TY - JOUR
T1 - Pharmacometric modeling to explore 4F-PCC dosing strategies for VKA reversal in patients with INR below 2
AU - Sarode, Ravi
AU - Fukutake, Katsuyuki
AU - Yasaka, Masahiro
AU - Tortorici, Michael A.
AU - Mangione, Antoinette
AU - Pfister, Marc
AU - Cuker, Adam
N1 - Funding Information:
Conflict-of-interest disclosure: R.S. served as a consultant for CSL Behring, Octapharma, and Portola and received institutional research funding from Siemens. M.A.T. and A.M. are employees of CSL Behring. M.P. is an employee of Certara. A.C. reports that his institution has received research funding on his behalf from Alexion, Bayer, Bioverativ, Novo Nordisk, Pfizer, Shire, Spark, and Syn-timmune and that he has served as a consultant for Genzyme, Kedrion, and Synergy. M.Y. has received lecture fees from Bayer, Bristol-Myers Squibb, and Daiichi-Sankyo. K.F. reports that his institution has received research funding on his behalf from Baxalta/ Shire, Bayer, Pfizer, CSL Behring, Novo Nordisk, Biogen/Bioverativ, Kaketsuken/KM Biologics, Japan Blood Products Organization, and Chugai Pharmaceutical; he has served as a consultant for Baxalta/ Shire, Bayer, CSL Behring, Novo Nordisk, Biogen/Bioverativ, Kaketsuken/KM Biologics, Chugai Pharmaceutical, SRL Inc., LSI Medience, Sekisui Medical, and Sysmex; and he has served as a speaker for Baxalta/Shire, Bayer, Pfizer, CSL Behring, Novo Nordisk, Biogen/Bioverativ, Kaketsuken/KM Biologics, Chugai Pharmaceutical, Siemens, Sekisui Medical, Fujirebio Inc., Torii Parmaceutical, MSD, Sysmex, Ortho Clinical Diagnostics, and Daiichi Sankyo.
Publisher Copyright:
© 2020 by The American Society of Hematology
PY - 2020/9
Y1 - 2020/9
N2 - The indicated dose of 4-factor prothrombin complex concentrate (4F-PCC) for urgent vitamin K antagonist (VKA) reversal in patients with an international normalized ratio (INR) of 2 to 4 is 25 IU/kg, but there is no indicated dose for INR,2. We explored 4F-PCC dosing strategies for baseline INR,2. Clinical trial data were used to develop pharmacometric models for Factor X (FX) and FII, accounting for covariates including baseline INR. FX and FII levels over time were simulated for mean baseline INR levels of the clinical trial participants plus baseline INRs 3.1, 1.9, and 1.6. For each INR, 200 virtual male patients were simulated to evaluate 4F-PCC doses of 35, 25, 20, 15, 12.5, and 10 IU/kg. Given an elevated bleeding risk with VKA therapy in Japanese vs Western populations, results were stratified by Japanese and non-Japanese patients. Target levels of FX and FII were $50% activity at 30 minutes after dosing in $80% of patients. FX- and FII-time models were developed with 1088 FX observations from 193 patients and 1074 FII observations from 192 patients. Model-based simulations indicated that at baseline INR 3.1, $80% of patients achieved $50% FX and FII activity with 25 IU/kg and 20 IU/kg 4F-PCC, respectively; at baseline INR 1.9, corresponding doses were 20 IU/kg and 15 IU/kg 4F-PCC, and at baseline INR 1.6, corresponding doses were 15 IU/kg, and 10 IU/kg 4F-PCC. Trends in Japanese and non-Japanese patients were similar. In conclusion, low 4F-PCC doses (15-20 IU/kg) may be sufficient to achieve hemostatic levels of FX and FII in Japanese and non-Japanese patients with baseline INR,2.
AB - The indicated dose of 4-factor prothrombin complex concentrate (4F-PCC) for urgent vitamin K antagonist (VKA) reversal in patients with an international normalized ratio (INR) of 2 to 4 is 25 IU/kg, but there is no indicated dose for INR,2. We explored 4F-PCC dosing strategies for baseline INR,2. Clinical trial data were used to develop pharmacometric models for Factor X (FX) and FII, accounting for covariates including baseline INR. FX and FII levels over time were simulated for mean baseline INR levels of the clinical trial participants plus baseline INRs 3.1, 1.9, and 1.6. For each INR, 200 virtual male patients were simulated to evaluate 4F-PCC doses of 35, 25, 20, 15, 12.5, and 10 IU/kg. Given an elevated bleeding risk with VKA therapy in Japanese vs Western populations, results were stratified by Japanese and non-Japanese patients. Target levels of FX and FII were $50% activity at 30 minutes after dosing in $80% of patients. FX- and FII-time models were developed with 1088 FX observations from 193 patients and 1074 FII observations from 192 patients. Model-based simulations indicated that at baseline INR 3.1, $80% of patients achieved $50% FX and FII activity with 25 IU/kg and 20 IU/kg 4F-PCC, respectively; at baseline INR 1.9, corresponding doses were 20 IU/kg and 15 IU/kg 4F-PCC, and at baseline INR 1.6, corresponding doses were 15 IU/kg, and 10 IU/kg 4F-PCC. Trends in Japanese and non-Japanese patients were similar. In conclusion, low 4F-PCC doses (15-20 IU/kg) may be sufficient to achieve hemostatic levels of FX and FII in Japanese and non-Japanese patients with baseline INR,2.
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U2 - 10.1182/BLOODADVANCES.2020002267
DO - 10.1182/BLOODADVANCES.2020002267
M3 - Article
C2 - 32898246
AN - SCOPUS:85091532592
SN - 2473-9529
VL - 4
SP - 4208
EP - 4216
JO - Blood advances
JF - Blood advances
IS - 17
ER -