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Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis
Background and objectives: Following the discovery of new drugs, physicians and pharmaceutical companies have become interested in examining patients’ mortality and morbidity rates. In this respect, the effects of methotrexate (MTX)+etanercept/infliximab (ETA/INF) therapy on the survival of rheumato...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503221/ https://www.ncbi.nlm.nih.gov/pubmed/31118865 http://dx.doi.org/10.2147/POR.S194408 |
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author | Akhlaghi, Saeed Sahebari, Maryam Mahmoodi, Mahmoud Yaseri, Mehdi Mansournia, Mohammad Ali Zeraati, Hojjat |
author_facet | Akhlaghi, Saeed Sahebari, Maryam Mahmoodi, Mahmoud Yaseri, Mehdi Mansournia, Mohammad Ali Zeraati, Hojjat |
author_sort | Akhlaghi, Saeed |
collection | PubMed |
description | Background and objectives: Following the discovery of new drugs, physicians and pharmaceutical companies have become interested in examining patients’ mortality and morbidity rates. In this respect, the effects of methotrexate (MTX)+etanercept/infliximab (ETA/INF) therapy on the survival of rheumatoid arthritis patients (RA) were evaluated in this study using marginal structural piecewise constant baseline hazard model. Patients and methods: According to the standard protocol, MTX is considered as the first-line treatment for RA patients. If there is no adequate response to MTX, biologic drugs will be added. To compare the survival rates of RA patients in MTX- and MTX+ETA/INF-treated groups, the piecewise constant baseline hazard model was fitted. Then, due to the existence of the time-dependent confounder (VAS) which was affected by previous treatment, the weight for each person-time was calculated via the inverse probability treatment weighting method. These weights were then used by marginal structural piecewise constant baseline hazard model. Finally, these models were compared. Results: The median (IQR) of the follow-up period in patients receiving MTX+ETN/INF and MTX was 11 (15.25) and 11 (31), respectively, and the 8-year survival rate was reported by 70% versus 68%, respectively. First, the piece-wise constant baseline hazard model was fitted. Fitting the given model showed that MTX+ETA/INF had a significant effect on patients’ survival (HR=0.789, 95% CI [0.634, 0.983]). Second, marginal structural piecewise constant baseline hazard model was fitted. But, the results of this model revealed that MTX+ETA/INF did not have a significant impact on patients’ survival (HR=0.968, 95% CI [0.860, 1.090]). Conclusion: Adjusting the pain score over time as a time-dependent confounder via marginal structural piecewise constant baseline hazard model, it has been demonstrated that MTX+ETA/INF does not have a significant effect on patients’ survival rates. Therefore, a significant difference can be found between survival rates of these groups using longitudinal studies. |
format | Online Article Text |
id | pubmed-6503221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-65032212019-05-22 Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis Akhlaghi, Saeed Sahebari, Maryam Mahmoodi, Mahmoud Yaseri, Mehdi Mansournia, Mohammad Ali Zeraati, Hojjat Pragmat Obs Res Original Research Background and objectives: Following the discovery of new drugs, physicians and pharmaceutical companies have become interested in examining patients’ mortality and morbidity rates. In this respect, the effects of methotrexate (MTX)+etanercept/infliximab (ETA/INF) therapy on the survival of rheumatoid arthritis patients (RA) were evaluated in this study using marginal structural piecewise constant baseline hazard model. Patients and methods: According to the standard protocol, MTX is considered as the first-line treatment for RA patients. If there is no adequate response to MTX, biologic drugs will be added. To compare the survival rates of RA patients in MTX- and MTX+ETA/INF-treated groups, the piecewise constant baseline hazard model was fitted. Then, due to the existence of the time-dependent confounder (VAS) which was affected by previous treatment, the weight for each person-time was calculated via the inverse probability treatment weighting method. These weights were then used by marginal structural piecewise constant baseline hazard model. Finally, these models were compared. Results: The median (IQR) of the follow-up period in patients receiving MTX+ETN/INF and MTX was 11 (15.25) and 11 (31), respectively, and the 8-year survival rate was reported by 70% versus 68%, respectively. First, the piece-wise constant baseline hazard model was fitted. Fitting the given model showed that MTX+ETA/INF had a significant effect on patients’ survival (HR=0.789, 95% CI [0.634, 0.983]). Second, marginal structural piecewise constant baseline hazard model was fitted. But, the results of this model revealed that MTX+ETA/INF did not have a significant impact on patients’ survival (HR=0.968, 95% CI [0.860, 1.090]). Conclusion: Adjusting the pain score over time as a time-dependent confounder via marginal structural piecewise constant baseline hazard model, it has been demonstrated that MTX+ETA/INF does not have a significant effect on patients’ survival rates. Therefore, a significant difference can be found between survival rates of these groups using longitudinal studies. Dove 2019-04-18 /pmc/articles/PMC6503221/ /pubmed/31118865 http://dx.doi.org/10.2147/POR.S194408 Text en © 2019 Akhlaghi et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Akhlaghi, Saeed Sahebari, Maryam Mahmoodi, Mahmoud Yaseri, Mehdi Mansournia, Mohammad Ali Zeraati, Hojjat Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title | Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title_full | Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title_fullStr | Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title_full_unstemmed | Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title_short | Casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
title_sort | casual effect of methotrexate+etanercept/infliximab on survival of patients with rheumatoid arthritis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503221/ https://www.ncbi.nlm.nih.gov/pubmed/31118865 http://dx.doi.org/10.2147/POR.S194408 |
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