-related cases (0.8 to 2%), with the addition of adjunctive therapy with anti-angiogenic agents reportedly increasing its prevalence to 3%. (Spec Care Dentist 36(4):231-236, 2016). The aim of this study is to report on DRONJ in cancer patients treated with DMB (Xgeva®, 120mg).

Case presentation: In this study, we identified four cases of ONJ among 74 patients receiving DMB therapy for metastatic cancer. Of the four patients, three had prostate cancer and one had breast cancer. Preceding tooth extraction within 2 months of the last DMB injection was found to be a risk factor for DRONJ. Pathological examination revealed that three patients had acute and chronic inflammation, including actinomycosis colonies. Among the four patients with DRONJ referred to us, three were successfully treated without complications and had no recurrence following surgical treatment, while one did not follow up. After healing, one patient experienced a recurrence at a different site. Sequestrectomy in conjunction with antibiotic therapy and cessation of DMB use proved to be effective in managing the condition, and the ONJ site healed after an average 5-month follow-up period.

Conclusion: Conservative surgery, along with antibiotic therapy and discontinuation of DMB, was found to be effective in managing the condition. Additional studies are needed to investigate the contribution of steroids and anticancer drugs to jaw bone necrosis, the prevalence of multicenter cases, and whether there is any drug interaction with DMB.

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肿瘤患者的denosumab相关颌骨坏死:回顾性描述性病例系列研究。
背景:Denosumab (DMB)是一种骨抗吸收药物,用于治疗骨质疏松症或骨转移癌。然而,denosumumab相关性颌骨骨坏死(DRONJ)已成为癌症患者的常见并发症。据估计,双膦酸盐相关病例(1.1 - 1.4%)和denosumumab相关病例(0.8 - 2%)中癌症患者颌骨骨坏死(ONJ)的患病率相似,据报道,加上抗血管生成药物的辅助治疗,其患病率增加到3%。(特殊护理牙医36(4):231-236,2016)。本研究的目的是报道DMB (Xgeva®,120mg)治疗的癌症患者的DRONJ。病例介绍:在这项研究中,我们在74例接受DMB治疗的转移性癌症患者中发现了4例ONJ。在这4名患者中,3人患有前列腺癌,1人患有乳腺癌。最后一次注射DMB后2个月内拔牙是发生DRONJ的危险因素。病理检查显示3例患者有急慢性炎症,包括放线菌菌落。转诊的4例DRONJ患者中,3例治疗成功,无并发症,手术治疗后无复发,1例未随访。愈合后,一名患者在不同部位复发。Sequestrectomy联合抗生素治疗和停止使用DMB被证明对控制病情是有效的,ONJ部位在平均5个月的随访期后愈合。结论:保守手术、抗生素治疗和停用DMB是治疗此病的有效方法。需要进一步的研究来调查类固醇和抗癌药物对颌骨坏死的作用,多中心病例的患病率,以及药物是否与DMB有相互作用。
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来源期刊
Maxillofacial Plastic and Reconstructive Surgery
Maxillofacial Plastic and Reconstructive Surgery DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.30
自引率
13.00%
发文量
37
审稿时长
13 weeks
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