Antiphospholipid antibody formation during immune checkpoint inhibition in patients with cancer: a prospective cohort study

Clicks: 1
ID: 323379
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal

Ranked #168 of 282 articles by views in European heart journal supplements : journal of the European Society of Cardiology

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 282 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Background Immune checkpoint inhibitors (ICIs) significantly improved survival in many cancer types. However, ICIs are associated with increased risk of venous (VTE) and arterial thromboembolism (ATE), and the underlying mechanisms are incompletely understood. We hypothesized that ICI therapy may induce antiphospholipid antibody development, contributing to hypercoagulability. Aim To evaluate changes in antiphospholipid antibody positivity and thrombin generation in patients with cancer initiating ICI therapy. Methods Data were used from ITHACA, a prospective cohort study including adults with cancer who underwent blood sampling at baseline and 3 months after starting ICI therapy. At both time points, lupus anticoagulant, anti-β2-glycoprotein I (anti-β2GPI) IgG/IgM, anticardiolipin IgG/IgM, and thrombin generation were measured. Primary outcome was development of antiphospholipid antibody positivity at 3 months. Secondary outcomes included changes in thrombin generation (endogenous thrombin potential (ETP) and peak height) and thromboembolic events. Results Forty patients initiating anti-PD-1 or anti-CTLA-4 therapy were included. Median age was 63 (interquartile range (IQR), 57-69), 80% were male, 5% used anticoagulation (Table 1). At baseline, three patients (8%) had positive anti-β2GPI or anticardiolipin antibodies versus two patients (5%) at 3 months (P=1.00). No patients had a positive lupus anticoagulant. ETP (935 vs 949 nM*min, P=0.65) and peak height (277 vs 279 nM, P=0.49) were similar at both timepoints (Figure 1). One patient developed VTE. Conclusion ICI therapy was not associated with development of antiphospholipid antibodies or changes in thrombin generation after 3 months. These findings suggest that the short-term risk of thromboembolic events after initiation of ICI therapy may not be mediated by antiphospholipid antibodies.
Reference Key
openalex_W7172331253 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors A Strijdhorst, D M Salet, J M Schoenaker, V Van Der Vegte, T T P Seijkens, H W M Van Laarhoven, R T Urbanus, N Van Es
Journal European heart journal supplements : journal of the European Society of Cardiology
Year 2026
DOI
10.1093/eurheartjsupp/suag097.017
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.