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Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency
PURPOSE: Intravenous IgG (IVIG) treatment wear-off is commonly experienced by patients, who report increased susceptibility to infection, and decreased quality of life towards the end of their 3- or 4-week dosing cycle, when serum IgG levels approach their trough. We quantified IVIG wear-off in term...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792336/ https://www.ncbi.nlm.nih.gov/pubmed/26910102 http://dx.doi.org/10.1007/s10875-016-0243-z |
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author | Rojavin, Mikhail A. Hubsch, Alphonse Lawo, John-Philip |
author_facet | Rojavin, Mikhail A. Hubsch, Alphonse Lawo, John-Philip |
author_sort | Rojavin, Mikhail A. |
collection | PubMed |
description | PURPOSE: Intravenous IgG (IVIG) treatment wear-off is commonly experienced by patients, who report increased susceptibility to infection, and decreased quality of life towards the end of their 3- or 4-week dosing cycle, when serum IgG levels approach their trough. We quantified IVIG wear-off in terms of treatment efficacy and patient well-being. METHODS: Data were collected from patients enrolled in three Phase III trials of Sandoglobulin® NF Liquid or Privigen®, treated every 3- or 4- weeks. Pooled analyses of raw patient data compared the rate of infection and other clinical outcomes during the course of the dosing cycle. Subjective symptoms of wear-off were quantified by comparing patient-reported overall well-being scores. RESULTS: The probability of a first infection in the final week of the IVIG cycle was 1.26 (95 % confidence intervals [CI]: 0.76–2.11; p = 0.3621) and 1.55 (95 % CI: 1.04–2.32; p = 0.0314) times higher than in the first week, for patients on a 3-week cycle and 4-week dosing cycles, respectively. Wear-off, as manifested by a decrease in overall well-being, was experienced in 10 % of all cycles and reported at least once by 61 % of the patients on a 3-week cycle, and 43 % of those on a 4-week cycle. CONCLUSIONS: These findings confirm the existence of decreased efficacy (treatment wear-off) towards the end of a 3–4 week IVIG dosing cycle, and provide a quantifiable evaluation to a phenomenon typically reported anecdotally. For patients experiencing wear-off, increasing the IgG dose or shortening the dosing interval and/or a switch to SCIG may be beneficial. |
format | Online Article Text |
id | pubmed-4792336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-47923362016-04-09 Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency Rojavin, Mikhail A. Hubsch, Alphonse Lawo, John-Philip J Clin Immunol Original Article PURPOSE: Intravenous IgG (IVIG) treatment wear-off is commonly experienced by patients, who report increased susceptibility to infection, and decreased quality of life towards the end of their 3- or 4-week dosing cycle, when serum IgG levels approach their trough. We quantified IVIG wear-off in terms of treatment efficacy and patient well-being. METHODS: Data were collected from patients enrolled in three Phase III trials of Sandoglobulin® NF Liquid or Privigen®, treated every 3- or 4- weeks. Pooled analyses of raw patient data compared the rate of infection and other clinical outcomes during the course of the dosing cycle. Subjective symptoms of wear-off were quantified by comparing patient-reported overall well-being scores. RESULTS: The probability of a first infection in the final week of the IVIG cycle was 1.26 (95 % confidence intervals [CI]: 0.76–2.11; p = 0.3621) and 1.55 (95 % CI: 1.04–2.32; p = 0.0314) times higher than in the first week, for patients on a 3-week cycle and 4-week dosing cycles, respectively. Wear-off, as manifested by a decrease in overall well-being, was experienced in 10 % of all cycles and reported at least once by 61 % of the patients on a 3-week cycle, and 43 % of those on a 4-week cycle. CONCLUSIONS: These findings confirm the existence of decreased efficacy (treatment wear-off) towards the end of a 3–4 week IVIG dosing cycle, and provide a quantifiable evaluation to a phenomenon typically reported anecdotally. For patients experiencing wear-off, increasing the IgG dose or shortening the dosing interval and/or a switch to SCIG may be beneficial. Springer US 2016-02-24 2016 /pmc/articles/PMC4792336/ /pubmed/26910102 http://dx.doi.org/10.1007/s10875-016-0243-z Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Rojavin, Mikhail A. Hubsch, Alphonse Lawo, John-Philip Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title | Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title_full | Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title_fullStr | Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title_full_unstemmed | Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title_short | Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency |
title_sort | quantitative evidence of wear-off effect at the end of the intravenous igg (ivig) dosing cycle in primary immunodeficiency |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792336/ https://www.ncbi.nlm.nih.gov/pubmed/26910102 http://dx.doi.org/10.1007/s10875-016-0243-z |
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