Low molecular weight heparin, therapy with dalteparin, and survival in advanced cancer: The fragmin advanced malignancy outcome study (FAMOUS)

被引:552
作者
Kakkar, AK
Levine, MN
Kadziola, Z
Lemoine, NR
Low, V
Patel, HK
Rustin, G
Thomas, M
Quigley, M
Williamson, RCN
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Surg Oncol & Technol, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, Fac Med, Canc Res UK Labs, London W12 0NN, England
[3] Hammersmith Hosp, Thrombosis Res Inst, London, England
[4] Hammersmith Hosp, Dept Surg, London, England
[5] Mt Vernon Hosp Canc Ctr, Northwood, Herts, England
[6] Bristol Royal Infirm & Gen Hosp, Dept Surg, Bristol, Avon, England
[7] Oldchurch Hosp, Dept Oncol, Romford RM7 0BE, Essex, England
[8] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
关键词
D O I
10.1200/JCO.2004.10.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose In experimental systems, interference with coagulation can affect tumor biology. Furthermore, it has been suggested that low molecular weight heparin therapy may prolong survival in patients with cancer. The primary aim of this study was to assess survival at 1 year of patients with advanced cancer. Patients and Methods Patients with advanced malignancy (N = 385) were randomly assigned to receive either a once-daily subcutaneous injection of dalteparin (5,000 IU), a low molecular weight heparin, or placebo for 1 year. Results The Kaplan-Meier survival estimates at 1, 2, and 3 years after randomization for patients receiving dalteparin were 46%, 27%, and 21%, respectively, compared with 41%, 18%, and 12%, respectively, for patients receiving placebo (P = .19). In an analysis not specified a priori, survival was examined in a subgroup of patients (dalteparin, n = 55; and placebo, n = 47) who had a better prognosis and who were alive 17 months after randomization. In these patients, Kaplan-Meier survival estimates at 2 and 3 years from randomization were significantly improved for patients receiving dalteparin versus placebo (78% v 55% and 60% v 36%, respectively, P = .03). The rates of symptomatic venous thromboembolism were 2.4% and 3.3% for dalteparin and placebo, respectively, with bleeding rates of 4.7% and 2.7%, respectively. Conclusion Dalteparin administration did not significantly improve 1-year survival rates in patients with advanced malignancy. However, the observed improved survival in a subgroup of patients with a better prognosis suggests a potential modifying effect of dalteparin on tumor biology. (C) 2004 by American Society of Clinical Oncology.
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页码:1944 / 1948
页数:5
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