Incidence of PTLD in Pediatric Renal Transplant Recipients Receiving Basiliximab, Calcineurin Inhibitor, Sirolimus and Steroids
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...
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| Published in | American journal of transplantation Vol. 8; no. 5; pp. 984 - 989 |
|---|---|
| Main Authors | , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Oxford, UK
Blackwell Publishing Ltd
01.05.2008
Blackwell |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1600-6135 1600-6143 1600-6143 |
| DOI | 10.1111/j.1600-6143.2008.02167.x |
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| Abstract | 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.
Pediatric renal transplant recipients were enrolled in a multi‐center, randomized, double‐blind trial of steroid withdrawal using basiliximab, calcineurin inhibitor, and sirolimus which was terminated due to a high incidence of post‐transplant lymphoproliferative disorder. |
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| AbstractList | 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.
Pediatric renal transplant recipients were enrolled in a multi‐center, randomized, double‐blind trial of steroid withdrawal using basiliximab, calcineurin inhibitor, and sirolimus which was terminated due to a high incidence of post‐transplant lymphoproliferative disorder. 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 < or =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 < or =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.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 < or =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 < or =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. 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 less than or equal to 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 less than or equal to 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. 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 < or =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 < or =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. |
| Author | Ho, M. Harmon, W. Grimm, P. Lindblad, R. Arar, M. Ikle, D. Liereman, D. McDonald, R. A. Wyatt, R. Bridges, N. Smith, J. M. |
| Author_xml | – sequence: 1 givenname: R. A. surname: McDonald fullname: McDonald, R. A. – sequence: 2 givenname: J. M. surname: Smith fullname: Smith, J. M. – sequence: 3 givenname: M. surname: Ho fullname: Ho, M. – sequence: 4 givenname: R. surname: Lindblad fullname: Lindblad, R. – sequence: 5 givenname: D. surname: Ikle fullname: Ikle, D. – sequence: 6 givenname: P. surname: Grimm fullname: Grimm, P. – sequence: 7 givenname: R. surname: Wyatt fullname: Wyatt, R. – sequence: 8 givenname: M. surname: Arar fullname: Arar, M. – sequence: 9 givenname: D. surname: Liereman fullname: Liereman, D. – sequence: 10 givenname: N. surname: Bridges fullname: Bridges, N. – sequence: 11 givenname: W. surname: Harmon fullname: Harmon, W. |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20323686$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/18416737$$D View this record in MEDLINE/PubMed |
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| Keywords | Antineoplastic agent Steroid Pediatrics Calcineurin inhibitor Sirolimus renal transplant Hemopathy Transplantation Epstein Barr virus Monoclonal antibody Homotransplantation Epidemiology Kidney Macrocycle Incidence pediatric Posttransplant lymphoproliferative disorder Surgery Immunotherapy Lymphoproliferative syndrome EBV Graft PTLD Protein synthesis inhibitor Child Gammaherpesvirinae Human Corticosteroid Herpesviridae Lactone Macrolide Infection Virus Immunomodulator Antibiotic Treatment Urinary system Basiliximab Viral disease Immunosuppressive agent Antibacterial agent |
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| References | 2001; 71 1993; 56 1990; 127 1997; 11 2002; 6 1995; 12 1969; 4 1969; 43 2004; 4 1999; 68 2002; 2 1986; 18 2007; 7 2006; 6 2005; 80 1969; 208 2001; 1 1995; S411 1996; 10 1985; 152 Kirk (10.1111/j.1600-6143.2008.02167.x_bib20) 2007; 7 Dharnidharka (10.1111/j.1600-6143.2008.02167.x_bib11) 2002; 2 Walker (10.1111/j.1600-6143.2008.02167.x_bib9) 1995; 12 Porter (10.1111/j.1600-6143.2008.02167.x_bib14) 1969; 208 Wehrenberg (10.1111/j.1600-6143.2008.02167.x_bib1) 1990; 127 Pereira (10.1111/j.1600-6143.2008.02167.x_bib13) 1969; 4 Dharnidharka (10.1111/j.1600-6143.2008.02167.x_bib7) 2004; 4 Humar (10.1111/j.1600-6143.2008.02167.x_bib21) 2006; 6 Penn (10.1111/j.1600-6143.2008.02167.x_bib15) 1986; 18 Dharnidharka (10.1111/j.1600-6143.2008.02167.x_bib3) 2001; 71 Ho (10.1111/j.1600-6143.2008.02167.x_bib10) 1985; 152 Mihalov (10.1111/j.1600-6143.2008.02167.x_bib4) 1996; 10 Cherikh (10.1111/j.1600-6143.2008.02167.x_bib16) 2001; 1 Cockfield (10.1111/j.1600-6143.2008.02167.x_bib8) 1993; 56 Kauffman (10.1111/j.1600-6143.2008.02167.x_bib19) 2005; 80 Ciancio (10.1111/j.1600-6143.2008.02167.x_bib5) 1997; 11 Dharnidharka (10.1111/j.1600-6143.2008.02167.x_bib6) 2002; 6 Robinson (10.1111/j.1600-6143.2008.02167.x_bib2) 1995; S411 Henle (10.1111/j.1600-6143.2008.02167.x_bib12) 1969; 43 Ellis (10.1111/j.1600-6143.2008.02167.x_bib17) 1999; 68 Kahan (10.1111/j.1600-6143.2008.02167.x_bib18) 2005; 80 |
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