Multistate modelling of probability of on-treatment clinical response and time remaining in response in patients with moderate-to-severe psoriasis treated with brodalumab or ustekinumab in the AMAGINE-2 and -3 studies (notice n° 604339)

détails MARC
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fixed length control field 02606cam a2200265 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250121155249.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Zachariae, Claus
Relator term author
245 00 - TITLE STATEMENT
Title Multistate modelling of probability of on-treatment clinical response and time remaining in response in patients with moderate-to-severe psoriasis treated with brodalumab or ustekinumab in the AMAGINE-2 and -3 studies
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2022.<br/>
500 ## - GENERAL NOTE
General note 45
520 ## - SUMMARY, ETC.
Summary, etc. BackgroundRelative changes in Psoriasis Area and Severity Index (PASI) are used as outcomes in psoriasis clinical trials but are limited when analysing long-term data and in routine practice. Absolute PASI may be more clinically useful. ObjectivesTo develop and implement a methodology for assessing the probability of achieving and maintaining a “response” in patients with psoriasis, defined using absolute PASI. Materials & MethodsThis analysis included pooled data from the Phase III AMAGINE-2 and -3 trials. Absolute PASI was described using all available data. Multistate modelling was used to compare the probabilities of achieving (absolute PASI = 0) and maintaining (absolute PASI ≤2) a response, and the time in the response state, in patients receiving brodalumab vs ustekinumab. ResultsHigher proportions of patients achieved lower absolute PASI over 52 weeks with brodalumab vs ustekinumab. The probability of achieving the response state was greater with brodalumab vs ustekinumab over 52 weeks (hazard ratio: 1.96; 95% confidence interval [CI]: 1.66–2.31, p&lt;0.001). At Week 52, there was a higher probability of being in response with brodalumab vs ustekinumab (81% [95% CI: 74–89%] vs 60% [95% CI: 54–67%], respectively). Mean time in response was longer with brodalumab (215 days; 95% CI: 197-233) vs ustekinumab (145 days; 95% CI: 130–160); a difference of 70 days (95% CI: 46–94; p&lt;0.001). ConclusionUsing a novel multistate modelling approach based on absolute PASI, we found that patients had a greater probability of achieving and maintaining a response with brodalumab vs ustekinumab.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element psoriasis
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element absolute PASI
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element ustekinumab
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element response
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element brodalumab
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element interleukin-17
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Mrowietz, Ulrich
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Strodl Andersen, Jens
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Puig, Lluís
Relator term author
786 0# - DATA SOURCE ENTRY
Note European Journal of Dermatology | 32 | 4 | 2022-07-01 | p. 530-535 | 1167-1122
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-european-journal-of-dermatology-2022-4-page-530?lang=en&redirect-ssocas=7080">https://shs.cairn.info/revue-european-journal-of-dermatology-2022-4-page-530?lang=en&redirect-ssocas=7080</a>

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