Interferon-Alpha And Survival In Metastatic Renal Carcinoma: Early Results Of A Randomised Controlled Trial

A Ritchie,Gareth Griffiths, Mahesh K. B. Parmar,Sophie D. Fosså,Peter Selby, Ma Cornbleet, G Sibley,Graham M. Mead,Stan B. Kaye, Owen,Rtd Oliver, Ph Smith,P Whelan,P A Cook, Pm Fayers,P Cook,J Webb,J Whitehead, A Lamont

LANCET(1999)

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摘要
Background Metastatic renal carcinoma has a 2-year survival of around 20% and is largely resistant to chemotherapy. The use of interferons in the treatment of metastatic renal carcinoma remains controversial. Although non-randomised studies suggest that biological therapy with interferons produces a small number of tumour responses, most clinicians judge such treatment to be ineffective. We have investigated the effect of treatment with interferon-alpha on survival inpatients with metastatic renal carcinoma.Methods In a multicentre, randomised trial, patients with metastatic renal carcinoma were randomly assigned subcutaneous interferon-alpha (three doses-5 MU, 5 MU, 10 MU-for the first week, then 10 MU three times per week for a further 11 weeks; n=174) or oral medroxyprogesterone acetate (MPA; 300 mg once daily for 12 weeks; n=176); The primary endpoint was overall survival. Analysis was by intention to treat. The trial used a triangular sequential design for early termination as soon as results were conclusive. The trial was stopped in November, 1997, when data were available for 335 patients (167 interferon-alpha, 168 MPA).Findings A total of 111 patients have died in the interferon-a group, and 125 patients have died in the MPA group. There was a 28% reduction in the risk of death in the interferon-alpha group (hazard ratio 0.72 [95% CI 0.55-0.94], p=0.017). Interferon-ol gave an improvement in 1-year survival of 12% (MPA 31% survival, interferon-alpha 43%), and an improvement in median survival of 2.5 months (MPA 6 months, interferon-alpha 8.5 months).Interpretation The benefit of treatment with interferon-oc should be weighed against the drug's toxic effects. Combination regimens of biological therapy and chemotherapy should now be compared with interferon-ce monotherapy in randomised controlled trials.
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