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Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study

PURPOSE: To evaluate the safety and tolerability of subcutaneous IgPro20 (Hizentra(®), CSL Behring, King of Prussia, PA, USA) administered at high infusion parameters (> 25 mL and > 25 mL/h per injection site) in patients with primary immunodeficiency. METHODS: The Hizentra(®) Label Optimizati...

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Autores principales: Anderson, John T., Bonagura, Vincent R., Cowan, Juthaporn, Hsu, Connie, Mustafa, S. Shahzad, Patel, Niraj C., Routes, John M., Sriaroon, Panida, Vinh, Donald C., Hofmann, Jutta H., Praus, Michaela, Rojavin, Mikhail A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858210/
https://www.ncbi.nlm.nih.gov/pubmed/33409867
http://dx.doi.org/10.1007/s10875-020-00912-5
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author Anderson, John T.
Bonagura, Vincent R.
Cowan, Juthaporn
Hsu, Connie
Mustafa, S. Shahzad
Patel, Niraj C.
Routes, John M.
Sriaroon, Panida
Vinh, Donald C.
Hofmann, Jutta H.
Praus, Michaela
Rojavin, Mikhail A.
author_facet Anderson, John T.
Bonagura, Vincent R.
Cowan, Juthaporn
Hsu, Connie
Mustafa, S. Shahzad
Patel, Niraj C.
Routes, John M.
Sriaroon, Panida
Vinh, Donald C.
Hofmann, Jutta H.
Praus, Michaela
Rojavin, Mikhail A.
author_sort Anderson, John T.
collection PubMed
description PURPOSE: To evaluate the safety and tolerability of subcutaneous IgPro20 (Hizentra(®), CSL Behring, King of Prussia, PA, USA) administered at high infusion parameters (> 25 mL and > 25 mL/h per injection site) in patients with primary immunodeficiency. METHODS: The Hizentra(®) Label Optimization (HILO) study was an open-label, parallel-arm, non-randomized study (NCT03033745) of IgPro20 using a forced upward titration design for infusion parameters. Patients experienced with pump-assisted IgPro20 infusions received weekly IgPro20 infusions at a stable dose in the Pump-Assisted Volume Cohort (N = 15; 25–50 mL per injection site) and in the Pump-Assisted Flow Rate Cohort (N = 18; 25–100 mL/h per injection site). Responder rates (percentage of patients who successfully completed ≥ 75% of planned infusions), safety outcomes, and serum immunoglobulin G (IgG) trough levels were evaluated. RESULTS: Responder rates were 86.7% (13/15, 25 mL) and 73.3% (11/15, 40 and 50 mL) in the Volume Cohort, and 77.8% (14/18, 25 and 50 mL/h), 66.7% (12/18, 75 mL/h), and 61.1% (11/18, 100 mL/h) in the Flow Rate Cohort. Infusion compliance was ≥ 90% in all patients in the Volume Cohort and in 83.3% of patients in the Flow Rate Cohort. The number of injection sites (Volume Cohort) and the infusion duration (Flow Rate Cohort) decreased with increasing infusion parameters. The rate of treatment-emergent adverse events per infusion was low (0.138 [Volume Cohort] and 0.216 [Flow Rate Cohort]). Serum IgG levels remained stable during the study. CONCLUSION: Pump-assisted IgPro20 infusions are feasible at 50 mL and 100 mL/h per injection site in treatment-experienced patients, which may result in fewer injection sites and shorter infusion times. TRIAL REGISTRATION: NCT03033745; registered January 27, 2017 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10875-020-00912-5.
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spelling pubmed-78582102021-02-11 Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study Anderson, John T. Bonagura, Vincent R. Cowan, Juthaporn Hsu, Connie Mustafa, S. Shahzad Patel, Niraj C. Routes, John M. Sriaroon, Panida Vinh, Donald C. Hofmann, Jutta H. Praus, Michaela Rojavin, Mikhail A. J Clin Immunol Original Article PURPOSE: To evaluate the safety and tolerability of subcutaneous IgPro20 (Hizentra(®), CSL Behring, King of Prussia, PA, USA) administered at high infusion parameters (> 25 mL and > 25 mL/h per injection site) in patients with primary immunodeficiency. METHODS: The Hizentra(®) Label Optimization (HILO) study was an open-label, parallel-arm, non-randomized study (NCT03033745) of IgPro20 using a forced upward titration design for infusion parameters. Patients experienced with pump-assisted IgPro20 infusions received weekly IgPro20 infusions at a stable dose in the Pump-Assisted Volume Cohort (N = 15; 25–50 mL per injection site) and in the Pump-Assisted Flow Rate Cohort (N = 18; 25–100 mL/h per injection site). Responder rates (percentage of patients who successfully completed ≥ 75% of planned infusions), safety outcomes, and serum immunoglobulin G (IgG) trough levels were evaluated. RESULTS: Responder rates were 86.7% (13/15, 25 mL) and 73.3% (11/15, 40 and 50 mL) in the Volume Cohort, and 77.8% (14/18, 25 and 50 mL/h), 66.7% (12/18, 75 mL/h), and 61.1% (11/18, 100 mL/h) in the Flow Rate Cohort. Infusion compliance was ≥ 90% in all patients in the Volume Cohort and in 83.3% of patients in the Flow Rate Cohort. The number of injection sites (Volume Cohort) and the infusion duration (Flow Rate Cohort) decreased with increasing infusion parameters. The rate of treatment-emergent adverse events per infusion was low (0.138 [Volume Cohort] and 0.216 [Flow Rate Cohort]). Serum IgG levels remained stable during the study. CONCLUSION: Pump-assisted IgPro20 infusions are feasible at 50 mL and 100 mL/h per injection site in treatment-experienced patients, which may result in fewer injection sites and shorter infusion times. TRIAL REGISTRATION: NCT03033745; registered January 27, 2017 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10875-020-00912-5. Springer US 2021-01-06 2021 /pmc/articles/PMC7858210/ /pubmed/33409867 http://dx.doi.org/10.1007/s10875-020-00912-5 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Anderson, John T.
Bonagura, Vincent R.
Cowan, Juthaporn
Hsu, Connie
Mustafa, S. Shahzad
Patel, Niraj C.
Routes, John M.
Sriaroon, Panida
Vinh, Donald C.
Hofmann, Jutta H.
Praus, Michaela
Rojavin, Mikhail A.
Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title_full Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title_fullStr Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title_full_unstemmed Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title_short Safety and Tolerability of Subcutaneous IgPro20 at High Infusion Parameters in Patients with Primary Immunodeficiency: Findings from the Pump-Assisted Administration Cohorts of the HILO Study
title_sort safety and tolerability of subcutaneous igpro20 at high infusion parameters in patients with primary immunodeficiency: findings from the pump-assisted administration cohorts of the hilo study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858210/
https://www.ncbi.nlm.nih.gov/pubmed/33409867
http://dx.doi.org/10.1007/s10875-020-00912-5
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