Effectiveness of cyclosporine A in patients with moderate to severe plaque psoriasis in a real-life clinical setting in Italy: the TRANSITION study.


Journal

The Journal of dermatological treatment
ISSN: 1471-1753
Titre abrégé: J Dermatolog Treat
Pays: England
ID NLM: 8918133

Informations de publication

Date de publication:
Feb 2022
Historique:
pubmed: 1 5 2020
medline: 16 2 2022
entrez: 1 5 2020
Statut: ppublish

Résumé

Cyclosporine A (CsA) is one of the systemic therapeutic options for moderate-to-severe psoriasis, based on its efficacy and rapidity of action. The current study investigated the response to CsA in patients with moderate-to-severe plaque psoriasis. TRANSITION was an observational, cross-sectional, multicentre study which evaluated the proportion of partial- and suboptimal-responders among patients with moderate-to-severe plaque psoriasis treated with continuous CsA for ≥12 weeks. Patients demonstrating a Psoriasis Area and Severity Index (PASI) response of ≥90, ≥75 and <90, ≥50 and <75 and <50 were defined as responders, suboptimal-responders, partial-responders, and non-responders, respectively. A total of 196 patients (mean age, 46.6 years; 62.8% males) from 14 sites in Italy were evaluated. At the study visit, the mean (SD) PASI score was 4.2(5.5) compared with 15.3(7.1) prior to the last CsA cycle. For response categories, 39.8%, 22.4%, 16.8%, and 20.9% of patients were responders, suboptimal-responders, partial-responders, and non-responders to CsA treatment. Overall, 28.6% of patients permanently discontinued treatment with CsA (lack of efficacy [10.2%], poor tolerability and voluntary discontinuation [3.6% each], and other [11.7%]). Patients were only partially satisfied with CsA treatment, reporting measurable impact on quality of life. Only 40% patients showed a satisfactory response to CsA.

Sections du résumé

BACKGROUND BACKGROUND
Cyclosporine A (CsA) is one of the systemic therapeutic options for moderate-to-severe psoriasis, based on its efficacy and rapidity of action. The current study investigated the response to CsA in patients with moderate-to-severe plaque psoriasis.
MATERIALS AND METHODS METHODS
TRANSITION was an observational, cross-sectional, multicentre study which evaluated the proportion of partial- and suboptimal-responders among patients with moderate-to-severe plaque psoriasis treated with continuous CsA for ≥12 weeks. Patients demonstrating a Psoriasis Area and Severity Index (PASI) response of ≥90, ≥75 and <90, ≥50 and <75 and <50 were defined as responders, suboptimal-responders, partial-responders, and non-responders, respectively.
RESULTS RESULTS
A total of 196 patients (mean age, 46.6 years; 62.8% males) from 14 sites in Italy were evaluated. At the study visit, the mean (SD) PASI score was 4.2(5.5) compared with 15.3(7.1) prior to the last CsA cycle. For response categories, 39.8%, 22.4%, 16.8%, and 20.9% of patients were responders, suboptimal-responders, partial-responders, and non-responders to CsA treatment. Overall, 28.6% of patients permanently discontinued treatment with CsA (lack of efficacy [10.2%], poor tolerability and voluntary discontinuation [3.6% each], and other [11.7%]).
CONCLUSION CONCLUSIONS
Patients were only partially satisfied with CsA treatment, reporting measurable impact on quality of life. Only 40% patients showed a satisfactory response to CsA.

Identifiants

pubmed: 32349568
doi: 10.1080/09546634.2020.1757017
doi:

Substances chimiques

Cyclosporine 83HN0GTJ6D

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

401-407

Auteurs

F Marsili (F)

Unit of Dermatology, Versilia Hospital, Lido di Camaiore, Lucca, Italy.

M Travaglini (M)

Centro per la cura della Psoriasi, Hospital "Di Summa-Perrino", Brindisi, Italy.

G Stinco (G)

Institute of Dermatology, Department of Medicine, University Hospital, Udine, Italy.

R Manzoni (R)

Division of Dermatology, Azienda Sanitaria Locale of Biella, Ponderano, Italy.

R Tiberio (R)

SCDU Dermatology, AOU Maggiore della Carità, Novara, Italy.

F Prignano (F)

Department of Health Science Dermatology Unit, University of Florence, Firenze, Italy.

A Mazzotta (A)

Dermatology Unit, San Camillo-Forlanini Hospital, Rome, Italy.

S P Cannavò (SP)

Dermatology Unit, University Hospital Policlinico "G. Martino", Messina, Italy.

A Cuccia (A)

Unit of Dermatology, San Donato Hospital, Arezzo, Italy.

M Germino (M)

Department of Dermatology, Hospital Policlinico Città di Udine, Udine, Italy.

M R Bongiorno (MR)

Dermatology Unit, University Hospital Policlinico "P. Giaccone", Palermo, Italy.

S Persechino (S)

Dermatology Unit, NESMOS Department, S. Andrea Hospital, University of Rome "Sapienza", Rome, Italy.

T Florio (T)

Dermatology Unit, Hospital Di Venere-Carbonara di Bari, Bari, Italy.

M Pettinato (M)

Dermatology Unit, University Hospital "Policlinico-Vittorio Emanuele", Catania, Italy.

M Tabanelli (M)

U.O.C. Dermatologia Ravenna AUSL Romagna, Ospedale Santa Maria delle Croci, Ravenna, Italy.

R Sarkar (R)

Novartis Pharma AG, Basel, Switzerland.

E Aloisi (E)

Novartis Farma SpA, Origgio, Italy.

M Bartezaghi (M)

Novartis Farma SpA, Origgio, Italy.

R Orsenigo (R)

Novartis Farma SpA, Origgio, Italy.

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