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1000 Titel
  • Ruxolitinib exposure in patients with acute and chronic graft versus host disease in routine clinical practice—a prospective single-center trial
1000 Autor/in
  1. Isberner, Nora |
  2. Kraus, Sabrina |
  3. Grigoleit, Götz Ulrich |
  4. Aghai, Fatemeh |
  5. Kurlbaum, Max |
  6. Zimmermann, Sebastian |
  7. Klinker, Hartwig |
  8. Scherf-Clavel, Oliver |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-09-10
1000 Erschienen in
1000 Quellenangabe
  • 88(6):973-983
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00280-021-04351-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536600/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!Knowledge on Ruxolitinib exposure in patients with graft versus host disease (GvHD) is scarce. The purpose of this prospective study was to analyze Ruxolitinib concentrations of GvHD patients and to investigate effects of CYP3A4 and CYP2C9 inhibitors and other covariates as well as concentration-dependent effects.!##!Methods!#!262 blood samples of 29 patients with acute or chronic GvHD who were administered Ruxolitinib during clinical routine were analyzed. A population pharmacokinetic model obtained from myelofibrosis patients was adapted to our population and was used to identify relevant pharmacokinetic properties and covariates on drug exposure. Relationships between Ruxolitinib exposure and adverse events were assessed.!##!Results!#!Median of individual mean trough serum concentrations was 39.9 ng/mL at 10 mg twice daily (IQR 27.1 ng/mL, range 5.6-99.8 ng/mL). Applying a population pharmacokinetic model revealed that concentrations in our cohort were significantly higher compared to myelofibrosis patients receiving the same daily dose (p < 0.001). Increased Ruxolitinib exposure was caused by a significant reduction in Ruxolitinib clearance by approximately 50%. Additional comedication with at least one strong CYP3A4 or CYP2C9 inhibitor led to a further reduction by 15% (p < 0.05). No other covariate affected pharmacokinetics significantly. Mean trough concentrations of patients requiring dose reduction related to adverse events were significantly elevated (p < 0.05).!##!Conclusion!#!Ruxolitinib exposure is increased in GvHD patients in comparison to myelofibrosis patients due to reduced clearance and comedication with CYP3A4 or CYP2C9 inhibitors. Elevated Ruxolitinib trough concentrations might be a surrogate for toxicity.
1000 Sacherschließung
lokal Cytochrome P-450 CYP3A Inhibitors/pharmacokinetics [MeSH]
lokal Aged [MeSH]
lokal Pyrimidines/pharmacokinetics [MeSH]
lokal CYP2C9
lokal Graft versus host disease
lokal Nitriles/pharmacokinetics [MeSH]
lokal Original Article
lokal Acute Disease [MeSH]
lokal Primary Myelofibrosis/drug therapy [MeSH]
lokal Male [MeSH]
lokal Nitriles/blood [MeSH]
lokal Tissue Distribution [MeSH]
lokal Chronic Disease [MeSH]
lokal Drug Interactions [MeSH]
lokal Pyrazoles/blood [MeSH]
lokal Toxicity
lokal Graft vs Host Disease/pathology [MeSH]
lokal Graft vs Host Disease/drug therapy [MeSH]
lokal Metabolic Clearance Rate [MeSH]
lokal Pyrazoles/pharmacokinetics [MeSH]
lokal Female [MeSH]
lokal Follow-Up Studies [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Prospective Studies [MeSH]
lokal Pyrimidines/blood [MeSH]
lokal Pyrimidines/administration
lokal Middle Aged [MeSH]
lokal Graft vs Host Disease/metabolism [MeSH]
lokal Pyrazoles/administration
lokal Cytochrome P-450 CYP2C9 Inhibitors/pharmacology [MeSH]
lokal Nitriles/administration
lokal Primary Myelofibrosis/metabolism [MeSH]
lokal CYP3A4
lokal Cytochrome P-450 CYP2C9/chemistry [MeSH]
lokal Prognosis [MeSH]
lokal Young Adult [MeSH]
lokal Cytochrome P-450 CYP3A/chemistry [MeSH]
lokal Primary Myelofibrosis/pathology [MeSH]
lokal Therapeutic drug monitoring
lokal Practice Patterns, Physicians'/statistics
lokal Ruxolitinib
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-7217-9191|https://frl.publisso.de/adhoc/uri/S3JhdXMsIFNhYnJpbmE=|https://frl.publisso.de/adhoc/uri/R3JpZ29sZWl0LCBHw7Z0eiBVbHJpY2g=|https://frl.publisso.de/adhoc/uri/QWdoYWksIEZhdGVtZWg=|https://frl.publisso.de/adhoc/uri/S3VybGJhdW0sIE1heA==|https://frl.publisso.de/adhoc/uri/WmltbWVybWFubiwgU2ViYXN0aWFu|https://frl.publisso.de/adhoc/uri/S2xpbmtlciwgSGFydHdpZw==|https://frl.publisso.de/adhoc/uri/U2NoZXJmLUNsYXZlbCwgT2xpdmVy
1000 Hinweis
  • DeepGreen-ID: d9592c1cfe454858b3e5977e847e5a70 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Erstellt am 2023-05-03T16:24:09.670+0200
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1000 Zuletzt bearbeitet Fri Oct 20 21:16:24 CEST 2023
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