Key result
Widespread TPO-RA adoption shows no increase in thrombosis risk among patients with primary ITP.
Why the study?
In patients with primary immune thrombocytopenia, the risk of thrombosis associated with thrombopoietin receptor agonists remains debated.
Does the widespread adoption of thrombopoietin receptor agonists (TPO-RAs) increase the risk of thrombosis in patients with primary immune thrombocytopenia?
Cohort (n=4,132)
No
Does the widespread adoption of thrombopoietin receptor agonists (TPO-RAs) increase the risk of thrombosis in patients with primary immune thrombocytopenia?
The widespread adoption of thrombopoietin receptor agonists in China for immune thrombocytopenia has not led to an overall increase in thrombotic events, though caution is still advised for patients with existing cardiovascular risk factors.
Answers are grounded in this paper and cite their sources.
Thrombosis rates unchanged after TPO-RA adoption in ITP; leaves open need for prospective trials to confirm safety and causality.
In patients with primary immune thrombocytopenia (ITP), the risk of thrombosis associated with thrombopoietin receptor agonists (TPO-RAs) remains debated. This study compared the thrombosis occurrence in ITP patients before and after the launch of TPO-RAs in China, to explore the relationship between TPO-RAs and thrombosis in ITP patients. Data from 2005 to 2017 were obtained from an article published by the Blood Disease Hospital, Chinese Academy of Medical Sciences in 2018. The present study included 1915 hospitalized patients in the same center from January 2018 to February 2025. Among these, thrombosis events occurred in 33 cases (1.72%). The incidence of arterial thrombosis was higher than that of venous thrombosis. Male gender, age over 40 years old, hypertension, diabetes, smoking, and TPO-RAs were associated with thrombosis. Neither platelet count nor stage of ITP showed a significant effect on thrombosis risk. Although the utilization rate of TPO-RAs increased significantly after 2018, no corresponding significant change in thrombosis incidence was observed. These findings suggest that thrombosis in ITP patients results from the interplay of multiple risk factors. While the widespread use of TPO-RAs does not appear to increase the overall risk of thrombosis in ITP patients, caution is still advised when administering these agents to patients with pre-existing thrombosis risk factors.
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Wang et al. (2026) conducted a cohort in Primary immune thrombocytopenia (ITP) (n=4,132). Widespread adoption of TPO-RAs (2018-2025 cohort) vs. Pre-widespread adoption of TPO-RAs (2005-2017 cohort) was evaluated on Incidence of thrombosis (p=0.421). The widespread adoption of TPO-RAs after 2018 did not increase the overall incidence of thrombosis in primary ITP patients compared to the pre-2018 period.
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