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Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma
Treatment of malignant tumors, such as rhabdomyosarcoma (RMS), can improve overall survival (OS). It is time-consuming and expensive for patients to obtain benefits from randomized controlled trials (RCTs) with OS as the primary end-point. Therefore, another surrogate end-point is necessary; however...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653385/ https://www.ncbi.nlm.nih.gov/pubmed/36371419 http://dx.doi.org/10.1038/s41598-022-23944-w |
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author | Kubota, Yuta Tanaka, Kazuhiro Kawano, Masanori Iwasaki, Tatsuya Itonaga, Ichiro Tsumura, Hiroshi |
author_facet | Kubota, Yuta Tanaka, Kazuhiro Kawano, Masanori Iwasaki, Tatsuya Itonaga, Ichiro Tsumura, Hiroshi |
author_sort | Kubota, Yuta |
collection | PubMed |
description | Treatment of malignant tumors, such as rhabdomyosarcoma (RMS), can improve overall survival (OS). It is time-consuming and expensive for patients to obtain benefits from randomized controlled trials (RCTs) with OS as the primary end-point. Therefore, another surrogate end-point is necessary; however, there is no report on the surrogacy analysis of RMS. In this study, we performed a systematic review of RCTs, involving patients with newly diagnosed RMS, and 11 RCTs were identified. We performed a meta-analysis to assess the surrogacy of intermediate end-points for OS. The correlations between surrogate end-points and OS were investigated using Spearman's rank correlation coefficient (ρ). The coefficient of determination (R(2)) was employed to measure the strength of the association. A total of 5183 patients were randomly allocated to 34 treatment groups. A marginal correlation (R(2) = 0.281, ρ = 0.445) between the hazard ratios (HRs) for event-free survival (EFS) and OS was observed. In patients with localized RMS, the EFS HR had a weaker correlation with OS HR in the sensitivity analysis than that in the primary analysis. Overall, the surrogacy of EFS for OS cannot be confirmed. |
format | Online Article Text |
id | pubmed-9653385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96533852022-11-15 Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma Kubota, Yuta Tanaka, Kazuhiro Kawano, Masanori Iwasaki, Tatsuya Itonaga, Ichiro Tsumura, Hiroshi Sci Rep Article Treatment of malignant tumors, such as rhabdomyosarcoma (RMS), can improve overall survival (OS). It is time-consuming and expensive for patients to obtain benefits from randomized controlled trials (RCTs) with OS as the primary end-point. Therefore, another surrogate end-point is necessary; however, there is no report on the surrogacy analysis of RMS. In this study, we performed a systematic review of RCTs, involving patients with newly diagnosed RMS, and 11 RCTs were identified. We performed a meta-analysis to assess the surrogacy of intermediate end-points for OS. The correlations between surrogate end-points and OS were investigated using Spearman's rank correlation coefficient (ρ). The coefficient of determination (R(2)) was employed to measure the strength of the association. A total of 5183 patients were randomly allocated to 34 treatment groups. A marginal correlation (R(2) = 0.281, ρ = 0.445) between the hazard ratios (HRs) for event-free survival (EFS) and OS was observed. In patients with localized RMS, the EFS HR had a weaker correlation with OS HR in the sensitivity analysis than that in the primary analysis. Overall, the surrogacy of EFS for OS cannot be confirmed. Nature Publishing Group UK 2022-11-12 /pmc/articles/PMC9653385/ /pubmed/36371419 http://dx.doi.org/10.1038/s41598-022-23944-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kubota, Yuta Tanaka, Kazuhiro Kawano, Masanori Iwasaki, Tatsuya Itonaga, Ichiro Tsumura, Hiroshi Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title | Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title_full | Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title_fullStr | Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title_full_unstemmed | Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title_short | Surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
title_sort | surrogacy analysis of intermediate end-points for overall survival in randomized controlled trials of rhabdomyosarcoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653385/ https://www.ncbi.nlm.nih.gov/pubmed/36371419 http://dx.doi.org/10.1038/s41598-022-23944-w |
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