TY - JOUR
T1 - Use of sirolimus and low-dose calcineurin inhibitor in lung transplant recipients with renal impairment
T2 - Results of a controlled pilot study
AU - Shitrit, David
AU - Rahamimov, Ruth
AU - Gidon, Sahar
AU - Bakal, Ilana
AU - Bargil-Shitrit, Ariella
AU - Milton, Saute
AU - Kramer, Mordechai R.
PY - 2005/4
Y1 - 2005/4
N2 - Background. Renal failure induced by calcineurin-inhibitor agents is a common complication of lung transplantation. Sirolimus, a macrolide immunosuppressant with a distinct mechanism of action, may prevent renal failure but was found to have a high infectious and toxicity rate in the only relevant study conducted so far. The aim of the present prospective pilot study was to assess the benefit of sirolimus combined with low-dose calcineurin inhibitors in this patient population. Methods. Sixteen lung transplant recipients with posttransplantation renal dysfunction were allocated to receive the standard immunosuppression regimen or a combination sirolimus/low-dose calcineurin-inhibitor regimen. Target trough levels of sirolimus were 4 to 8 ng/mL. Tacrolimus was tapered down to target trough levels of 4 to 8 ng/mL and cyclosporine to 80 to 120 ng/mL. Duration of follow-up was 18 months. Results. At the end of follow-up, the sirolimus group showed a significant improvement in creatinine clearance (42.6 mL/min vs. 32.5 mL/min, P = 0.05), whereas the control group showed a significant reduction (32.3 mL/min vs. 40.3 mL/min, P = 0.02). The difference between the groups was statistically significant (P < 0.0001). Acute rejection episodes occurred in 2 patients in the sirolimus group and 1 patient in the control group (P = NS). Pneumonia developed in 6 study patients and 4 controls; all responded to antibiotics. Conclusion. Sirolimus combined with low-dose calcineurin inhibitors appears to be a safe and effective alternative immunosuppressive therapy to sirolimus alone in lung transplant recipients with renal failure. Graft function is preserved, and infection and drug toxicity rates are low.
AB - Background. Renal failure induced by calcineurin-inhibitor agents is a common complication of lung transplantation. Sirolimus, a macrolide immunosuppressant with a distinct mechanism of action, may prevent renal failure but was found to have a high infectious and toxicity rate in the only relevant study conducted so far. The aim of the present prospective pilot study was to assess the benefit of sirolimus combined with low-dose calcineurin inhibitors in this patient population. Methods. Sixteen lung transplant recipients with posttransplantation renal dysfunction were allocated to receive the standard immunosuppression regimen or a combination sirolimus/low-dose calcineurin-inhibitor regimen. Target trough levels of sirolimus were 4 to 8 ng/mL. Tacrolimus was tapered down to target trough levels of 4 to 8 ng/mL and cyclosporine to 80 to 120 ng/mL. Duration of follow-up was 18 months. Results. At the end of follow-up, the sirolimus group showed a significant improvement in creatinine clearance (42.6 mL/min vs. 32.5 mL/min, P = 0.05), whereas the control group showed a significant reduction (32.3 mL/min vs. 40.3 mL/min, P = 0.02). The difference between the groups was statistically significant (P < 0.0001). Acute rejection episodes occurred in 2 patients in the sirolimus group and 1 patient in the control group (P = NS). Pneumonia developed in 6 study patients and 4 controls; all responded to antibiotics. Conclusion. Sirolimus combined with low-dose calcineurin inhibitors appears to be a safe and effective alternative immunosuppressive therapy to sirolimus alone in lung transplant recipients with renal failure. Graft function is preserved, and infection and drug toxicity rates are low.
KW - Calcineurin-inhibitor
KW - Lung transplantation
KW - Rejection
KW - Renal function
KW - Sirolimus
UR - http://www.scopus.com/inward/record.url?scp=16244395775&partnerID=8YFLogxK
U2 - 10.1111/j.1523-1755.2005.00224.x
DO - 10.1111/j.1523-1755.2005.00224.x
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C2 - 15780099
AN - SCOPUS:16244395775
SN - 0085-2538
VL - 67
SP - 1471
EP - 1475
JO - Kidney International
JF - Kidney International
IS - 4
ER -