TY - JOUR
T1 - Everolimus-facilitated calcineurin inhibitor reduction in Asian de novo kidney transplant recipients
T2 - 2-year results from the subgroup analysis of the TRANSFORM study
AU - Watarai, Yoshihiko
AU - Danguilan, Romina
AU - Casasola, Concesa
AU - Chang, Shen Shin
AU - Ruangkanchanasetr, Prajej
AU - Kee, Terence
AU - Wong, Hin Seng
AU - Kenmochi, Takashi
AU - Amante, Angel Joaquin
AU - Shu, Kuo Hsiung
AU - Ingsathit, Atiporn
AU - Bernhardt, Peter
AU - Hernandez-Gutierrez, Maria Pilar
AU - Han, Duck Jong
AU - Kim, Myoung Soo
N1 - Funding Information:
The authors thank Dhaval Gupta, Aparajita Mandal, and Sushant Thakur of Novartis Healthcare Pvt Ltd India, for providing medical writing support, which was funded by Novartis Pharma AG, Basel, Switzerland in accordance with Good Publication Practice (GPP3) guidelines (http://www.ismpp.org/gpp3).
Funding Information:
Yoshihiko Watarai has received consulting honoraria and travel grants from Novartis, Astellas, and Chugai Pharma. Romina Danguilan has received speaker's honoraria from Novartis, Astellas, MSD, Sanofi, Macropharma, and Pharmalink. Concesa Casasola, Shen‐Shin Chang, Prajej Ruangkanchanasetr, Terence Kee, Hin Seng Wong, Takashi Kenmochi, Angel Joaquin Amante, Kuo‐Hsiung Shu, Atiporn Ingsathit, Duck Jong Han, and Myoung Soo Kim have no conflict of interest. Peter Bernhardt and Maria Pilar Hernandez‐Gutierrez are employees of Novartis.
Publisher Copyright:
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2021/10
Y1 - 2021/10
N2 - Objective: We analyzed the efficacy and safety of an everolimus with reduced-exposure calcineurin inhibitor (EVR+rCNI) versus mycophenolic acid with standard-exposure CNI (MPA+sCNI) regimen in Asian patients from the TRANSFORM study. Methods: In this 24-month, open-label study, de novo kidney transplant recipients (KTxRs) were randomized (1:1) to receive EVR+rCNI or MPA+sCNI, along with induction therapy and corticosteroids. Results: Of the 2037 patients randomized in the TRANSFORM study, 293 were Asian (EVR+rCNI, N = 136; MPA+sCNI, N = 157). At month 24, EVR+rCNI was noninferior to MPA+sCNI for the binary endpoint of estimated glomerular filtration rate (eGFR) < 50 ml/min/1.73 m2 or treated biopsy-proven acute rejection (27.0% vs. 29.2%, P =.011 for a noninferiority margin of 10%). Graft loss and death were reported for one patient each in both arms. Mean eGFR was higher in EVR+rCNI versus MPA+sCNI (72.2 vs. 66.3 ml/min/1.73 m2, P =.0414) even after adjusting for donor type and donor age (64.3 vs. 59.3 ml/min/1.73 m2, P =.0582). Overall incidence of adverse events was comparable. BK virus (4.4% vs. 12.1%) and cytomegalovirus (4.4% vs. 13.4%) infections were significantly lower in the EVR+rCNI arm. Conclusion: This subgroup analysis in Asian de novo KTxRs demonstrated that the EVR+rCNI versus MPA+sCNI regimen provides comparable antirejection efficacy, better renal function, and reduced viral infections (NCT01950819).
AB - Objective: We analyzed the efficacy and safety of an everolimus with reduced-exposure calcineurin inhibitor (EVR+rCNI) versus mycophenolic acid with standard-exposure CNI (MPA+sCNI) regimen in Asian patients from the TRANSFORM study. Methods: In this 24-month, open-label study, de novo kidney transplant recipients (KTxRs) were randomized (1:1) to receive EVR+rCNI or MPA+sCNI, along with induction therapy and corticosteroids. Results: Of the 2037 patients randomized in the TRANSFORM study, 293 were Asian (EVR+rCNI, N = 136; MPA+sCNI, N = 157). At month 24, EVR+rCNI was noninferior to MPA+sCNI for the binary endpoint of estimated glomerular filtration rate (eGFR) < 50 ml/min/1.73 m2 or treated biopsy-proven acute rejection (27.0% vs. 29.2%, P =.011 for a noninferiority margin of 10%). Graft loss and death were reported for one patient each in both arms. Mean eGFR was higher in EVR+rCNI versus MPA+sCNI (72.2 vs. 66.3 ml/min/1.73 m2, P =.0414) even after adjusting for donor type and donor age (64.3 vs. 59.3 ml/min/1.73 m2, P =.0582). Overall incidence of adverse events was comparable. BK virus (4.4% vs. 12.1%) and cytomegalovirus (4.4% vs. 13.4%) infections were significantly lower in the EVR+rCNI arm. Conclusion: This subgroup analysis in Asian de novo KTxRs demonstrated that the EVR+rCNI versus MPA+sCNI regimen provides comparable antirejection efficacy, better renal function, and reduced viral infections (NCT01950819).
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U2 - 10.1111/ctr.14415
DO - 10.1111/ctr.14415
M3 - Article
C2 - 34216395
AN - SCOPUS:85115321900
SN - 0902-0063
VL - 35
JO - Clinical Transplantation
JF - Clinical Transplantation
IS - 10
M1 - e14415
ER -