PO053 | PLATELET AGGREGATION AND THROMBIN GENERATION IN MULTIPLE MYELOMA: A PROSPECTIVE STUDY
Abstract
Background and Aims. Multiple Myeloma (MM) is a plasma cell dyscrasia characterized by the clonal proliferation of plasma cells, which is associated with a significantly increased risk of both thrombotic and hemorrhagic complications. This ongoing prospective observational study aims to characterize platelet function and thrombin generation (TGA) in patients with newly diagnosed MM and to assess the impact of first-line therapy on these parameters. Methods. To date, eighteen patients with newly diagnosed MM have been enrolled. Platelet function was evaluated using closure time (PFA200) and light transmission aggregometry (Born method) with four agonists: ADP (5 µM), Epinephrine (Epi) (10 µM), Collagen (Coll) (2 µg/ml), and Arachidonic Acid (AA) (1 mM). Thrombin generation (TGA) was assessed using the Calibrated Automated Thrombogram (CAT) assay. Baseline results were compared with historical healthy control cohorts. Intra-patient analysis was performed on 11 patients after four cycles of induction therapy (D-VTd or DRd). Statistical analysis was performed using R software (version 4.4). Comparisons between patients and controls were performed using the Wilcoxon rank-sum test and Pearson’s Chi-square test. For paired data the Wilcoxon signed-rank test was employed. Statistical significance was set at p < 0.05. Results. In this interim analysis, at diagnosis, MM patients exhibited significantly lower platelet aggregation compared to controls for ADP (p=0.008), Epinephrine (p=0.004), and Arachidonic Acid (p=0.026). Procoagulant markers were significantly elevated: vWF:Ag (p=0.002) and vWF:RCo (p=0.009), while Factor VIII (p=0.065) showed a trend toward elevation. TGA analysis revealed significantly prolonged Lag Time (p=0.021) and significantly higher ETP (p=0.009), Peak (p=0.003), and Velocity Index (p=0.014) in MM patients (Table 1). Following therapy, most parameters remained stable, showing persistence of high thrombin generation, elevated vWF/FVIII levels, and impaired platelet function. Only Mean Platelet Volume (MPV) showed a significant decrease (7.85 fl vs. 7.30 fl, p=0.024). Conclusions. This study highlights the coexistence of hypercoagulability and platelet dysfunction in MM. Based on these preliminary results, the reduction of tumor burden and the treatment do not seem to modify the evaluated parameters.
Related
- Platelet-released polyphosphate controls thrombin generation.
- PO021 | PLATELETS MATTER: THROMBIN GENERATION IN PLATELET‐RICH PLASMA VERSUS PLATELET-POOR-PLASMA UNDER NON-REPLACEMENT THERAPIES IN HAEMOPHILIA
- PO052 | VALIDATION OF THROMBIN GENERATION MEASUREMENT IN PLATELET- RICH-PLASMA: EVOLUTION IN THE ST GENESIA® SYSTEM
- Adjunctive Autologous Platelet-Rich Plasma Activated with Autologous Thrombin Serum for a Refractory Below-Knee Amputation Stump Wound: A Case Report.
- Interindividual variability in platelet aggregation among aspirin-treated patients: a large retrospective analysis
BibTeX
@article{biglietto2026po053,
title = {{PO053 | PLATELET AGGREGATION AND THROMBIN GENERATION IN MULTIPLE MYELOMA: A PROSPECTIVE STUDY}},
author = {Mario Biglietto},
journal = {Bleeding, Thrombosis and Vascular Biology},
year = {2026},
month = oct,
url = {https://www.btvb.org/btvb/article/view/869},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - PO053 | PLATELET AGGREGATION AND THROMBIN GENERATION IN MULTIPLE MYELOMA: A PROSPECTIVE STUDY
AU - Mario Biglietto
PY - 2026
DA - 2026/10/26
JO - Bleeding, Thrombosis and Vascular Biology
UR - https://www.btvb.org/btvb/article/view/869
AB - Background and Aims. Multiple Myeloma (MM) is a plasma cell dyscrasia characterized by the clonal proliferation of plasma cells, which is associated with a significantly increased risk of both thrombotic and hemorrhagic complications. This ongoing prospective observational study aims to characterize platelet function and thrombin generation (TGA) in patients with newly diagnosed MM and to assess the impact of first-line therapy on these parameters. Methods. To date, eighteen patients with newly diagnosed MM have been enrolled. Platelet function was evaluated using closure time (PFA200) and light transmission aggregometry (Born method) with four agonists: ADP (5 µM), Epinephrine (Epi) (10 µM), Collagen (Coll) (2 µg/ml), and Arachidonic Acid (AA) (1 mM). Thrombin generation (TGA) was assessed using the Calibrated Automated Thrombogram (CAT) assay. Baseline results were compared with historical healthy control cohorts. Intra-patient analysis was performed on 11 patients after four cycles of induction therapy (D-VTd or DRd). Statistical analysis was performed using R software (version 4.4). Comparisons between patients and controls were performed using the Wilcoxon rank-sum test and Pearson’s Chi-square test. For paired data the Wilcoxon signed-rank test was employed. Statistical significance was set at p < 0.05. Results. In this interim analysis, at diagnosis, MM patients exhibited significantly lower platelet aggregation compared to controls for ADP (p=0.008), Epinephrine (p=0.004), and Arachidonic Acid (p=0.026). Procoagulant markers were significantly elevated: vWF:Ag (p=0.002) and vWF:RCo (p=0.009), while Factor VIII (p=0.065) showed a trend toward elevation. TGA analysis revealed significantly prolonged Lag Time (p=0.021) and significantly higher ETP (p=0.009), Peak (p=0.003), and Velocity Index (p=0.014) in MM patients (Table 1). Following therapy, most parameters remained stable, showing persistence of high thrombin generation, elevated vWF/FVIII levels, and impaired platelet function. Only Mean Platelet Volume (MPV) showed a significant decrease (7.85 fl vs. 7.30 fl, p=0.024). Conclusions. This study highlights the coexistence of hypercoagulability and platelet dysfunction in MM. Based on these preliminary results, the reduction of tumor burden and the treatment do not seem to modify the evaluated parameters.
SN - 2785-5309
ER -