@article{1014e88778e94b9fb9b33e45fdf536ca,
title = "Personalizing treatment in end-stage kidney disease: deciding between haemodiafiltration and haemodialysis based on individualized treatment effect prediction",
abstract = "Background: Previous studies suggest that haemodiafiltration reduces mortality compared with haemodialysis in patients with end-stage kidney disease (ESKD), but the controversy surrounding its benefits remains and it is unclear to what extent individual patients benefit from haemodiafiltration. This study is aimed to develop and validate a treatment effect prediction model to determine which patients would benefit most from haemodiafiltration compared with haemodialysis in terms of all-cause mortality.Methods: Individual participant data from four randomized controlled trials comparing haemodiafiltration with haemodialysis on mortality were used to derive a Royston-Parmar model for the prediction of absolute treatment effect of haemodiafiltration based on pre-specified patient and disease characteristics. Validation of the model was performed using internal-external cross validation.Results: The median predicted survival benefit was 44 (Q1-Q3: 44-46) days for every year of treatment with haemodiafiltration compared with haemodialysis. The median survival benefit with haemodiafiltration ranged from 2 to 48 months. Patients who benefitted most from haemodiafiltration were younger, less likely to have diabetes or a cardiovascular history and had higher serum creatinine and albumin levels. Internal-external cross validation showed adequate discrimination and calibration.Conclusion: Although overall mortality is reduced by haemodiafiltration compared with haemodialysis in ESKD patients, the absolute survival benefit can vary greatly between individuals. Our results indicate that the effects of haemodiafiltration on survival can be predicted using a combination of readily available patient and disease characteristics, which could guide shared decision-making.",
keywords = "haemodiafiltration, haemodialysis, treatment effect heterogeneity, treatment effect prediction",
author = "{van Kruijsdijk}, {Rob C M} and Vernooij, {Robin W M} and Bots, {Michiel L} and Peters, {Sanne A E} and Dorresteijn, {Jannick A N} and Visseren, {Frank L J} and Blankestijn, {Peter J} and Debray, {Thomas P A}",
note = "Funding Information: The authors of the four studies were financially supported by the EuDial working group. EuDial is an official working group of the European Renal Association (ERA, https://www.era-online. org/en/eudial/). No industry funding was received for any part of or activity related to the present analysis. The Turkish HDF study was supported by European Nephrology and Dialysis Institute with an unrestricted grant. The study was performed in Fresenius Medical Care haemodialysis clinics in Turkey. ESHOL was supported by The Catalan Society of Nephrology and by grants from Fresenius Medical Care and Gambro through the Catalan Society of Nephrology. The CONTRAST study was supported by a grant from the Dutch Kidney Foundation (Nierstichting Nederland Grant C02.2019), and unrestricted grants from Fresenius Medical Care, Netherlands, and Gambro Lundia AB, Sweden. Additional support was received from the Dr E.E. Twiss Fund, Roche Netherlands, the International Society of Nephrology/Baxter Extramural Grant Program, and the Netherlands Organization for Health Research and Development (ZONMw Grant 170882802). The French HDF study was supported by a national grant from the Health Ministry (Programme Hospitalier de Recherche Clinique, PHRC) as a means to improve the care and outcome of elderly chronic disease patients. RWMV, PJB, and MLB are funded by the CONVINCE study (European Union's Horizon 2020 research and innovation programme under grant agreement No 754803). Publisher Copyright: {\textcopyright} 2022 The Author(s). Published by Oxford University Press on behalf of the ERA.",
year = "2022",
month = oct,
doi = "10.1093/ckj/sfac153",
language = "English",
volume = "15",
pages = "1924--1931",
journal = "Clinical Kidney Journal",
issn = "2048-8505",
publisher = "Oxford University Press",
number = "10",
}