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Multiple Pulmonary Metastases of Recurrent Giant Cell Tumor of Bone with Expression of VEGFR-2 Successfully Controlled by Denosumab and Apatinib: A Case Report and Literature Review

Journal

CANCER MANAGEMENT AND RESEARCH
Volume 13, Issue -, Pages 4447-4454

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/CMAR.S312846

Keywords

giant cell tumor of bone; pulmonary metastasis; VEGFR-2; denosumab; apatinib

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Funding

  1. Chengdu Science and Technology Program Projects [2017-CY02 -00032-GX]
  2. National Natural Science Foundation of China [81801852]
  3. National Key Research and Development Program of China [2017YFB0702604]

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Giant cell tumor of bone is a rare, benign but locally aggressive bone tumor with a high tendency for local recurrence and lung metastasis. Currently, an optimal treatment strategy has not been established, although Denosumab and Apatinib may be effective treatment options.
Giant cell tumor of bone (GCTB) is a rare, benign, but locally aggressive bone tumor. It has a high tendency for local recurrence, which may increase the incidence of lung metastasis. Currently, an optimal treatment strategy has not been established because of the rarity of pulmonary metastatic GCTB. Denosumab is the preferred regimen for unresectable metastatic lesions; however, there are no alternative treatment options when patients are resistant to denosumab. Apatinib is a small-molecule tyrosine kinase inhibitor that selectively competes for the vascular endothelial growth factor receptor 2 (VEGFR-2) ATP binding site, and several studies have analyzed the effectiveness of apatinib in advanced or metastatic tumors. However, there is no report of apatinib as an anti-angiogenesis therapy for pulmonary metastatic GCTB to date. Here, we present a case of a 26-year-old female who was diagnosed with recurrent and pulmonary metastatic GCTB. Immunohistochemical (IHC) staining indicated that the tumor cells were positive for VEGFR-2. Denosumab was administered to control the metastases; nevertheless, disease progression was confirmed after four months of treatment. Given the IHC results and rapid disease progression, apatinib was added to the treatment strategy. After 42 months of treatment, the patient showed noticeable symptomatic improvement and considerable tumor shrinkage.

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