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. Author manuscript; available in PMC: 2022 Jan 21.
Published in final edited form as: Nat Rev Cardiol. 2020 Mar 30;17(8):474–502. doi: 10.1038/s41569-020-0348-1
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.