| Literature DB >> 28573819 |
Tomás J González-López1, María T Alvarez-Román2, Cristina Pascual3, Blanca Sánchez-González4, Fernando Fernández-Fuentes5, Gloria Pérez-Rus3, José A Hernández-Rivas6, Silvia Bernat7, José M Bastida8, María P Martínez-Badas9, Violeta Martínez-Robles10, Inmaculada Soto11, Pavel Olivera12, Estefanía Bolaños13, Rafael Alonso14, Laura Entrena15, Marta Gómez-Nuñez16, Arancha Alonso17, María Yera Cobo18, Isabel Caparrós19, María Tenorio20, Esther Arrieta-Cerdán21, Elsa Lopez-Ansoar22, Javier García-Frade23, José R González-Porras8.
Abstract
Eltrombopag is a second-line treatment in primary immune thrombocytopenia (ITP). However, its role in secondary ITP is unknown. We evaluated the efficacy and safety of eltrombopag in secondary ITP in daily clinical practice. Eighty-seven secondary ITP patients (46 with ITP secondary to autoimmune syndromes, 23 with ITP secondary to a neoplastic disease subtype: lymphoproliferative disorders [LPDs] and 18 with ITP secondary to viral infections) who had been treated with eltrombopag were retrospectively evaluated. Forty-four patients (38%) had a platelet response, including 40 (35%) with complete responses. Median time to platelet response was 15 days (95% confidence interval, 7-28 days), and was longer in the LPD-ITP group. Platelet response rate was significantly lower in the LPD-ITP than in other groups. However, having achieved response, there were no significant differences between the durable response of the groups. Forty-three patients (49·4%) experienced adverse events (mainly grade 1-2), the commonest being hepatobiliary laboratory abnormalities. There were 10 deaths in this case series, all of which were related to pre-existing medical conditions. In routine clinical practice, eltrombopag is effective and well-tolerated in unselected patients with ITP secondary to both immune and infectious disorders. However, the response rate in LPD-ITP is low.Entities:
Keywords: efficacy; eltrombopag; immune thrombocytopenia; safety; thrombopoietin
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Year: 2017 PMID: 28573819 DOI: 10.1111/bjh.14788
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998