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Post Transplant lymphoproliferative disorders (PTLD), the most common neoplasms in transplanted children are mostly associated with Epstein-Barr virus (EBV). The aims of our study were: 1. To describe, in a cohort of kidney transplant patients (KTx), cumulative incidence, incidence rate, time of onset (early <1 yr vs. late >1 yr), and clinical and histopathological characteristics of PTLD; 2. To compare patient and graft survival between those with and without PTLD and, in those EBV negative, association between peri-transplant administration of rituximab and primary EBV infection, EBV loads, and development of PTLD.
Retrospective, observational and descriptive analysis including 1072 consecutive KTx recipients between Dec,1988 and Aug,2023. PTLD was diagnosed according to the WHO Criteria (2008/2016). To investigate association between rituximab given in the peri KTx period and the appearance of PTLD, we included EBV negative patients given rituximab.
PTLD was diagnosed in 39 patients (Table 1). Cumulative incidence over the period was 3.64%. Before 2011 (Era1), when viral load was not monitored, it was 5,4% (n=34/627), while after (Era2) it dropped to 1.12% (n=5/445) (p<.001) Incidence rate was 3.6 per 100 p/y in E1 and 0.5 episodes per 100 p/y in E2. Median time from KTx to PTLD diagnosis was 27 months (IQR: 12.4-63.7). Ten pt developed early disease at 4.2 mth (IQR: 3-6) and 29 late, at 31 mth (IQR: 16-67) (p=.0008). On histological examination, plasmocytic hyperplasia was observed in 20 pt, hyperplasia follicular: two, infectious mononucleosis: three, polymorphic: five, monomorphic lesions: 8, Hodgkin’s lymphoma: one. Main affected organ was tonsils: 24, other nodes: 7, small bowel: 4, brain: 2, liver: 1; pancreas: 1. Patients EBV negative pre KTx, had a mean 10.6 times higher risk (CI:95%: 5-21; p<.0001) of developing PTLD, compared to those EBV positive. The 1-, 3-, and 5-yr pat survival with and without PTLD were 94.8%, 92% and 86,4%; and 99%, 97.6% and 96.3%, respectively (p=.001). The 1-, 3-, and 5-yr graft survival rate were 92.3%, 89,6%, and 87% and 93,4%, 86% and 81,5%, respectively (p=.35). Twelve pt EBV negative received Rituximab (375mg/m2) in the peri KTx (Table 2). None increased EBV loads or developed PTLD.
Incidence of PTLD decreased in this cohort. Administration of peri KTx Rituximab in EBV negative recipients was associated with absence of PTLD during follow-up period.