Vnitr Lek 2016, 62(6):449-452

Long-term treatment of venous thromboembolism in patients with cancer

Jan ©mrha1,2,*, Petr Kessler3, Hynek Poul3, Michaela Harudová3
1 Interní oddělení Nemocnice Pelhřimov, p.o.
2 Kardiologické oddělení Nemocnice Jihlava, p.o.
3 Oddělení hematologie a transfuziologie Nemocnice Pelhřimov p.o.

Background:
The treatment with low-molecular-weight heparin (LMWH) is recommended for patients with cancer associated thrombosis (CAT) during the first 6 months; the initial therapeutic dose can be reduced to 60-75 % after one month. The therapy should be reevaluated after 6 month and subsequent therapy using LMWH or warfarin is recommended indefinitely, unless the cancer is resolved or any major contraindications arise.

Aims:
To analyze the usage of various treatment modalities in CAT patients after the initial 6 month period according to the course of cancer.

Patients and methods:
87 patients with CAT were followed prospectively during the treatment period. The proportion of patients, in whom LMWH was replaced by warfarin during the first 6 months and during the entire follow up, was analyzed in relation to the course of the cancer. The χ2 test and χ2 test with Yates correction were used for the statistical evaluation.

Results:
The median follow-up was 445 days, mean duration of follow up was 743 days. 6 months after the diagnosis of thrombosis 9/30 (31.0 %) patients with complete remission (CR) of the cancer were treated with warfarin, while only 3/12 (25 %), 0/9 (0 %) and 1/13 (7.7 %) of the patients with partial remission (PR), stable disease (SD) and progression, respectively, were treated with warfarin. Patients with CR and PR were more frequently treated with warfarin than patients with SD or progression (P = 0.02). 13 patients died during the first 6 months, and 8 patients were followed less than 6 months. During the entire follow up, 25/30 (83.3 %) patients with CR switched to warfarin, while only 5/12 (41.7 %), 1/9 (11.1 %) and 1/13 (7.7 %) patients with PR, SD, and progression, respectively, were treated with warfarin. The proportion of patients with CR which switched to warfarin was higher, than the proportion of patients with PR (P = 0.007), with SD (P = 0.0003), and with progression (P < 0.0001). Median time from thrombosis onset to the switch from LMWH to warfarin was 219 days in patients in complete remission after 6 months and was not reached in patients in PR,SD, and progression.

Conclusions:
The course of malignant disease is important for the choice of appropriate therapy of CAT after the initial period of LMWH therapy. The patients achieving complete remission are more prone to switch from LMWH to warfarin.

Keywords: cancer; low-molecular-weight-heparin; venous thromboembolism; warfarin

Received: February 25, 2016; Accepted: April 26, 2016; Published: June 1, 2016  Show citation

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©mrha J, Kessler P, Poul H, Harudová M. Long-term treatment of venous thromboembolism in patients with cancer. Vnitr Lek. 2016;62(6):449-452.
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References

  1. Heit JA, Silverstein MD, Mohr DN et al. Risk factors for deep vein thrombosis and pulmonary embolism: a population-based case-control study. Arch Intern Med 2000; 160(6): 809-815. Go to original source... Go to PubMed...
  2. Palareti G, Legnani C, Lee AY et al. A comparison of the safety and efficacy of oral anticoagulation for the treatment of venous thromboembolic disease in patients with or without malignancy. Thromb Haemost 2000; 84(5): 805-810. Go to original source... Go to PubMed...
  3. Konstantinides S, Torbicki A, Agnelli G et al. [Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC)]. 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism Eur Heart J 2014; 35(43): 3033-69, 3069a-3069. Dostupné z WWW: <http://eurheartj.oxfordjournals.org/content/ehj/35/43/3033.full.pdf>. Erratum in Corrigendum to: 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism. [Eur Heart J 2015]. Corrigendum to: 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism. [Eur Heart J 2015] Go to original source... Go to PubMed...
  4. Lee AY, Levine MN, Baker RI et al. Randomized Comparison of Low-Molecular-Weight Heparin versus Oral Anticoagulant Therapy for the Prevention of Recurrent Venous Thromboembolism in Patients with Cancer (CLOT) Investigators: Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. N Engl J Med 2003; 349(2): 146-153. Go to original source... Go to PubMed...
  5. Lee AY, Bauersachs R, Janas MS et al. CATCH: a randomised clinical trial comparing long-term tinzaparin versus warfarin for treatment of acute venous thromboembolism in cancer patients. BMC Cancer 2013; 13: 284. Dostupné z DOI: <http://dx.doi.org/10.1186/1471-2407-13-284>. Go to original source... Go to PubMed...
  6. Cronin-Fenton DP, Søndergaard F, Pedersen LA et al. Hospitalisation for venous thromboembolism in cancer patients and the general population: a population-based cohort study in Denmark, 1997-2006. Br J Cancer 2010; 103(7): 947-953. Go to original source... Go to PubMed...
  7. Lee AY, Rickles FR, Julian JA et al. Randomized comparison of low molecular weight heparin and coumarin derivatives on the survival of patients with cancer and venous thromboembolism. J Clin Oncol 2005; 23(10): 2123-2129. Go to original source... Go to PubMed...
  8. Prandoni P. The treatment of cancer-associated venous thromboembolism in the era of the novel oral anticoagulants. Expert Opin Pharmacother 2015; 16(16):2391-2394. Go to original source... Go to PubMed...
  9. Akl EA, Barba M, Rohilla S et al. Anticoagulation for the long term treatment of venous thromboembolism in patients with cancer. Cochrane Database Syst Rev 2008; 16(2): CD006650. Dostupné z DOI: <http://dx.doi.org/10.1002/14651858.CD006650.pub2>. Go to original source... Go to PubMed...
  10. Meyer G, Marjanovic Z, Valcke J et al. Comparison of low-molecular-weight heparin and warfarin for the secondary prevention of venous thromboembolism in patients with cancer: a randomized controlled study. Arch Intern Med 2002; 162(15): 1729-1735. Go to original source... Go to PubMed...
  11. Hull RD, Pineo GF, Brant RF et al. [LITE Trial Investigators]. Long-term low-molecular-weight heparin versus usual care in proximal-vein thrombosis patients with cancer. Am J Med 2006; 119(12): 1062-1072. Go to original source... Go to PubMed...
  12. Francis CW, Kessler CM, Goldhaber SZ et al. Treatment of venous thromboembolism in cancer patients with dalteparin for up to 12 months: the DALTECAN Study. J Thromb Haemost 2015; 13(6): 1028-1035. Go to original source... Go to PubMed...
  13. Noble S, Matzdorff A, Maraveyas A et al. Assessing patients' anticoagulation preferences for the treatment of cancer-associated thrombosis using conjoint methodology. Haematologica 2015; 100(11): 1486-1492. Go to original source... Go to PubMed...
  14. van der Hulle T, den Exter PL, Planquette B et al. Risk of recurrent venous thromboembolism and major hemorrhage in incidental pulmonary embolism among treated and untreated patients: a pooled analysis of 926 patients. J Thromb Haemost 2016; 14(1): 105-113. Go to original source... Go to PubMed...
  15. Vedovati MC, Germini F, Agnelli G et al. Direct oral anticoagulants in patients with VTE and cancer: a systematic review and meta-analysis. Chest 2015; 147(2): 475-483. Go to original source... Go to PubMed...
  16. van Es N, Coppens M, Schulman S. Direct oral anticoagulants compared with vitamin K antagonists for acute venous thromboembolism: evidence from phase 3 trials. Blood 2014; 124(12): 1968-1975. Go to original source... Go to PubMed...




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