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Vol. 120, No. 1, 2008
Issue release date: October 2008
Section title: Original Paper
Acta Haematol 2008;120:36–46
(DOI:10.1159/000155234)

Post-Transplant Lymphoproliferative Disorders after Heart or Kidney Transplantation at a Single Centre: Presentation and Response to Treatment

Aversa S.M.L. · Stragliotto S. · Marino D. · Calabrese F. · Rigotti P. · Marchini F. · Gambino A. · Feltrin G. · Boso C. · Canova F. · Soldà C. · Mazzarotto R. · Burra P.
aDivision of Medical Oncology and bDepartment of Radiotherapy, Istituto Oncologico Veneto, IRCCS, cDepartment of Medical Sciences and Special Therapies, dKidney and Pancreas Transplantation Unit, Department of Medical and Surgical Sciences, eDepartment of Cardiothoracic Sciences and fDepartment of Surgical and Gastroenterological Science, University of Padua, Padua, Italy

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: 5/7/2008
Accepted: 6/30/2008
Published online: 9/16/2008

Number of Print Pages: 11
Number of Figures: 3
Number of Tables: 5

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: http://www.karger.com/AHA

Abstract

Post-transplant lymphoproliferative disorders (PTLD) is a serious complication after solid organ transplantation. Reduction of immunosuppression (RI) alone is not able to control the disease. We report a prospective analysis of 30 patients with PTLD after heart or kidney transplantation. Only 5 of 30 patients, treated solely with RI, obtained a complete response. Five patients were treated heterogeneously; in the remaining 20, the efficacy and safety of a weekly anthracycline-based chemotherapy were assessed. Sixteen patients obtained a complete remission. One death was related to treatment. With a median follow-up of 36 months, 3-year overall survival was 63.3% and 57% for the entire group and the chemotherapy-treated group, respectively. Moreover, 4 second neoplasms were observed in the chemotherapeutic group. In this study, we demonstrated that most PTLD need other treatment than RI and a weekly regimen is manageable and has a favourable impact on long-term survival.


Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: 5/7/2008
Accepted: 6/30/2008
Published online: 9/16/2008

Number of Print Pages: 11
Number of Figures: 3
Number of Tables: 5

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: http://www.karger.com/AHA


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Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in goverment regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
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