Pharmacokinetics of Efmoroctocog alfa by Two-Compartment Model Highlights Hemophilia A Patients with Biphasic Decay, Long Mean Residence Time, and Beta Half-Life

被引:0
作者
Morfini, Massimo [1 ]
Peyvandi, Flora [2 ]
Mancuso, Maria Elisa [3 ]
Marchesini, Emanuela [4 ]
Tagliaferri, Annarita [5 ]
Gualtierotti, Roberta [2 ]
Castaman, Giancarlo [6 ]
Pollio, Berardino [7 ]
Santoro, Cristina [8 ]
Banov, Luisa [9 ]
Napolitano, Mariasanta [10 ]
Preti, Paola Stefania [11 ]
Santoro, Rita Carlotta [12 ]
Coppola, Antonio [5 ]
Linari, Silvia [6 ]
Santagostino, Elena [13 ]
Bernardi, Francesco [14 ]
机构
[1] Italian Assoc Hemophilia Ctr AICE, I-20120 Milan, Italy
[2] Univ Milan, Fdn IRCSS CaGranda Maggiore Hosp, Dept Pathophysiol & Transplantat, Angelo Bianchi Bonomi, I-20120 Milan, Italy
[3] IRCCS Humanitas Res Hosp, Ctr Thrombosis & Hemorrhag Dis, I-20142 Milan, Italy
[4] Santa Maria Misericordia Univ Hosp, Hemophilia Ctr Internal & Cardiovasc Med, I-06100 Perugia, Italy
[5] Univ Hosp Parma, Reg Reference Ctr Inherited Bleeding Disorders, I-43100 Parma, Italy
[6] Careggi Univ Hosp, Ctr Bleeding Disorders & Coagulat, Dept Oncol, I-50139 Florence, Italy
[7] Regina Margher Children Hosp, Reg Reference Ctr Inherited Bleeding & Thrombot Di, Transfus Med, I-10100 Turin, Italy
[8] Univ Hosp Policlin Umberto I, Dept Hematol, I-00100 Rome, Italy
[9] IRCCS Ist Giannina Gaslini, Reg Reference Ctr Hemorrhag Dis, I-16100 Genoa, Italy
[10] Univ Palermo, Thrombosis & Hemostasis Reference Reg Ctr, Hematol Unit, I-90100 Palermo, Italy
[11] Univ Pavia, Dept Internal Med & Therapeut, I-27100 Pavia, Italy
[12] Azienda Osped Pugliese Ciaccio, Reg Reference Ctr Hemophilia & Coagulat Dis, I-88100 Catanzaro, Italy
[13] SOBI, SE-11276 Stockholm, Sweden
[14] Univ Ferrara, Dept Life Sci & Biotechnol, Sect Biochem & Mol Biol, I-44121 Ferrara, Italy
关键词
rFVIIIFc; Hemophilia A; pharmacokinetics; one compartment model; two compartment model; non-compartmental analysis; Efmoroctocog alfa; RECOMBINANT FACTOR-VIII; FC FUSION PROTEIN; CONCENTRATE;
D O I
10.3390/jcm13174986
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Objectives: A compartmental pharmacokinetics (PK) analysis of new extended half-life FVIII concentrates has never been performed in a large cohort of hemophilia patients. An improved PK analysis of individual outcomes may help to tailor hemophilia replacement treatment. Methods: PK outcomes after the infusion of a standard single dose of Efmoroctocog alfa were collected from 173 patients with severe/moderately severe hemophilia A in 11 Italian hemophilia centers. Factor VIII clotting activity (FVIII:C) was measured by one-stage clotting assay (OSA) in all patients, and chromogenic substrate assay (CSA) in a subgroup (n = 52). Fifty patients underwent a comparative PK assessment with standard half-life (SHL) recombinant FVIII (rFVIII) products. Non-compartmental analysis (NCA), one compartment model (OCM), and TCM were used to analyze the decay curves of all patients, and one-way paired ANOVA to compare the PK outcomes. Results: All 173 PKs conformed to the NCA and OCM, but only 106 (61%) conformed to the TCM based on the biphasic features of their decay curves. According to the TCM, the Beta HL and MRT of rFVIIIFc were 20.42 +/- 7.73 and 25.64 +/- 7.61 h, respectively. ANOVA analysis of the outcomes from the three PK models showed significant differences in clearance, half-life (HL), and mean residence time (MRT) (p < 0.001 for all parameters). As anticipated, the HL and MRT of rFVIIIFc were longer than those of SHL rFVIII. Comparing OSA with CSA outcomes, Cmax resulted higher when measured by CSA (p = 0.05) and, according to TCM, Beta HL resulted longer when measured by OSA (p = 0.03). FVIII:C trough levels obtained with SHL concentrates were significantly lower than those obtained with rFVIIIFc at each post-infusion time point. Conclusions: In a large group of hemophilia A (HA) patients, three different PK models confirmed the improved pharmacokinetic (PK) characteristics of rFVIIIFc, compared with standard half-life rFVIII concentrates. The TCM only fits two-thirds of the PKs, highlighting their biphasic decay and a long Beta half-life. In these patients, the TCM would be preferable to properly evaluate individual PK features.
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共 32 条
  • [1] ALLAIN JP, 1976, NOUV PRESSE MED, V5, P1047
  • [2] BARRETT KE, 1967, LANCET, V1, P191
  • [3] BRETTLER DB, 1990, BLOOD, V76, P254
  • [4] BRINKHOUS KM, 1947, P SOC EXP BIOL MED, V66, P117
  • [5] Long-term outcomes with emicizumab prophylaxis for hemophilia A with or without FVIII inhibitors from the HAVEN 1-4 studies
    Callaghan, Michael U.
    Negrier, Claude
    Paz-Priel, Ido
    Chang, Tiffany
    Chebon, Sammy
    Lehle, Michaela
    Mahlangu, Johnny
    Young, Guy
    Kruse-Jarres, Rebecca
    Mancuso, Maria Elisa
    Niggli, Markus
    Howard, Monet
    Bienz, Nives Selak
    Shima, Midori
    Jimenez-Yuste, Victor
    Schmitt, Christophe
    Asikanius, Elina
    Levy, Gallia G.
    Pipe, Steven W.
    Oldenburg, Johannes
    [J]. BLOOD, 2021, 137 (16) : 2231 - 2242
  • [6] Draper N. R., 1998, Applied Regression Analysis
  • [7] Gabrielsson J., 2006, PK and PD Data Analysis: Concepts and Applications, V4th ed.
  • [8] Gabrielsson Johan, 2012, Methods Mol Biol, V929, P377
  • [9] Measuring FVIII activity of glycopegylated recombinant factor VIII, N8-GP, with commercially available one-stage clotting and chromogenic assay kits: a two-centre study
    Hillarp, A.
    Bowyer, A.
    Ezban, M.
    Persson, P.
    Kitchen, S.
    [J]. HAEMOPHILIA, 2017, 23 (03) : 458 - 465
  • [10] The pharmacokinetics of a B-domain truncated recombinant factor VIII, turoctocog alfa (NovoEight®), in patients with hemophilia A
    Jimenez-Yuste, V.
    Lejniece, S.
    Klamroth, R.
    Suzuki, T.
    Santagostino, E.
    Karim, F. A.
    Saugstrup, T.
    Moss, J.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, 13 (03) : 370 - 379