Combination of calcineurin and mTOR inhibitors in kidney transplantation: a propensity score analysis based on current clinical practice.
Calcineurin
Calcineurin Inhibitors
/ adverse effects
Graft Rejection
/ prevention & control
Graft Survival
Humans
Immunosuppressive Agents
/ adverse effects
Kidney Transplantation
/ adverse effects
Mycophenolic Acid
/ adverse effects
Propensity Score
TOR Serine-Threonine Kinases
Tacrolimus
/ adverse effects
Kidney transplantation
Propensity score
Rejection
Survival
mTOR inhibitors
Journal
Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
14
09
2019
accepted:
18
11
2019
pubmed:
20
12
2019
medline:
19
8
2021
entrez:
20
12
2019
Statut:
ppublish
Résumé
The TRANSFORM study demonstrated that an immunosuppression based on a combination of calcineurin inhibitors and de-novo mTOR inhibitors (mTORi) is safe and effective in kidney transplant recipients. However, data that validate this approach in clinical practice are currently missing. Analysis of 401 kidney transplant recipients transplanted from June 2013 to December 2016. All patients received tacrolimus with prednisone in combination with either mycophenolate (n = 186) or mTORi (either everolimus or sirolimus, n = 215). A propensity score to receive mTORi was calculated based on the inverse probability of treatment weighting (IPTW) from the following parameters: age and sex of donor and recipient, BMI, previous transplants, diabetes, cPRA, dialysis before transplantation, dialysis vintage, type of donor, ABO-incompatibility, HLA-mismatches, induction and ischemia time. Median follow-up was 2.6 [1.9; 3.7] years. Cox-regression analysis suggests good results for mTORi versus MPA in terms of 1-year biopsy-proven acute rejection (BPAR, P = 0.063), 1-year graft loss (P = 0.025) and patient survival (P < 0.001). Results observed for BPAR and graft failure were largely attributed to those patients that would have been excluded by the TRANSFORM because of some exclusion criteria (52.9% of the population, P = 0.003 for 1-year BPAR and P = 0.040 for graft loss). In patients who met selection criteria for TRANSFORM, no effect of treatment for BPAR or graft failure was observed, while the beneficial effect on overall survival persisted. In a real-life setting, a protocol based on de-novo mTORi with tacrolimus and prednisone could be employed as a standard immunosuppressive regimen and was associated with good outcomes.
Identifiants
pubmed: 31853792
doi: 10.1007/s40620-019-00675-2
pii: 10.1007/s40620-019-00675-2
doi:
Substances chimiques
Calcineurin Inhibitors
0
Immunosuppressive Agents
0
MTOR protein, human
EC 2.7.1.1
TOR Serine-Threonine Kinases
EC 2.7.11.1
Calcineurin
EC 3.1.3.16
Mycophenolic Acid
HU9DX48N0T
Tacrolimus
WM0HAQ4WNM
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM