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Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions
The first analysis of the MRC RE01 trial in metastatic renal carcinoma identified a 28% reduction in the hazard of death for patients treated with interferon-α compared with medroxyprogesterone acetate (MPA). No subgroup was identified in which treatment with interferon-α was more or less effective...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410187/ https://www.ncbi.nlm.nih.gov/pubmed/14970855 http://dx.doi.org/10.1038/sj.bjc.6601622 |
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author | Royston, P Sauerbrei, W Ritchie, A |
author_facet | Royston, P Sauerbrei, W Ritchie, A |
author_sort | Royston, P |
collection | PubMed |
description | The first analysis of the MRC RE01 trial in metastatic renal carcinoma identified a 28% reduction in the hazard of death for patients treated with interferon-α compared with medroxyprogesterone acetate (MPA). No subgroup was identified in which treatment with interferon-α was more or less effective than MPA. We used a new approach based on fractional polynomials to investigate the updated data from this trial for the possible interaction of treatment with prognostic factors. In the spirit of hypothesis generation, we considered 10 possible prognostic variables, of which white cell count (WCC) was found to influence the effectiveness of interferon treatment. In patients treated with MPA, there was no prognostic effect of WCC, whereas, in patients treated with interferon, the risk of dying increased significantly with WCC level. We defined subgroups of patients based on WCC levels and estimated a hazard ratio of 0.53 in favour of interferon in patients with WCC <6.5 × 10(9), whereas for patients with WCC >10 × 10(9) the risk appears to be similar between the treatment groups, or even slightly raised in the interferon group. Since our results are derived from flexible statistical models, they may be interpreted as a new hypothesis and require validation in independent data. |
format | Text |
id | pubmed-2410187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24101872009-09-10 Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions Royston, P Sauerbrei, W Ritchie, A Br J Cancer Clinical The first analysis of the MRC RE01 trial in metastatic renal carcinoma identified a 28% reduction in the hazard of death for patients treated with interferon-α compared with medroxyprogesterone acetate (MPA). No subgroup was identified in which treatment with interferon-α was more or less effective than MPA. We used a new approach based on fractional polynomials to investigate the updated data from this trial for the possible interaction of treatment with prognostic factors. In the spirit of hypothesis generation, we considered 10 possible prognostic variables, of which white cell count (WCC) was found to influence the effectiveness of interferon treatment. In patients treated with MPA, there was no prognostic effect of WCC, whereas, in patients treated with interferon, the risk of dying increased significantly with WCC level. We defined subgroups of patients based on WCC levels and estimated a hazard ratio of 0.53 in favour of interferon in patients with WCC <6.5 × 10(9), whereas for patients with WCC >10 × 10(9) the risk appears to be similar between the treatment groups, or even slightly raised in the interferon group. Since our results are derived from flexible statistical models, they may be interpreted as a new hypothesis and require validation in independent data. Nature Publishing Group 2004-02-23 2004-02-17 /pmc/articles/PMC2410187/ /pubmed/14970855 http://dx.doi.org/10.1038/sj.bjc.6601622 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Royston, P Sauerbrei, W Ritchie, A Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title | Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title_full | Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title_fullStr | Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title_full_unstemmed | Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title_short | Is treatment with interferon-α effective in all patients with metastatic renal carcinoma? A new approach to the investigation of interactions |
title_sort | is treatment with interferon-α effective in all patients with metastatic renal carcinoma? a new approach to the investigation of interactions |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410187/ https://www.ncbi.nlm.nih.gov/pubmed/14970855 http://dx.doi.org/10.1038/sj.bjc.6601622 |
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