Early onset post-transplant lymphoproliferative disease is associated with allograft localization

被引:68
作者
Bakker, NA
van Imhoff, GW
Verschuuren, EAM
van Son, WJ
van der Heide, JJH
Veeger, NJGM
Kluin, PM
Kluin-Nelemans, HC
机构
[1] Univ Groningen Hosp, Dept Hematol, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen Hosp, Dept Pulm Dis, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen Hosp, Dept Nephrol, NL-9700 RB Groningen, Netherlands
[4] Univ Groningen Hosp, Dept Pathol, NL-9700 RB Groningen, Netherlands
关键词
allograft; IPI; prognosis; PTLD;
D O I
10.1111/j.1399-0012.2005.00342.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Post-transplant lymphoproliferative disease (PTLD) is a major complication after solid organ transplantation. We analyzed incidence, patient characteristics, clinical presentation, and prognostic factors for treatment outcome and survival of PTLD patients transplanted at our center. Records from adult kidney and lung transplant recipients, transplanted between January 1985 and December 2002 with a histologically confirmed diagnosis of PTLD, were retrieved. Histology was reviewed and prognostic factors for treatment outcome were evaluated by multivariable analysis. Of 1354 kidney and 206 lung transplants, PTLD was diagnosed in 40 transplant recipients (2.6%). Lung transplant recipients had a significantly higher incidence of PTLD (8.3%) than kidney transplant recipients (1.7%). Sites of presentation were highly heterogeneous. Notably, PTLD localized in the allograft occurred significantly earlier after transplantation than PTLD localized outside the allograft (p = 0.001). This was true for lung (p = 0.006) as well as for kidney transplant recipients (p = 0.03). In multivariable Cox regression, performance status (p = 0.01) and advanced stage (p = 0.04) were factors negatively predictive for response to first-line treatment. Only performance status remained as negative predictive factor for survival (p = 0.002) and freedom from tumor progression (p = 0.01). In conclusion, the allograft is significantly more often involved as primary site of PTLD presentation during the first post-transplant year. This may have clinical consequences and give new insights in pathogenesis of PTLD. Performance status and stage are important risk factors for outcome of PTLD.
引用
收藏
页码:327 / 334
页数:8
相关论文
共 33 条
[1]   Anti-B-cell monoclonal antibody treatment of severe posttransplant B-lymphoproliferative disorder: Prognostic factors and long-term outcome [J].
Benkerrou, M ;
Jais, JP ;
Leblond, V ;
Durandy, A ;
Sutton, L ;
Bordigoni, P ;
Garnier, JL ;
Le Bidois, J ;
Le Deist, F ;
Blanche, S ;
Fischer, A .
BLOOD, 1998, 92 (09) :3137-3147
[2]  
Birkeland SA, 1995, TRANSPLANT P, V27, P3467
[3]   CHRONIC ANTIGENIC-STIMULATION FROM THE GRAFT AS A POSSIBLE ONCOGENIC FACTOR AFTER RENAL-TRANSPLANT [J].
BIRKELAND, SA .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 1983, 17 (03) :355-359
[4]   Immunosuppression and the risk of post-transplant malignancy among cadaveric first kidney transplant recipients [J].
Bustami, RT ;
Ojo, AO ;
Wolfe, RA ;
Merion, RM ;
Bennett, WM ;
McDiarmid, SV ;
Leichtman, AB ;
Held, PJ ;
Port, FK .
AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 (01) :87-93
[5]  
CARBONE PP, 1971, CANCER RES, V31, P1860
[6]  
Choquet Sylvain, 2002, Recent Results Cancer Res, V159, P67
[7]  
Dotti G, 2000, TRANSPLANTATION, V69, P827
[8]   Humanized anti-CD20 monoclonal antibody (Rituximab) treatment for post-transplant lymphoproliferative disorder [J].
Ganne, V ;
Siddiqi, N ;
Kamaplath, B ;
Chang, CC ;
Cohen, EP ;
Bresnahan, BA ;
Hariharan, S .
CLINICAL TRANSPLANTATION, 2003, 17 (05) :417-422
[9]   A single-centre experience of post-renal transplant lymphoproliferative disorder [J].
Herzig, KA ;
Juffs, HG ;
Norris, D ;
Brown, AM ;
Gill, D ;
Hawley, CM ;
Cobcroft, R ;
Petrie, JB ;
Marlton, P ;
Thomson, D ;
Campbell, SB ;
Nicol, DL ;
Johnson, DW .
TRANSPLANT INTERNATIONAL, 2003, 16 (07) :529-536
[10]  
HOWARD TK, 1992, TRANSPLANTATION, V53, P1145