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骨巨细胞瘤的恶性肿瘤:地舒单抗开放性 2 期研究分析。

Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab.

机构信息

Chemotherapy Unit, IRCCS Istituto Ortopedico Rizzoli, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), Bologna University, 40136, Bologna, Italy.

David Geffen School of Medicine, UCLA Health System, 200 UCLA Medical Plaza Suite 165-57, Los Angeles, CA, 90095, USA.

出版信息

BMC Cancer. 2021 Jan 22;21(1):89. doi: 10.1186/s12885-020-07739-8.

Abstract

BACKGROUND

Giant cell tumor of bone (GCTB) is a rare osteoclastogenic stromal tumor. GCTB can rarely undergo malignant transformation. This post hoc analysis evaluated and classified malignancies in patients with GCTB who received denosumab.

METHODS

This analysis was conducted on patients with pathologically confirmed GCTB and measurable active disease treated with denosumab 120 mg subcutaneously once every 4 weeks, with loading doses on study days 8 and 15, as part of a phase 2, open-label, multicenter study. We identified potential cases of malignancy related to GCTB through an independent multidisciplinary review or medical history, associated imaging or histopathologic reports, and disease course. The findings were summarized and no statistical analysis was performed.

RESULTS

Twenty of five hundred twenty-six patients (3.8%) who received at least one dose of denosumab were misdiagnosed with GCTB that was later discovered to be malignancies: five primary malignant GCTB, five secondary malignant GCTB, four sarcomatous transformations, and six patients with other malignancies (giant cell-rich osteosarcoma, undifferentiated pleomorphic sarcoma, spindle cell sarcoma, osteogenic sarcoma, phosphaturic mesenchymal tumor of mixed connective tissue type, and fibrosarcoma/malignant fibrous histiocytoma). Many malignancies were present before denosumab was initiated (8 definitive cases, 7 likely cases), excluding potential involvement of denosumab in these cases. Signs associated with potential misdiagnoses of GCTB included poor mineralization with denosumab treatment, rapid relapse in pain, or a failure of the typical dramatic improvement in pain normally observed with denosumab.

CONCLUSIONS

Although rare, GCTB can undergo malignant transformation, and rates in this study were consistent with previous reports. Signs of poor mineralization or lack of response to denosumab treatment may warrant close monitoring.

TRIAL REGISTRATION

clinicaltrials.gov , ( NCT00680992 ). Registered May 20, 2008.

摘要

背景

骨巨细胞瘤(GCTB)是一种罕见的破骨细胞源性基质肿瘤。GCTB 很少发生恶性转化。本事后分析评估并分类了接受地舒单抗治疗的 GCTB 患者的恶性肿瘤。

方法

本分析纳入了接受皮下注射地舒单抗 120mg、每 4 周 1 次,研究第 8 天和第 15 天给予负荷剂量的病理证实的 GCTB 且存在可测量活跃疾病的患者,该研究为一项 2 期、开放标签、多中心研究。我们通过独立的多学科审查或病史、相关影像学或组织病理学报告以及疾病过程,确定了与 GCTB 相关的恶性肿瘤的潜在病例。总结了研究结果,未进行统计学分析。

结果

526 例接受至少 1 剂地舒单抗治疗的患者中,有 20 例(3.8%)被误诊为 GCTB,后发现为恶性肿瘤:5 例原发性恶性 GCTB、5 例继发性恶性 GCTB、4 例肉瘤样转化、6 例其他恶性肿瘤(巨细胞丰富型骨肉瘤、未分化多形性肉瘤、梭形细胞肉瘤、成骨肉瘤、混合结缔组织型磷酸尿嘧啶间充质肿瘤、纤维肉瘤/恶性纤维组织细胞瘤)。许多恶性肿瘤在开始用地舒单抗治疗前就已存在(8 例明确病例、7 例可能病例),排除了地舒单抗在这些病例中的潜在参与。与 GCTB 潜在误诊相关的迹象包括:地舒单抗治疗时矿化不良、疼痛迅速复发或通常与地舒单抗治疗相关的疼痛明显改善失败。

结论

尽管罕见,但 GCTB 可能发生恶性转化,本研究中的发生率与既往报告一致。矿化不良或对地舒单抗治疗无反应的迹象可能需要密切监测。

试验注册

clinicaltrials.gov(NCT00680992)。2008 年 5 月 20 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/156c/7824947/aa0dc4e39125/12885_2020_7739_Fig1_HTML.jpg

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