ABATACEPT CORRELATES WITH LOWER CARE UTILIZATION IN PATIENTS WITH COMMON VARIABLE AND COMMON IMMUNE DEFICIENCIES

Primary immune deficiency (PID) patients with autoinflammatory disease have higher morbidity/mortality, yet we lack FDA-approved therapies for care. We investigated clinical use of abatacept and associated outcomes among PID patients. We performed a retrospective review of patients with Internationa...

Full description

Saved in:
Bibliographic Details
Published inAnnals of allergy, asthma, & immunology Vol. 133; no. 6; p. S65
Main Authors Jogdand, A., Hong, J., Pak, A., Digiacomo, D., Barmettler, S., Farmer, J.
Format Journal Article
LanguageEnglish
Published Elsevier Inc 01.11.2024
Online AccessGet full text

Cover

Loading…
More Information
Summary:Primary immune deficiency (PID) patients with autoinflammatory disease have higher morbidity/mortality, yet we lack FDA-approved therapies for care. We investigated clinical use of abatacept and associated outcomes among PID patients. We performed a retrospective review of patients with International Classification of Diseases (ICD)-10 coded diagnoses of common variable immunodeficiency (CVID, D83*) and/or combined immunodeficiency (CID, D81.*) at two separate tertiary care centers. We analyzed the association of abatacept therapy with care utilization (defined as unique hospital admissions), comparing timepoints pre- to post-abatacept therapy by paired t-test (p<0.05). We identified 44 unique patients with CVID/CID who received abatacept at any timepoint. This cohort was predominantly female (84%), non-Hispanic (91%), White (95%), and without identified CTLA4, LRBA, or DEF6 mutations (84%). The primary indications for abatacept use were inflammatory arthritis (55%) and autoimmune enteropathy (AIE, 25%). The median abatacept dose was 625 mg monthly (intravenous, 67%), with a median duration of treatment of 18 (IQR: 4.5-48) months. Care utilization was high in the cohort overall (median 4 (IQR: 2-12) total hospital admissions), with most admissions occurring in the AIE subgroup in the two-year period closely preceding abatacept start. In CVID/CID patients with AIE, abatacept therapy was associated with fewer hospital admissions in the 2-year post-initiation period (median 2; IQR:0-3) compared to the two-year pre-abatacept period (median 3; IQR: 1-7), p=0.03. Abatacept may improve care utilization in CVID/CID patients with AIE. Future work will investigate the impact of abatacept on global autoinflammatory disease score in CVID/CID patients.
ISSN:1081-1206
DOI:10.1016/j.anai.2024.08.216