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April 26, 2012
Two recent studies have reported on the possible utility of assessing pre-treatment neutrophil-to-lymphocyte ratio (NLR) as a prognostic factor in mRCC.
April 26, 2012
A small phase II study of tandutinib (MLN518), a selective inhibitor of type III tyrosine receptor kinases (FLT3), has concluded that the novel agent has no clinical activity and excessive toxicity, and should not be developed further for mRCC.
March 31, 2012
Patients with papillary renal cell carcinoma, the second most common kidney cancer subtype, face a low risk of tumour recurrence and cancer-related death after surgery.
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Improved outcome with concomitant angiotensin inhibitors

Clinical outcomes may be improved in sunitinib-treated mRCC patients who receive concomitant therapy with an angiotensin inhibitor (ACE inhibitor or angiotensin II receptor inhibitor) (Keizman et al. Eur J Cancer 2011; 47: 1955-1961. www.ncbi.nlm.nih.gov/pubmed/21600760. Preliminary data presented at ASCO 2011 by Kim et al. J Clin Oncol 2011; 29(suppl): e15008).

The retrospective study analysed data from 127 mRCC patients treated with sunitinib 50 mg, 4 weeks on/2 weeks off, during the period 2004-2010. Patients were categorized as an angiotensin inhibitor user or non-user. The two groups were balanced with respect to clinical prognostic factors.

The objective response rate (PR + SD) in angiotensin inhibitor users versus non-users was 86% vs. 72%. The proportion with progressive disease was 14% vs. 28%, respectively. Median PFS was 13 versus 6 months. Median OS was 30 versus 23 months.

It has been speculated that agents that block the angiotensin cascade may have anti-tumour effects. Laboratory studies have reported that angiotensin types 1 and 2 receptors are overexpressed in renal clear-cell carcinoma (Dolley-Hitze et al. Br J Cancer 2010; 103: 1698-1705; www.ncbi.nlm.nih.gov/pubmed/21102591 free full text at www.ncbi.nlm.nih.gov/pmc/articles/PMC2994218/pdf/6605866a.pdf).

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