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Which outcome measures in SLE clinical trials best reflect medical judgment?

OBJECTIVES: To compare two measures of systemic lupus erythematosus (SLE) response: the British Isles Lupus Assessment Group (BILAG)-based Composite Lupus Assessment (BICLA) and the Systemic Lupus Responder Index (SRI) against a clinician's assessment of improvement. METHODS: Ninety-one lupus p...

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Autores principales: Thanou, Aikaterini, Chakravarty, Eliza, James, Judith A, Merrill, Joan T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225744/
https://www.ncbi.nlm.nih.gov/pubmed/25396057
http://dx.doi.org/10.1136/lupus-2013-000005
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author Thanou, Aikaterini
Chakravarty, Eliza
James, Judith A
Merrill, Joan T
author_facet Thanou, Aikaterini
Chakravarty, Eliza
James, Judith A
Merrill, Joan T
author_sort Thanou, Aikaterini
collection PubMed
description OBJECTIVES: To compare two measures of systemic lupus erythematosus (SLE) response: the British Isles Lupus Assessment Group (BILAG)-based Composite Lupus Assessment (BICLA) and the Systemic Lupus Responder Index (SRI) against a clinician's assessment of improvement. METHODS: Ninety-one lupus patients were identified with two visits at which Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and BILAG had been scored and with active disease (SLEDAI≥6) at the first visit. A physician rated the disease activity at the second visit as clinically significant improvement, no change or worsening. SRI and BICLA were scored both with and without the medication criteria often used in trials to restrict response definitions. RESULTS: 68 patients were considered improved, 17 same and 6 worse at follow-up. SRI versus BICLA, performed without considering medication changes, captured physician-rated improvement with 85% vs 76% sensitivity and 74% vs 78% specificity. With medication limits both instruments had 37% sensitivity and 96% specificity for physician-assessed improvement. Seven patients considered improved by the clinician met the BICLA but not the SRI definition of improvement by failing to achieve a four-point improvement in SLEDAI. 13 clinician-rated responders met SRI but not BICLA by improving in less than all organs. CONCLUSIONS: Shortfalls of SRI and BICLA may be due to BICLA only requiring partial improvement but in all organs versus SRI requiring full improvement in some manifestation(s) and not all organs. SRI and BICLA with medication restrictions are less likely to denote response when the physician disagrees and could provide stringent proof of efficacy in appropriately powered clinical trials.
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spelling pubmed-42257442014-11-13 Which outcome measures in SLE clinical trials best reflect medical judgment? Thanou, Aikaterini Chakravarty, Eliza James, Judith A Merrill, Joan T Lupus Sci Med Epidemiology and Outcomes OBJECTIVES: To compare two measures of systemic lupus erythematosus (SLE) response: the British Isles Lupus Assessment Group (BILAG)-based Composite Lupus Assessment (BICLA) and the Systemic Lupus Responder Index (SRI) against a clinician's assessment of improvement. METHODS: Ninety-one lupus patients were identified with two visits at which Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and BILAG had been scored and with active disease (SLEDAI≥6) at the first visit. A physician rated the disease activity at the second visit as clinically significant improvement, no change or worsening. SRI and BICLA were scored both with and without the medication criteria often used in trials to restrict response definitions. RESULTS: 68 patients were considered improved, 17 same and 6 worse at follow-up. SRI versus BICLA, performed without considering medication changes, captured physician-rated improvement with 85% vs 76% sensitivity and 74% vs 78% specificity. With medication limits both instruments had 37% sensitivity and 96% specificity for physician-assessed improvement. Seven patients considered improved by the clinician met the BICLA but not the SRI definition of improvement by failing to achieve a four-point improvement in SLEDAI. 13 clinician-rated responders met SRI but not BICLA by improving in less than all organs. CONCLUSIONS: Shortfalls of SRI and BICLA may be due to BICLA only requiring partial improvement but in all organs versus SRI requiring full improvement in some manifestation(s) and not all organs. SRI and BICLA with medication restrictions are less likely to denote response when the physician disagrees and could provide stringent proof of efficacy in appropriately powered clinical trials. BMJ Publishing Group 2014-04-01 /pmc/articles/PMC4225744/ /pubmed/25396057 http://dx.doi.org/10.1136/lupus-2013-000005 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Epidemiology and Outcomes
Thanou, Aikaterini
Chakravarty, Eliza
James, Judith A
Merrill, Joan T
Which outcome measures in SLE clinical trials best reflect medical judgment?
title Which outcome measures in SLE clinical trials best reflect medical judgment?
title_full Which outcome measures in SLE clinical trials best reflect medical judgment?
title_fullStr Which outcome measures in SLE clinical trials best reflect medical judgment?
title_full_unstemmed Which outcome measures in SLE clinical trials best reflect medical judgment?
title_short Which outcome measures in SLE clinical trials best reflect medical judgment?
title_sort which outcome measures in sle clinical trials best reflect medical judgment?
topic Epidemiology and Outcomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225744/
https://www.ncbi.nlm.nih.gov/pubmed/25396057
http://dx.doi.org/10.1136/lupus-2013-000005
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