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Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review
Despite advances in treating Systemic lupus erythematosus (SLE), a proportion of patients continue to face significant morbidity and mortality. Haemopoietic stem cell transplant (HSCT) has been recognized as an option for such patients. We analysed the evidence on efficacy and safety of HSCT in pati...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751808/ https://www.ncbi.nlm.nih.gov/pubmed/31548842 http://dx.doi.org/10.1186/s13223-019-0373-y |
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author | de Silva, Nipun Lakshitha Seneviratne, Suranjith L. |
author_facet | de Silva, Nipun Lakshitha Seneviratne, Suranjith L. |
author_sort | de Silva, Nipun Lakshitha |
collection | PubMed |
description | Despite advances in treating Systemic lupus erythematosus (SLE), a proportion of patients continue to face significant morbidity and mortality. Haemopoietic stem cell transplant (HSCT) has been recognized as an option for such patients. We analysed the evidence on efficacy and safety of HSCT in patients with SLE. A database search was done for articles on HSCT in SLE up to July 2017 in PUBMED, Cochrane library, LILACS and clinical trial registration databases to select prospective or retrospective studies with 8 or more patients. Of the 732 search results from the PUBMED, Cochrane and LILACS database search, following duplicate removal, 15 studies were eligible for detailed assessment. Findings of an additional trial were obtained from the clinical trial registration database. Data were extracted on study design, patient characteristics, nature of intervention, outcomes, complications and study quality. Case reports and small case series were summarised without detailed qualitative analysis. Most of the studies showed remission in the majority of patients. Relapse of the original disease increased with longer follow-up. Common adverse effects included: infections and secondary autoimmune disorders. Short follow up period and lack of randomised controlled trials were the main limitations restricting the generalizability of study results. A meta-analysis was not performed due to heterogeneity of studies. Although HSCT is a viable option in SLE, its exact clinical utility needs to be further evaluated in well-designed studies. |
format | Online Article Text |
id | pubmed-6751808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67518082019-09-23 Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review de Silva, Nipun Lakshitha Seneviratne, Suranjith L. Allergy Asthma Clin Immunol Review Despite advances in treating Systemic lupus erythematosus (SLE), a proportion of patients continue to face significant morbidity and mortality. Haemopoietic stem cell transplant (HSCT) has been recognized as an option for such patients. We analysed the evidence on efficacy and safety of HSCT in patients with SLE. A database search was done for articles on HSCT in SLE up to July 2017 in PUBMED, Cochrane library, LILACS and clinical trial registration databases to select prospective or retrospective studies with 8 or more patients. Of the 732 search results from the PUBMED, Cochrane and LILACS database search, following duplicate removal, 15 studies were eligible for detailed assessment. Findings of an additional trial were obtained from the clinical trial registration database. Data were extracted on study design, patient characteristics, nature of intervention, outcomes, complications and study quality. Case reports and small case series were summarised without detailed qualitative analysis. Most of the studies showed remission in the majority of patients. Relapse of the original disease increased with longer follow-up. Common adverse effects included: infections and secondary autoimmune disorders. Short follow up period and lack of randomised controlled trials were the main limitations restricting the generalizability of study results. A meta-analysis was not performed due to heterogeneity of studies. Although HSCT is a viable option in SLE, its exact clinical utility needs to be further evaluated in well-designed studies. BioMed Central 2019-09-18 /pmc/articles/PMC6751808/ /pubmed/31548842 http://dx.doi.org/10.1186/s13223-019-0373-y Text en © The Author(s) 2019 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review de Silva, Nipun Lakshitha Seneviratne, Suranjith L. Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title | Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title_full | Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title_fullStr | Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title_full_unstemmed | Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title_short | Haemopoietic stem cell transplantation in Systemic lupus erythematosus: a systematic review |
title_sort | haemopoietic stem cell transplantation in systemic lupus erythematosus: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751808/ https://www.ncbi.nlm.nih.gov/pubmed/31548842 http://dx.doi.org/10.1186/s13223-019-0373-y |
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