| Anticoagulant regimen | Preferred timing with respect to cancer therapy | Drugs and dosing | Reversibility | Drug-drug interactions | Reduced renal function | Reduced liver function | Cost | Comments |
|---|---|---|---|---|---|---|---|---|
| VKAs | Before and after | Coumadin, dosing according to INR | Vitamin K, fresh frozen plasma or prothrombin complex concentrate | +++ | Preferred if severe end-stage renal disease without haemodialysis | Not required | Low | Inconvenience owing to the need for recurrent INR checks |
| LMWH | During | Enoxaparin 1 mg/kg subcutaneously twice daily; dalteparin 200 U/kg subcutaneously daily | Protamine (but unlike with unfractionated heparin, it does not completely abolish the anti-factor Xa activity of LMWH) | + | Caution if eGFR <30 ml/min; monitor factor Xa levels | Not required | High | Heparin-induced thrombocytopenia; discomfort with injections; challenging long-term treatment |
| NOACs | Before and after | Rivaroxaban 20 mg orally daily; endoxaban 60 mg orally daily; dabigatran 150 mg orally twice daily; apixaban 5 mg orally twice daily | Idarucizumab (Praxbind) for dabigatran; andexanet alfa (Andexxa), if available, for apixaban or rivaroxaban; or four-factor prothrombin complex concentrate for all other NOACs | +++ | Reduce rivaroxaban dosage to 15 mg daily; reduce endoxaban dosage to 30 mg daily if eGFR is 15–50 ml/min; reduce dabigatran dosage to 75 mg twice daily if eGFR is 15–30 ml/min; reduce apixaban dosage to 2.5 mg twice daily if serum creatinine level is ≥1.5 mg/dl and either age ≥80 years or weight ≤60 kg | Not recommended with moderate-to-severe (rivaroxaban and endoxaban) or severe (apixaban) liver dysfunction (Child-Pugh class B/C and class C) | High | Lack of ample experience and publications in patients with cancer; concerns for use in patients with gastrointestinal (and genitourinary) tract lesions |
egFR, estimated glomerular filtration rate; INR, international normalized ratio.