4.7 Article

Association between treatment effects on disease progression end points and overall survival in clinical studies of patients with metastatic renal cell carcinoma

期刊

BRITISH JOURNAL OF CANCER
卷 107, 期 7, 页码 1059-1068

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NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2012.367

关键词

metastatic; progression; renal cell carcinoma; survival

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资金

  1. Novartis Pharmaceuticals Corp.
  2. Florham Park, NJ, USA
  3. Novartis
  4. GlaxoSmithKline
  5. Amgen

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BACKGROUND: The relationship between progression-free survival and time to progression (PFS/TTP) and overall survival (OS) has been demonstrated in a variety of solid tumours but not in metastatic renal cell carcinoma (mRCC). METHODS: A systematic literature search was conducted to identify controlled trials of cytokine or targeted therapies for mRCC reporting information on treatment effects on PFS/TTP and OS for one or more comparison. The associations between treatment effects on PFS/TTP and OS were analysed using linear regression. RESULTS: Thirty-one studies representing 10 943 patients, 75 treatment groups, and 41 comparisons were identified. The correlation coefficient between the negative log of the hazard ratio (HR) for PFS/TTP ( - In HRPFS/TTP) vs the negative log of the HR for OS ( - In HROS) was 0.80 (P < 0.0001). In linear regression, the coefficient on - In HRPFS/TTP vs - In HROS was 0.64 (95% confidence interval (CI): 0.470.81; R-2 = 0.63), suggesting each 10% relative risk reduction (RRR) for PFS/TTP was associated with a 6% RRR for OS. A 1-month gain in median PFS/TTP was associated with a 1.17-month gain in median OS (95% CI: 0.59,1.76; R-2 = 0.28). CONCLUSION: In trials of treatments for mRCC, treatment effects on PFS/TTP are strongly associated with treatment effects on OS. British Journal of Cancer (2012) 107, 1059-1068. doi:10.1038/bjc.2012.367 www.bjcancer.com Published online 30 August 2012 (c) 2012 Cancer Research UK

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