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Reduction of Immunosuppression as Initial Therapy for Posttransplantation Lymphoproliferative Disorder ★
Author(s) -
Reshef R.,
Vardhanabhuti S.,
Luskin M. R.,
Heitjan D. F.,
Hadjiliadis D.,
Goral S.,
Krok K. L.,
Goldberg L. R.,
Porter D. L.,
Stadtmauer E. A.,
Tsai D. E.
Publication year - 2011
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/j.1600-6143.2010.03387.x
Subject(s) - medicine , immunosuppression , lymphoproliferative disorders , gastroenterology , stage (stratigraphy) , adjuvant , surgery , post transplant lymphoproliferative disorder , lymphoma , rituximab , paleontology , biology
Reduction of immunosuppression (RI) is commonly used to treat posttransplant lymphoproliferative disorder (PTLD) in solid organ transplant recipients. We investigated the efficacy, safety and predictors of response to RI in adult patients with PTLD. Sixty‐seven patients were managed with RI alone and 30 patients were treated with surgical excision followed by adjuvant RI. The response rate to RI alone was 45% (complete response—37%, partial response—8%). The relapse rate in complete responders was 17%. Adjuvant RI resulted in a 27% relapse rate. The acute rejection rate following RI‐containing strategies was 32% and a second transplant was feasible without relapse of PTLD. The median survival was 44 months in patients treated with RI alone and 9.5 months in patients who remained on full immunosuppression (p = 0.07). Bulky disease, advanced stage and older age predicted lack of response to RI. Survival analysis demonstrated predictors of poor outcome—age, dyspnea, B symptoms, LDH level, hepatitis C, bone marrow and liver involvement. Patients with none or one of these factors had a 3‐year overall survival of 100% and 79%, respectively. These findings support the use of RI alone in low‐risk PTLD and suggest factors that predict response and survival.