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Increasing Tacrolimus Time-in-Therapeutic Range Is Associated with Less Cellular Rejection in Lung Transplant Recipients.

C. Ensor, K. Harrigan, R. Venkataramanan, M. Morrell, C. Moore, J. Hayanga, M. Crespo, J. DCunha, A. Zeevi, J. McDyer.

University of Pittsburgh, Pittsburgh, PA.

Meeting: 2016 American Transplant Congress

Abstract number: 150

Keywords: Immunosuppression

Session Information

Session Name: Concurrent Session: Lung Transplant: Moving the Field Forward

Session Type: Concurrent Session

Date: Sunday, June 12, 2016

Session Time: 4:30pm-6:00pm

 Presentation Time: 5:18pm-5:30pm

Location: Room 313

Purpose: To describe the effect of tacrolimus (FK) time-in-therapeutic range (TTR) on incidence of cellular rejection (ACR) within the first year after lung transplantation (LT).

Methods: Single-center, retrospective cohort study of adult LT recipients (LTRs) on FK in year-one. Protocol trough targets were: 12-15 ng/mL for 6 months followed by 10-12 ng/mL for 6 months. FK percent TTR was calculated using Rosendaal linear interpolation method. Percent of levels-in-therapeutic range (LTR) was also calculated. Patients were grouped by TTR above and below 30%. Primary outcome was ACR burden (composite rejection standardization score (CRSS), range 0-6). Secondary outcome included high-grate ACR burden (CRSS > 2). Normality was assessed and univariate and multivariate parametric and nonparametric approaches were used where appropriate. Risk was assigned using univariate and multivariate logistic regression.

Results: 292 LTRs were included. Baseline demographics including bilateral lung (p=0.96), sex (p=.17), age (p=0.54), LAS (p=0.95), sensitized (p=0.55), induction agent (p=0.69), or azole antifungal use (p=0.1) were not different between groups. Mean year-one TTR and LTR were 22.1% (SD 10.1%) and 20% (SD 6.8%) respectively. Number of ACR events were not numerically different between groups (p=0.44). Each increase in TTR by 10% resulted in significantly lower burden of ACR events (OR 0.74, 95%CI 0.68-0.81, p<0.001); which remained significant when adjusting for lymphodepleting induction with alemtuzumab (LIA) and age (OR 0.81, 95%CI 0.66-0.995, p=0.045). Each increase in LTR by 10% resulted in significantly lower burden of ACR events (OR 0.72, 5%CI 0.65-0.79, p<0.001); which did not remain significant when adjusting for LIA and age (OR 0.81, 95%CI 0.62-1.07, p=0.14). TTR over 30% was associated with significantly less high-grade ACR (OR: 0.1, 95%CI 0.02-0.41, p=0.001); which remained significant when adjusting for LIA and age (OR: 0.1, 95%CI 0.22-0.46, p=0.003). LTR over 20% was associated with significantly less high-grade ACR (OR: 0.28, 5%CI 0.15-0.53, p<0.001); which remained significant when adjusting for LIA and age (OR: 0.15, 95%CI 0.06-0.4, p<0.001).

Conclusion: Increasing FK TTR is significantly associated with decreasing incidence and severity of ACR events within the first year after LT; even when adjusting for lymphodepletion and age.

CITATION INFORMATION: Ensor C, Harrigan K, Venkataramanan R, Morrell M, Moore C, Hayanga J, Crespo M, DCunha J, Zeevi A, McDyer J. Increasing Tacrolimus Time-in-Therapeutic Range Is Associated with Less Cellular Rejection in Lung Transplant Recipients. Am J Transplant. 2016;16 (suppl 3).

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To cite this abstract in AMA style:

Ensor C, Harrigan K, Venkataramanan R, Morrell M, Moore C, Hayanga J, Crespo M, DCunha J, Zeevi A, McDyer J. Increasing Tacrolimus Time-in-Therapeutic Range Is Associated with Less Cellular Rejection in Lung Transplant Recipients. [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/increasing-tacrolimus-time-in-therapeutic-range-is-associated-with-less-cellular-rejection-in-lung-transplant-recipients/. Accessed May 10, 2025.

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