Cargando…
Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis
PURPOSE: Inflammatory breast cancer (IBC) is a rare, aggressive and special subtype of primary breast cancer. We aimed to establish competing-risks nomograms to predict the IBC-specific death (BCSD) and other-cause-specific death (OCSD) of IBC patients. METHODS: We extracted data on primary IBC pati...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141985/ https://www.ncbi.nlm.nih.gov/pubmed/34013802 http://dx.doi.org/10.1177/15330338211016371 |
_version_ | 1783696482883338240 |
---|---|
author | Xu, Fengshuo Yang, Jin Han, Didi Huang, Qiao Li, Chengzhuo Zheng, Shuai Wang, Hui Lyu, Jun |
author_facet | Xu, Fengshuo Yang, Jin Han, Didi Huang, Qiao Li, Chengzhuo Zheng, Shuai Wang, Hui Lyu, Jun |
author_sort | Xu, Fengshuo |
collection | PubMed |
description | PURPOSE: Inflammatory breast cancer (IBC) is a rare, aggressive and special subtype of primary breast cancer. We aimed to establish competing-risks nomograms to predict the IBC-specific death (BCSD) and other-cause-specific death (OCSD) of IBC patients. METHODS: We extracted data on primary IBC patients from the SEER (Surveillance, Epidemiology, and End Results) database by applying specific inclusion and exclusion criteria. Cumulative incidence function (CIF) was used to calculate the cumulative incidence rates and Gray’s test was used to evaluate the difference between groups. Fine-Gray proportional subdistribution hazard method was applied to identify the independent predictors. We then established nomograms to predict the 1-, 3-, and 5-year cumulative incidence rates of BCSD and OCSD based on the results. The calibration curves and concordance index (C-index) were adopted to validate the nomograms. RESULTS: We enrolled 1699 eligible IBC patients eventually. In general, the 1-, 3-, and 5-years cumulative incidence rates of BCSD were 15.3%, 41.0%, and 50.7%, respectively, while those of OCSD were 3.0%, 5.1%, and 7.4%. The following 9 variables were independent predictive factors for BCSD: race, lymph node ratio (LNR), AJCC M stage, histological grade, ER (estrogen receptor) status, PR (progesterone receptor) status, HER-2 (human epidermal growth factor-like receptor 2) status, surgery status, and radiotherapy status. Meanwhile, age, ER, PR and chemotherapy status could predict OCSD independently. These factors were integrated for the construction of the competing-risks nomograms. The results of calibration curves and C-indexes indicated the nomograms had good performance. CONCLUSIONS: Based on the SEER database, we established the first competing-risks nomograms to predict BCSD and OCSD of IBC patients. The good performance indicated that they could be incorporated in clinical practice to provide references for clinicians to make individualized treatment strategies. |
format | Online Article Text |
id | pubmed-8141985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-81419852021-06-04 Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis Xu, Fengshuo Yang, Jin Han, Didi Huang, Qiao Li, Chengzhuo Zheng, Shuai Wang, Hui Lyu, Jun Technol Cancer Res Treat Original Article PURPOSE: Inflammatory breast cancer (IBC) is a rare, aggressive and special subtype of primary breast cancer. We aimed to establish competing-risks nomograms to predict the IBC-specific death (BCSD) and other-cause-specific death (OCSD) of IBC patients. METHODS: We extracted data on primary IBC patients from the SEER (Surveillance, Epidemiology, and End Results) database by applying specific inclusion and exclusion criteria. Cumulative incidence function (CIF) was used to calculate the cumulative incidence rates and Gray’s test was used to evaluate the difference between groups. Fine-Gray proportional subdistribution hazard method was applied to identify the independent predictors. We then established nomograms to predict the 1-, 3-, and 5-year cumulative incidence rates of BCSD and OCSD based on the results. The calibration curves and concordance index (C-index) were adopted to validate the nomograms. RESULTS: We enrolled 1699 eligible IBC patients eventually. In general, the 1-, 3-, and 5-years cumulative incidence rates of BCSD were 15.3%, 41.0%, and 50.7%, respectively, while those of OCSD were 3.0%, 5.1%, and 7.4%. The following 9 variables were independent predictive factors for BCSD: race, lymph node ratio (LNR), AJCC M stage, histological grade, ER (estrogen receptor) status, PR (progesterone receptor) status, HER-2 (human epidermal growth factor-like receptor 2) status, surgery status, and radiotherapy status. Meanwhile, age, ER, PR and chemotherapy status could predict OCSD independently. These factors were integrated for the construction of the competing-risks nomograms. The results of calibration curves and C-indexes indicated the nomograms had good performance. CONCLUSIONS: Based on the SEER database, we established the first competing-risks nomograms to predict BCSD and OCSD of IBC patients. The good performance indicated that they could be incorporated in clinical practice to provide references for clinicians to make individualized treatment strategies. SAGE Publications 2021-05-20 /pmc/articles/PMC8141985/ /pubmed/34013802 http://dx.doi.org/10.1177/15330338211016371 Text en © The Author(s) 2021 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Xu, Fengshuo Yang, Jin Han, Didi Huang, Qiao Li, Chengzhuo Zheng, Shuai Wang, Hui Lyu, Jun Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title | Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title_full | Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title_fullStr | Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title_full_unstemmed | Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title_short | Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis |
title_sort | nomograms for estimating cause-specific death rates of patients with inflammatory breast cancer: a competing-risks analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141985/ https://www.ncbi.nlm.nih.gov/pubmed/34013802 http://dx.doi.org/10.1177/15330338211016371 |
work_keys_str_mv | AT xufengshuo nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT yangjin nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT handidi nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT huangqiao nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT lichengzhuo nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT zhengshuai nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT wanghui nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis AT lyujun nomogramsforestimatingcausespecificdeathratesofpatientswithinflammatorybreastcanceracompetingrisksanalysis |