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Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study
Background This study aims to develop functional nomograms to predict specific distant metastatic sites and overall survival (OS) of colorectal cancer (CRC) patients. Methods CRC case data were retrospectively recruited from a large population‐based public dataset. Nomograms were developed to predic...
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Published in: | Clinical and translational medicine 2020-03, Vol.10 (1), p.169-181 |
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creator | Mo, Shaobo Cai, Xin Zhou, Zheng Li, Yaqi Hu, Xiang Ma, Xiaoji Zhang, Long Cai, Sanjun Peng, Junjie |
description | Background
This study aims to develop functional nomograms to predict specific distant metastatic sites and overall survival (OS) of colorectal cancer (CRC) patients.
Methods
CRC case data were retrospectively recruited from a large population‐based public dataset. Nomograms were developed to predict the probabilities of specific distant metastatic sites and OS of CRC patients. The performance of nomogram was evaluated with the concordance index (C‐index), calibration curves, area under the curve (AUC), and decision curve analysis (DCA).
Results
A total of 142 343 cases were included in the current study. On the basis of univariate and multivariate analyses, clinicopathological features were correlated with specific distant metastatic sites and survival outcomes and were used to establish nomograms. The nomograms showed excellent accuracy in predicting specific distant metastatic sites. The C‐indexes for the prediction of liver, lung, bone, and brain metastases were 0.82 (95% confidence interval (CI), 0.81‐0.83), 0.80 (95% CI, 0.78‐0.81), 0.83 (95% CI, 0.79‐0.86), and 0.73 (95% CI, 0.72‐0.84), respectively. Then, a prognostic nomogram integrating clinicopathological features and specific distant metastatic sites was established to predict 1‐, 3‐, and 5‐year OS of CRC, with AUCs of 0.764 (95% CI, 0.741‐0.783), 0.762 (95% CI, 0.745‐0.781), and 0.745 (95% CI, 0.730‐0.761), respectively. DCA showed that the prognostic nomogram had a better clinical application value than current TNM staging system.
Conclusions
Based on clinicopathological features, original nomograms were constructed for clinicians to predict specific distant metastatic sites and OS of CRC patients. These models could help to support the postoperative personalized assessment. |
doi_str_mv | 10.1002/ctm2.20 |
format | article |
fullrecord | <record><control><sourceid>wiley_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_0215a9148f3745c58811b3b9688809dc</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_0215a9148f3745c58811b3b9688809dc</doaj_id><sourcerecordid>CTM220</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4010-9d5fad825529a10539ae5e837ef3c9d6d1b3d2956370ba21c362e72701093c83</originalsourceid><addsrcrecordid>eNp1kc1u1DAQxyMEolWpeAPkGwe0rT_ixOaAVK34qFTgsndrYk-CKyeO7OxWe-sj8AA8HU-Cy5aqPeCLZ8b__280nqp6zegZo5Sf22XkZ5w-q445pWzFBG-eP4qPqtOcr2k5qta65S-rI8ElVZS3x9Wvb3GMQ4Ixkz4mMid03i5-Gkie0freW-J8XmBayIgLlGgppewXzAQmR-IOE4RA8jbt_A4CiT2xMcSEdimZhcliwRYXTkt-Ty5IgDQgmeO8DaUap9-3PzvI6EhCCCW5iSk4kpet27-qXvQQMp7e3yfV5tPHzfrL6ur758v1xdXK1pTRlXayB6e4lFwDo1JoQIlKtNgLq13jWCcc17IRLe2AMysaji1vi1cLq8RJdXnAugjXZk5-hLQ3Ebz5W4hpMJDK2AEN5UyCZrXqRVtLK5ViBd7pRilFtbOF9eHAmrfdiM6Wqcv_PIE-fZn8DzPEnWl5TZXkBfD2ALAp5pywf_Ayau7Wbe7WbTgtyjePWz3o_i23CN4dBDc-4P5_HLPefOUF9wcI67iL</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study</title><source>Wiley Online Library Open Access</source><source>Springer Nature - SpringerLink Journals - Fully Open Access </source><source>PubMed Central</source><creator>Mo, Shaobo ; Cai, Xin ; Zhou, Zheng ; Li, Yaqi ; Hu, Xiang ; Ma, Xiaoji ; Zhang, Long ; Cai, Sanjun ; Peng, Junjie</creator><creatorcontrib>Mo, Shaobo ; Cai, Xin ; Zhou, Zheng ; Li, Yaqi ; Hu, Xiang ; Ma, Xiaoji ; Zhang, Long ; Cai, Sanjun ; Peng, Junjie</creatorcontrib><description>Background
This study aims to develop functional nomograms to predict specific distant metastatic sites and overall survival (OS) of colorectal cancer (CRC) patients.
Methods
CRC case data were retrospectively recruited from a large population‐based public dataset. Nomograms were developed to predict the probabilities of specific distant metastatic sites and OS of CRC patients. The performance of nomogram was evaluated with the concordance index (C‐index), calibration curves, area under the curve (AUC), and decision curve analysis (DCA).
Results
A total of 142 343 cases were included in the current study. On the basis of univariate and multivariate analyses, clinicopathological features were correlated with specific distant metastatic sites and survival outcomes and were used to establish nomograms. The nomograms showed excellent accuracy in predicting specific distant metastatic sites. The C‐indexes for the prediction of liver, lung, bone, and brain metastases were 0.82 (95% confidence interval (CI), 0.81‐0.83), 0.80 (95% CI, 0.78‐0.81), 0.83 (95% CI, 0.79‐0.86), and 0.73 (95% CI, 0.72‐0.84), respectively. Then, a prognostic nomogram integrating clinicopathological features and specific distant metastatic sites was established to predict 1‐, 3‐, and 5‐year OS of CRC, with AUCs of 0.764 (95% CI, 0.741‐0.783), 0.762 (95% CI, 0.745‐0.781), and 0.745 (95% CI, 0.730‐0.761), respectively. DCA showed that the prognostic nomogram had a better clinical application value than current TNM staging system.
Conclusions
Based on clinicopathological features, original nomograms were constructed for clinicians to predict specific distant metastatic sites and OS of CRC patients. These models could help to support the postoperative personalized assessment.</description><identifier>ISSN: 2001-1326</identifier><identifier>EISSN: 2001-1326</identifier><identifier>DOI: 10.1002/ctm2.20</identifier><identifier>PMID: 32508027</identifier><language>eng</language><publisher>United States: John Wiley and Sons Inc</publisher><subject>colorectal cancer ; decision curve analysis ; distant metastasis ; nomogram ; overall survival</subject><ispartof>Clinical and translational medicine, 2020-03, Vol.10 (1), p.169-181</ispartof><rights>2020 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics</rights><rights>2020 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4010-9d5fad825529a10539ae5e837ef3c9d6d1b3d2956370ba21c362e72701093c83</citedby><cites>FETCH-LOGICAL-c4010-9d5fad825529a10539ae5e837ef3c9d6d1b3d2956370ba21c362e72701093c83</cites><orcidid>0000-0002-0371-4960</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240852/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240852/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,27923,27924,46051,46475,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32508027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mo, Shaobo</creatorcontrib><creatorcontrib>Cai, Xin</creatorcontrib><creatorcontrib>Zhou, Zheng</creatorcontrib><creatorcontrib>Li, Yaqi</creatorcontrib><creatorcontrib>Hu, Xiang</creatorcontrib><creatorcontrib>Ma, Xiaoji</creatorcontrib><creatorcontrib>Zhang, Long</creatorcontrib><creatorcontrib>Cai, Sanjun</creatorcontrib><creatorcontrib>Peng, Junjie</creatorcontrib><title>Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study</title><title>Clinical and translational medicine</title><addtitle>Clin Transl Med</addtitle><description>Background
This study aims to develop functional nomograms to predict specific distant metastatic sites and overall survival (OS) of colorectal cancer (CRC) patients.
Methods
CRC case data were retrospectively recruited from a large population‐based public dataset. Nomograms were developed to predict the probabilities of specific distant metastatic sites and OS of CRC patients. The performance of nomogram was evaluated with the concordance index (C‐index), calibration curves, area under the curve (AUC), and decision curve analysis (DCA).
Results
A total of 142 343 cases were included in the current study. On the basis of univariate and multivariate analyses, clinicopathological features were correlated with specific distant metastatic sites and survival outcomes and were used to establish nomograms. The nomograms showed excellent accuracy in predicting specific distant metastatic sites. The C‐indexes for the prediction of liver, lung, bone, and brain metastases were 0.82 (95% confidence interval (CI), 0.81‐0.83), 0.80 (95% CI, 0.78‐0.81), 0.83 (95% CI, 0.79‐0.86), and 0.73 (95% CI, 0.72‐0.84), respectively. Then, a prognostic nomogram integrating clinicopathological features and specific distant metastatic sites was established to predict 1‐, 3‐, and 5‐year OS of CRC, with AUCs of 0.764 (95% CI, 0.741‐0.783), 0.762 (95% CI, 0.745‐0.781), and 0.745 (95% CI, 0.730‐0.761), respectively. DCA showed that the prognostic nomogram had a better clinical application value than current TNM staging system.
Conclusions
Based on clinicopathological features, original nomograms were constructed for clinicians to predict specific distant metastatic sites and OS of CRC patients. These models could help to support the postoperative personalized assessment.</description><subject>colorectal cancer</subject><subject>decision curve analysis</subject><subject>distant metastasis</subject><subject>nomogram</subject><subject>overall survival</subject><issn>2001-1326</issn><issn>2001-1326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>DOA</sourceid><recordid>eNp1kc1u1DAQxyMEolWpeAPkGwe0rT_ixOaAVK34qFTgsndrYk-CKyeO7OxWe-sj8AA8HU-Cy5aqPeCLZ8b__280nqp6zegZo5Sf22XkZ5w-q445pWzFBG-eP4qPqtOcr2k5qta65S-rI8ElVZS3x9Wvb3GMQ4Ixkz4mMid03i5-Gkie0freW-J8XmBayIgLlGgppewXzAQmR-IOE4RA8jbt_A4CiT2xMcSEdimZhcliwRYXTkt-Ty5IgDQgmeO8DaUap9-3PzvI6EhCCCW5iSk4kpet27-qXvQQMp7e3yfV5tPHzfrL6ur758v1xdXK1pTRlXayB6e4lFwDo1JoQIlKtNgLq13jWCcc17IRLe2AMysaji1vi1cLq8RJdXnAugjXZk5-hLQ3Ebz5W4hpMJDK2AEN5UyCZrXqRVtLK5ViBd7pRilFtbOF9eHAmrfdiM6Wqcv_PIE-fZn8DzPEnWl5TZXkBfD2ALAp5pywf_Ayau7Wbe7WbTgtyjePWz3o_i23CN4dBDc-4P5_HLPefOUF9wcI67iL</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Mo, Shaobo</creator><creator>Cai, Xin</creator><creator>Zhou, Zheng</creator><creator>Li, Yaqi</creator><creator>Hu, Xiang</creator><creator>Ma, Xiaoji</creator><creator>Zhang, Long</creator><creator>Cai, Sanjun</creator><creator>Peng, Junjie</creator><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0371-4960</orcidid></search><sort><creationdate>202003</creationdate><title>Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study</title><author>Mo, Shaobo ; Cai, Xin ; Zhou, Zheng ; Li, Yaqi ; Hu, Xiang ; Ma, Xiaoji ; Zhang, Long ; Cai, Sanjun ; Peng, Junjie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4010-9d5fad825529a10539ae5e837ef3c9d6d1b3d2956370ba21c362e72701093c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>colorectal cancer</topic><topic>decision curve analysis</topic><topic>distant metastasis</topic><topic>nomogram</topic><topic>overall survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mo, Shaobo</creatorcontrib><creatorcontrib>Cai, Xin</creatorcontrib><creatorcontrib>Zhou, Zheng</creatorcontrib><creatorcontrib>Li, Yaqi</creatorcontrib><creatorcontrib>Hu, Xiang</creatorcontrib><creatorcontrib>Ma, Xiaoji</creatorcontrib><creatorcontrib>Zhang, Long</creatorcontrib><creatorcontrib>Cai, Sanjun</creatorcontrib><creatorcontrib>Peng, Junjie</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ: Directory of Open Access Journals</collection><jtitle>Clinical and translational medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mo, Shaobo</au><au>Cai, Xin</au><au>Zhou, Zheng</au><au>Li, Yaqi</au><au>Hu, Xiang</au><au>Ma, Xiaoji</au><au>Zhang, Long</au><au>Cai, Sanjun</au><au>Peng, Junjie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study</atitle><jtitle>Clinical and translational medicine</jtitle><addtitle>Clin Transl Med</addtitle><date>2020-03</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>169</spage><epage>181</epage><pages>169-181</pages><issn>2001-1326</issn><eissn>2001-1326</eissn><abstract>Background
This study aims to develop functional nomograms to predict specific distant metastatic sites and overall survival (OS) of colorectal cancer (CRC) patients.
Methods
CRC case data were retrospectively recruited from a large population‐based public dataset. Nomograms were developed to predict the probabilities of specific distant metastatic sites and OS of CRC patients. The performance of nomogram was evaluated with the concordance index (C‐index), calibration curves, area under the curve (AUC), and decision curve analysis (DCA).
Results
A total of 142 343 cases were included in the current study. On the basis of univariate and multivariate analyses, clinicopathological features were correlated with specific distant metastatic sites and survival outcomes and were used to establish nomograms. The nomograms showed excellent accuracy in predicting specific distant metastatic sites. The C‐indexes for the prediction of liver, lung, bone, and brain metastases were 0.82 (95% confidence interval (CI), 0.81‐0.83), 0.80 (95% CI, 0.78‐0.81), 0.83 (95% CI, 0.79‐0.86), and 0.73 (95% CI, 0.72‐0.84), respectively. Then, a prognostic nomogram integrating clinicopathological features and specific distant metastatic sites was established to predict 1‐, 3‐, and 5‐year OS of CRC, with AUCs of 0.764 (95% CI, 0.741‐0.783), 0.762 (95% CI, 0.745‐0.781), and 0.745 (95% CI, 0.730‐0.761), respectively. DCA showed that the prognostic nomogram had a better clinical application value than current TNM staging system.
Conclusions
Based on clinicopathological features, original nomograms were constructed for clinicians to predict specific distant metastatic sites and OS of CRC patients. These models could help to support the postoperative personalized assessment.</abstract><cop>United States</cop><pub>John Wiley and Sons Inc</pub><pmid>32508027</pmid><doi>10.1002/ctm2.20</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-0371-4960</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | colorectal cancer decision curve analysis distant metastasis nomogram overall survival |
title | Nomograms for predicting specific distant metastatic sites and overall survival of colorectal cancer patients: A large population‐based real‐world study |
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