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1000 Titel
  • Approach to the patient with eosinophilia in the era of tyrosine kinase inhibitors and biologicals
1000 Autor/in
  1. Lübke, Johannes |
  2. Metzgeroth, Georgia |
  3. Reiter, Andreas |
  4. Schwaab, Juliana |
1000 Verlag
  • Springer US
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-07-22
1000 Erschienen in
1000 Quellenangabe
  • 19(5):208-222
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s11899-024-00738-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11416429/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Purpose of Review</jats:title> <jats:p>In this review, we aim to explore the optimal approach to patients presenting with eosinophilia, considering recent advances in diagnostic and therapeutic strategies. Specifically, we focus on the integration of novel therapies into clinical practice to improve patient outcomes.</jats:p> </jats:sec><jats:sec> <jats:title>Recent Findings</jats:title> <jats:p>Advanced insights into the clinical and genetic features of eosinophilic disorders have prompted revisions in diagnostic criteria by the World Health Organization classification (WHO-HAEM5) and the International Consensus Classification (ICC). These changes reflect a growing understanding of disease pathogenesis and the development of targeted treatment options. The therapeutic landscape now encompasses a range of established and novel therapies. For reactive conditions, drugs targeting the eosinophilopoiesis, such as those aimed at interleukin-5 or its receptor, have demonstrated significant potential in decreasing blood eosinophil levels and minimizing disease flare-ups and relapse. These therapies have the potential to mitigate the side effects commonly associated with prolonged use of oral corticosteroids or immunosuppressants. Myeloid and lymphoid neoplasms with eosinophilia and tyrosine kinase (TK) gene fusions are managed by various TK inhibitors with variable efficacy.</jats:p> </jats:sec><jats:sec> <jats:title>Summary</jats:title> <jats:p>Diagnosis and treatment rely on a multidisciplinary approach. By incorporating novel treatment options into clinical practice, physicians across different disciplines involved in the management of eosinophilic disorders can offer more personalized and effective care to patients. However, challenges remain in accurately diagnosing and risk-stratifying patients, as well as in navigating the complexities of treatment selection.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Protein-Tyrosine Kinases/antagonists
lokal Biological Products/therapeutic use [MeSH]
lokal Humans [MeSH]
lokal Eosinophilia/drug therapy [MeSH]
lokal CEL
lokal Disease Management [MeSH]
lokal Protein Kinase Inhibitors/therapeutic use [MeSH]
lokal Tyrosine Kinase Inhibitors [MeSH]
lokal Eosinophilia
lokal MLN-TK
lokal Article
lokal Hypereosinophilia
lokal Topical Collection on Myeloproliferative Neoplasms
lokal Biological Products/adverse effects [MeSH]
lokal HES
lokal Protein Kinase Inhibitors/adverse effects [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TMO8YmtlLCBKb2hhbm5lcw==|https://frl.publisso.de/adhoc/uri/TWV0emdlcm90aCwgR2VvcmdpYQ==|https://frl.publisso.de/adhoc/uri/UmVpdGVyLCBBbmRyZWFz|https://frl.publisso.de/adhoc/uri/U2Nod2FhYiwgSnVsaWFuYQ==
1000 Hinweis
  • DeepGreen-ID: 5b58465454b241848e324c00e69ee963 ; 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)
1000 Label
1000 Förderer
  1. Wilhelm Sander-Stiftung |
  2. Medizinische Fakultät Mannheim der Universität Heidelberg |
1000 Fördernummer
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  2. -
1000 Förderprogramm
  1. -
  2. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Wilhelm Sander-Stiftung |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Medizinische Fakultät Mannheim der Universität Heidelberg |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6489628.rdf
1000 Erstellt am 2025-02-03T08:41:02.134+0100
1000 Erstellt von 322
1000 beschreibt frl:6489628
1000 Zuletzt bearbeitet 2025-07-30T08:26:45.534+0200
1000 Objekt bearb. Wed Jul 30 08:26:45 CEST 2025
1000 Vgl. frl:6489628
1000 Oai Id
  1. oai:frl.publisso.de:frl:6489628 |
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