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A large observational study of patients with primary immune thrombocytopenia receiving romiplostim in European clinical practice

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F17%3A43912199" target="_blank" >RIV/00216208:11120/17:43912199 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064173:_____/17:N0000024

  • Result on the web

    <a href="http://dx.doi.org/10.1111/ejh.12807" target="_blank" >http://dx.doi.org/10.1111/ejh.12807</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/ejh.12807" target="_blank" >10.1111/ejh.12807</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A large observational study of patients with primary immune thrombocytopenia receiving romiplostim in European clinical practice

  • Original language description

    OBJECTIVE: Romiplostim has maintained long-term platelet counts in patients with immune thrombocytopenia (ITP) for up to 5 years in clinical studies. This prospective observational study aimed to describe romiplostim utilisation and outcomes in European clinical practice. METHODS: Adults with primary ITP who received romiplostim in routine care were eligible. RESULTS: Three-hundred and forty patients were eligible for analysis, of whom 299 (88%) completed the two-year observation period. The median age was 62 years, with 43% of patients aged GREATER-THAN OR EQUAL TO65 years, and two-thirds of patients initiated romiplostim before splenectomy. The median average weekly dose of romiplostim was 2.8 μg/kg. The median baseline platelet count was 20 x 10(9) /L, which increased after 2 weeks of romiplostim treatment and remained &gt;50 x 10(9) /L thereafter. After romiplostim initiation, there was a decrease in rates of grade GREATER-THAN OR EQUAL TO3 bleeding events (from 12 to 2 per 100 patient-years) and ITP-related hospitalisations (from 87 to 33 per 100 patient-years). The rate of thrombotic events was 2 per 100 patient-years and bone marrow fibrosis occurred in two patients. CONCLUSIONS: Romiplostim dosing, effectiveness, and safety in an unselected real-world ITP population seemed comparable with that observed in clinical studies.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    European Journal of Haematology

  • ISSN

    0902-4441

  • e-ISSN

  • Volume of the periodical

    98

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    112-120

  • UT code for WoS article

    000393167400002

  • EID of the result in the Scopus database

    2-s2.0-84994344530