Plasma Biomarkers of Risk for Death in a Multicenter Phase 3 trial with Uniform Transplant Characteristics Post-Allogeneic HCT

Publication Type
Journal Article
Year of Publication
2017
Authors
Abu Zaid, M; Wu, J; Wu, C; Logan, BR; Yu, J; Cutler, C; Antin, JH; Paczesny, S; Choi, SW
Secondary
Blood
Volume
129
Start Page
162
Pagination
162-170
Date Published
01/2017
Keywords
allogeneic hematopoietic cell transplantation (HCT); graft-versus-host disease (GVHD) prophylaxis; matched-related allogeneic hematopoietic cell transplantation (HCT); tacrolimus/methotrexate (Tac/Mtx); tacrolimus/sirolimus (Tac/Sir)
Abstract

A phase 3 clinical trial (BMT CTN 0402) comparing tacrolimus/sirolimus (Tac/Sir) versus tacrolimus/methotrexate (Tac/Mtx) as graft-versus-host disease (GVHD) prophylaxis after matched-related allogeneic hematopoietic cell transplantation (HCT) recently showed no difference between study arms in acute GVHD-free survival. Within this setting of a prospective, multicenter study with uniform GVHD prophylaxis, conditioning regimen, and donor source, we explored the correlation of 10 previously identified biomarkers with clinical outcomes after allogeneic HCT. We measured biomarkers from plasma samples collected in 211 patients using ELISA (Tac/Sir=104, Tac/Mtx=107). High suppression of tumorigenicity-2 (ST2) and T cell immunoglobulin mucin-3 (TIM3) at day 28 correlated with 2-year non-relapse mortality in multivariate analysis (P=0.0050, P=0.0075, respectively) and in a proportional hazards model with time-dependent covariates (adjusted hazard ratio [HR]: 2.43 [1.49-3.95], P=0.0038 and 4.87 [2.53-9.34], P<0.0001, respectively). High ST2 and TIM3 correlated with overall survival. Chemokine (C-X-C motif) ligand 9 (CXCL9) levels above the median were associated with chronic GVHD compared with levels below the median in a time-dependent proportional hazard analysis (P=0.0069). Low L-Ficolin was associated with hepatic veno-occlusive disease (P=0.0053, AUC=0.80). We confirmed the correlation of plasma-derived proteins, previously assessed in single-center cohorts, with clinical outcomes after allogeneic HCT within this prospective, multicenter study.