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Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients
Introduction: Fibromyalgia (FM) is a chronic disorder characterized by widespread pain with an enormous symptom burden. Its treatment efficacy is limited. Its pathogenesis involves immune dysregulation, which includes interleukin-6 (IL-6) production. Methods: We herein reported a case series of FM p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376766/ https://www.ncbi.nlm.nih.gov/pubmed/37509414 http://dx.doi.org/10.3390/biomedicines11071774 |
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author | Tang, Kuo-Tung Liao, Tsai-Ling Chen, Yi-Hsing Chen, Der-Yuan Lai, Kou-Lung |
author_facet | Tang, Kuo-Tung Liao, Tsai-Ling Chen, Yi-Hsing Chen, Der-Yuan Lai, Kou-Lung |
author_sort | Tang, Kuo-Tung |
collection | PubMed |
description | Introduction: Fibromyalgia (FM) is a chronic disorder characterized by widespread pain with an enormous symptom burden. Its treatment efficacy is limited. Its pathogenesis involves immune dysregulation, which includes interleukin-6 (IL-6) production. Methods: We herein reported a case series of FM patients receiving subcutaneous tocilizumab at our institution. FM symptoms were evaluated by the revised Fibromyalgia Impact Questionnaire (FIQR), which included pain level, and the fibromyalgianess scale based on the 2016 criteria of the American College of Rheumatology (ACR). FM symptoms were compared using the Wilcoxon signed-rank test. Neutrophils from primary FM patients and matched healthy controls were also isolated for transcriptome analysis. Results: We presented a total of two primary and four secondary FM patients who had received subcutaneous tocilizumab for a minimum of 12 weeks. All patients had severe symptoms despite standard treatments. Patients’ FIQR and fibromyalgianess both dropped at 4 and 12 weeks. Four (67%) of them reached a pain reduction of ≥30% at 4 weeks, and three (50%) reached a pain reduction of ≥30% at 12 weeks. Possible differentially expressed genes were identified in primary FM patients when compared with controls and after tocilizumab treatment. Conclusions: FM patients likely benefited from subcutaneous tocilizumab therapy. A randomized controlled trial is needed to verify its efficacy. |
format | Online Article Text |
id | pubmed-10376766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103767662023-07-29 Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients Tang, Kuo-Tung Liao, Tsai-Ling Chen, Yi-Hsing Chen, Der-Yuan Lai, Kou-Lung Biomedicines Case Report Introduction: Fibromyalgia (FM) is a chronic disorder characterized by widespread pain with an enormous symptom burden. Its treatment efficacy is limited. Its pathogenesis involves immune dysregulation, which includes interleukin-6 (IL-6) production. Methods: We herein reported a case series of FM patients receiving subcutaneous tocilizumab at our institution. FM symptoms were evaluated by the revised Fibromyalgia Impact Questionnaire (FIQR), which included pain level, and the fibromyalgianess scale based on the 2016 criteria of the American College of Rheumatology (ACR). FM symptoms were compared using the Wilcoxon signed-rank test. Neutrophils from primary FM patients and matched healthy controls were also isolated for transcriptome analysis. Results: We presented a total of two primary and four secondary FM patients who had received subcutaneous tocilizumab for a minimum of 12 weeks. All patients had severe symptoms despite standard treatments. Patients’ FIQR and fibromyalgianess both dropped at 4 and 12 weeks. Four (67%) of them reached a pain reduction of ≥30% at 4 weeks, and three (50%) reached a pain reduction of ≥30% at 12 weeks. Possible differentially expressed genes were identified in primary FM patients when compared with controls and after tocilizumab treatment. Conclusions: FM patients likely benefited from subcutaneous tocilizumab therapy. A randomized controlled trial is needed to verify its efficacy. MDPI 2023-06-21 /pmc/articles/PMC10376766/ /pubmed/37509414 http://dx.doi.org/10.3390/biomedicines11071774 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Tang, Kuo-Tung Liao, Tsai-Ling Chen, Yi-Hsing Chen, Der-Yuan Lai, Kou-Lung Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title | Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title_full | Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title_fullStr | Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title_full_unstemmed | Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title_short | Subcutaneous Tocilizumab May Be Effective in Refractory Fibromyalgia Patients |
title_sort | subcutaneous tocilizumab may be effective in refractory fibromyalgia patients |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376766/ https://www.ncbi.nlm.nih.gov/pubmed/37509414 http://dx.doi.org/10.3390/biomedicines11071774 |
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