The effects of low molecular weight heparins on venous thromboembolism and survival in patients with cancer

被引:15
作者
Lee, Agnes Y. Y. [1 ,2 ]
机构
[1] Hamilton Hlth Sci Henderson Hosp, Hamilton, ON L8V 1C3, Canada
[2] McMaster Univ, Dept Med, Hamilton, ON, Canada
关键词
low molecular weight heparin; neoplasm; venous thrombosis; thromboembolism;
D O I
10.1016/S0049-3848(07)70140-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Monotherapy with low molecular weight heparin (LMWH) is superior to vitamin K antagonists in preventing recurrent venous thromboembolism (VTE) in patients with cancer and may improve the survival of patients with less advanced malignancies. These agents are also the preferred anticoagulants for primary prophylaxis in medical and surgical patients in hospital. Despite their limitations, LMWHs have improved the quality of care and quality of life in patients with VTE. Recent research has also explored the role of LMWH as anticancer agents. Evidence from experimental studies have demonstrated inhibitory effects of LMWH on various processes that are necessary for tumour growth and progression while results from clinical trials have shown a reduction in overall mortality in patients treated with LMWH. However, because of [imitations and differences in study designs as well as small sample sizes, it remains uncertain whether the reduction in mortality is real and whether LMWH achieve this effect through inhibition of coagulation, non-anticoagulant mechanisms or both. Multiple anticancer mechanisms, including inhibition of tumour angiogenesis, interference with tumour cell adhesion, and suppression of tumour cell invasion, have been demonstrated in experimental models with LMWH, but none have been confirmed in vivo in humans. This review will, briefly summarize the data on the treatment of VTE in cancer patients with LMWH and discuss the experimental and clinical data on its possible anticancer effects. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:S121 / S127
页数:7
相关论文
共 48 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]  
[Anonymous], 2004, COCHRANE DATABASE SY, DOI DOI 10.1002/14651858.CD001100.PUB2
[3]   Signaling of the tissue factor coagulation pathway in angiogenesis and cancer [J].
Belting, M ;
Ahamed, J ;
Ruf, W .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (08) :1545-1550
[4]  
Berry D, 2004, CHEM BIOL, V11, P487, DOI 10.1016/j.chembiol.2004.03.023
[5]   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
[6]   Fondaparinux or Enoxaparin for the initial treatment of symptomatic deep venous thrombosis -: A randomized trial [J].
Büller, HR ;
Davidson, BL ;
Decousus, H ;
Gallus, A ;
Gent, M ;
Piovella, F ;
Prins, MH ;
Raskob, G ;
Segers, AEM ;
Cariou, R ;
Leeuwenkamp, O ;
Lensing, AWA .
ANNALS OF INTERNAL MEDICINE, 2004, 140 (11) :867-873
[7]  
Büller HR, 2003, NEW ENGL J MED, V349, P1695
[8]   Effect of a low molecular weight heparin molecule, dalteparin, on cellular apoptosis and inflammatory process in an incisional wound-healing model [J].
Civelek, Ali ;
Ak, Koray ;
Kurtkaya, Ozlem ;
Tekeli, Atike ;
Isbir, Selim ;
Nargileci, Erol ;
Arsan, Sinan ;
Sav, Aydin .
SURGERY TODAY, 2007, 37 (05) :406-411
[9]   Improved cancer mortality with low-molecular-weight heparin treatment: A review of the evidence [J].
Cosgrove, RH ;
Zacharski, LR ;
Racine, E ;
Andersen, JC .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2002, 28 (01) :79-87
[10]   Thrombin signalling and protease-activated receptors [J].
Coughlin, SR .
NATURE, 2000, 407 (6801) :258-264