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Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics
OBJECTIVE: To describe the size and variability of non-inferiority margins used in non-inferiority trials of medications with primary outcomes involving mortality, and to examine the association between trial characteristics and non-inferiority margin size. DESIGN: Systematic review. DATA SOURCES: M...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061825/ https://www.ncbi.nlm.nih.gov/pubmed/33879485 http://dx.doi.org/10.1136/bmjopen-2020-044480 |
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author | Pong, Sandra Urner, Martin Fowler, Robert A Mitsakakis, Nicholas Seto, Winnie Hutchison, James S Science, Michelle Daneman, Nick |
author_facet | Pong, Sandra Urner, Martin Fowler, Robert A Mitsakakis, Nicholas Seto, Winnie Hutchison, James S Science, Michelle Daneman, Nick |
author_sort | Pong, Sandra |
collection | PubMed |
description | OBJECTIVE: To describe the size and variability of non-inferiority margins used in non-inferiority trials of medications with primary outcomes involving mortality, and to examine the association between trial characteristics and non-inferiority margin size. DESIGN: Systematic review. DATA SOURCES: Medline, Medline In Process, Medline Epub Ahead of Print and Embase Classic+Embase databases from January 1989 to December 2019. ELIGIBILITY CRITERIA: Prospective non-inferiority randomised controlled trials comparing pharmacological therapies, with primary analyses for non-inferiority and primary outcomes involving mortality alone or as part of a composite outcome. Trials had to prespecify non-inferiority margins as absolute risk differences or relative to risks of outcome and provide a baseline risk of primary outcome in the control intervention. RESULTS: 3992 records were screened, 195 articles were selected for full text review and 111 articles were included for analyses. 82% of trials were conducted in thrombosis, infectious diseases or oncology. Mortality was the sole primary outcome in 23 (21%) trials, and part of a composite primary outcome in 88 (79%) trials. The overall median non-inferiority margin was an absolute risk difference of 9% (IQR 4.2%–10%). When non-inferiority margins were expressed relative to the baseline risk of primary outcome in control groups, the median relative non-inferiority margin was 1.5 (IQR 1.3–1.7). In multivariable regression analyses examining the association between trial characteristics (medical specialty, inclusion of paediatric patients, mortality as a sole or part of a composite primary outcome, presence of industry funding) and non-inferiority margin size, only medical specialty was significantly associated with non-inferiority margin size. CONCLUSION: Absolute and relative non-inferiority margins used in published trials comparing medications are large, allowing conclusions of non-inferiority in the context of large differences in mortality. Accepting the potential for large increases in outcomes involving mortality while declaring non-inferiority is a challenging methodological issue in the conduct of non-inferiority trials. |
format | Online Article Text |
id | pubmed-8061825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-80618252021-05-11 Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics Pong, Sandra Urner, Martin Fowler, Robert A Mitsakakis, Nicholas Seto, Winnie Hutchison, James S Science, Michelle Daneman, Nick BMJ Open Research Methods OBJECTIVE: To describe the size and variability of non-inferiority margins used in non-inferiority trials of medications with primary outcomes involving mortality, and to examine the association between trial characteristics and non-inferiority margin size. DESIGN: Systematic review. DATA SOURCES: Medline, Medline In Process, Medline Epub Ahead of Print and Embase Classic+Embase databases from January 1989 to December 2019. ELIGIBILITY CRITERIA: Prospective non-inferiority randomised controlled trials comparing pharmacological therapies, with primary analyses for non-inferiority and primary outcomes involving mortality alone or as part of a composite outcome. Trials had to prespecify non-inferiority margins as absolute risk differences or relative to risks of outcome and provide a baseline risk of primary outcome in the control intervention. RESULTS: 3992 records were screened, 195 articles were selected for full text review and 111 articles were included for analyses. 82% of trials were conducted in thrombosis, infectious diseases or oncology. Mortality was the sole primary outcome in 23 (21%) trials, and part of a composite primary outcome in 88 (79%) trials. The overall median non-inferiority margin was an absolute risk difference of 9% (IQR 4.2%–10%). When non-inferiority margins were expressed relative to the baseline risk of primary outcome in control groups, the median relative non-inferiority margin was 1.5 (IQR 1.3–1.7). In multivariable regression analyses examining the association between trial characteristics (medical specialty, inclusion of paediatric patients, mortality as a sole or part of a composite primary outcome, presence of industry funding) and non-inferiority margin size, only medical specialty was significantly associated with non-inferiority margin size. CONCLUSION: Absolute and relative non-inferiority margins used in published trials comparing medications are large, allowing conclusions of non-inferiority in the context of large differences in mortality. Accepting the potential for large increases in outcomes involving mortality while declaring non-inferiority is a challenging methodological issue in the conduct of non-inferiority trials. BMJ Publishing Group 2021-04-20 /pmc/articles/PMC8061825/ /pubmed/33879485 http://dx.doi.org/10.1136/bmjopen-2020-044480 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Research Methods Pong, Sandra Urner, Martin Fowler, Robert A Mitsakakis, Nicholas Seto, Winnie Hutchison, James S Science, Michelle Daneman, Nick Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title | Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title_full | Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title_fullStr | Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title_full_unstemmed | Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title_short | Testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
title_sort | testing for non-inferior mortality: a systematic review of non-inferiority margin sizes and trial characteristics |
topic | Research Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061825/ https://www.ncbi.nlm.nih.gov/pubmed/33879485 http://dx.doi.org/10.1136/bmjopen-2020-044480 |
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