Immunosuppression with generic tacrolimus in liver and kidney transplantation—systematic review and meta‐analysis on biopsy‐proven acute rejection and bioequivalence
Autor: | Peter Schemmer, Gudrun Pregartner, Judith Kahn |
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Rok vydání: | 2020 |
Předmět: |
Adult
Graft Rejection kidney medicine.medical_specialty Biopsy medicine.medical_treatment Urology 030230 surgery Bioequivalence liver Lower risk Tacrolimus 03 medical and health sciences 0302 clinical medicine medicine Humans generic immunosuppression Kidney transplantation Immunosuppression Therapy Transplantation medicine.diagnostic_test business.industry Immunosuppression medicine.disease Kidney Transplantation Therapeutic Equivalency Meta-analysis 030211 gastroenterology & hepatology Meta‐Analysis business Immunosuppressive Agents |
Zdroj: | Transplant International |
ISSN: | 1432-2277 0934-0874 |
Popis: | Summary While rejection prevention with innovator tacrolimus (Tac) is one of the key factors for long‐lasting graft function, the use of generic Tac is still under debate. Thus, we performed a systematic review and meta‐analysis to provide an overview on the current body of evidence for the effect of generic Tac in adult liver (LT) and kidney transplantation (KT) with focus on both biopsy‐proven acute rejection (BPAR) and bioequivalence. A systematic literature search for trials comparing generic versus innovator Tac was conducted accordingly. Seventeen studies (5 LT, 11 KT, 1 LT/KT) including 1412 patients were identified. About 92.9% (13/14; 5/5 LT, 8/9 KT) of studies reported the same or lower BPAR with generics (pooled RR: 0.84, 95% CI: 0.65–1.09); however, de novo studies showed a significantly lower risk with generic Tac (RR: 0.75, 95% CI: 0.63–0.90), whereas conversion studies showed increased risk (RR: 1.93, 95% CI: 1.00–3.70). Bioequivalence was demonstrated primarily in studies on conversion. The current evidence is mostly based on observational data and studies showing some risk of bias. In conclusion, whereas overall there was no significant difference in terms of BPAR, there is some evidence suggesting lower BPAR risk with generic Tac for de novo use. |
Databáze: | OpenAIRE |
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