4.7 Article

Risk of thrombosis with anti-phospholipid syndrome in systemic lupus erythematosus treated with thrombopoietin-receptor agonists

Journal

RHEUMATOLOGY
Volume 57, Issue 8, Pages 1432-1438

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/key119

Keywords

immune thrombocytopenia; systemic lupus erythematosus; antiphospholipid syndrome; thrombopoietin-receptor agonists; thrombosis events; adverse events

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Objectives. The use of thrombopoietin-receptor agonists (TPO-RAs) has increased as a second-line therapy in ITP, but the efficacy and safety of such drugs has not been evaluated in SLE-associated ITP. Methods. This was a multicentre retrospective cohort study from 2009 to 2016. Participating centres (n = 11) were secondary-or tertiary-care hospitals belonging to the French national network for adult ITP. Results. We included 18 patients with SLE-ITP treated with TPO-RAs; 10 (55%) had aPL, 5 (27%) showing definite APS. Except for one patient, all (94%) achieved response with TPO-RAs overall. After a median follow-up of 14.7 months with TPO-RAs, four arterial thrombosis events (including one catastrophic APS) occurred in four patients. Two venous thrombosis events occurred in a patient without APS or aPLs. Conclusion. Our results suggest that aPLs should be systematically screened before TPO-RA initiation in patients with SLE. With aPL positivity, alternative therapy should be discussed (if possible), especially in patients with definite APS or suboptimal adherence to anti-coagulation therapy.

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