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  3. Use of eltrombopag in aplastic anemia in Europe.
 

Use of eltrombopag in aplastic anemia in Europe.

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BORIS DOI
10.7892/boris.133197
Date of Publication
June 2019
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Ecsedi, Matyas
Lengline, Étienne
Knol-Bout, Cora
Bosman, Paul
Eikema, Dirk-Jan
Afanasyev, Boris
Maschan, Alexei
Dreger, Peter
Halkes, Constantijn J M
Drexler, Beatrice
Cortelezzi, Agostino
Drénou, Bernard
Patriarca, Andrea
Bruno, Benedetto
Onofrillo, Daniela
Lanino, Edoardo
Pulanic, Drazen
Serventi-Seiwerth, Ranka
Garnier, Alice
Ljungman, Per
Bonifazi, Francesca
Giammarco, Sabrina
Tournilhac, Olivier
Pioltelli, Pietro
Rovó, Alicia
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Risitano, Antonio M
de Latour, Régis Peffault
Dufour, Carlo
Passweg, Jakob
Subject(s)

600 - Technology::610...

Series
Annals of hematology
ISSN or ISBN (if monograph)
0939-5555
Publisher
Springer-Verlag
Language
English
Publisher DOI
10.1007/s00277-019-03652-8
PubMed ID
30915499
Uncontrolled Keywords

Aplastic anemia Eltro...

Description
Eltrombopag (ELT), an oral thrombopoietin receptor agonist, has recently emerged as a promising new drug for the treatment of aplastic anemia (AA). How ELT is used outside of clinical trials in the real-world setting and results of this treatment are not known. We conducted therefore a retrospective survey on the use of ELT in AA among EBMT member centers. We analyzed the 134 patients reported in our survey together with 46 patients recently published by Lengline et al. The median follow-up from start of ELT treatment was 15.3 months, with 85.6% patients alive at last follow-up. Importantly, only 28.9% of our patients received ELT according to the FDA/EMA label as monotherapy in the relapsed/refractory setting, whereas 16.7% received ELT upfront. The overall response rate in our cohort was 62%, very similar to the results of the pivotal ELT trial. In multivariate analysis, combination therapy with ELT/cyclosporine/ATG and response to previous therapy were associated with response. Overall survival was favorable with a 1-year survival from ELT start of 87.4%. We identified age, AA severity before ELT start and response to ELT as variables significantly associated with OS. Two patients transformed to MDS; other adverse events were mostly benign. In sum, ELT is used widely in Europe to treat AA patients, mostly in the relapsed/refractory setting. Response to ELT is similar to the clinical trial data across different age groups, treatment lines, and treatment combinations and results in favorable survival.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/182094
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s00277-019-03652-8.pdftextAdobe PDF475.72 KBpublisherpublishedOpen
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