Abstract
Background: Everolimus has been approved for second-line treatment of patients with metstatic renal cell carcinoma (mRCC) after failure of sorafenib or suni-tinib. The purpose of this retrospective study was to assess the efficacy and safety of everolimus in Taiwanese patients with mRCC. Methods: Between March 2009 and August 2011, 24 mRCC patients treated with everolimus were analyzed. Prior to everolimus, each patient had received therapy with at least one vascular endothelial growth factor receptor-tyrosine kinas inhibitor. Progression-free survival (PFS) and overall survival (OS) were estimated according to the Kaplan-Meier method. Results Fifteen patients (62.5%) achieved stable disease. The median PFS was 7.1 months (95% confidence interval, 3.6-10.5 months). The median OS was 20.7 months (95% confidence interval, 5.0-36.4 months). The most frequent non-hematological adverse events with everolimus were mucositis, rash, epis-taxis and pneumonitis. Conclusions: Everolimus is an effective second-line treatment for Taiwanese patients with mRCC The toxicity is tolerable and manageable.
| Original language | English |
|---|---|
| Pages (from-to) | 402-407 |
| Number of pages | 6 |
| Journal | Chang Gung Medical Journal |
| Volume | 35 |
| Issue number | 5 |
| Publication status | Published - 2012 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Everolimus
- Mammalian target of rapamycin (mTOR) inhibitor
- Renal cell cancer
ASJC Scopus subject areas
- General Medicine
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