Abstract

PurposePrimary immunodeficiency diseases (PIDDs) are a heterogenous group of disorders characterized by intrinsic impairment in the immune system. Most patients with PIDD require life-long immunoglobulin G replacement therapy, which has been shown to reduce the rate of infections and, related hospitalizations and reduce health-related quality of life (HRQOL). Here, treatment satisfaction and HRQOL in patients with PIDD was evaluated upon switching from intravenous (IVIG) or subcutaneous immunoglobulins (SCIGs) to 20% SCIG (Hizentra®), and during long-term steady-state Hizentra® treatment.MethodsAnalyses were based on two pivotal (switch) and four extension/follow-up (maintenance) Phase III studies of Hizentra® conducted in Europe (EU), Japan (JP), and the United States (US). Two validated questionnaires were used: Life Quality Index (LQI) for assessment of IgG-specific perceptions of HRQOL and Short Form 36 version 2 (SF-36v2).ResultsIn the EU and JP switch studies, there was significant and meaningful improvement from Screening in LQI domain scores at all time points, largely driven by patients switching from IVIG to SCIG. In the EU switch study, there were also significant increases in mean SF-36v2 domain scores for Physical Function and General Health from Screening to Week 12. These improvements were observed also at Week 24. Overall, LQI and SF-36v2 domain scores were generally sustained in the maintenance studies.ConclusionsThese results showed that switching patients from IVIG to SCIG improves patient self-reported health status and IgG-specific HRQOL perception. The maintenance studies generally showed no deterioration of this improved health status over a long follow-up period.

Highlights

  • Primary immunodeficiency diseases (PIDDs) consist of a heterogenous group of disorders in which there is an intrinsicElectronic supplementary material The online version of this article contains supplementary material, which is available to authorized users.Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan 4 Frontier Science, Kincraig, Scotland, UK impairment in the body’s immune system [1, 2]

  • These results showed that switching patients from IVIG to subcutaneous immunoglobulins (SCIGs) improves patient self-reported health status and immunoglobulin G (IgG)-specific health-related quality of life (HRQOL) perception

  • The maintenance studies generally showed no deterioration of this improved health status over a long follow-up period

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Summary

Introduction

Primary immunodeficiency diseases (PIDDs) consist of a heterogenous group of disorders in which there is an intrinsic. While up to 300 types of PIDD are recognized, common variable immunodeficiency and X-linked agammaglobulinemia are two of the most common [1, 2]. PIDD imposes a significant disease burden on patients, including limitations in work, play, and normal physical activity [4]. In comparison with healthy children and adults, patients with PIDD experience measurably lower general health with higher hospitalization rates and increased physical, school, and social activity limitation [5,6,7]. Patients with PIDD fare even worse than those with other chronic conditions with respect to general health perceptions [8, 9]

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