Evidence map›Paper›PMID 41680879›Full record

ArticleThrombosis journal2026

Hematologic safety of caplacizumab in immune-mediated thrombotic thrombocytopenic purpura: insights from platelet-related signal detection in the FAERS database.

Zhenqi Liu, Xu Ye

Abstract read
In one paragraph

Article in Thrombosis journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Zhenqi LiuDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, 510220, China.
Xu YeDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, 510220, China. yexu2000@yeah.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCaplacizumab, a nanobody targeting von Willebrand factor, has transformed the management of immune-mediated thrombotic thrombocytopenic purpura (iTTP) by rapidly restoring platelet counts and improving survival. However, comprehensive real-world evidence regarding its hematologic safety profile remains limited.

methodsWe conducted a post-marketing pharmacovigilance study using reports from the U.S. FDA Adverse Event Reporting System (FAERS) from 2019 to Q1 2025. Disproportionality analyses were performed using four signal-detection algorithms-reporting odds ratio (ROR), proportional reporting ratio (PRR), Bayesian confidence propagation neural network (BCPNN), and multi-item gamma Poisson shrinker (MGPS)-with false discovery rate adjustment. Time-to-onset was assessed among reports with available dates, and Weibull modeling was applied to characterize onset patterns.

resultsA total of 1,306 caplacizumab-related reports were identified, predominantly involving adult female patients with iTTP. Frequently reported adverse events included hematologic and hemorrhagic events (e.g., epistaxis and thrombocytopenia), as well as fatigue and laboratory abnormalities. Significant positive signals were consistently observed for bleeding-related preferred terms across multiple algorithms. The median time to onset was 10 days after treatment initiation, and Weibull modeling suggested an early-failure pattern, indicating greater susceptibility during the initial treatment cycles.

conclusionsIn FAERS post-marketing data, caplacizumab-associated adverse events were mainly bleeding-related, generally predictable, and tended to occur early during therapy. Close clinical and laboratory monitoring-particularly of hematologic parameters-during the initial treatment period is warranted to balance bleeding vigilance with therapeutic efficacy. These findings provide real-world evidence to inform hematologists about the safety profile of caplacizumab in iTTP management.

Indexed as

CaplacizumabFAERSHematologic safetyImmune-mediated thrombotic thrombocytopenic purpuraReal-world evidence

Identifiers

PMID41680879
PMCPMC12998118

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