Nomograms for Estimating Cause-Specific Death Rates of Patients With Inflammatory Breast Cancer: A Competing-Risks Analysis

被引:9
|
作者
Xu, Fengshuo [1 ,2 ]
Yang, Jin [3 ]
Han, Didi [1 ,2 ]
Huang, Qiao [4 ]
Li, Chengzhuo [1 ,2 ]
Zheng, Shuai [1 ,5 ]
Wang, Hui [2 ]
Lyu, Jun [1 ,2 ]
机构
[1] Jinan Univ, Dept Clin Res, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Publ Hlth, Hlth Sci Ctr, Xian, Shaanxi, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Sch Populat Med & Publ Hlth, Beijing, Peoples R China
[4] Wuhan Univ, Ctr Evidence Based & Translat Med, Zhongnan Hosp, Wuhan, Peoples R China
[5] Shaanxi Univ Chinese Med, Sch Publ Hlth, Xianyang, Shaanxi, Peoples R China
关键词
inflammatory breast cancer; competing-risks analysis; SEER; cause-specific death; nomogram; CAUSE-SPECIFIC MORTALITY; LONG-TERM; SURVIVAL; EPIDEMIOLOGY; EXPERIENCE; MANAGEMENT; BIOLOGY;
D O I
10.1177/15330338211016371
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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-year 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.
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页数:12
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