72
Views
5
CrossRef citations to date
0
Altmetric
Drug Evaluation

Denosumab for treating giant cell tumor of bone

, & , MD PhD
 

Abstract

Introduction: Giant cell tumor of bone (GCTB) is usually a locally aggressive tumor with low metastatic potential. Giant cells are known to express receptor activator of NF-κB ligand (RANKL) and are responsible for its aggressive osteolytic nature. Overexpression of RANKL by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated giant cells.

Areas covered: In patients with high-risk or locally advanced/surgically unsalvageable GCTB or in rare cases of metastatic disease, systemic targeted therapy with the RANKL inhibitor – monoclonal antibody denosumab – is highly effective and may lead to long-term responses or down staging facilitating resection of the tumor. Several studies with denosumab in patients with advanced or unresectable GCTB have shown objective reductions of bone destruction and clinical benefits. The literature focusing on denosumab and GCTB is reviewed here and the most important questions related to the future management of GCTB are discussed.

Expert opinion: Denosumab, which inhibits RANK – RANKL interaction, is a new promising actor among molecular-targeted therapeutic agents for GCTB. Ideally, all patients should be treated with local/intralesional excision followed by adjuvant treatment or preceded by neoadjuvant denosumab in selected cases, achieving joint salvage and optimal function outcome.

Declaration of interest

P Rutkowski has served as a member of an advisory board for Amgen and received honoraria for lectures for Amgen. A Pienkowski has received a travel grant from Amgen. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

Notes

This box summarizes key points contained in the article.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.