Association between calcineurin inhibitor blood concentrations and outcomes after allogeneic hematopoietic cell transplantation

Abstract

To determine whether calcineurin inhibitor (CNI) blood concentrations within the first month after allogeneic hematopoietic cell transplantation (HCT) correlated with the incidence of graft-versus-host disease (GVHD) and other outcomes, we retrospectively analyzed data from 1181 patients with hematologic malignancies who had HCT from HLA-matched related (n = 634) or unrelated (n = 547) donors at a single institution between 2001 and 2009. After myeloablative HCT (n = 774), higher CNI concentrations were not associated with lower risks of acute or chronic GVHD (aGVHD, cGVHD). After nonmyeloablative HCT (n = 407), higher cyclosporine concentrations were associated with decreased risks of grade 2-4 and 3-4 aGVHD (hazard ratio [HR] per 100 ng/mL change in cyclosporine concentrations, 0.7; 95% confidence interval [CI], 0.6-0.82; and HR, 0.66, 95% CI, 0.49-0.9, respectively), nonrelapse mortality (HR, 0.6, 95% CI, 0.41-0.88), and overall mortality (HR, 0.83, 95% CI, 0.71-0.99). Cyclosporine concentrations were not associated with risks of cGVHD and recurrent malignancy after nonmyeloablative HCT. Among patients given tacrolimus after nonmyeloablative HCT, a similar trend of CNI-associated GVHD-protection was observed. Higher CNI concentrations were not associated with apparent renal toxicity. We conclude that higher cyclosporine concentrations relatively early after nonmyeloablative HCT confer protection against aGVHD that translates into reduced risks of nonrelapse and overall mortality.

Figure 1

Association of mean week 2 CSP (A and B) and TAC (C and D) concentrations with the cumulative incidence of grade 2–4 (A and C) and grade 3–4 (B and D) acute GVHD after HCT with nonmyeloablative conditioning. CNI concentrations were divided according to quartiles.

Figure 2

Correlation of mean week 2 CNI concentrations in patients treated with CSP (A and C) or TAC (B and D) with the maximal change in GFR during the first 4 weeks after HCT with myeloablative conditioning (A and B) or nonmyeloablative conditioning (C and D).