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Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results

IMPORTANCE: Interpreting randomized clinical trials (RCTs) and their clinical relevance is challenging when P values are either marginally above or below the P = .05 threshold. OBJECTIVE: To use the concept of reverse fragility index (RFI) to provide a measure of confidence in the neutrality of RCT...

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Autores principales: Khan, Muhammad Shahzeb, Fonarow, Gregg C., Friede, Tim, Lateef, Noman, Khan, Safi U., Anker, Stefan D., Harrell, Frank E., Butler, Javed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407075/
https://www.ncbi.nlm.nih.gov/pubmed/32756927
http://dx.doi.org/10.1001/jamanetworkopen.2020.12469
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author Khan, Muhammad Shahzeb
Fonarow, Gregg C.
Friede, Tim
Lateef, Noman
Khan, Safi U.
Anker, Stefan D.
Harrell, Frank E.
Butler, Javed
author_facet Khan, Muhammad Shahzeb
Fonarow, Gregg C.
Friede, Tim
Lateef, Noman
Khan, Safi U.
Anker, Stefan D.
Harrell, Frank E.
Butler, Javed
author_sort Khan, Muhammad Shahzeb
collection PubMed
description IMPORTANCE: Interpreting randomized clinical trials (RCTs) and their clinical relevance is challenging when P values are either marginally above or below the P = .05 threshold. OBJECTIVE: To use the concept of reverse fragility index (RFI) to provide a measure of confidence in the neutrality of RCT results when assessed from the clinical perspective. DESIGN, SETTING, AND PARTICIPANTS: In this cross-sectional study, a MEDLINE search was conducted for RCTs published from January 1, 2013, to December 31, 2018, in JAMA, the New England Journal of Medicine (NEJM), and The Lancet. Eligible studies were phase 3 and 4 trials with 1:1 randomization and statistically nonsignificant binary primary end points. Data analysis was performed from August 1, 2019, to August 31, 2019. EXPOSURES: Single vs multicenter enrollment, total number of events, private vs government funding, placebo vs active control, and time to event vs frequency data. MAIN OUTCOMES AND MEASURES: The primary outcome was the median RFI with interquartile range (IQR) at the P = .05 threshold. Secondary outcomes were the number of RCTs in which the number of participants lost to follow-up was greater than the RFI; the median RFI with IQR at different P value thresholds; the median reverse fragility quotient with IQR; and the correlation between sample sizes, number of events, and P values of the RCT and RFI. RESULTS: Of the 167 RCTs included, 76 (46%) were published in the NEJM, 50 (30%) in JAMA, and 41 (24%) in The Lancet. The median (IQR) sample size was 970 (470-3427) participants, and the median (IQR) number of events was 251 (105-570). The median (IQR) RFI at the P = .05 threshold was 8 (5-13). Fifty-seven RCTs (34%) had an RFI of 5 or lower, and in 68 RCTs (41%) the number of participants lost to follow-up was greater than the RFI. Trials with P values ranging from P = .06 to P = .10 had a median (IQR) RFI of 3 (2-4). When compared, median (IQR) RFIs were not statistically significant for single-center vs multicenter enrollment (5 [4-13] vs 8 [5-13]; P = .41), private vs government-funded studies (9 [5-13] vs 8 [5-13]; P = .34), and time-to-event primary end points vs frequency data (9 [5-14] vs 7 [4-13]; P = .43). The median (IQR) RFI at the P = .01 threshold was 12 (7-19) and at the P = .005 threshold was 14 (9-21). CONCLUSIONS AND RELEVANCE: This cross-sectional study found that a relatively small number of events (median of 8) had to change to move the primary end point of an RCT from nonsignificant to statistically significant. These findings emphasize the nuance required when interpreting trial results that did not meet prespecified significance thresholds.
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spelling pubmed-74070752020-08-13 Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results Khan, Muhammad Shahzeb Fonarow, Gregg C. Friede, Tim Lateef, Noman Khan, Safi U. Anker, Stefan D. Harrell, Frank E. Butler, Javed JAMA Netw Open Original Investigation IMPORTANCE: Interpreting randomized clinical trials (RCTs) and their clinical relevance is challenging when P values are either marginally above or below the P = .05 threshold. OBJECTIVE: To use the concept of reverse fragility index (RFI) to provide a measure of confidence in the neutrality of RCT results when assessed from the clinical perspective. DESIGN, SETTING, AND PARTICIPANTS: In this cross-sectional study, a MEDLINE search was conducted for RCTs published from January 1, 2013, to December 31, 2018, in JAMA, the New England Journal of Medicine (NEJM), and The Lancet. Eligible studies were phase 3 and 4 trials with 1:1 randomization and statistically nonsignificant binary primary end points. Data analysis was performed from August 1, 2019, to August 31, 2019. EXPOSURES: Single vs multicenter enrollment, total number of events, private vs government funding, placebo vs active control, and time to event vs frequency data. MAIN OUTCOMES AND MEASURES: The primary outcome was the median RFI with interquartile range (IQR) at the P = .05 threshold. Secondary outcomes were the number of RCTs in which the number of participants lost to follow-up was greater than the RFI; the median RFI with IQR at different P value thresholds; the median reverse fragility quotient with IQR; and the correlation between sample sizes, number of events, and P values of the RCT and RFI. RESULTS: Of the 167 RCTs included, 76 (46%) were published in the NEJM, 50 (30%) in JAMA, and 41 (24%) in The Lancet. The median (IQR) sample size was 970 (470-3427) participants, and the median (IQR) number of events was 251 (105-570). The median (IQR) RFI at the P = .05 threshold was 8 (5-13). Fifty-seven RCTs (34%) had an RFI of 5 or lower, and in 68 RCTs (41%) the number of participants lost to follow-up was greater than the RFI. Trials with P values ranging from P = .06 to P = .10 had a median (IQR) RFI of 3 (2-4). When compared, median (IQR) RFIs were not statistically significant for single-center vs multicenter enrollment (5 [4-13] vs 8 [5-13]; P = .41), private vs government-funded studies (9 [5-13] vs 8 [5-13]; P = .34), and time-to-event primary end points vs frequency data (9 [5-14] vs 7 [4-13]; P = .43). The median (IQR) RFI at the P = .01 threshold was 12 (7-19) and at the P = .005 threshold was 14 (9-21). CONCLUSIONS AND RELEVANCE: This cross-sectional study found that a relatively small number of events (median of 8) had to change to move the primary end point of an RCT from nonsignificant to statistically significant. These findings emphasize the nuance required when interpreting trial results that did not meet prespecified significance thresholds. American Medical Association 2020-08-05 /pmc/articles/PMC7407075/ /pubmed/32756927 http://dx.doi.org/10.1001/jamanetworkopen.2020.12469 Text en Copyright 2020 Khan MS et al. JAMA Network Open. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Khan, Muhammad Shahzeb
Fonarow, Gregg C.
Friede, Tim
Lateef, Noman
Khan, Safi U.
Anker, Stefan D.
Harrell, Frank E.
Butler, Javed
Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title_full Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title_fullStr Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title_full_unstemmed Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title_short Application of the Reverse Fragility Index to Statistically Nonsignificant Randomized Clinical Trial Results
title_sort application of the reverse fragility index to statistically nonsignificant randomized clinical trial results
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407075/
https://www.ncbi.nlm.nih.gov/pubmed/32756927
http://dx.doi.org/10.1001/jamanetworkopen.2020.12469
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