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Risk of VTE – when is anticoagulation required treatment of VTE – what is optimum anticoagulant survival advantage with heparins new anticoagulants – how.

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Presentation on theme: "Risk of VTE – when is anticoagulation required treatment of VTE – what is optimum anticoagulant survival advantage with heparins new anticoagulants – how."— Presentation transcript:

1 risk of VTE – when is anticoagulation required treatment of VTE – what is optimum anticoagulant survival advantage with heparins new anticoagulants – how do they differ and what implications are there for patients with cancer Cancer, venous thrombosis & new anticoagulants

2 risk of VTE – when is anticoagulation required treatment of VTE – what is optimum anticoagulant survival advantage with heparins new anticoagulants – how do they differ and what implications are there for patients with cancer new drugs - oral, direct inhibitors, predictable pharmacokinetics and pharmacodynamics, few side effects, few drug interactions, single dose for all (?) palliative care - if more effective and easy to use (safer) then lower threshold for intervention cost - cf warfarin & heparin (NICE & PCTs) Cancer, venous thrombosis & new anticoagulants

3 CancerThrombosis

4 CancerThrombosis risk of VTE 5x greater in patients with cancer 1 to 2% of patients with cancer develop VTE within 2 years 10% of consecutive patients with VTE have cancer 1/7 cancer patients dying in hospital die of PE

5 Determinants of venous thrombosis risk in cancer patients Tumour stage Tumour type Therapy Surgery Chemotherapy Radiotherapy Hormonal Other Prothrombotic abnormalities

6 Blom et al JAMA 2005;293:715 Malignancies and risk of venous thrombosis (MEGA) time from diagnosis of cancer - years Odds Ratio Risk of VTE

7 Chew et al Arch Int Med 2006;166:458 Incidence of VTE and its effect on survival among patients with common cancers KM plot of incidence of VTE within 2 years of cancer diagnosis metastatic disease at diagnosis regional disease at diagnosis

8 Development and validation of predictive model for chemotherapy-associated thrombosis Khorana et al Blood 2008;111:4902

9 CancerThrombosis 1 year mortality increased in patients with VTE compared to patients with same cancer without VTE cancer growth promoted by TF, thrombin, fibrin, platelet activation

10 Hutten et al J Clin Oncol 2000;18:3078 Recurrent thromboembolisl and bleeding in patients with VTE in relation to malignancy and achieved INR

11 Prandoni et al Blood 2002;100:3484 Recurrent VTE and bleeding during anticoagulant treatment in patients with cancer and venous thrombosis

12 Meyer et al Arch Int Med 2002;162:1729 Comparison of LMWH & warfarin for prevention of recurrent VTE in patients with cancer major bleeding & symptomatic recurrent VTE death from all causes 146 enoxaparin VKA enoxaparin 6 months5-7 days enoxaparin

13 Lee et al NEJM 2003;349:146 LMWH v VKA for prevention of recurrent VTE in patients with cancer CLOT Investigators Symptomatic recurrent VTEdeath from all causes 672 dalteparin VKA dalteparin 6 months5-7 days dalteparin

14 Hull et al Am J Med 2006;119:1062 Long-term LMWH v UFH/VKA in proximal vein thrombosis in patients with cancer Symptomatic recurrent VTE survival 200 tinzaparin VKA tinzaparin 3 months6 days UFH

15 Buller et al J Thromb Haemostas 2007;5:246 Cancer and thrombosis effect of heparin on survival heparins v placebo A = all patients, B = limited disease patients

16 Lee et al J Clin Oncol 2005;23:2123 Cancer and thrombosis effect of heparin on survival (CLOT study) dalteparin v warfarin

17 Properties of traditional & new anticoagulants OralPredictable Fixed No routine No food/drug response dosing monitoring interactions Ideal+ + + + + VKA+ UF heparin+ LMWH + + + + fondaparinux + + + + lepirudin+ dabigatran+ + + + + rivaroxaban+ + + + + apixaban+ + + + +

18 Properties of traditional & new anticoagulants noreversibleno placental not HITTtransferimmunogenic Ideal+++ + VKA++ + UF heparin++ LMWH-/++ fondaparinux++ + lepirudin+? dabigatran+? + rivaroxaban++ + apixaban+? +

19 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin

20 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin heparin

21 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin warfarin

22 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin fondaparinux idraparinux

23 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin dabigatran

24 TF / VIIa XIX IXa Xa Va VIIIa IIa fibrinogenfibrin rivaroxaban apixaban

25 Vitamin KVitamin K epoxide inactive vitamin K dependent factors biologically active forms VK epoxide reductase Warfarin

26 Gage, ASH 2006

27 White, R. H. et. al. Ann Intern Med 1995;122:40-42 Decrease in the international normalized ratio (INR) over time after discontinuation of warfarin therapy

28 Antithrombin RCL- IIa

29 AT-Protease-Heparin Complexes

30

31 Dabigatran base-IIa

32 Dabigatran Clinical trial patients: >38,000 Plasma levels correlate with clotting time PT, APTT Dose response for efficacy Yes Dose response for bleeding Yes Bioavailability 6.5% Absorption (C max) 2 hrs t1/2 12-14 hrs KD 7 x 10 M Metabolism (active drug) not inactivated Excretion Renal 80%, accumulation when GFR < 50ml/min Drug interactions amiodarone -10

33 Rivaroxaban Clinical trial patients: >45,000 Plasma levels correlate with clotting time PT Dose response for efficacy yes Dose response for bleeding yes Bioavailability >80% Absorption (C max) 3 hrs t1/2 7 - 11 hrs KD 3 x 10 M metabolism 67% liver, can be used in liver disease if no coagulapathy Excretion 33% renal,minimal renal, no accum. If GFR > 15ml/min Drug interactions HIV protease inhibitors azole antifungals -10

34 New oral anticoagulants dabigatranrivaroxabanapixaban OrthopaedicRENOVATERECORDADVANCE VTE prophylaxisREMODELI - IV REMOBILISE AFRELYROCKETARISTOTLE VTE treatmentRE-COVEREINSTEIN REMEDY RESONATE ACSREDEEMATLASAPPRAISE Medical-MAGELLANADOPT prophylaxis Surgical (non-ortho)--- VTE prophylaxis

35 RE-COVER: Dabigatran versus warfarin in the treatment of VTE Schulman et al NEJM 2009;361:2342 2539 dabigatran warfarin 6 months5-7 days heparin

36 RE-COVER: Dabigatran versus warfarin in VTE Schulman et al NEJM 2009;361:2342

37 VAN GOGH: Idraparinux versus standard therapy for venous thromboembolic disease Van Gogh Investigators NEJM 2007;357:1094 2904 DVT 2215 PE Idraparinux VKA 3 -6 months5-7 days Idra heparin

38 Reversibility of Idrabiotaparinux by intravenous avidin Paty et al J Thromb Haemostas 2010;8:722

39 Reversibility of Idrabiotaparinux by intravenous avidin The EQUINOX Investigators J Thromb Haemostas 2010;epub


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