Utility of the Dermatology Life Quality Index at initiation or switching of biologics in real-life Japanese patients with plaque psoriasis: Results from the ProLOGUE study.


Journal

Journal of dermatological science
ISSN: 1873-569X
Titre abrégé: J Dermatol Sci
Pays: Netherlands
ID NLM: 9011485

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 08 10 2020
revised: 27 12 2020
accepted: 03 01 2021
pubmed: 27 1 2021
medline: 27 7 2021
entrez: 26 1 2021
Statut: ppublish

Résumé

Plaque psoriasis significantly affects patients' health-related quality of life. To aid treatment decisions, not only objective assessment by physicians but also subjective assessment by patients is important. To assess the significance of Dermatology Life Quality Index (DLQI) evaluation at the time of biologics introduction in clinical practice in Japanese patients with plaque psoriasis. This was a single-arm, open-label, multicenter study. At baseline, Psoriasis Area and Severity Index (PASI) and DLQI scores were measured and stratified based on DLQI scores ≥6/≤5 and PASI scores ≤10/>10. Other patient-reported outcomes assessed included EQ-5D-5L, itch numerical rating scale (NRS), skin pain NRS, Generalized Anxiety Disorder-7 (GAD-7), Patient Health Questionnaire-8 (PHQ-8), Sleep Problem Index-II (SPI-II), and Treatment Satisfaction Questionnaire for Medication-9 (TSQM-9). Of the 73 enrolled patients, 23 had PASI scores ≤10. Those with PASI/DLQI scores >10/≥6 had a significantly higher median PASI score than those with PASI/DLQI scores >10/≤5 (p = 0.0125). Regardless of PASI scores (>10/≤10), median itch NRS and GAD-7 scores were significantly higher in patients with DLQI scores ≥6 than in those with DLQI scores ≤5 (itch NRS, p = 0.0361 and p = 0.0086, respectively; GAD-7, p = 0.0167 and p = 0.0273, respectively). Patients with PASI/DLQI scores ≤10/≥6 had significantly higher skin pain NRS (p = 0.0292) and PHQ-8 (p = 0.0255) scores and significantly lower median SPI-II scores (p = 0.0137) and TSQM-9 Effectiveness domain scores (p = 0.0178) than those with PASI/DLQI scores ≤10/≤5. DLQI may be useful for assessing patients' concerns that cannot be identified by PASI alone while initiating biologics or switching from other biologics in clinical practice.

Sections du résumé

BACKGROUND BACKGROUND
Plaque psoriasis significantly affects patients' health-related quality of life. To aid treatment decisions, not only objective assessment by physicians but also subjective assessment by patients is important.
OBJECTIVE OBJECTIVE
To assess the significance of Dermatology Life Quality Index (DLQI) evaluation at the time of biologics introduction in clinical practice in Japanese patients with plaque psoriasis.
METHODS METHODS
This was a single-arm, open-label, multicenter study. At baseline, Psoriasis Area and Severity Index (PASI) and DLQI scores were measured and stratified based on DLQI scores ≥6/≤5 and PASI scores ≤10/>10. Other patient-reported outcomes assessed included EQ-5D-5L, itch numerical rating scale (NRS), skin pain NRS, Generalized Anxiety Disorder-7 (GAD-7), Patient Health Questionnaire-8 (PHQ-8), Sleep Problem Index-II (SPI-II), and Treatment Satisfaction Questionnaire for Medication-9 (TSQM-9).
RESULTS RESULTS
Of the 73 enrolled patients, 23 had PASI scores ≤10. Those with PASI/DLQI scores >10/≥6 had a significantly higher median PASI score than those with PASI/DLQI scores >10/≤5 (p = 0.0125). Regardless of PASI scores (>10/≤10), median itch NRS and GAD-7 scores were significantly higher in patients with DLQI scores ≥6 than in those with DLQI scores ≤5 (itch NRS, p = 0.0361 and p = 0.0086, respectively; GAD-7, p = 0.0167 and p = 0.0273, respectively). Patients with PASI/DLQI scores ≤10/≥6 had significantly higher skin pain NRS (p = 0.0292) and PHQ-8 (p = 0.0255) scores and significantly lower median SPI-II scores (p = 0.0137) and TSQM-9 Effectiveness domain scores (p = 0.0178) than those with PASI/DLQI scores ≤10/≤5.
CONCLUSION CONCLUSIONS
DLQI may be useful for assessing patients' concerns that cannot be identified by PASI alone while initiating biologics or switching from other biologics in clinical practice.

Identifiants

pubmed: 33495058
pii: S0923-1811(21)00002-5
doi: 10.1016/j.jdermsci.2021.01.002
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Biological Products 0
brodalumab 6ZA31Y954Z

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

185-193

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest S. Imafuku and T. Kakuma have received grants and meeting travel fees related to the submitted work from Kyowa Kirin. K. Murotani, K. Ito, C. Ohata, F. Yamazaki, T. Miyagi, H. Takahashi, Y. Okubo, H. Saeki, M. Honma, Y. Tada, T. Mabuchi, M. Higashiyama, S. Kobayashi, Y. Hashimoto, and M. Seishima have received grants related to the submitted work from Kyowa Kirin. Y. Kanai and T. Nomura are employees of Kyowa Kirin.

Auteurs

Shinichi Imafuku (S)

Department of Dermatology, Fukuoka University Faculty of Medicine, Fukuoka, Japan. Electronic address: dermatologist@mac.com.

Yasumasa Kanai (Y)

Medical Affairs, Kyowa Kirin Co., Ltd., Tokyo, Japan.

Kenta Murotani (K)

Biostatistics Center, Kurume University, Fukuoka, Japan.

Takanobu Nomura (T)

Medical Affairs, Kyowa Kirin Co., Ltd., Tokyo, Japan.

Kei Ito (K)

Department of Dermatology, JR Sapporo Hospital, Sapporo, Hokkaido, Japan.

Chika Ohata (C)

Department of Dermatology, Osaka General Medical Center, Osaka, Japan.

Fumikazu Yamazaki (F)

Department of Dermatology, Kansai Medical University, Osaka, Japan.

Takuya Miyagi (T)

Department of Dermatology, University of the Ryukyus, Okinawa, Japan.

Hidetoshi Takahashi (H)

Takagi Dermatological Clinic, Hokkaido, Japan.

Yukari Okubo (Y)

Department of Dermatology, Tokyo Medical University, Tokyo, Japan.

Hidehisa Saeki (H)

Department of Dermatology, Nippon Medical School, Tokyo, Japan.

Masaru Honma (M)

Department of Dermatology, Asahikawa Medical University, Hokkaido, Japan.

Yayoi Tada (Y)

Department of Dermatology, Teikyo University School of Medicine, Tokyo, Japan.

Tomotaka Mabuchi (T)

Department of Dermatology, Tokai University School of Medicine, Kanagawa, Japan.

Mari Higashiyama (M)

Department of Dermatology, Nippon Life Hospital, Osaka, Japan.

Satomi Kobayashi (S)

Department of Dermatology, Seibo International Catholic Hospital, Tokyo, Japan.

Yuki Hashimoto (Y)

Department of Dermatology, Toho University School of Medicine, Tokyo, Japan.

Mariko Seishima (M)

Department of Dermatology, Gifu University Graduate School of Medicine, Gifu, Japan.

Tatsuyuki Kakuma (T)

Biostatistics Center, Kurume University, Fukuoka, Japan.

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