The effect of low-molecular-weight heparin on cancer survival. A systematic review and meta-analysis of randomized trials

被引:165
作者
Lazo-Langner, A.
Goss, G. D.
Spaans, J. N.
Rodger, M. A.
机构
[1] Univ Ottawa, Ottawa Hosp, Civic Parkdale Clin, Div Hematol, Ottawa, ON K1Y 1J8, Canada
[2] Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON K1Y 1J8, Canada
[3] Univ Ottawa, Ottawa Hosp Reg Canc Ctr, Div Med Oncol, Ottawa, ON K1Y 1J8, Canada
[4] Ottawa Hlth Res Inst, Clin Epidemiol Program, Ottawa, ON, Canada
关键词
cancer; low-molecular-weight heparin; meta-analysis; randomized trial; survival; systematic review;
D O I
10.1111/j.1538-7836.2007.02427.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Low-molecular-weight heparins (LMWH) have an antitumor effect in vitro and in experimental animal models of malignancy. Retrospective data suggest that it might improve survival in cancer patients. Objectives: To evaluate the effect of LMWH compared to placebo or no anticoagulant intervention on the survival of cancer patients. Methods: We conducted a systematic review of randomized trials specifically evaluating the impact of LMWH on the survival of cancer patients. Data sources were: MEDLINE, EMBASE, HealthSTAR, Cochrane library, gray literature and cross-referencing from reference lists. Data extraction was performed by one reviewer, and accuracy was independently verified by a second reviewer. Meta-analysis was conducted using: (i) odds ratio (OR) and relative risk (RR); (ii) survival rates using censored endpoints; and (iii) hazard ratios (HR). Results: The pooled HR in all patients was 0.83 (95% CI 0.70-0.99; P = 0.03), and in patients with advanced disease it was 0.86 (95% CI 0.74-0.99; P = 0.04), both in favor of the LMWH group. The results of the OR, RR and survival meta-analysis consistently favored the LMWH group. Sensitivity analyses according to tumor type were not conducted, because of a lack of information. Conclusions: LMWH improves overall survival in cancer patients, even in those with advanced disease. Additional trials are required to define the tumor types, disease stages and dosing schedules most likely to provide the greatest survival benefit.
引用
收藏
页码:729 / 737
页数:9
相关论文
共 61 条
[1]   A randomized clinical trial of combination chemotherapy with and without low-molecular-weight heparin in small cell lung cancer [J].
Altinbas, M ;
Coskun, HS ;
Er, O ;
Ozkan, M ;
Eser, B ;
Unal, A ;
Cetin, M ;
Soyuer, S .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (08) :1266-1271
[2]   Odds ratios should be avoided when events are common [J].
Altman, DG ;
Deeks, JJ ;
Sackett, DL .
BRITISH MEDICAL JOURNAL, 1998, 317 (7168) :1318-1318
[3]  
[Anonymous], J THROMB HAEMOST
[4]  
Baker Stuart G, 2003, BMC Med Res Methodol, V3, P10
[5]   Antitumor and antimetastatic effect of warfarin and heparins [J].
Bobek, V ;
Kovarík, J .
BIOMEDICINE & PHARMACOTHERAPY, 2004, 58 (04) :213-219
[6]   The MET oncogene drives a genetic programme linking cancer to haemostasis [J].
Boccaccio, C ;
Sabatino, G ;
Medico, E ;
Girolami, F ;
Follenzi, A ;
Reato, G ;
Sottile, A ;
Naldini, L ;
Comoglio, PM .
NATURE, 2005, 434 (7031) :396-400
[7]   Heparin and cancer revisited: Mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis [J].
Borsig, L ;
Wong, R ;
Feramisco, J ;
Nadeau, DR ;
Varki, NM ;
Varki, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3352-3357
[8]   A RANDOMIZED TRIAL OF ANTICOAGULATION WITH WARFARIN AND OF ALTERNATING CHEMOTHERAPY IN EXTENSIVE SMALL-CELL LUNG-CANCER BY THE CANCER AND LEUKEMIA GROUP-B [J].
CHAHINIAN, AP ;
PROPERT, KJ ;
WARE, JH ;
ZIMMER, B ;
PERRY, MC ;
HIRSH, V ;
SKARIN, A ;
KOPEL, S ;
HOLLAND, JF ;
COMIS, RL ;
GREEN, MR .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (08) :993-1002
[9]   SOME METHODS FOR STRENGTHENING THE COMMON X2 TESTS [J].
COCHRAN, WG .
BIOMETRICS, 1954, 10 (04) :417-451
[10]   Low-molecular-weight heparin and cancer survival: Review of the literature and pooled analysis of 1,726 patients treated for at least three months [J].
Conti, S ;
Guercini, F ;
Iorio, A .
PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2003, 33 (04) :197-201