Safety of everolimus with reduced calcineurin inhibitor exposure in de novo kidney transplants: An analysis from the randomized transform study
on behalf of the TRANSFORM Investigators
(2019) Transplantation, volume 103, issue 9, pp. 1953 - 1963
(Article)
Abstract
Background. The safety profiles of standard therapy versus everolimus with reduced-exposure calcineurin inhibitor (CNI) therapy using contemporary protocols in de novo kidney transplant recipients have not been compared in detail. Methods. TRANSFORM was a randomized, international trial in which de novo kidney transplant patients were randomized to everolimus with reduced-exposure
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CNI (N = 1014) or mycophenolic acid (MPA) with standard-exposure CNI (N = 1012), both with induction and corticosteroids. Results. Within the safety population (everolimus 1014, MPA 1012), adverse events with a suspected relation to study drug occurred in 62.9% versus 59.2% of patients given everolimus or MPA, respectively (P = 0.085). Hyperlipidemia, interstitial lung disease, peripheral edema, proteinuria, stomatitis/mouth ulceration, thrombocytopenia, and wound healing complications were more frequent with everolimus, whereas diarrhea, nausea, vomiting, leukopenia, tremor, and insomnia were more frequent in the MPA group. The incidence of viral infections (17.2% versus 29.2%; P < 0.001), cytomegalovirus (CMV) infections (8.1% versus 20.1%; P < 0.001), CMV syndrome (13.6% versus 23.0%, P = 0.044), and BK virus (BKV) infections (4.3% versus 8.0%, P < 0.001) were less frequent with everolimus. CMV infection was less common with everolimus versus MPA after adjusting for prophylaxis therapy in the D+/R- subgroup (P < 0.001). Study drug was discontinued more frequently due to rejection or impaired healing with everolimus, and more often due to BKV infection or BKV nephropathy with MPA. Conclusions. De novo everolimus with reduced-exposure CNI yielded a comparable incidence, though a distinctly different pattern, of adverse events versus current standard of care. Both regimens are safe and effective, yet their distinct profiles may enable tailoring for individual kidney transplant recipients.
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Keywords: Transplantation
ISSN: 0041-1337
Publisher: Lippincott Williams & Wilkins
Note: Funding Information: Amgen. J.M.C. has received honoraria from Sandoz and Novartis and travel grants from Chiesi. The institution of C.S. has received research grants from Novartis and Astellas. V.D.G. has received consulting honoraria from Pfizer and travel grants from Pfizer and EMS. H-D.U. has received advisory board and speaker’s honoraria from Amgen, Astellas, Shire, and Vifor. G.R. has received honoraria from Astellas and Novartis. D.K. has received consulting and speaker’s honoraria from Astellas and Novartis, travel grants from Astellas and Novartis, and research grants from Astellas. M.B. has received travel grants from Novartis. F.C. has received consulting honoraria and travel grants from Novartis, Astellas, Pfizer, and Bristol Myers Squibb. M.P.H.G. and P.B. are employees of Novartis. S.C. has received institutional research funding, travel support, or consulting honoraria from Novartis, Astellas, and Alexion. D.Y.K., M.A.B., and M.S.K. declare no conflicts of interest. Funding Information: H.T-S. has received consulting honoraria and travel grants from Novartis, Pfizer, BMS, and Roche, and his institution has received research grants from Novartis, Pfizer, BMS, Roche, Veloxis, and Teraclone. J.P. has received consulting honoraria from Novartis and Chiesi, travel grants from Novartis and Chiesi, and his institution has received research grants from Novartis, Astellas, Chiesi, and Amgen. O.V. has received consulting honoraria from Alexion, Chiesi, travel grants from Sanofi, and his institution has received research grants from Novartis, Alexion, and Teva. N.B-J. has received honoraria from Novartis, Astellas, Chiesi, Roche, Amgen, Abbvie, Fresenius Medical Care, and Teva. E.C. has received travel grants from Novartis, Roche, Astellas, Chiesi, and Funding Information: The TRANSFORM study was funded by Novartis Pharma AG, Basel, Switzerland. Medical writing support was funded by Novartis. Publisher Copyright: Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.
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