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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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PFS with First-Line Therapy Prognostic for OS IN mRCC

REPORT FROM THE AMERICAN SOCIETY OF CLINICAL ONCOLOGY (ASCO) ANNUAL MEETING, CHICAGO, IL, JUNE 3-7, 2011 - A retrospective study of 119 mRCC patients treated with a first-line VEGF-targeted therapy has found that PFS is prognostic for overall survival (Seidel et al. J Clin Oncol 2011; 29(suppl): 4591;http://www.asco.org/ASCOv2/Meetings/Abstracts?&vmview=abst_detail_view&confID=102&abstractID=77895).

A majority of subjects received first-line treatment with sunitinib; other treatments included sorafenib, axitinib, and bevacizumab + interferon-alfa or everolimus. Best response was evaluated in 95 subjects and included complete remission in 6%, partial remission in 19%, stable disease in 48% and progressive disease in 26%. Median PFS with first-line therapy was 8.1 months; median OS was 22.7 months. The median OS in patients with PFS ≤ 6 or >6 months was 12 and 33 months, respectively.

PFS >6 months during first-line treatment, good MSKCC score and treatment with second-line therapy were independent prognostic factors for prolonged OS. The authors concluded that response to first-line VEGF therapy may inform clinical decision-making when selecting subsequent treatments.

These findings align with those reported in a recent analysis by Heng et al. at the University of Calgary (Heng et al. Cancer 2011; 117: 2637-2642; www.ncbi.nlm.nih.gov/pubmed/21656741). In their study, a proportional hazards model was used to evaluate the utility of PFS for predicting OS. Data were obtained from 1,158 mRCC patients at 12 centres with a median follow-up of 30.6 months.

Overall, the median PFS was 7.6 months; median OS was 19.7 months. Both PFS at 3 and 6 months were predictive of OS. For the 3-month PFS, OS was 7.8 versus 23.6 months for patients who progressed compared to those who did not progress (p<0.0001; adjusted hazard ratio 3.05). For 6-month PFS, OS was 8.6 versus 26.0 months for the two groups, respectively (p<0.0001; adjusted HR 2.96). PFS at 9 and 12 months were also predictive of OS.
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