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Authors Luo Y, Tang F, Wang Y, Zhou Y, Min L, Zhang W, Shi R, Duan H, Tu C
Received 8 January 2018
Accepted for publication 30 March 2018
Published 5 July 2018 Volume 2018:10 Pages 1901—1906
DOI https://doi.org/10.2147/CMAR.S161871
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Andrew Yee
Peer reviewer comments 3
Editor who approved publication: Professor Luzhe Sun
Background: Giant
cell tumor (GCT) of bone is an intermittent and locally aggressive tumor with
increasing pulmonary metastatic potential. In this study, we evaluated the
interim clinical outcome of denosumab in patients with pulmonary metastatic
GCT.
Materials and
methods: We retrospectively reviewed seven
patients with pulmonary metastatic GCT who received denosumab treatment after
local tumor surgery during January 2014 and July 2016. Denosumab treatment for
all patients lasted for at least 12 months. Serial chest computerized
tomography scan was used to monitor the drug response and RECIST 1.1 standard
was used to evaluate the therapeutic efficacy.
Results: All patients experienced chest pain relief in the first month of
treatment. Three patients showed partial response. Four patients got stable
disease after denosumab treatment. Adverse events included one patient with
hypocalcemia and two patients with fever. No treatment-related deaths were
reported. No patient with metastatic disease progression was found during an average
of 28.6 months follow-up period.
Conclusion: We presented a promising interim clinical outcome using denosumab
to treat patients with pulmonary metastatic GCT. Denosumab might be considered
as the first-line treatment for patients with inoperable metastatic pulmonary
GCT. However, Phase II clinical study with larger number of patients and longer
follow-up period is needed to detect the further efficacy and safety of this
drug for lung metastatic GCT.
Keywords: denosumab, giant cell tumor of bone, pulmonary metastasis, RANKL,
recurrence