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Pharmacodynamics of natalizumab extended interval dosing in MS

OBJECTIVE: To determine if the concentration and saturation of natalizumab (NTZ) administration at extended interval dosing (EID; every 5–8 weeks) over 18 months is able to be maintained in the range considered adequate to sustain the clinical efficacy of NTZ. METHODS: In a cross-sectional assessmen...

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Autores principales: Zhovtis Ryerson, Lana, Li, Xiaochun, Goldberg, Judith D., Hoyt, Tamara, Christensen, Angel, Metzger, Ryan R., Kister, Ilya, Foley, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057061/
https://www.ncbi.nlm.nih.gov/pubmed/32019876
http://dx.doi.org/10.1212/NXI.0000000000000672
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author Zhovtis Ryerson, Lana
Li, Xiaochun
Goldberg, Judith D.
Hoyt, Tamara
Christensen, Angel
Metzger, Ryan R.
Kister, Ilya
Foley, John
author_facet Zhovtis Ryerson, Lana
Li, Xiaochun
Goldberg, Judith D.
Hoyt, Tamara
Christensen, Angel
Metzger, Ryan R.
Kister, Ilya
Foley, John
author_sort Zhovtis Ryerson, Lana
collection PubMed
description OBJECTIVE: To determine if the concentration and saturation of natalizumab (NTZ) administration at extended interval dosing (EID; every 5–8 weeks) over 18 months is able to be maintained in the range considered adequate to sustain the clinical efficacy of NTZ. METHODS: In a cross-sectional assessment of patients with multiple sclerosis (MS) who received standard interval dosing (every 4 weeks) or EID, serum NTZ concentrations were measured using ELISA, and α(4)-integrin receptor saturations were analyzed via cytometry, in blood samples obtained at trough timepoints. RESULTS: Trough serum concentration was above the “therapeutic” concentration of 2.0 μg/mL in 72% of EID patients. Trough saturation was above the “therapeutic” 50% threshold in 79% of EID-treated patients. Our model predicted that at least 9 NTZ infusions/year are required to maintain adequate trough saturation and concentration levels. Higher body mass index (BMI) was a predictor of suboptimal trough saturation on EID NTZ. CONCLUSIONS: Trough α4-integrin receptor saturation >50% correlated with high clinical efficacy of NTZ in previous studies. A continual treatment with EID maintains receptor saturation and concentration that are in the “therapeutic range” for most patients. This finding provides biological plausibility for the clinical efficacy of NTZ EID. Patients with higher BMI may require closer clinical and MRI follow-up.
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spelling pubmed-70570612020-03-13 Pharmacodynamics of natalizumab extended interval dosing in MS Zhovtis Ryerson, Lana Li, Xiaochun Goldberg, Judith D. Hoyt, Tamara Christensen, Angel Metzger, Ryan R. Kister, Ilya Foley, John Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To determine if the concentration and saturation of natalizumab (NTZ) administration at extended interval dosing (EID; every 5–8 weeks) over 18 months is able to be maintained in the range considered adequate to sustain the clinical efficacy of NTZ. METHODS: In a cross-sectional assessment of patients with multiple sclerosis (MS) who received standard interval dosing (every 4 weeks) or EID, serum NTZ concentrations were measured using ELISA, and α(4)-integrin receptor saturations were analyzed via cytometry, in blood samples obtained at trough timepoints. RESULTS: Trough serum concentration was above the “therapeutic” concentration of 2.0 μg/mL in 72% of EID patients. Trough saturation was above the “therapeutic” 50% threshold in 79% of EID-treated patients. Our model predicted that at least 9 NTZ infusions/year are required to maintain adequate trough saturation and concentration levels. Higher body mass index (BMI) was a predictor of suboptimal trough saturation on EID NTZ. CONCLUSIONS: Trough α4-integrin receptor saturation >50% correlated with high clinical efficacy of NTZ in previous studies. A continual treatment with EID maintains receptor saturation and concentration that are in the “therapeutic range” for most patients. This finding provides biological plausibility for the clinical efficacy of NTZ EID. Patients with higher BMI may require closer clinical and MRI follow-up. Lippincott Williams & Wilkins 2020-02-03 /pmc/articles/PMC7057061/ /pubmed/32019876 http://dx.doi.org/10.1212/NXI.0000000000000672 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Zhovtis Ryerson, Lana
Li, Xiaochun
Goldberg, Judith D.
Hoyt, Tamara
Christensen, Angel
Metzger, Ryan R.
Kister, Ilya
Foley, John
Pharmacodynamics of natalizumab extended interval dosing in MS
title Pharmacodynamics of natalizumab extended interval dosing in MS
title_full Pharmacodynamics of natalizumab extended interval dosing in MS
title_fullStr Pharmacodynamics of natalizumab extended interval dosing in MS
title_full_unstemmed Pharmacodynamics of natalizumab extended interval dosing in MS
title_short Pharmacodynamics of natalizumab extended interval dosing in MS
title_sort pharmacodynamics of natalizumab extended interval dosing in ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057061/
https://www.ncbi.nlm.nih.gov/pubmed/32019876
http://dx.doi.org/10.1212/NXI.0000000000000672
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