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地诺单抗治疗后骨良性巨细胞瘤的恶性肉瘤样转化:病例报告的文献综述

Malignant Sarcomatous Transformation of Benign Giant Cell Tumor of Bone after Treatment with Denosumab Therapy: A Literature Review of Reported Cases.

作者信息

Alaqaili Sadiq I, Abduljabbar Abbas M, Altaho Ali J, Khan Abdulrahman A, Alherabi Jawaher A

机构信息

Miscellaneous, Alfaisal University, Riyadh, SAU.

Emergency Medicine, Dammam University, Qatif, SAU.

出版信息

Cureus. 2018 Dec 28;10(12):e3792. doi: 10.7759/cureus.3792.

Abstract

Giant cell tumor of bone (GCTB) is a biologically benign and locally aggressive tumor that most often affects the epiphyseal and metaphyseal sites of long bones in the young adult population. Overexpression of receptor activator of nuclear factor kappa B ligand (RANKL) by cancerous mesenchymal stromal cells stimulates a signal transduction cascade that recruits and activates multinucleated osteoclast-like giant cells, resulting in pathologic bone resorption. Denosumab, an RANKL inhibitor that blocks the RANKL-mediated osteoclast activation, has been recently approved by the United States Food and Drug Administration (FDA) for the treatment of aggressive GCTB. Although uncommon, several studies reported drug-related malignant morphological transformation of benign GCTB following treatment with denosumab therapy. The aim of the article was to review the clinicopathological characteristics of all the reported cases of malignant sarcomatous transformation of GCTB after treatment with denosumab therapy in patients without any history of prior exposure to radiotherapy.

摘要

骨巨细胞瘤(GCTB)是一种生物学行为为良性但具有局部侵袭性的肿瘤,最常累及年轻成年人群长骨的骨骺和干骺端部位。癌性间充质基质细胞中核因子κB受体活化因子配体(RANKL)的过表达会刺激信号转导级联反应,该反应会募集并激活多核破骨细胞样巨细胞,从而导致病理性骨吸收。地诺单抗是一种RANKL抑制剂,可阻断RANKL介导的破骨细胞活化,最近已被美国食品药品监督管理局(FDA)批准用于治疗侵袭性GCTB。尽管并不常见,但有几项研究报告了地诺单抗治疗后良性GCTB发生与药物相关的恶性形态学转变。本文的目的是回顾所有报道的在无放疗史患者中接受地诺单抗治疗后GCTB发生恶性肉瘤样转变病例的临床病理特征。

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