Incidence of PTLD in pediatric renal transplant recipients receiving basiliximab, calcineurin inhibitor, sirolimus and steroids

被引:132
作者
McDonald, R. A. [1 ,2 ,3 ]
Smith, J. M. [1 ,2 ,3 ]
Ho, M. [4 ]
Lindblad, R. [4 ]
Ikle, D. [5 ]
Grimm, P. [6 ]
Wyatt, R. [7 ]
Arar, M. [8 ]
Liereman, D. [9 ]
Bridges, N. [10 ]
Harmon, W. [11 ]
机构
[1] Univ Washington, Seattle, WA 98195 USA
[2] Childrens Hosp, Seattle, WA USA
[3] Reg Med Ctr, Seattle, WA USA
[4] EMMES Corp, Rockville, MD USA
[5] PPD Inc, Wilmington, NC USA
[6] Univ Calif San Diego, San Diego, CA 92103 USA
[7] Bonheur Childrens Med Ctr, Memphis, TN USA
[8] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA
[9] British Columbia Childrens Hosp, Vancouver, BC V6H 3V4, Canada
[10] NIAID, Bethesda, MD 20892 USA
[11] Childrens Hosp, Boston, MA 02115 USA
关键词
EBV; pediatric; PTLD; renal transplant;
D O I
10.1111/j.1600-6143.2008.02167.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Pediatric renal transplant recipients were enrolled in a multicenter, randomized, double-blind trial of steroid withdrawal. Subjects received basiliximab, calcineurin inhibitor, sirolimus and steroids. Of 274 subjects enrolled, 19 (6.9%) subjects developed posttransplant lymphoproliferative disorder (PTLD). The relative hazard (RH) for PTLD was 5.3-fold higher in children aged <= 5 versus those > 12 years (p = 0.0017). EBV seronegative subjects had a 4.7-fold higher RH compared to EBV positive subjects (p = 0.02). Among EBV donor+/recipient- (D+/R-) subjects, the RH increased by 6.1-fold (p = 0.0001). In a multivariate model, risk factors included recipient age <= 5 years (RH 3.2, 95% CI: 1.1-9.6, p = 0.034) and EBV D+/R- status (RH 7.7, 95% CI: 1.6-35.9, p = 0.010). Of 19 patients with PTLD, 17 are alive with functioning grafts and 2 lost their grafts, 1 of whom subsequently died of recurrent PTLD. This 'robust' immunosuppression protocol was associated with low rejection rates but an unacceptably high incidence of PTLD. The combination of basiliximab, calcineurin inhibitor, sirolimus and steroids resulted in over-immunosuppression in a high-risk pediatric population and we do not recommend its use. Future studies must include routine viral monitoring to permit early identification of viral activity and a protocol driven reduction of immunosuppression aimed at avoiding complications.
引用
收藏
页码:984 / 989
页数:6
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