ArticleAmerican journal of hematology2025
Efficacy and Thrombotic Risk of Thrombopoietin Receptor Agonists for Immune Thrombocytopenia Secondary to Systemic Lupus and Antiphospholipid Syndrome: French Experience With 80 Patients.
Article in American journal of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.
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Who cites it
6 citing papers in PubMed, 1 synthesis or guideline pooled it.
- The thrombotic burden of high-risk immune thrombocytopenia patients receiving second-line treatments: a systematic review.Rheumatology (Oxford, England) · 2026Pooled it
- Advances and Clinical Applications of Thrombopoietic Agents.Current medical science · 2026Review
- Nasal Mucosal Necrosis in a Patient with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review.Journal of clinical medicine · 2026Article
- Thrombosis in adult primary immune thrombocytopenia in Korea: incidence and risk factors in a 20-year retrospective cohort.Annals of hematology · 2026Article
- Comparison of Evans syndrome and isolated autoimmune cytopenias in SLE: a retrospective study.Lupus science & medicine · 2026Article
- Efficacy and Thrombotic Risk of Thrombopoietin Receptor Agonists for Immune Thrombocytopenia Secondary to Systemic Lupus and Antiphospholipid Syndrome: French Experience With 80 Patients.American journal of hematology · 2025Article
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Authors and funding
18 authors.
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Abstract
Only few data are available regarding the efficacy and safety of thrombopoietin receptor agonists (TPO-RAs) for treating systemic lupus erythematosus (SLE) and/or antiphospholipid syndrome (APS)-associated immune thrombocytopenia (ITP). We retrospectively assessed the efficacy and safety of TPO-RAs in 80 adults with ITP in three subgroups: (1) 37 patients with definite or incomplete SLE and no antiphospholipid antibodies (APAs), (2) 27 patients with definite or incomplete SLE associated with APAs and no history of arterial or venous thrombotic events (TEs) and (3) 16 patients with APS. In total, 39 (48.8%) patients received eltrombopag, 14 (17.5%) romiplostim and 27 (33.8%) both TPO-RAs sequentially. The overall response of ITP was 78.8%. In total, 17 (21.3%) patients had 21 TEs (7 venous and 14 arterials, including 3 catastrophic APS); 3 were fatal. The rate of TEs was 8.1% in the SLE or lupus without APAs group, 22.2% in the SLE or lupus with APAs group and 50% in the APS group. In 12 patients, TPO-RAs were continued after TE onset, combined with an anticoagulant (n = 12) and/or an antiplatelet agent (n = 3). Only one TE relapse occurred in the nine patients with TPO-RAs maintained and combined with an anticoagulant after TE. TPO-RAs may be effective safe in ITP associated with SLE and no APAs. Their use should be carefully considered in the presence of thrombotic risk factors and/or APA positivity and should be avoided in patients with definite APS. When a TE occurs, risk of relapse is low with maintenance of the TPO-RA combined with anticoagulation.
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