The use of adalimumab, etanercept, golimumab and infliximab in rheumatic pathologies: variation between label dosage and real-world use


Por: Martinez-Cutillas J, Alerany-Pardo C, Borrás-Blasco J, Broto-Sumalla A, Burgos A, Climent-Bolta C, Escudero-Vilaplana V, Fernández-Fuente MA, Ferrit-Martin M, Gómez-Germá P, Martínez-Sesmero JM, Mayorga-Pérez J, Menchén-Viso B, Merino-Alonso J, Polache J and Sánchez-Guerrero A

Publicada: 3 sep 2015 Ahead of Print: 14 may 2015
Resumen:
Rheumatoid arthritis (AR), psoriatic arthritis (PSA) and ankylosing spondylitis (AS) are autoimmune systemic diseases characterized by inflammation, pain and joint degeneration. The objective of this study is to evaluate, under the actual conditions of use, dosing patterns of adalimumab, etanercept, golimumab and infliximab in these pathologies, and compare them with the label regimens recommended, as well as evaluating the financial implications of these regimen modifications. The study population included all adult patients diagnosed with RA, PSA or AS who had been treated with adalimumab, etanercept, golimumab and infliximab for at least 6 months between 1 January 2011 and 31 December 2013. The main variable of this study was to assess the dose dispensed for drugs administered subcutaneously and the dose prepared/administered for drugs administered intravenously, and the annual costs of the treatment. A total of 5,428 episodes were included. The mean weekly dose was lower than the standard dose in the three pathologies studied in the patients treated with adalimumab and etanercept (84.3% vs 81.2% for RA, 85.0% vs 78.0% for PSA and 87.8% vs 81.6% for AS). The drugs with highest dose optimization in RA are etanercept (46.3%) followed by adalimumab (46%); however, the highest percentage of patients with major dose optimization corresponds to etanercept (11.6%). Both in the PA and the AS group, we also observed that etanercept is the drug more optimized, corresponding to 53.9 and 43% of patients, respectively. By contrast, 48.5% of patients with RA treated with infliximab required dose intensification; however, infliximab dose intensification in PSA and AS is not so pronounced. The practice of optimization of dose regimens in patients with rheumatic diseases under treatment with anti-TNF is spreading among professionals, resulting in annual cost reduction in the treatment of rheumatic arthropathies. However, long term follow-up will be necessary to assess the influence of this optimization on health outcomes.

Filiaciones:
Martinez-Cutillas J:
 a 1 Hospital Universitari Vall d'Hebron, Pharmacy, Barcelona, 08035, Spain

Alerany-Pardo C:
 a 1 Hospital Universitari Vall d'Hebron, Pharmacy, Barcelona, 08035, Spain

:
 b 2 Hospital de Sagunto, Pharmacy, Avda Ramon y Cajal s/n, Sagunto 46520 (Valencia), Spain

Broto-Sumalla A:
 c 3 Consorci Sanitari Terrassa, Pharmacy, Terrassa, Spain

Burgos A:
 d 4 Hospital General de Alicante, Pharmacy, Alicante, Spain

Climent-Bolta C:
 e 5 Hospital Clínic de Barcelona, Pharmacy, Barcelona, Spain

Escudero-Vilaplana V:
 f 6 Hospital Universitario Gregorio Marañon, Pharmacy, Madrid, Spain

Fernández-Fuente MA:
 g 7 Hospital Universitari de Salamanca, Pharmacy, Salamanca, Spain

Ferrit-Martin M:
 h 8 Hospital Universitario Virgen de las Nieves, Pharmacy, Granada, Spain

Gómez-Germá P:
 i 9 Hospital de Jerez, Pharmacy, Jerez, Spain

Martínez-Sesmero JM:
 j 10 Hospital Virgen de la Salud de Toledo, Pharmacy, Toledo, Spain

Mayorga-Pérez J:
 k 11 Hospital Universitario Marques de Valdecilla, Pharmacy, Santander, Spain

Menchén-Viso B:
 l 12 Hospital Puerta de Hierro, Pharmacy, Madrid, Spain

Merino-Alonso J:
 m 13 Hospital Universitario Ntra Sra de Candelaria, Pharmacy, Santa Cruz de Tenerife, Spain

Polache J:
 d 4 Hospital General de Alicante, Pharmacy, Alicante, Spain

Sánchez-Guerrero A:
 l 12 Hospital Puerta de Hierro, Pharmacy, Madrid, Spain
ISSN: 14737167





EXPERT REVIEW OF PHARMACOECONOMICS & OUTCOMES RESEARCH
Editorial
TAYLOR & FRANCIS LTD, 4 PARK SQUARE, MILTON PARK, ABINGDON OX14 4RN, OXON, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 15 Número: 5
Páginas: 851-858
WOS Id: 000369414900002
ID de PubMed: 25972066

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