Key result
TPO-RAs linked to ~21 percentage points less subsequent treatment vs. splenectomy in immune thrombocytopenia.
Why the study?
Although splenectomy and TPO-RAs are recommended second-line therapies for ITP, real-world tailoring of these treatments to patient characteristics is often unclear.
Does the use of TPO-RAs compared to splenectomy as second-line therapy improve time to next treatment and safety in patients with immune thrombocytopenia?
Cohort (n=504)
Yes
Does the use of TPO-RAs compared to splenectomy as second-line therapy improve time to next treatment and safety in patients with immune thrombocytopenia?
Absolute Event Rate: 61.4% vs 82.3%
In a real-world Korean cohort of ITP patients, second-line TPO-RAs were associated with a longer time to next treatment after 24 months compared to splenectomy, but with earlier onset of venous thromboembolism.
Matched claims data show no early superiority of splenectomy versus TPO-RAs in ITP; leaves open optimal sequencing pending prospective trials.
Background Splenectomy and thrombopoietin receptor agonists (TPO-RAs) are recommended second-line therapies for immune thrombocytopenia (ITP). Although guidelines recommend tailoring second-line treatments to patient characteristics, this approach is often unclear in real-world practice. Objectives We examined claims-based time to next treatment (TTNT) and safety outcomes after splenectomy or TPO-RA as a second-line therapy using nationally representative Korean claims data. Methods Patients diagnosed with ITP between 2002 and 2021 were included. From the eligible cohort, we identified patients whose index second-line treatment was splenectomy (group 1) or TPO-RA without prior splenectomy (group 2). Propensity score matching was performed between patients in both groups who had received corticosteroids as first-line treatment. Results After matching, 447 group 1 and 57 group 2 patients were analyzed. Subsequent treatment was administered to 82.3% and 61.4% of patients in groups 1 and 2, respectively. Median TTNTs were 5.80 and 3.03 months in groups 1 and 2, respectively. Estimated TTNT curves diverged after 24 months, with a longer TTNT observed in the TPO-RA group. Pneumococcal infections occurred in 3.1% of patients in group 1 and none in group 2. Venous thromboembolism (VTE) occurred in 10.5% and 15.7% of patients in groups 1 and 2, respectively. The observed time to VTE was shorter in group 2 than in group 1. Conclusion Patients treated with TPO-RAs as a second-line therapy were associated with a longer TTNT after 24 months, whereas VTE occurred earlier in the TPO-RA group. However, these findings should be interpreted with caution because of residual confounding.
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Lim et al. (2026) conducted a cohort in Immune thrombocytopenia (ITP) (n=504). Thrombopoietin receptor agonists (TPO-RAs) vs. Splenectomy was evaluated on Subsequent treatment administration. Second-line therapy with TPO-RAs for immune thrombocytopenia was associated with a lower rate of subsequent treatment (61.4% vs 82.3%) and a longer time to next treatment compared to splenectomy.
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