TUMOR NECROSIS FACTOR (TNF)-BLOCKER DOSE ESCALATION AMONG PATIENTS WITH RHEUMATOID ARTHRITIS (RA) IN A LARGE MANAGED CARE POPULATION IN THE UNITED STATES

Author(s)

Fisher M1, Watson C2, Gandra SR2, Chen YW1, Fox KM31HealthCore, Inc., Wilmington, DE, USA, 2Amgen, Inc., Thousand Oaks, CA, USA, 3Strategic Healthcare Solutions, LLC, Monkton, MD, USA

OBJECTIVES:  To estimate dose escalation rates of etanercept, adalimumab, and infliximab for RA patients initiating and continuing TNF-blockers METHODS:  This retrospective analysis in the HealthCore Integrated Research Database identified adult (18-64 years) RA patients with ≥1 claim for etanercept, adalimumab, or infliximab between July 1, 2007 and January 31, 2010 (first claim=index).  Patients were continuously enrolled for 6 months prior to index; patients with TNF-blocker claims within 6 months prior to index were considered continuing therapy.  Patients with other indicated conditions or contraindicated to RA biologic therapy were excluded.  Dose escalation, assessed over a 12-month period of continuous treatment (<60-day gap), was defined as: 1) 2+ instances in which subsequent doses were ≥130% of index dose or 2) any instances with increased number of syringe/vial or shortened dosing interval. RESULTS:  Overall, 3868 patients were included (mean age 50.1 years; 74.4% female).  Among new patients (932 etanercept; 267 adalimumab; 292 infliximab), 4.4%, 9.0%, and 42.5% of etanercept, adalimumab, and infliximab patients, respectively, had 2+ instances of dose escalation (P<0.001 for all 2-way comparisons).  Most new patients (85.3% etanercept; 92.1% adalimumab; N/A infliximab) initiated therapy at recommended dose; of these patients, 2.3%, 12.6%, and 59.9% of etanercept, adalimumab, and infliximab patients, respectively, increased by ≥1 syringe/vial or shortened dosing frequency.  Among continuing patients (1078 etanercept; 480 adalimumab; 819 infliximab), 6.0%, 16.9%, and 29.1% of etanercept, adalimumab, and infliximab patients, respectively, had 2+ instances of dose escalation (P<0.0001 for all 2-way comparisons).  Most continuing patients (93.5% etanercept; 95.6% adalimumab; N/A infliximab) received the index dose at recommended dose; of these, 4.1%, 19.6%, and 79.5% of etanercept, adalimumab, and infliximab patients, respectively, increased by ≥1 syringe/vial or shortened dosing frequency. CONCLUSIONS:  Etanercept had lower dose escalation rates for new and continuing patients compared with adalimumab and infliximab in a large US managed care plan.

Conference/Value in Health Info

2012-06, ISPOR 2012, Washington, D.C., USA

Value in Health, Vol. 15, No. 4 (June 2012)

Code

PMS70

Topic

Health Service Delivery & Process of Care

Topic Subcategory

Prescribing Behavior

Disease

Musculoskeletal Disorders

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