Development and Validation of Web-Based Nomograms for Predicting Cause-Specific Mortality in Surgically Resected Nonmetastatic Invasive Breast Cancer: A Population-Based Study
Background This study aims to build nomograms to predict overall survival (OS) and breast cancer-specific death (BCSD) in resected nonmetastatic invasive breast cancer. Patients and Methods Patients extracted from surveillance, epidemiology, and end results database between 2010 and 2014 were analyz...
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Veröffentlicht in: | Annals of surgical oncology 2021-10, Vol.28 (11), p.6537-6550 |
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creator | Chen, Guangyong Jia, Mei Zeng, Qingpeng Zhang, Huiming |
description | Background
This study aims to build nomograms to predict overall survival (OS) and breast cancer-specific death (BCSD) in resected nonmetastatic invasive breast cancer.
Patients and Methods
Patients extracted from surveillance, epidemiology, and end results database between 2010 and 2014 were analyzed. Through multivariate Cox regression and Fine and Gray competing risks regression, independent predictive factors were identified and integrated to build nomograms for predicting OS and BCSD. The models were validated by bootstrap resampling and an independent cohort. Additionally, the models’ performance was measured by the Harrell’s C-index, calibrate curve, and time-dependent receiver operating characteristic (ROC) curves.
Results
In total, 110,180 cases were identified and enrolled in the analysis, with 83,450 in the training cohort and 26,730 in the validation cohort. Several independent predictive factors for OS and BCSD were identified and integrated to construct the nomograms. The C-indexes in the training cohort and validation cohort were 0.759 and 0.772 for predicting OS, and 0.857 and 0.856 for predicting BCSD, respectively. The nomogram models were well calibrated, and the time-dependent ROC curves verified the superiority of our models for clinical usefulness. Significant differences in the OS and BCSD curves were also observed when stratifying patients into several different risk groups. For convenient access, we deployed these proposed nomograms into web-based calculators.
Conclusions
We established and validated novel nomograms for individualized prediction of OS and BCSD in resected nonmetastatic invasive breast cancer. These nomograms perform better than previous models and could be easily accessed easily by clinicians. |
doi_str_mv | 10.1245/s10434-021-10129-4 |
format | Article |
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This study aims to build nomograms to predict overall survival (OS) and breast cancer-specific death (BCSD) in resected nonmetastatic invasive breast cancer.
Patients and Methods
Patients extracted from surveillance, epidemiology, and end results database between 2010 and 2014 were analyzed. Through multivariate Cox regression and Fine and Gray competing risks regression, independent predictive factors were identified and integrated to build nomograms for predicting OS and BCSD. The models were validated by bootstrap resampling and an independent cohort. Additionally, the models’ performance was measured by the Harrell’s C-index, calibrate curve, and time-dependent receiver operating characteristic (ROC) curves.
Results
In total, 110,180 cases were identified and enrolled in the analysis, with 83,450 in the training cohort and 26,730 in the validation cohort. Several independent predictive factors for OS and BCSD were identified and integrated to construct the nomograms. The C-indexes in the training cohort and validation cohort were 0.759 and 0.772 for predicting OS, and 0.857 and 0.856 for predicting BCSD, respectively. The nomogram models were well calibrated, and the time-dependent ROC curves verified the superiority of our models for clinical usefulness. Significant differences in the OS and BCSD curves were also observed when stratifying patients into several different risk groups. For convenient access, we deployed these proposed nomograms into web-based calculators.
Conclusions
We established and validated novel nomograms for individualized prediction of OS and BCSD in resected nonmetastatic invasive breast cancer. These nomograms perform better than previous models and could be easily accessed easily by clinicians.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-021-10129-4</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Breast cancer ; Epidemiology ; Global Health Services Research ; Invasiveness ; Medicine ; Medicine & Public Health ; Nomograms ; Oncology ; Patients ; Population studies ; Population-based studies ; Risk groups ; Surgery ; Surgical Oncology</subject><ispartof>Annals of surgical oncology, 2021-10, Vol.28 (11), p.6537-6550</ispartof><rights>Society of Surgical Oncology 2021</rights><rights>Society of Surgical Oncology 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-84a6cea2570a9025cab63fb7e7e2968e9e92c95c8678c5f4e5e2200f95ab1c953</citedby><cites>FETCH-LOGICAL-c352t-84a6cea2570a9025cab63fb7e7e2968e9e92c95c8678c5f4e5e2200f95ab1c953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1245/s10434-021-10129-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1245/s10434-021-10129-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Chen, Guangyong</creatorcontrib><creatorcontrib>Jia, Mei</creatorcontrib><creatorcontrib>Zeng, Qingpeng</creatorcontrib><creatorcontrib>Zhang, Huiming</creatorcontrib><title>Development and Validation of Web-Based Nomograms for Predicting Cause-Specific Mortality in Surgically Resected Nonmetastatic Invasive Breast Cancer: A Population-Based Study</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><description>Background
This study aims to build nomograms to predict overall survival (OS) and breast cancer-specific death (BCSD) in resected nonmetastatic invasive breast cancer.
Patients and Methods
Patients extracted from surveillance, epidemiology, and end results database between 2010 and 2014 were analyzed. Through multivariate Cox regression and Fine and Gray competing risks regression, independent predictive factors were identified and integrated to build nomograms for predicting OS and BCSD. The models were validated by bootstrap resampling and an independent cohort. Additionally, the models’ performance was measured by the Harrell’s C-index, calibrate curve, and time-dependent receiver operating characteristic (ROC) curves.
Results
In total, 110,180 cases were identified and enrolled in the analysis, with 83,450 in the training cohort and 26,730 in the validation cohort. Several independent predictive factors for OS and BCSD were identified and integrated to construct the nomograms. The C-indexes in the training cohort and validation cohort were 0.759 and 0.772 for predicting OS, and 0.857 and 0.856 for predicting BCSD, respectively. The nomogram models were well calibrated, and the time-dependent ROC curves verified the superiority of our models for clinical usefulness. Significant differences in the OS and BCSD curves were also observed when stratifying patients into several different risk groups. For convenient access, we deployed these proposed nomograms into web-based calculators.
Conclusions
We established and validated novel nomograms for individualized prediction of OS and BCSD in resected nonmetastatic invasive breast cancer. These nomograms perform better than previous models and could be easily accessed easily by clinicians.</description><subject>Breast cancer</subject><subject>Epidemiology</subject><subject>Global Health Services Research</subject><subject>Invasiveness</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nomograms</subject><subject>Oncology</subject><subject>Patients</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>Risk groups</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1u3CAURq2qkZq_F8gKqZtsSAEDNtkl07SNlLZRpk2XiMHXIyIbXMAjzVP1FUtmIkXqoivQ5dzDJ31VdUbJBWVcfEiU8JpjwiimhDKF-ZvqkIoy4rKlb8udyBYrJsW76iilJ0JoUxNxWP35CBsYwjSCz8j4Dj2awXUmu-BR6NEvWOFrk6BD38IY1tGMCfUhovsInbPZ-TVamDkBXk5gXe8s-hpiLoq8Rc6j5RzXzpph2KIHSGDzTuRHyCbl8olFt35jktsAuo5QZsXmLcRLdIXuwzQPuyAvCZZ57rYn1UFvhgSnL-dx9fPTzY_FF3z3_fPt4uoO21qwjFtupAXDREOMIkxYs5J1v2qgAaZkCwoUs0rYVjatFT0HAYwR0ithVrQ81MfV-d47xfB7hpT16JKFYTAewpw0E5wIqmTNC_r-H_QpzNGXdIVqhJSCK1YotqdsDClF6PUU3WjiVlOinzvU-w516VDvOtTP6nq_lArs1xBf1f_Z-gu9PqF4</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Chen, Guangyong</creator><creator>Jia, Mei</creator><creator>Zeng, Qingpeng</creator><creator>Zhang, Huiming</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20211001</creationdate><title>Development and Validation of Web-Based Nomograms for Predicting Cause-Specific Mortality in Surgically Resected Nonmetastatic Invasive Breast Cancer: A Population-Based Study</title><author>Chen, Guangyong ; Jia, Mei ; Zeng, Qingpeng ; Zhang, Huiming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-84a6cea2570a9025cab63fb7e7e2968e9e92c95c8678c5f4e5e2200f95ab1c953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Breast cancer</topic><topic>Epidemiology</topic><topic>Global Health Services Research</topic><topic>Invasiveness</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nomograms</topic><topic>Oncology</topic><topic>Patients</topic><topic>Population studies</topic><topic>Population-based studies</topic><topic>Risk groups</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Guangyong</creatorcontrib><creatorcontrib>Jia, Mei</creatorcontrib><creatorcontrib>Zeng, Qingpeng</creatorcontrib><creatorcontrib>Zhang, Huiming</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Guangyong</au><au>Jia, Mei</au><au>Zeng, Qingpeng</au><au>Zhang, Huiming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Validation of Web-Based Nomograms for Predicting Cause-Specific Mortality in Surgically Resected Nonmetastatic Invasive Breast Cancer: A Population-Based Study</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><date>2021-10-01</date><risdate>2021</risdate><volume>28</volume><issue>11</issue><spage>6537</spage><epage>6550</epage><pages>6537-6550</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Background
This study aims to build nomograms to predict overall survival (OS) and breast cancer-specific death (BCSD) in resected nonmetastatic invasive breast cancer.
Patients and Methods
Patients extracted from surveillance, epidemiology, and end results database between 2010 and 2014 were analyzed. Through multivariate Cox regression and Fine and Gray competing risks regression, independent predictive factors were identified and integrated to build nomograms for predicting OS and BCSD. The models were validated by bootstrap resampling and an independent cohort. Additionally, the models’ performance was measured by the Harrell’s C-index, calibrate curve, and time-dependent receiver operating characteristic (ROC) curves.
Results
In total, 110,180 cases were identified and enrolled in the analysis, with 83,450 in the training cohort and 26,730 in the validation cohort. Several independent predictive factors for OS and BCSD were identified and integrated to construct the nomograms. The C-indexes in the training cohort and validation cohort were 0.759 and 0.772 for predicting OS, and 0.857 and 0.856 for predicting BCSD, respectively. The nomogram models were well calibrated, and the time-dependent ROC curves verified the superiority of our models for clinical usefulness. Significant differences in the OS and BCSD curves were also observed when stratifying patients into several different risk groups. For convenient access, we deployed these proposed nomograms into web-based calculators.
Conclusions
We established and validated novel nomograms for individualized prediction of OS and BCSD in resected nonmetastatic invasive breast cancer. These nomograms perform better than previous models and could be easily accessed easily by clinicians.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1245/s10434-021-10129-4</doi><tpages>14</tpages></addata></record> |
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subjects | Breast cancer Epidemiology Global Health Services Research Invasiveness Medicine Medicine & Public Health Nomograms Oncology Patients Population studies Population-based studies Risk groups Surgery Surgical Oncology |
title | Development and Validation of Web-Based Nomograms for Predicting Cause-Specific Mortality in Surgically Resected Nonmetastatic Invasive Breast Cancer: A Population-Based Study |
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