Treatment Approach for DVT in Cancer Patients – Thread by
Treatment Approach for DVT in Cancer Patients – Thread by @sujeethemat
Q1. You have a patient with dx of cancer & DVT and u need to start anticoagulation. Your approach?
A1. Treatment approach
Immediate anticoagulation (1-3 weeks) followed by continued anticoagulation (3-6 m)— thehematologist.org.in (@hematologist_in) April 16, 2023
Q1. You have a patient with dx of cancer & DVT and u need to start anticoagulation. Your approach?
A1. Treatment approach Immediate anticoagulation (1-3 weeks) followed by continued anticoagulation (3-6 m).
Q2. Which drugs you will choose for Immediate anticoagulation?
A2. Either low molecular weight (LMW) heparin or a direct oral anticoagulant (DOAC) can be used.
Q3. Why not UFH?
A3. LMWH is possibly superior to UFH in the initial treatment of VTE in people with cancer. The evidence comes from a meta-analysis of 15 randomized controlled trials in cancer patients receiving anticoagulation for VTE (PMID: 29363105.
Q4. Is there any data to support use of DOAC for immediate treatment in cancer patients with DVT, as traditionally UFH or LMWH were considered only options?
A4. Yes!! Data is there.
DATA
[1] Apixaban Vs LMWH (dalteparin) in a RCT CARAVAGGIO trial showed similar efficacy and bleeding rates.
[2] Rivaroxaban vs LMWH (dalteparin) in pilot sudy (n = 406) SELECT-D showed similar efficacy but increased non major bleeding in patients with GI cancer with rivaroxaban
Treatment approach Immediate anticoagulation (1-3 weeks) followed by continued anticoagulation (3-6 m)
In above points we talked about Immediate anticoagulation.
Now for continued Anticoagulation >> Continued use of the DOAC (apixaban or rivaroxaban) or LMW heparin can be done!!
5. Why not the cheaper warfarin?
A5.
[1] Drug interactions, malnutrition and liver dysfunction can lead to wide fluctuations in INR.
[2] RCTs (CLOT trial) and meta-analyses have shown superior efficacy of LMWH in patients with VTE in patients with active cancer (vs warfarin).
NOTE >> For patients with renal insufficiency (eg, crcl <30 mL/min), in whom LMWH (and fondaparinux) is contraindicated and DOACs have not been investigated, IV UFH is preferred, although some experts administer renally dosed enoxaparin with monitoring of antifactor Xa levels.
Q6. What about Platelet cutoffs for these drugs?
A6.
1. Platelet >50,000/microL is not a contraindication
2. Platelet <20,000/microL is a contraindication.
3. Platelet 20,000 – 50,000/microL, the decision to anticoagulant should be individualized and based upon the risk assessment
Q7. How will you administer enoxaparin?
A7. 1.5 mg/kg SC once daily or 1 mg/kg SC twice daily (up to 3-6 months). If you want to start oral ie DOAC after 1-3 weeks, then start apixaban or rivaroxaban at continued anticoagulation doses only after a minimum of 7 days of enoxaparin.
NOTE: Renally dosed enoxaparin (to be given when crcl <30 ml/min) – 1 mg/kg SC OD [ideally with monitoring of antifactor Xa Levels]
Q8. How will you administer dalteparin (LMWH) ?
A8. 200 international units IU/kg daily during month 1, then 150 IU/kg daily for months 2 to 6
Q9. What is dose for Rivaroxaban when it is started form 1st day?
A9. Rivaroxaban dose > Immediate anticoagulation by 15 mg twice daily for three weeks, then for continued anticoagulation with 20 mg once daily for (3-6 months).