Post-transplantation lymphoproliferative disease in heart and heart-lung transplant recipients: 30-year experience at Stanford University

被引:96
作者
Gao, SZ
Chaparro, SV
Perlroth, M
Montoya, JG
Miller, JL
DiMiceli, S
Hastie, T
Oyer, PE
Schroeder, J
机构
[1] Stanford Univ, Med Ctr, Sch Med, Div Cardiovasc Med, Stanford, CA 94305 USA
[2] Stanford Univ, Med Ctr, Dept Med, Div Infect Dis, Stanford, CA 94305 USA
[3] Stanford Univ, Med Ctr, Div Biostat, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[4] Stanford Univ, Med Ctr, Dept Surg, Div Thorac Surg, Stanford, CA 94305 USA
关键词
D O I
10.1016/S1053-2498(02)01229-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Post-transplantation lymphoproliferative disease (PTLD) is an important source of morbidity and mortality in transplant recipients, with a reported incidence of 0.8% to 20%. Risk factors are thought to include immunosuppressive agents and viral infection. This study attempts to evaluate the impact of different immunosuppressive regimens, ganciclovir prophylaxis and other potential risk factors in the development of PTLD. Methods: We reviewed the records of 1,026 (874 heart, 152 heart-lung) patients who underwent transplantation at Stanford between 1968 and 1997. Of these, 57 heart and 8 heart-lung recipients developed PTLD. During this interval, 4 different immunosuppressive regimens were utilized sequentially. In January 1987, ganciclovir prophylaxis for cytomegalovirus serologic-positive patients was introduced. Other potential risk factors evaluated included age, gender, prior cardiac diagnoses, HLA match, rejection frequency and calcium-channel blockade. Results: No correlation of development of PTLD was found with different immunosuppression regimens consisting of azathioprine, prednisone, cyclosporine, OKT3 induction, tacrolimus and mycophenolate mofetil. A trend suggesting an influence of ganciclovir on the prevention of PTLD was not statistically significant (p = 0.12). Recipient age and rejection frequency, as well as high-dose cyclosporine immunosuppression, were significantly (p < 0.02) associated with PTLD development. The prevalence of PTLD at 13.3 years was 15%. Conclusions: The overall incidence of PTLD was 6.3%. It was not altered by sequential modifications in treatment regimens. Younger recipient age and higher rejection frequency were associated with increased PTLD occurrence. The 15% prevalence of PTLD in 58 long-term survivors was unexpectedly high.
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页码:505 / 514
页数:10
相关论文
共 32 条
[1]  
[Anonymous], 1967, Presse Med, V75, P2815
[2]  
ARMITAGE JM, 1991, J HEART LUNG TRANSPL, V10, P877
[3]  
Badley A D, 1996, Liver Transpl Surg, V2, P375, DOI 10.1002/lt.500020508
[4]  
BASGOZ N, 1995, INFECT DIS CLIN N AM, V9, P901
[5]   Preventing acute rejection, Epstein-Barr virus infection, and posttransplant lymphoproliferative disorders after kidney transplantation: Use of aciclovir and mycophenolate mofetil in a steroid-free immunosuppressive protocol [J].
Birkeland, SA ;
Andersen, HK ;
Hamilton-Dutoit, SJ .
TRANSPLANTATION, 1999, 67 (09) :1209-1214
[6]  
Boubenider S, 1997, J NEPHROL, V10, P136
[7]   Posttransplantation lymphoproliferative disorders in pediatric thoracic organ recipients [J].
Boyle, GJ ;
Michaels, MG ;
Webber, SA ;
Knisely, AS ;
Kurland, G ;
Cipriani, LA ;
Griffith, BP ;
Fricker, FJ .
JOURNAL OF PEDIATRICS, 1997, 131 (02) :309-313
[8]  
Brumbaugh J, 1985, J Heart Transplant, V4, P307
[9]  
Chadburn A, 1997, SEMIN DIAGN PATHOL, V14, P15
[10]  
Ciancio G, 1997, CLIN TRANSPLANT, V11, P243