| Literature DB >> 31570488 |
Carlo Visco1,2, Francesco Rodeghiero1,3, Alessandra Romano4, Federica Valeri5, Michele Merli6, Giulia Quaresimini7, Stefano Volpetti8, Roberto M Santi9, Giuseppe Carli1, Elisa Lucchini8,10, Francesco Passamonti6, Alessandro Rambaldi7, Giovanna Motta4, Alessandra Borchiellini5, Emanuele S G d'Amore11, Marco Ruggeri1.
Abstract
Immune thrombocytopenia (ITP) secondary to chronic lymphoproliferative disorders (LPDs) is poorly responsive to conventional treatments. We conducted a multicenter phase 2 prospective 24-week study in 18 patients with ITP secondary to LPDs to assess the safety and efficacy of eltrombopag. Responsive patients entered an extension study for up to 5 years. For inclusion, patients should not require cytotoxic treatment and should have a platelet count <30 × 109/L or have symptoms of bleeding. Eltrombopag was initiated at 50 mg/day, with a maximum of 150 mg/day. The primary end point was platelet response after 4 weeks. Median age was 70 years (range, 43-83 years), and 14 patients had chronic lymphocytic leukemia, 2 had classic Hodgkin lymphoma, and 2 had Waldenström macroglobulinemia. All patients had received previous ITP treatments. Response rate at week 4 was 78% (95% confidence interval [CI], 58%-97%), with 50% of patients having a complete response (CR) (95% CI, 43%-57%); respective results at week 24 were 59% (95% CI, 36%-82%) with 30% reaching a CR (95% CI, 8%-52%). Median exposure to eltrombopag was 16 months; median dose at week 4 was 50 mg/day (range, 25-100 mg/day), and at week 24, it was 50 mg/day (range, 25-150 mg/day). No grade >2 adverse events were reported. Eltrombopag is active and well tolerated in ITP secondary to LPDs. This trial was registered at www.clinicaltrials.gov as #NCT01610180.Entities:
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Year: 2019 PMID: 31570488 DOI: 10.1182/blood.2019001617
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113