Abstract

ABSTRACT: Introduction The aim of our study is to explore the relationship of rabbit anti-thymocyte globulin (R-ATG) on development of post-transplant lymphoproliferative disease (PTLD) and its aggressive forms (monomorphic PTLD and Hodgkin lymphoma) in renal transplant recipients. Methodology All patients diagnosed with PTLD post-renal transplant in the United States’ Organ Procurement and Transplantation Network from 2003 till 2013 and followed up till 2017 were retrospectively reviewed. Multi-variable logistic regression analysis assessed association of R-ATG to development of PTLD and its aggressive form. Results Risk of developing PTLD post renal transplant is 1.35%. In comparison to interleukin-2 blocker induction therapy, R-ATG is associated with increased risk of development of PTLD (Odds Ratio = 1.48, confidence interval ranges from 1.04 to 2.11, p = .02) and is associated with higher risk of development of aggressive PTLD (Odds Ratio = 1.83, confidence interval ranges from 1.001 to 3.34, p = .04). Conclusion We conclude that R-ATG induction is associated with a higher risk of PTLD and its aggressive form (monomorphic PTLD and Hodgkin lymphoma). Careful monitoring for development of PTLD in renal transplant recipients receiving R-ATG induction therapy is advised.

Highlights

  • The aim of our study is to explore the relationship of rabbit anti-thymocyte globulin (R-ATG) on development of post-transplant lymphoproliferative disease (PTLD) and its aggressive forms in renal transplant recipients

  • The aim of our study is to explore the relationship between R-ATG and development of PTLD and its aggressive forms in renal transplant recipients

  • All renal transplant patients registered in organ procurement and transplantation network (OPTN) from January 2003 until January 2013, received R-ATG or interleukin-2 receptor antagonist induction therapies and discharged on calcineurin inhibitors maintenance therapy were retrospectively reviewed

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Summary

Introduction

The aim of our study is to explore the relationship of rabbit anti-thymocyte globulin (R-ATG) on development of post-transplant lymphoproliferative disease (PTLD) and its aggressive forms (monomorphic PTLD and Hodgkin lymphoma) in renal transplant recipients. Post-transplant lymphoproliferative disease (PTLD) is one of the most common cancers occurring after solid organ transplantation, accounting for almost 20% of all cancers [1,2] It is affected by the type and dose of immunosuppression regimens and is often associated with poor prognosis [3]. Rabbit anti-thymocyte globulin (R-ATG) has been reported to increase the risk of PTLD in solid organ transplant recipients and hematopoietic stem cell transplant (HSCT) [7,8,9]. According to the 2008 World Health Organization (WHO) classification there are 4 subtypes of PTLD: 1. Early hyperplastic lesions characterized by polyclonal B cell proliferation without malignant transformation presenting as infectious mononucleosis-like acute illness

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