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Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients

Due to insufficient quantitative evaluation of the clinic-pathological features and prognosis of young colorectal cancer (CRC) with mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRC), the aim of our study was to develop a nomogram to identify the prognostic predictors for overall sur...

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Autores principales: Wang, Baochun, Zeng, Juntao, Liu, Yuren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639454/
https://www.ncbi.nlm.nih.gov/pubmed/30692229
http://dx.doi.org/10.1042/BSR20181863
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author Wang, Baochun
Zeng, Juntao
Liu, Yuren
author_facet Wang, Baochun
Zeng, Juntao
Liu, Yuren
author_sort Wang, Baochun
collection PubMed
description Due to insufficient quantitative evaluation of the clinic-pathological features and prognosis of young colorectal cancer (CRC) with mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRC), the aim of our study was to develop a nomogram to identify the prognostic predictors for overall survival (OS) in this patient population. We retrospectively evaluated the patient records of MAC and SRC patients aged ≤ 40 years. Kaplan–Meier analysis and log-rank testing were performed to estimate OS. A nomogram predicting OS was created for risk quantitation and decision tree analysis was performed for patient grouping. With a median follow-up of 36.5 months, we included a total of 90 young CRC patients for analysis. The overall cumulate 5-year OS rate was 57.7% (95% confidence interval (CI): 45.1–68.5%). The estimated 5-year OS was 62.9% (95% CI: 48.5–74.3%) for MAC and 37.3% (95% CI: 14.4–61.2%) for SRC (P=0.021). The recurrence rate was significantly greater in the SRC group compared with the mucinous group (52.4 compared with 26.1%, P=0.047). In the multivariate Cox regression model, preoperative carcinoembryonic antigen (CEA) levels and cycles of adjuvant chemotherapy (CT) were found to be an independent prognostic factor for OS (hazard ratio (HR): 2.43; 95% CI: 1.13–5.62, P=0.024; HR: 0.21; 95% CI: 0.083–0.57, P=0.002, respectively). Nomograms predicting 3- and 5-year OS were established that performed well (concordance index (c-indexes) of 0.636, 95% CI: 0.549–723) for OS. For MAC and SRC disease, a greater proportion of young patients present with advanced disease, and the prognosis for young SRC patients is poorer than MAC. Furthermore, preoperative CEA levels and cycles of adjuvant CT seem to independently affect the OS in this patient population.
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spelling pubmed-66394542019-07-29 Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients Wang, Baochun Zeng, Juntao Liu, Yuren Biosci Rep Research Articles Due to insufficient quantitative evaluation of the clinic-pathological features and prognosis of young colorectal cancer (CRC) with mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRC), the aim of our study was to develop a nomogram to identify the prognostic predictors for overall survival (OS) in this patient population. We retrospectively evaluated the patient records of MAC and SRC patients aged ≤ 40 years. Kaplan–Meier analysis and log-rank testing were performed to estimate OS. A nomogram predicting OS was created for risk quantitation and decision tree analysis was performed for patient grouping. With a median follow-up of 36.5 months, we included a total of 90 young CRC patients for analysis. The overall cumulate 5-year OS rate was 57.7% (95% confidence interval (CI): 45.1–68.5%). The estimated 5-year OS was 62.9% (95% CI: 48.5–74.3%) for MAC and 37.3% (95% CI: 14.4–61.2%) for SRC (P=0.021). The recurrence rate was significantly greater in the SRC group compared with the mucinous group (52.4 compared with 26.1%, P=0.047). In the multivariate Cox regression model, preoperative carcinoembryonic antigen (CEA) levels and cycles of adjuvant chemotherapy (CT) were found to be an independent prognostic factor for OS (hazard ratio (HR): 2.43; 95% CI: 1.13–5.62, P=0.024; HR: 0.21; 95% CI: 0.083–0.57, P=0.002, respectively). Nomograms predicting 3- and 5-year OS were established that performed well (concordance index (c-indexes) of 0.636, 95% CI: 0.549–723) for OS. For MAC and SRC disease, a greater proportion of young patients present with advanced disease, and the prognosis for young SRC patients is poorer than MAC. Furthermore, preoperative CEA levels and cycles of adjuvant CT seem to independently affect the OS in this patient population. Portland Press Ltd. 2019-07-19 /pmc/articles/PMC6639454/ /pubmed/30692229 http://dx.doi.org/10.1042/BSR20181863 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Wang, Baochun
Zeng, Juntao
Liu, Yuren
Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title_full Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title_fullStr Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title_full_unstemmed Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title_short Using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
title_sort using nomograms to predict prognostic factors in young colorectal mucinous and signet-ring cell adenocarcinoma patients
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639454/
https://www.ncbi.nlm.nih.gov/pubmed/30692229
http://dx.doi.org/10.1042/BSR20181863
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