Cargando…
A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma
AIMS: Hematological markers that can be used for prognosis prediction for stage I lung adenocarcinoma (LUAD) are still lacking. Here, we examined the prognostic value of a combination of the red cell distribution width (RDW) and carcinoembryonic antigen (CEA), namely, the RDW-CEA score (RCS), in sta...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945661/ https://www.ncbi.nlm.nih.gov/pubmed/36814297 http://dx.doi.org/10.1186/s12957-023-02945-7 |
_version_ | 1784892183289004032 |
---|---|
author | Xu, Hengliang Zhao, Guangqiang Lin, Jixing Ye, Qianwen Xiang, Jia Yan, Bing |
author_facet | Xu, Hengliang Zhao, Guangqiang Lin, Jixing Ye, Qianwen Xiang, Jia Yan, Bing |
author_sort | Xu, Hengliang |
collection | PubMed |
description | AIMS: Hematological markers that can be used for prognosis prediction for stage I lung adenocarcinoma (LUAD) are still lacking. Here, we examined the prognostic value of a combination of the red cell distribution width (RDW) and carcinoembryonic antigen (CEA), namely, the RDW-CEA score (RCS), in stage I LUAD. MATERIALS AND METHODS: A retrospective study with 154 patients with stage I LUAD was conducted. Patients were divided into RCS 1 (decreased RDW and CEA), RCS 2 (decreased RDW and increased CEA, increased RDW and decreased CEA), and RCS 3 (increased RDW and CEA) subgroups based on the best optimal cutoff points of RDW and CEA for overall survival (OS). The differences in other clinicopathological parameters among RCS subgroups were calculated. Disease-free survival (DFS) and OS among these groups were determined by Kaplan–Meier analysis, and risk factors for outcome were calculated by a Cox proportional hazards model. RESULTS: Seventy, 65, and 19 patients were assigned to the RCS 1, 2, and 3 subgroups, respectively. Patients ≥ 60 years (P < 0.001), male sex (P = 0.004), T(2) stage (P = 0.004), and IB stage (P = 0.006) were more significant in the RCS 2 or 3 subgroups. The RCS had a good area under the curve (AUC) for predicting DFS (AUC = 0.81, P < 0.001) and OS (AUC = 0.93, P < 0.001). The DFS (log-rank = 33.26, P < 0.001) and OS (log-rank = 42.05, P < 0.001) were significantly different among RCS subgroups, with RCS 3 patients displaying the worst survival compared to RCS 1 or 2 patients. RCS 3 was also an independent risk factor for both DFS and OS. CONCLUSIONS: RCS is a useful prognostic indicator in stage I LUAD patients, and RCS 3 patients have poorer survival. However, randomized controlled trials are needed to validate our findings in the future. |
format | Online Article Text |
id | pubmed-9945661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99456612023-02-23 A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma Xu, Hengliang Zhao, Guangqiang Lin, Jixing Ye, Qianwen Xiang, Jia Yan, Bing World J Surg Oncol Research AIMS: Hematological markers that can be used for prognosis prediction for stage I lung adenocarcinoma (LUAD) are still lacking. Here, we examined the prognostic value of a combination of the red cell distribution width (RDW) and carcinoembryonic antigen (CEA), namely, the RDW-CEA score (RCS), in stage I LUAD. MATERIALS AND METHODS: A retrospective study with 154 patients with stage I LUAD was conducted. Patients were divided into RCS 1 (decreased RDW and CEA), RCS 2 (decreased RDW and increased CEA, increased RDW and decreased CEA), and RCS 3 (increased RDW and CEA) subgroups based on the best optimal cutoff points of RDW and CEA for overall survival (OS). The differences in other clinicopathological parameters among RCS subgroups were calculated. Disease-free survival (DFS) and OS among these groups were determined by Kaplan–Meier analysis, and risk factors for outcome were calculated by a Cox proportional hazards model. RESULTS: Seventy, 65, and 19 patients were assigned to the RCS 1, 2, and 3 subgroups, respectively. Patients ≥ 60 years (P < 0.001), male sex (P = 0.004), T(2) stage (P = 0.004), and IB stage (P = 0.006) were more significant in the RCS 2 or 3 subgroups. The RCS had a good area under the curve (AUC) for predicting DFS (AUC = 0.81, P < 0.001) and OS (AUC = 0.93, P < 0.001). The DFS (log-rank = 33.26, P < 0.001) and OS (log-rank = 42.05, P < 0.001) were significantly different among RCS subgroups, with RCS 3 patients displaying the worst survival compared to RCS 1 or 2 patients. RCS 3 was also an independent risk factor for both DFS and OS. CONCLUSIONS: RCS is a useful prognostic indicator in stage I LUAD patients, and RCS 3 patients have poorer survival. However, randomized controlled trials are needed to validate our findings in the future. BioMed Central 2023-02-22 /pmc/articles/PMC9945661/ /pubmed/36814297 http://dx.doi.org/10.1186/s12957-023-02945-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Xu, Hengliang Zhao, Guangqiang Lin, Jixing Ye, Qianwen Xiang, Jia Yan, Bing A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title | A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title_full | A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title_fullStr | A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title_full_unstemmed | A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title_short | A combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage I lung adenocarcinoma |
title_sort | combined preoperative red cell distribution width and carcinoembryonic antigen score contribute to prognosis prediction in stage i lung adenocarcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945661/ https://www.ncbi.nlm.nih.gov/pubmed/36814297 http://dx.doi.org/10.1186/s12957-023-02945-7 |
work_keys_str_mv | AT xuhengliang acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT zhaoguangqiang acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT linjixing acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT yeqianwen acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT xiangjia acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT yanbing acombinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT xuhengliang combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT zhaoguangqiang combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT linjixing combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT yeqianwen combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT xiangjia combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma AT yanbing combinedpreoperativeredcelldistributionwidthandcarcinoembryonicantigenscorecontributetoprognosispredictioninstageilungadenocarcinoma |