Literature DB >> 30744465

First line treatment of adult patients with primary immune thrombocytopenia: a real-world study.

Liang Wang1,2,3, Lei Xu2, Hongyuan Hao4, A J Gerard Jansen5, Guoqiang Liu2, Honglei Li2, Xinguang Liu1, Yajing Zhao1, Jun Peng1,3,6, Ming Hou1,3,7.   

Abstract

Immune thrombocytopenia (ITP) is an autoimmune disease with a mild to severe risk of bleeding complications. First line treatment includes corticosteroids, immunoglobulins, or other. In this large cohort study, first-line strategies for treatment-naive adult primary ITP was studied in a real-world setting. Records from all adult ITP patients who received first-line treatment between January 2010 and December 2017 at Qilu Hospital were reviewed retrospectively (n = 699). During the study period, 271 patients were treated with high-dose dexamethasone (HDD) and 289 patients were treated with conventional prednisone (alone or in combination with other drugs). Initial responses were similar for the two groups (88.56% vs. 86.51%, P = 0.462), but patients in the HDD group responded earlier than the prednisone group (3 days vs. 5 days, P < 0.001). The sustained response (SR) at 6 months was lower in the HDD group than in the prednisone group (35.4% vs. 47.1%, P = 0.040). However, the SR at 12 months and at the end of our follow-up were not significantly different between the groups. Overall duration of response (DOR) in the prednisone group was longer than in the HDD group throughout the follow-up period (P = 0.007). However, the incidence of SR and overall DOR were not significantly different between the HDD group and the prednisone 3 months group (prednisone terminated within 3 months). The presence of anti-GPIb-IX autoantibodies was a predictive factor for a poor initial response to corticosteroids therapy (P < 0.05). However, neither of the two antiplatelet autoantibodies were correlated with the opportunity to achieve SR and overall DOR in both groups throughout the follow-up period (P > 0.05). Adverse events were more frequent and long-lasting in the prednisone group. Our study showed that HDD provided an effective and more rapid response as initial treatment of ITP, with comparable long-term prognosis and better tolerance when compared with conventional PDN (less than 3 months) in the real-world setting.

Entities:  

Keywords:  Dexamethasone; efficacy; first-line treatment; immune thrombocytopenia; prednisone; real-world

Mesh:

Substances:

Year:  2019        PMID: 30744465     DOI: 10.1080/09537104.2019.1572875

Source DB:  PubMed          Journal:  Platelets        ISSN: 0953-7104            Impact factor:   3.862


  2 in total

1.  Efficacy and steroid-sparing effect of tacrolimus in patients with autoimmune cytopenia.

Authors:  Ruoxi Zhang; Miao Chen; Chen Yang; Bing Han
Journal:  Ann Hematol       Date:  2022-09-06       Impact factor: 4.030

2.  COVID-19-associated immune thrombocytopenia.

Authors:  Gienke Bomhof; Pim G N J Mutsaers; Frank W G Leebeek; Peter A W Te Boekhorst; Johannes Hofland; F Nanne Croles; A J Gerard Jansen
Journal:  Br J Haematol       Date:  2020-06-08       Impact factor: 8.615

  2 in total

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