A multicenter retrospective case-control study on Suspension of TNF-inhibitors and Outcomes in Psoriatic patients (STOP study).


Journal

Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia
ISSN: 1827-1820
Titre abrégé: G Ital Dermatol Venereol
Pays: Italy
ID NLM: 8102852

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 27 9 2018
medline: 31 12 2019
entrez: 26 9 2018
Statut: ppublish

Résumé

There is limited information on patients undergoing withdrawal after long-term treatment with anti-TNF alpha drugs and their clinical evolution during the post-interruption period in real-life settings. The purpose of the present retrospective case-control study was to provide a clearer insight into the clinical management of psoriatic patients with adequate response to long-term adalimumab, etanercept and infliximab treatment once these biologic agents are interrupted. A total of 270 patients undergoing anti-TNF alpha agents discontinuation and 253 controls treated with a continuous regimen were enrolled. The primary endpoint was the change in disease activity in each study group over six months (or until treatment of psoriatic recurrence) as measured by the PASI score every month. Then, we evaluated the rate of and time to relapse, the rate of clinical worsening (PASI≥5) and the clinical variables influencing the loss of response. Our study showed that about 50% of patients achieving a long-term and optimal response to the aforementioned anti-TNF alpha agents did not experience any relapse over a 6-month follow-up period after withdrawal. We also observed that subjects displaying a complete remission (PASI=0) at anti-TNF alpha therapy withdrawal experienced less frequently disease worsening and/or relapse compared to subjects having a PASI>0. Our findings confirmed that all three anti-TNF alpha agents tend to retain their effectiveness upon re-administration in case of recurrence, even if they have been previously used for long time.

Sections du résumé

BACKGROUND
There is limited information on patients undergoing withdrawal after long-term treatment with anti-TNF alpha drugs and their clinical evolution during the post-interruption period in real-life settings. The purpose of the present retrospective case-control study was to provide a clearer insight into the clinical management of psoriatic patients with adequate response to long-term adalimumab, etanercept and infliximab treatment once these biologic agents are interrupted.
METHODS
A total of 270 patients undergoing anti-TNF alpha agents discontinuation and 253 controls treated with a continuous regimen were enrolled. The primary endpoint was the change in disease activity in each study group over six months (or until treatment of psoriatic recurrence) as measured by the PASI score every month. Then, we evaluated the rate of and time to relapse, the rate of clinical worsening (PASI≥5) and the clinical variables influencing the loss of response.
RESULTS
Our study showed that about 50% of patients achieving a long-term and optimal response to the aforementioned anti-TNF alpha agents did not experience any relapse over a 6-month follow-up period after withdrawal. We also observed that subjects displaying a complete remission (PASI=0) at anti-TNF alpha therapy withdrawal experienced less frequently disease worsening and/or relapse compared to subjects having a PASI>0.
CONCLUSIONS
Our findings confirmed that all three anti-TNF alpha agents tend to retain their effectiveness upon re-administration in case of recurrence, even if they have been previously used for long time.

Identifiants

pubmed: 30251810
pii: S0392-0488.18.06156-4
doi: 10.23736/S0392-0488.18.06156-4
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0
Tumor Necrosis Factor-alpha 0
Infliximab B72HH48FLU
Adalimumab FYS6T7F842
Etanercept OP401G7OJC

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

392-399

Auteurs

Giuseppe Stinco (G)

Department of Medical Area, Institute of Dermatology, University of Udine, Udine, Italy - giuseppe.stinco@uniud.it.

Nicola Balato (N)

Unit of Dermatology, Department of Clinical Medicine and Surgery, Federico II University of Naples, Naples, Italy.

Cinzia Buligan (C)

Department of Medical Area, Institute of Dermatology, University of Udine, Udine, Italy.

Anna Campanati (A)

Unit of Dermatology, Department of Clinical and Molecular Sciences, Polytechnic Marche University, Ancona, Italy.

Stefano Dastoli (S)

Department of Health Sciences, Institute of Dermatology, University Magna Graecia, Catanzaro, Italy.

Nicola Di Meo (N)

Department of Dermatology, University of Trieste, Trieste, Italy.

Paolo Gisondi (P)

Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy.

Francesco Lacarrubba (F)

Dermatology Clinic, University of Catania, Catania, Italy.

Maria L Musumeci (ML)

Dermatology Clinic, University of Catania, Catania, Italy.

Maddalena Napolitano (M)

Unit of Dermatology, Department of Clinical Medicine and Surgery, Federico II University of Naples, Naples, Italy.

Annamaria Offidani (A)

Unit of Dermatology, Department of Clinical and Molecular Sciences, Polytechnic Marche University, Ancona, Italy.

Leonardo Pescitelli (L)

Section of Dermatology, Department of Surgery and Translational Medicine, University of Florence, Florence, Italy.

Stefano Piaserico (S)

Unit of Dermatology, Department of Medicine, University of Padua, Padua, Italy.

Angelo Piccirillo (A)

Department of Dermatology, San Carlo Hospital, Potenza, Italy.

Francesca Prignano (F)

Section of Dermatology, Department of Surgery and Translational Medicine, University of Florence, Florence, Italy.

Enzo Errichetti (E)

Department of Medical Area, Institute of Dermatology, University of Udine, Udine, Italy.

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