Cargando…
Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts
BACKGROUND: Approximately 10% of stage I colorectal cancer (CRC) patients experience unfavorable clinical outcomes after surgery. However, little is known about the subset of stage I patients who are predisposed to high risk of recurrence or death. Previous evidence was limited by small sample sizes...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814451/ https://www.ncbi.nlm.nih.gov/pubmed/36600277 http://dx.doi.org/10.1186/s12916-022-02693-7 |
_version_ | 1784864136544387072 |
---|---|
author | Wu, Qingbin Chen, Pengju Shu, Chi Chen, Lin Jin, Zechuan Huang, Jun Wang, Xin Li, Xue Wei, Mingtian Yang, Tinghan Deng, Xiangbing Wu, Aiwen He, Yazhou Wang, Ziqiang |
author_facet | Wu, Qingbin Chen, Pengju Shu, Chi Chen, Lin Jin, Zechuan Huang, Jun Wang, Xin Li, Xue Wei, Mingtian Yang, Tinghan Deng, Xiangbing Wu, Aiwen He, Yazhou Wang, Ziqiang |
author_sort | Wu, Qingbin |
collection | PubMed |
description | BACKGROUND: Approximately 10% of stage I colorectal cancer (CRC) patients experience unfavorable clinical outcomes after surgery. However, little is known about the subset of stage I patients who are predisposed to high risk of recurrence or death. Previous evidence was limited by small sample sizes and lack of validation. METHODS: We aimed to identify early indicators and develop a risk stratification model to inform prognosis of stage I patients by employing two large prospective cohorts. Prognostic factors for stage II tumors, including T stage, number of nodes examined, preoperative carcinoma embryonic antigen (CEA), lymphovascular invasion, perineural invasion (PNI), and tumor grade were investigated in the discovery cohort, and significant findings were further validated in the other cohort. We adopted disease-free survival (DFS) as the primary outcome for maximum statistical power and recurrence rate and overall survival (OS) as secondary outcomes. Hazard ratios (HRs) were estimated from Cox proportional hazard models, which were subsequently utilized to develop a multivariable model to predict DFS. Predictive performance was assessed in relation to discrimination, calibration and net benefit. RESULTS: A total of 728 and 413 patients were included for discovery and validation. Overall, 6.7% and 4.1% of the patients developed recurrences during follow-up. We identified consistent significant effects of PNI and higher preoperative CEA on inferior DFS in both the discovery (PNI: HR = 4.26, 95% CI: 1.70–10.67, p = 0.002; CEA: HR = 1.46, 95% CI: 1.13–1.87, p = 0.003) and the validation analysis (PNI: HR = 3.31, 95% CI: 1.01–10.89, p = 0.049; CEA: HR = 1.58, 95% CI: 1.10–2.28, p = 0.014). They were also significantly associated with recurrence rate. Age at diagnosis was a prominent determinant of OS. A prediction model on DFS using Age at diagnosis, CEA, PNI, and number of LYmph nodes examined (ACEPLY) showed significant discriminative performance (C-index: 0.69, 95% CI:0.60–0.77) in the external validation cohort. Decision curve analysis demonstrated added clinical benefit of applying the model for risk stratification. CONCLUSIONS: PNI and preoperative CEA are useful indicators for inferior survival outcomes of stage I CRC. Identification of stage I patients at high risk of recurrence is feasible using the ACEPLY model, although the predictive performance is yet to be improved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02693-7. |
format | Online Article Text |
id | pubmed-9814451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98144512023-01-06 Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts Wu, Qingbin Chen, Pengju Shu, Chi Chen, Lin Jin, Zechuan Huang, Jun Wang, Xin Li, Xue Wei, Mingtian Yang, Tinghan Deng, Xiangbing Wu, Aiwen He, Yazhou Wang, Ziqiang BMC Med Research Article BACKGROUND: Approximately 10% of stage I colorectal cancer (CRC) patients experience unfavorable clinical outcomes after surgery. However, little is known about the subset of stage I patients who are predisposed to high risk of recurrence or death. Previous evidence was limited by small sample sizes and lack of validation. METHODS: We aimed to identify early indicators and develop a risk stratification model to inform prognosis of stage I patients by employing two large prospective cohorts. Prognostic factors for stage II tumors, including T stage, number of nodes examined, preoperative carcinoma embryonic antigen (CEA), lymphovascular invasion, perineural invasion (PNI), and tumor grade were investigated in the discovery cohort, and significant findings were further validated in the other cohort. We adopted disease-free survival (DFS) as the primary outcome for maximum statistical power and recurrence rate and overall survival (OS) as secondary outcomes. Hazard ratios (HRs) were estimated from Cox proportional hazard models, which were subsequently utilized to develop a multivariable model to predict DFS. Predictive performance was assessed in relation to discrimination, calibration and net benefit. RESULTS: A total of 728 and 413 patients were included for discovery and validation. Overall, 6.7% and 4.1% of the patients developed recurrences during follow-up. We identified consistent significant effects of PNI and higher preoperative CEA on inferior DFS in both the discovery (PNI: HR = 4.26, 95% CI: 1.70–10.67, p = 0.002; CEA: HR = 1.46, 95% CI: 1.13–1.87, p = 0.003) and the validation analysis (PNI: HR = 3.31, 95% CI: 1.01–10.89, p = 0.049; CEA: HR = 1.58, 95% CI: 1.10–2.28, p = 0.014). They were also significantly associated with recurrence rate. Age at diagnosis was a prominent determinant of OS. A prediction model on DFS using Age at diagnosis, CEA, PNI, and number of LYmph nodes examined (ACEPLY) showed significant discriminative performance (C-index: 0.69, 95% CI:0.60–0.77) in the external validation cohort. Decision curve analysis demonstrated added clinical benefit of applying the model for risk stratification. CONCLUSIONS: PNI and preoperative CEA are useful indicators for inferior survival outcomes of stage I CRC. Identification of stage I patients at high risk of recurrence is feasible using the ACEPLY model, although the predictive performance is yet to be improved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02693-7. BioMed Central 2023-01-04 /pmc/articles/PMC9814451/ /pubmed/36600277 http://dx.doi.org/10.1186/s12916-022-02693-7 Text en © The Author(s) 2022 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 Article Wu, Qingbin Chen, Pengju Shu, Chi Chen, Lin Jin, Zechuan Huang, Jun Wang, Xin Li, Xue Wei, Mingtian Yang, Tinghan Deng, Xiangbing Wu, Aiwen He, Yazhou Wang, Ziqiang Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title | Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title_full | Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title_fullStr | Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title_full_unstemmed | Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title_short | Survival outcomes of stage I colorectal cancer: development and validation of the ACEPLY model using two prospective cohorts |
title_sort | survival outcomes of stage i colorectal cancer: development and validation of the aceply model using two prospective cohorts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814451/ https://www.ncbi.nlm.nih.gov/pubmed/36600277 http://dx.doi.org/10.1186/s12916-022-02693-7 |
work_keys_str_mv | AT wuqingbin survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT chenpengju survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT shuchi survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT chenlin survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT jinzechuan survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT huangjun survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT wangxin survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT lixue survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT weimingtian survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT yangtinghan survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT dengxiangbing survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT wuaiwen survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT heyazhou survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts AT wangziqiang survivaloutcomesofstageicolorectalcancerdevelopmentandvalidationoftheaceplymodelusingtwoprospectivecohorts |