Posttransplant Lymphoproliferative Disease Following Pancreas Transplantation: A 40 Year Single‐Center Experience

Author:

Matar Abraham J.1ORCID,Finger Erik B.1ORCID,Maakaron Joseph2,Minja Emmanuel1,Ramanathan Karthik1,Humphreville Vanessa1,Rao Joseph S.1,Fisher Jessica1ORCID,Sutherland David E. R.1,Matas Arthur J.1ORCID,Kandaswamy Raja1

Affiliation:

1. Department of Surgery Division of Transplantation University of Minnesota Minneapolis Minnesota USA

2. Department of Medicine Division of Hematology, Oncology, and Transplantation University of Minnesota Minneapolis Minnesota USA

Abstract

ABSTRACTBackgroundChronic immunosuppression following pancreas transplantation carries significant risk, including posttransplant lymphoproliferative disease (PTLD). We sought to define the incidence, risk factors, and long‐term outcomes of PTLD following pancreas transplantation at a single center.MethodsAll adult pancreas transplants between February 1, 1983 and December 31, 2023 at the University of Minnesota were reviewed, including pancreas transplant alone (PTA), simultaneous pancreas–kidney transplants (SPK), and pancreas after kidney transplants (PAK).ResultsAmong 2353 transplants, 110 cases of PTLD were identified, with an overall incidence of 4.8%. 17.3% were diagnosed within 1 year of transplant, 32.7% were diagnosed within 5 years, and 74 (67.3%) were diagnosed after 5 years. The overall 30‐year incidence of PTLD did not differ by transplant type—7.4% for PTA, 14.2% for SPK, and 19.4% for PAK (p = 0.3). In multivariable analyses, older age and Epstein‐Barr virus seronegativity were risk factors for PTLD, and PTLD was a risk factor for patient death. PTLD‐specific mortality was 32.7%, although recipients with PTLD had similar median posttransplant survival compared to those without PTLD (14.9 year vs. 15.6 year, p = 0.9).ConclusionsPTLD following pancreas transplantation is associated with significant mortality. Although the incidence of PTLD has decreased over time, a high index of suspicion for PTLD following PTx should remain in EBV‐negative recipients.

Publisher

Wiley

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