Dosing Strategy of Immunoglobulin (IgG) Replacement Therapies in Obese and Overweight Patients with Primary Immunodeficiency Diseases (PIDDs): A Meta‐Analysis of Clinical Trials

Author:

Zhou Tingting1,Tegenge Million A.2ORCID,Golding Basil3,Scott John1

Affiliation:

1. Office of Biostatistics and Pharmacovigilance Center for Biologics Evaluation and Research US Food and Drug Administration Silver Spring MD USA

2. Office of Clinical Evaluation Office of Therapeutic Products Center for Biologics Evaluation and Research US Food and Drug Administration Silver Spring MD USA

3. Office of Plasma Protein Therapeutics Office of Therapeutic Products Center for Biologics Evaluation and Research US Food and Drug Administration Silver Spring MD USA

Abstract

AbstractThe current dosing strategy of immune globulin products for the treatment of primary immunodeficiency diseases (PIDDs) in the USA is based on total body weight (BW). The aim of our study was to assess the relationship between dose and trough level, and to determine whether an alternative dosing strategy should be considered for patients who are overweight or obese. We analyzed data in a total of 533 patients from 11 studies. We modeled the relationship between trough level and dose per week using a linear mixed model. We used an over‐dispersed Poisson model to model the relationship between infection and trough level. In these analyses, we then combined the study‐specific treatment effects using a random‐effect or fixed‐effect model. The mean administered dose per week was 9.77, 14.00, or 18.17 g in patients who were normal weight, overweight, or obese, respectively. Compared with a patient of normal weight, a 1 g increase in dose per week in a patient who was overweight was associated with a smaller increase in the trough level, 0.08 g/L less (95%CI –0.14 to –0.03 g/L), and a 1 g increase in dose per week in a patient who was obese was associated with a much smaller increase in trough level, 0.01 g/L less (95% CI –0.07 to 0.06 g/L). Last, for a 1 unit (g/L) increase in trough level, the expected number of infections remained the same, with a multiplicative factor of 1.01 (95%CI 0.98‐1.04). Overall, we found no compelling evidence to justify a reconsideration of the current dosing strategy based on total BW for patients with PIDDs who are overweight or obese.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference21 articles.

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5. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

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