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Serum protein electrophoresis abnormalities in adult solid organ transplant patients with post-transplant lymphoproliferative disorder*

Authors :
John E. Tomaszewski
Edward A. Stadtmauer
Kim M. Olthoff
Vivek N. Ahya
Susan C. Brozena
Richard L. Hodinka
David L. Porter
Nicole A. Aqui
Robert M. Kotloff
Selina M. Luger
Roy D. Bloom
Donald E. Tsai
Thomas R. Klumpp
Stephen J. Schuster
Sunita D. Nasta
Source :
Clinical Transplantation. 19:644-652
Publication Year :
2005
Publisher :
Wiley, 2005.

Abstract

Post-transplant lymphoproliferative disorder (PTLD) is an Epstein-Barr virus (EBV) associated malignancy that occurs in the setting of pharmacologic immunosuppression used after organ transplantation. The presence of monoclonal gammopathy (MG) after organ transplantation is a risk factor for the development of PTLD. We retrospectively explored the characteristics of serum protein electrophoresis (SPEP) in 38 adult solid organ transplant patients with biopsy proven PTLD and SPEP. Twenty-three (61%) had MG with nine (24%) showing multiple MG. Background gammaglobulin levels were abnormal in 13 (34%) patients with five (13%) and eight (21%) having polyclonal hypergammaglobulinemia or hypogammaglobulinemia, respectively. Hypogammaglobulinemia was correlated with the presence of MG (p = 0.01) and polymorphic B-cell hyperplasia histology (p = 0.01). No correlation between SPEP findings and overall survival were noted. With median follow-up of 116 wk (range 2-261 wk), 21 (55%) patients are alive with 20 (53%) in complete remission. Response to reduction in immunosuppression was correlated with improved overall survival (262 wk vs. 68 wk, p = 0.003). Persistence of MG after complete response of the PTLD did not predict relapse. There is a high incidence of MG and gammaglobulin abnormalities in patients with PTLD.

Details

ISSN :
13990012 and 09020063
Volume :
19
Database :
OpenAIRE
Journal :
Clinical Transplantation
Accession number :
edsair.doi.dedup.....b3b94c19bc70800ea278a2d2997f13e1
Full Text :
https://doi.org/10.1111/j.1399-0012.2005.00388.x