Presented in part at the American Society of Clinical Oncology Venous Thrombosis Guideline Committee Meeting, July 2006.
A meta-analysis and systematic review of the efficacy and safety of anticoagulants as cancer treatment †
Impact on survival and bleeding complications
Article first published online: 17 JUL 2007
Copyright © 2007 American Cancer Society
Volume 110, Issue 5, pages 1149–1161, 1 September 2007
How to Cite
Kuderer, N. M., Khorana, A. A., Lyman, G. H. and Francis, C. W. (2007), A meta-analysis and systematic review of the efficacy and safety of anticoagulants as cancer treatment . Cancer, 110: 1149–1161. doi: 10.1002/cncr.22892
- Issue published online: 20 AUG 2007
- Article first published online: 17 JUL 2007
- Manuscript Accepted: 5 MAY 2007
- Manuscript Revised: 21 MAR 2007
- Manuscript Received: 25 JAN 2007
- American Society of Clinical Oncology
- National Institutes of Health. Grant Number: T32HL07152-30
- National Cancer Institute. Grant Number: 1K23 CA120587-01A1
- low-molecular-weight heparin;
- randomized controlled trials;
Preclinical evidence suggests that anticoagulants, in particular the low-molecular-weight heparins (LMWH), exert an antitumor effect, whereas clinical trials have reported conflicting results. The authors conducted a comprehensive, systematic review and meta-analysis of the evidence from randomized controlled trials (RCTs), to evaluate the impact of anticoagulants on survival and safety in cancer patients without venous thromboembolism.
A comprehensive systematic literature review of RCTs was performed without language restrictions through May 2006 with subsequent updates to the end of 2006, including an exhaustive search of electronic databases, major conference proceedings, article references, and content experts. Two reviewers extracted data independently. Primary study outcomes were 1-year overall mortality and all bleeding complications. Major and fatal bleeding complications were secondary outcomes.
Across all 11 studies that were identified, anticoagulation significantly decreased 1-year overall mortality with a relative risk (RR) of 0.905 (95% confidence interval [95% CI], 0.847–0.967; P = .003). The RR for mortality was 0.877 (95% CI, 0.789–0.975; P = .015) for LMWH, compared with an RR of 0.942 (95% CI, 0.854–1.040; P = .239) for warfarin, resulting in an absolute risk difference (ARD) of 8% for LMWH and an ARD of 3% for warfarin. Improved survival with anticoagulation may be dependent on tumor type. Major bleeding episodes occurred less frequently in patients who received LMWH (ARD, 1%) compared with patients who received warfarin (ARD, 11.5%; P < .0001). Overall, fatal bleeding occurred rarely (ARD, 0.32%; P = .542).
Anticoagulants, particularly LMWH, significantly improved overall survival in cancer patients without venous thrombosis while increasing the risk for bleeding complications. However, given the limitations of available data, the use of anticoagulants as antineoplastic therapy cannot be recommended until additional RCTs confirm these results. Cancer 2007. © 2007 American Cancer Society.