Abstract
Bone destruction is mediated by osteoclasts, whose formation, function, and survival requires the receptor activator of NF-kB ligand (RANKL). Denosumab is a fully human monoclonal antibody to RANKL, thereby inhibiting osteoclast-mediated bone destruction, and blocks the vicious cycle of cancer-mediated bone disease. In breast cancer patients with bone metastases, denosumab was superior to zoledronic acid in delaying time to first on-study skeletal-related event (SRE; HR∈=∈0.82; P∈=∈0.01 superiority) and time to first and subsequent on-study SREs (HR∈=∈0. 77; P∈=∈0.001). Overall survival, disease progression, and serious adverse events were similar between groups.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1-4 |
| Number of pages | 4 |
| Journal | Current oncology reports |
| Volume | 13 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- Oncology
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