{"title":"美国导管原位癌与浸润性癌乳腺癌死亡率的趋势","authors":"Hyuna Sung, Chenxi Jiang, Ismail Jatoi, Ahmedin Jemal","doi":"10.1186/s13058-025-02068-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Breast ductal carcinoma in situ (DCIS), considered a non-obligate precursor to invasive breast cancer, has been widely studied; however, trends in death rate from DCIS remain undocumented.</p><p><strong>Methods: </strong>To examine the trend in death rate from DCIS among women (age at death, 40 + years) in the US, we quantified annual percent changes (APCs) and average APCs in age-standardized death rates using the Surveillance, Epidemiology, and End Results Program (SEER) 8 incidence-based mortality database and Joinpoint regression. The trend was quantified from 2000 to 2021, capturing deaths among women diagnosed between 1975 and 2021 and allowing for a 25-year follow-back period before each death year. Additionally, we employed the SEER 12 to assess disparities in death rates from DCIS by race and ethnicity during 2017-2021, based on diagnoses from 1992-2021. Trends in death rates from invasive breast cancer were analysed similarly.</p><p><strong>Results: </strong>Death rate from DCIS increased by 2.43% annually (95% confidence interval [CI] = 1.34-3.54) from 2000-2015, and then plateaued, leading to an overall statistically non-significant increase from 2000-2021 (1.01% per year; 95%CI = -0.20-2.24). This trend was in stark contrast with an average of 1.61% annual decrease in death rates for invasive breast cancer (95%CI = -1.95 to -1.27). From 2016-2021, death rate from DCIS was 87% higher among non-Hispanic Black women than non-Hispanic White women (2.98 vs 1.60 per 100,000), a relatively larger disparity than the 39% estimated for death rate from invasive cancer (55.96 vs 40.28 per 100,000).</p><p><strong>Conclusions: </strong>Distinct epidemiologic patterns in death rates between DCIS and invasive breast cancer highlight important implications for understanding the natural history and management of these malignancies.</p>","PeriodicalId":49227,"journal":{"name":"Breast Cancer Research","volume":"27 1","pages":"164"},"PeriodicalIF":5.6000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12465744/pdf/","citationCount":"0","resultStr":"{\"title\":\"Trends in breast cancer death rates from ductal carcinoma in situ versus invasive cancer in the United States.\",\"authors\":\"Hyuna Sung, Chenxi Jiang, Ismail Jatoi, Ahmedin Jemal\",\"doi\":\"10.1186/s13058-025-02068-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Breast ductal carcinoma in situ (DCIS), considered a non-obligate precursor to invasive breast cancer, has been widely studied; however, trends in death rate from DCIS remain undocumented.</p><p><strong>Methods: </strong>To examine the trend in death rate from DCIS among women (age at death, 40 + years) in the US, we quantified annual percent changes (APCs) and average APCs in age-standardized death rates using the Surveillance, Epidemiology, and End Results Program (SEER) 8 incidence-based mortality database and Joinpoint regression. The trend was quantified from 2000 to 2021, capturing deaths among women diagnosed between 1975 and 2021 and allowing for a 25-year follow-back period before each death year. Additionally, we employed the SEER 12 to assess disparities in death rates from DCIS by race and ethnicity during 2017-2021, based on diagnoses from 1992-2021. Trends in death rates from invasive breast cancer were analysed similarly.</p><p><strong>Results: </strong>Death rate from DCIS increased by 2.43% annually (95% confidence interval [CI] = 1.34-3.54) from 2000-2015, and then plateaued, leading to an overall statistically non-significant increase from 2000-2021 (1.01% per year; 95%CI = -0.20-2.24). This trend was in stark contrast with an average of 1.61% annual decrease in death rates for invasive breast cancer (95%CI = -1.95 to -1.27). From 2016-2021, death rate from DCIS was 87% higher among non-Hispanic Black women than non-Hispanic White women (2.98 vs 1.60 per 100,000), a relatively larger disparity than the 39% estimated for death rate from invasive cancer (55.96 vs 40.28 per 100,000).</p><p><strong>Conclusions: </strong>Distinct epidemiologic patterns in death rates between DCIS and invasive breast cancer highlight important implications for understanding the natural history and management of these malignancies.</p>\",\"PeriodicalId\":49227,\"journal\":{\"name\":\"Breast Cancer Research\",\"volume\":\"27 1\",\"pages\":\"164\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12465744/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Breast Cancer Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s13058-025-02068-9\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breast Cancer Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13058-025-02068-9","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
Trends in breast cancer death rates from ductal carcinoma in situ versus invasive cancer in the United States.
Background: Breast ductal carcinoma in situ (DCIS), considered a non-obligate precursor to invasive breast cancer, has been widely studied; however, trends in death rate from DCIS remain undocumented.
Methods: To examine the trend in death rate from DCIS among women (age at death, 40 + years) in the US, we quantified annual percent changes (APCs) and average APCs in age-standardized death rates using the Surveillance, Epidemiology, and End Results Program (SEER) 8 incidence-based mortality database and Joinpoint regression. The trend was quantified from 2000 to 2021, capturing deaths among women diagnosed between 1975 and 2021 and allowing for a 25-year follow-back period before each death year. Additionally, we employed the SEER 12 to assess disparities in death rates from DCIS by race and ethnicity during 2017-2021, based on diagnoses from 1992-2021. Trends in death rates from invasive breast cancer were analysed similarly.
Results: Death rate from DCIS increased by 2.43% annually (95% confidence interval [CI] = 1.34-3.54) from 2000-2015, and then plateaued, leading to an overall statistically non-significant increase from 2000-2021 (1.01% per year; 95%CI = -0.20-2.24). This trend was in stark contrast with an average of 1.61% annual decrease in death rates for invasive breast cancer (95%CI = -1.95 to -1.27). From 2016-2021, death rate from DCIS was 87% higher among non-Hispanic Black women than non-Hispanic White women (2.98 vs 1.60 per 100,000), a relatively larger disparity than the 39% estimated for death rate from invasive cancer (55.96 vs 40.28 per 100,000).
Conclusions: Distinct epidemiologic patterns in death rates between DCIS and invasive breast cancer highlight important implications for understanding the natural history and management of these malignancies.
期刊介绍:
Breast Cancer Research, an international, peer-reviewed online journal, publishes original research, reviews, editorials, and reports. It features open-access research articles of exceptional interest across all areas of biology and medicine relevant to breast cancer. This includes normal mammary gland biology, with a special emphasis on the genetic, biochemical, and cellular basis of breast cancer. In addition to basic research, the journal covers preclinical, translational, and clinical studies with a biological basis, including Phase I and Phase II trials.