TY - JOUR
T1 - Different eGFR decline thresholds and renal effects of canagliflozin
T2 - Data from the CANVAS program
AU - Oshima, Megumi
AU - Neal, Bruce
AU - Toyama, Tadashi
AU - Ohkuma, Toshiaki
AU - Li, Qiang
AU - de Zeeuw, Dick
AU - Heerspink, Hiddo J.L.
AU - Mahaffey, Kenneth W.
AU - Fulcher, Gregory
AU - Canovatchel, William
AU - Matthews, David R.
AU - Perkovic, Vlado
N1 - Funding Information:
K.W. Mahaffey reports grants from Afferent; grants and personal fees from Amgen; grants from Apple, Inc.; grants from AstraZeneca; grants from Cardiva Medical, Inc.; grants from Ferring; grants from Google (Verily); grants from Johnson & Johnson; grants from Luitpold; grants from Medtronic; grants from Merck; grants from the National Institutes of Health; grants from Novartis; grants from Sanofi; grants from St. Jude; personal fees from Abbott; personal fees from AstraZeneca; personal fees from Baim Institute; personal fees from Boehringer Ingelheim; personal fees from Elsevier; personal fees from Johnson & Johnson; personal fees from Medscape; personal fees from Myokardia; personal fees from the National Institutes of Health; personal fees from Novartis; personal fees from Novo Nordisk; personal fees from Portola; personal fees from Regeneron; personal fees from SmartMedics; personal fees from Anthos; personal fees from CSL Behring; personal fees from Intermountain Health; personal fees from Mount Sinai; personal fees from Mundi Pharma; personal fees from Sanofi; and personal fees from Theravance, outside the submitted work. W. Cano-vatchel is a full-time employee of Janssen Global Services, LLC. D. de Zeeuw reports serving on advisory boards and/or as a speaker for Bayer, Boehringer Ingelheim, Fresenius, Mundipharma, and Mitsubishi Tanabe; serving on steering committees and/or as a speaker for AbbVie and Janssen; and serving on data safety and monitoring committees for Bayer. G. Fulcher reports receiving research support from Novo Nordisk and serving on advisory boards and as a consultant for Janssen, Novo Nordisk, Boehringer Ingelheim, and Merck Sharp and Dohme. H.J.L. Heerspink has served as a consultant for AbbVie, Astellas, AstraZeneca, Boehringer Ingelheim, Fresenius, Gilead, Janssen, Merck, and Mitsubishi Tanabe and has received grant support from Abb-Vie, AstraZeneca, Boehringer Ingelheim, and Janssen. Q. Li reports being a full-time employee of The George Institute for Global Health. D.R. Mat-thews has received research support from Janssen; has served on advisory boards and as a consultant for Novo Nordisk, Novartis, Sanofi-Aventis, Janssen, and Servier; and has given lectures for Novo Nordisk, Servier, Sanofi-Aventis, Novartis, Janssen, Mitsubishi Tanabe, and Aché Laboratories. B. Neal is supported by an Australian National Health and Medical Research Council Principal Research Fellowship; holds a research grant for this study from Janssen; and has held research grants for other large-scale cardiovascular outcome trials from Roche, Servier, and Merck Schering Plough. B. Neal’s institution has received consultancy, honoraria, or travel support for contributions he has made to advisory boards and/or the continuing medical education programs of Abbott, Janssen, Novartis, Pfizer, Roche, and Servier. T. Ohkuma is supported by the John Chalmers Clinical Research Fellowship of The George Institute for Global Health. M. Oshima is supported by the Japan Society for the Promotion of Science Program for Fostering Globally Talented Researchers. V. Perkovic has received fees for advisory boards, steering committee roles, or scientific presentations from AbbVie, Astellas, AstraZeneca, Bayer, Baxter, BMS, Boehringer Ingelheim, Dimerix, Durect, Eli Lilly, Gilead, GSK, Janssen, Merck, Mitsubishi Tanabe, Mundi-pharma, Novartis, Novo Nordisk, Pfizer, Pharmalink, Relypsa, Retrophin, Sa-nofi, Servier, Vifor, and Tricida. T. Toyama is supported by the Japan Society for the Promotion of Science Program for Fostering Globally Talented Researchers, outside the submitted work.
Funding Information:
Technical editorial assistance was provided by Elizabeth Meucci of MedErgy, and it was funded by Janssen Global Services, LLC. Cana-gliflozin has been developed by Janssen Research & Development, LLC in collaboration with Mitsubishi Tanabe Pharma Corporation.
Publisher Copyright:
Copyright © 2020 by the American Society of Nephrology
PY - 2020/10
Y1 - 2020/10
N2 - Background Traditionally, clinical trials evaluating effects of a new therapy with creatinine-based renal end points use doubling of serum creatinine (equivalent to a 57% eGFR reduction), requiring large sample sizes. Methods To assess whether eGFR declines,57% could detect canagliflozin's effects on renal outcomes, we conducted a post hoc study comparing effects of canagliflozin versus placebo on composite renal outcomes using sustained 57%, 50%, 40%, or 30% eGFR reductions in conjunction with ESKD and renal death. Because canagliflozin causes an acute reversible hemodynamic decline in eGFR, we made estimates using all eGFR values as well as estimates that excluded early measures of eGFR influenced by the acute hemodynamic effect. Results Among the 10,142 participants, 93 (0.9%), 161 (1.6%), 352 (3.5%), and 800 (7.9%) participants recorded renal outcomes on the basis of 57%, 50%, 40%, or 30% eGFR reduction, respectively, during a mean follow-up of 188 weeks. Compared with a 57% eGFR reduction (risk ratio [RR], 0.51; 95% confidence interval [95% CI], 0.34 to 0.77), the effect sizes were progressively attenuated when using 50% (RR, 0.61; 95% CI, 0.45 to 0.83), 40% (RR, 0.70; 95% CI, 0.57 to 0.86), or 30% (RR, 0.81; 95% CI, 0.71 to 0.93) eGFR reductions. In analyses that controlled for the acute hemodynamic fall in eGFR, effect sizes were comparable, regardless of whether a 57%, 50%, 40%, or 30% eGFR reduction was used. Estimated sample sizes for studies on the basis of lesser eGFR reductions were much reduced by controlling for this early hemodynamic effect. Conclusions Declines in eGFR,57% may provide robust estimates of canagliflozin's effects on renal outcomes if the analysis controls for the drug's acute hemodynamic effect.
AB - Background Traditionally, clinical trials evaluating effects of a new therapy with creatinine-based renal end points use doubling of serum creatinine (equivalent to a 57% eGFR reduction), requiring large sample sizes. Methods To assess whether eGFR declines,57% could detect canagliflozin's effects on renal outcomes, we conducted a post hoc study comparing effects of canagliflozin versus placebo on composite renal outcomes using sustained 57%, 50%, 40%, or 30% eGFR reductions in conjunction with ESKD and renal death. Because canagliflozin causes an acute reversible hemodynamic decline in eGFR, we made estimates using all eGFR values as well as estimates that excluded early measures of eGFR influenced by the acute hemodynamic effect. Results Among the 10,142 participants, 93 (0.9%), 161 (1.6%), 352 (3.5%), and 800 (7.9%) participants recorded renal outcomes on the basis of 57%, 50%, 40%, or 30% eGFR reduction, respectively, during a mean follow-up of 188 weeks. Compared with a 57% eGFR reduction (risk ratio [RR], 0.51; 95% confidence interval [95% CI], 0.34 to 0.77), the effect sizes were progressively attenuated when using 50% (RR, 0.61; 95% CI, 0.45 to 0.83), 40% (RR, 0.70; 95% CI, 0.57 to 0.86), or 30% (RR, 0.81; 95% CI, 0.71 to 0.93) eGFR reductions. In analyses that controlled for the acute hemodynamic fall in eGFR, effect sizes were comparable, regardless of whether a 57%, 50%, 40%, or 30% eGFR reduction was used. Estimated sample sizes for studies on the basis of lesser eGFR reductions were much reduced by controlling for this early hemodynamic effect. Conclusions Declines in eGFR,57% may provide robust estimates of canagliflozin's effects on renal outcomes if the analysis controls for the drug's acute hemodynamic effect.
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U2 - 10.1681/ASN.2019121312
DO - 10.1681/ASN.2019121312
M3 - Article
C2 - 32694216
AN - SCOPUS:85092281670
SN - 1046-6673
VL - 31
SP - 2446
EP - 2456
JO - Journal of the American Society of Nephrology : JASN
JF - Journal of the American Society of Nephrology : JASN
IS - 10
ER -