69
Views
9
CrossRef citations to date
0
Altmetric
Original Research

Evaluation of thrombosis-related biomarkers before and after therapy in patients with multiple myeloma

, , , , , , , & show all
Pages 1-7 | Published online: 19 Jan 2018

Figures & data

Figure 1 Randomization and follow-up of patients included in the trial.

Notes: A total of 91 patients underwent randomization: 23 were assigned to treatment with Mel-P, 31 with bortezomib, and 37 with lenalidomide.
Abbreviation: Mel-P, melphalan and prednisone.
Figure 1 Randomization and follow-up of patients included in the trial.

Table 1 Plasma levels of cytokines, PDMP, and soluble factors

Figure 2 Changes in the plasma levels of TNFα, HMGB1, and PDMP before and after treatments.

Notes: Data are shown as mean ± SD. p-value, patients versus controls.
Abbreviations: Mel-P, melphalan and prednisone; Bor, bortezomib; Len, lenalidomide; TNFα, tumor necrosis factor α; HMGB1, high mobility group box protein 1; PDMP, platelet-derived microparticle; NS, not significant.
Figure 2 Changes in the plasma levels of TNFα, HMGB1, and PDMP before and after treatments.

Figure 3 Changes in the plasma levels of sVCAM-1, PAI-1, and sEPCR before and after treatments.

Notes: Data are shown as mean ± SD. p-value, patients versus controls.
Abbreviations: Mel-P, melphalan and prednisone; Bor, bortezomib; Len, lenalidomide; sVCAM-1, soluble vascular cell adhesion molecule-1; PAI-1, plasminogen activator inhibitor-1; sEPCR, soluble endothelial protein C receptor; NS, not significant.
Figure 3 Changes in the plasma levels of sVCAM-1, PAI-1, and sEPCR before and after treatments.

Figure 4 Changes in HMGB1 (A), sVCAM-1 (B), PAI-1 (C), and PDMP (D) before and after treatment of patients with higher levels of sEPCR.

Notes: Data are shown as mean ± SD. p-value, before versus 3 or 6 months after treatment began.
Abbreviations: HMGB1, high mobility group box protein 1; sVCAM-1, soluble vascular cell adhesion molecule-1; PAI-1, plasminogen activator inhibitor-1; PDMP, platelet-derived microparticles; Mel-P, melphalan and prednisone; Bor, bortezomib; Len, lenalidomide; NS, not significant; M, months.
Figure 4 Changes in HMGB1 (A), sVCAM-1 (B), PAI-1 (C), and PDMP (D) before and after treatment of patients with higher levels of sEPCR.

Table 2 Changes in the plasma levels of PDMP, soluble factors, and cytokines/chemokines before and after all treatments of patients with elevated sEPCR