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Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis
BACKGROUND: Research on the correlation between circulating tumor cells (CTCs) and gastric cancer (GC) has increased rapidly in recent years. However, whether CTCs are associated with GC patient prognosis is highly controversial. OBJECTIVE: This study aims to evaluate the value of CTCs to predict th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331349/ https://www.ncbi.nlm.nih.gov/pubmed/37435560 http://dx.doi.org/10.1177/17588359231183678 |
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author | Jin, Tao Liang, Pan-Ping Chen, Ze-Hua He, Feng-Jun Li, Ze-Dong Chen, Zheng-Wen Hu, Jian-Kun Yang, Kun |
author_facet | Jin, Tao Liang, Pan-Ping Chen, Ze-Hua He, Feng-Jun Li, Ze-Dong Chen, Zheng-Wen Hu, Jian-Kun Yang, Kun |
author_sort | Jin, Tao |
collection | PubMed |
description | BACKGROUND: Research on the correlation between circulating tumor cells (CTCs) and gastric cancer (GC) has increased rapidly in recent years. However, whether CTCs are associated with GC patient prognosis is highly controversial. OBJECTIVE: This study aims to evaluate the value of CTCs to predict the prognosis of GC patients. DESIGN: A meta-analysis. DATA SOURCES AND METHODS: We searched the PubMed, Embase, and Cochrane Library databases for studies that reported the prognostic value of CTCs in GC patients before October 2022. The association between CTCs and overall survival (OS) and disease-free survival (DFS)/recurrence-free survival (RFS) and progression-free survival (PFS) of GC patients was assessed. Subgroup analyses were stratified by sampling times (pre-treatment and post-treatment), detection targets, detection method, treatment method, tumor stage, region, and HR (Hazard Ratio) extraction methods. Sensitivity analysis was performed by removing individual studies to assess the stability of the results. Publication bias was evaluated using funnel plots, Egger’s test, and Begg’s test. RESULTS: We initially screened 2000 studies, of which 28 were available for further analysis, involving 2383 GC patients. The pooled analysis concluded that the detection of CTCs was associated with poor OS (HR = 1.933, 95% CI 1.657–2.256, p < 0.001), DFS/RFS (HR = 3.228, 95% CI 2.475–4.211, p < 0.001), and PFS (HR = 3.272, 95% CI 1.970–5.435, p < 0.001). Furthermore, the subgroup analysis stratified by tumor stage (p < 0.01), HR extraction methods (p < 0.001), detection targets (p < 0.001), detection method (p < 0.001), sampling times (p < 0.001), and treatment method (p < 0.001) all showed that CTC detection was associated with poor OS and DFS/RFS for GC patients. Furthermore, the study showed that CTCs were associated with the poor DFS/RFS of GC when CTCs were detected for patients from Asian or No-Asian regions (p < 0.05). In addition, higher CTCs predicted poorer OS for GC patients who are from Asian regions (p < 0.001), but without statistical difference for GC patients from No-Asian regions (p = 0.490). CONCLUSION: CTC detection in peripheral blood was associated with poor OS, DFS/RFS, and PFS in patients with GC. |
format | Online Article Text |
id | pubmed-10331349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-103313492023-07-11 Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis Jin, Tao Liang, Pan-Ping Chen, Ze-Hua He, Feng-Jun Li, Ze-Dong Chen, Zheng-Wen Hu, Jian-Kun Yang, Kun Ther Adv Med Oncol Liquid Biopsy in Gastrointestinal Cancers: circulating tumor DNA (ctDNA) and circulating tumor cell (CTC)-based precision oncology BACKGROUND: Research on the correlation between circulating tumor cells (CTCs) and gastric cancer (GC) has increased rapidly in recent years. However, whether CTCs are associated with GC patient prognosis is highly controversial. OBJECTIVE: This study aims to evaluate the value of CTCs to predict the prognosis of GC patients. DESIGN: A meta-analysis. DATA SOURCES AND METHODS: We searched the PubMed, Embase, and Cochrane Library databases for studies that reported the prognostic value of CTCs in GC patients before October 2022. The association between CTCs and overall survival (OS) and disease-free survival (DFS)/recurrence-free survival (RFS) and progression-free survival (PFS) of GC patients was assessed. Subgroup analyses were stratified by sampling times (pre-treatment and post-treatment), detection targets, detection method, treatment method, tumor stage, region, and HR (Hazard Ratio) extraction methods. Sensitivity analysis was performed by removing individual studies to assess the stability of the results. Publication bias was evaluated using funnel plots, Egger’s test, and Begg’s test. RESULTS: We initially screened 2000 studies, of which 28 were available for further analysis, involving 2383 GC patients. The pooled analysis concluded that the detection of CTCs was associated with poor OS (HR = 1.933, 95% CI 1.657–2.256, p < 0.001), DFS/RFS (HR = 3.228, 95% CI 2.475–4.211, p < 0.001), and PFS (HR = 3.272, 95% CI 1.970–5.435, p < 0.001). Furthermore, the subgroup analysis stratified by tumor stage (p < 0.01), HR extraction methods (p < 0.001), detection targets (p < 0.001), detection method (p < 0.001), sampling times (p < 0.001), and treatment method (p < 0.001) all showed that CTC detection was associated with poor OS and DFS/RFS for GC patients. Furthermore, the study showed that CTCs were associated with the poor DFS/RFS of GC when CTCs were detected for patients from Asian or No-Asian regions (p < 0.05). In addition, higher CTCs predicted poorer OS for GC patients who are from Asian regions (p < 0.001), but without statistical difference for GC patients from No-Asian regions (p = 0.490). CONCLUSION: CTC detection in peripheral blood was associated with poor OS, DFS/RFS, and PFS in patients with GC. SAGE Publications 2023-07-08 /pmc/articles/PMC10331349/ /pubmed/37435560 http://dx.doi.org/10.1177/17588359231183678 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Liquid Biopsy in Gastrointestinal Cancers: circulating tumor DNA (ctDNA) and circulating tumor cell (CTC)-based precision oncology Jin, Tao Liang, Pan-Ping Chen, Ze-Hua He, Feng-Jun Li, Ze-Dong Chen, Zheng-Wen Hu, Jian-Kun Yang, Kun Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title | Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title_full | Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title_fullStr | Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title_full_unstemmed | Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title_short | Association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
title_sort | association between circulating tumor cells in the peripheral blood and the prognosis of gastric cancer patients: a meta-analysis |
topic | Liquid Biopsy in Gastrointestinal Cancers: circulating tumor DNA (ctDNA) and circulating tumor cell (CTC)-based precision oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331349/ https://www.ncbi.nlm.nih.gov/pubmed/37435560 http://dx.doi.org/10.1177/17588359231183678 |
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