Real-World Analysis of Therapeutic Patterns in Patients Affected by Rheumatoid Arthritis in Italy: A Focus on Baricitinib.

Baricitinib Biologic DMARDs Real-world study Rheumatoid arthritis Targeted synthetic DMARDs Treatment patterns

Journal

Rheumatology and therapy
ISSN: 2198-6576
Titre abrégé: Rheumatol Ther
Pays: England
ID NLM: 101674543

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 29 04 2020
pubmed: 20 7 2020
medline: 20 7 2020
entrez: 20 7 2020
Statut: ppublish

Résumé

The objective of this study was to evaluate treatment patterns in patients with rheumatoid arthritis (RA), with a focus on the utilization of baricitinib, an oral highly selective Janus kinase 1 and 2 inhibitor, in an Italian real-world setting. This observational retrospective analysis was based on data collected in selected Italian administrative databases. Patients aged ≥ 18 years with a diagnosis of RA defined by hospitalization discharge diagnosis (International Classification of Diseases, Ninth Revision, Clinical Modification code 714.0) or by disease exemption code 006 for RA in 2018 were included. The index date (ID) was defined as the date of first prescription for a drug indicated for RA during the inclusion period. Patients without a prescription for biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) before the ID were considered to be b/tsDMARD naïve. A further analysis was performed on patients only receiving baricitinib. A total of 41,290 RA patients were enrolled, of whom 55.6% were not treated with conventional synthetic DMARDs (csDMARDs) or b/tsDMARDs, 39.4% were receiving therapy with csDMARDs, and 5.0% were using b/tsDMARDs. In the latter group, 2.7% (n = 56) were receiving therapy with baricitinib. In 2018, 13.2% of csDMARD-treated patients switched to b/tsDMARDs, of whom 4.3% (n = 93) of these switched to baricitinib. In total, 149 patients (mean age ± standard deviation 57.6 ± 12.1; 12.8% male) had a baricitinib prescription, of whom 51% were b/tsDMARD naïve. At baseline, 61.7% of baricitinib users were receiving combination therapy with csDMARDs plus corticosteroids, 26.2% were receiving combination therapy with corticosteroids, and 8.1% were receiving combination therapy with csDMARDs; 4% were receiving baricitinib monotherapy. During follow-up, the proportion of patients receiving baricitinib monotherapy increased to 38.9%, while 26.9, 18.8, and 15.4% of baricitinib users received combination therapy with corticosteroids, csDMARDs plus corticosteroids, and csDMARDs, respectively. This study provides a current view of the treatment patterns in Italian patients with RA in a real-world setting of daily clinical practice, with a focus on baricitinib utilization.

Identifiants

pubmed: 32683611
doi: 10.1007/s40744-020-00218-3
pii: 10.1007/s40744-020-00218-3
pmc: PMC7410892
doi:

Types de publication

Journal Article

Langues

eng

Pagination

657-665

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Auteurs

Valentina Perrone (V)

Clicon S.r.l. Health Economics and Outcomes Research, Ravenna, Italy. valentina.perrone@clicon.it.

Serena Losi (S)

Eli Lilly Italy S.p.A., Sesto Fiorentino, Italy.

Veronica Rogai (V)

Eli Lilly Italy S.p.A., Sesto Fiorentino, Italy.

Silvia Antonelli (S)

Eli Lilly Italy S.p.A., Sesto Fiorentino, Italy.

Walid Fakhouri (W)

Eli Lilly and Company Limited, Windlesham, Surrey, UK.

Massimo Giovannitti (M)

Eli Lilly Italy S.p.A., Rome, Italy.

Elisa Giacomini (E)

Clicon S.r.l. Health Economics and Outcomes Research, Ravenna, Italy.

Diego Sangiorgi (D)

Clicon S.r.l. Health Economics and Outcomes Research, Ravenna, Italy.

Luca Degli Esposti (L)

Clicon S.r.l. Health Economics and Outcomes Research, Ravenna, Italy.

Classifications MeSH