Evidence map›Paper›PMID 39196490›Full record

ArticleBlood research2024

Evaluation of FVIII pharmacokinetic profiles in Korean hemophilia A patients assessed with myPKFiT: a retrospective chart review.

Young-Shil Park, Ki-Young Yoo, Sang Kyu Park, Taiju Hwang, Aeran Jung, Eun Jin Choi

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Article in Blood research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Young-Shil ParkDepartment of Pediatrics, Kyung Hee University Hospital, Gangdong, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-6643-4245
Ki-Young YooKorea Hemophilia Foundation Clinic, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-1470-3519
Sang Kyu ParkKorea Hemophilia Foundation Clinic, Busan, Republic of Korea.ORCID http://orcid.org/0000-0003-2458-981X
Taiju HwangKorea Hemophilia Foundation Clinic, Gwangju, Republic of Korea.ORCID http://orcid.org/0000-0002-1752-1967
Aeran JungMedical Affairs, Takeda Pharmaceuticals Korea Co., Ltd, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0003-4723-5253
Eun Jin ChoiDepartment of Pediatrics, Daegu Catholic University Medical Center, 33 Duryugongwon-Ro 17-Gil, Nam-Gu, Daegu, 42472, Republic of Korea. ejchoi2@cu.ac.kr.ORCID http://orcid.org/0000-0001-7116-8538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to investigate the pharmacokinetics (PK) of factor VIII (FVIII) in Korean patients, as limited information is available on the PK of FVIII in this population.

methodsWe collected the FVIII PK results from patients with moderate-to-severe hemophilia A using myPKFiT. PK variations were assessed according to age, blood type, inhibitor history, von Willebrand factor antigen (vWF:Ag) level, and body mass index. Additionally, the correlation between the PK profile and prophylaxis regimen was specifically analyzed for each product in severe cases.

resultsThe PK data of 48 and 81 patients treated with octocog alfa and rurioctocog alfa pegol, respectively, were obtained. The median half-lives of octocog alfa and rurioctocog alfa pegol were 9.9 (range: 6.3-15.2) h and 15.3 (range: 10.4-23.9) h, respectively. The PK profiles for each product did not differ according to age group; however, blood type-O patients had shorter half-lives and time to 1% compared to non-blood type-O patients. In regression analysis, the PK of octocog alfa showed a statistically significant difference according to age, whereas the PK of rurioctocog alfa pegol correlated with vWF:Ag. Only the frequency of rurioctocog alfa pegol use showed a statistically significant difference in relation to time to 1%, although the coefficient of determination was small.

conclusionThis study confirmed significant interpatient variation in the PK of FVIII among Korean patients with hemophilia A. To achieve optimized prophylaxis, personalizing the regimen based on the PK profile of each individual patient is essential.

Indexed as

FVIIIHemophilia AKoreanPharmacokineticsProphylaxis

Identifiers

PMID39196490
PMCPMC11358568

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