{"title":"西班牙/拉丁裔和非西班牙裔白人结直肠癌患者的指数窗c反应蛋白和癌胚抗原与5年全因死亡率:一项回顾性生物标志物队列研究","authors":"Freddy Martinez, Raphael E Cuomo","doi":"10.1080/20565623.2026.2743711","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>To examine index-window carcinoembryonic antigen (CEA), C-reactive protein (CRP), and five-year recorded mortality by ethnicity in colorectal cancer.</p><p><strong>Patients and methods: </strong>This retrospective University of California Health Data Warehouse cohort included Hispanic/Latino and non-Hispanic White adults indexed during 2012-2020 with both biomarkers measured within ±30 days and complete covariates. Linear regression modeled log(CEA + 0.1); Cox regression modeled recorded all-cause mortality.</p><p><strong>Results: </strong>Among 345 patients, 143 deaths were recorded. Hispanic/Latino ethnicity was associated with higher log(CEA + 0.1) (β = 0.743; robust 95% confidence interval [CI], 0.202-1.285; P = 0.007). The mortality association was nonsignificant (hazard ratio [HR], 0.723; 95% CI, 0.483-1.084; P = 0.117). Higher log(CEA + 0.1) (HR, 1.266; 95% CI, 1.174-1.366; P < 0.001) and log(CRP + 0.1) (HR, 1.134; 95% CI, 1.037-1.239; P = 0.006) were associated with mortality.</p><p><strong>Conclusions: </strong>In this biomarker-selected cohort, Hispanic/Latino patients had higher recorded CEA without a statistically significant ethnic-group mortality difference. Confirmation requires clinically characterized cohorts with stage, treatment, biomarker timing, verified assay comparability, and complete mortality ascertainment.</p>","PeriodicalId":12568,"journal":{"name":"Future Science OA","volume":"12 1","pages":"2743711"},"PeriodicalIF":2.5000,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13652077/pdf/","citationCount":"0","resultStr":"{\"title\":\"Index-window C-reactive protein and carcinoembryonic antigen and five-year all-cause mortality in Hispanic/Latino and non-Hispanic White patients with colorectal cancer: a retrospective biomarker cohort study.\",\"authors\":\"Freddy Martinez, Raphael E Cuomo\",\"doi\":\"10.1080/20565623.2026.2743711\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>To examine index-window carcinoembryonic antigen (CEA), C-reactive protein (CRP), and five-year recorded mortality by ethnicity in colorectal cancer.</p><p><strong>Patients and methods: </strong>This retrospective University of California Health Data Warehouse cohort included Hispanic/Latino and non-Hispanic White adults indexed during 2012-2020 with both biomarkers measured within ±30 days and complete covariates. Linear regression modeled log(CEA + 0.1); Cox regression modeled recorded all-cause mortality.</p><p><strong>Results: </strong>Among 345 patients, 143 deaths were recorded. Hispanic/Latino ethnicity was associated with higher log(CEA + 0.1) (β = 0.743; robust 95% confidence interval [CI], 0.202-1.285; P = 0.007). The mortality association was nonsignificant (hazard ratio [HR], 0.723; 95% CI, 0.483-1.084; P = 0.117). Higher log(CEA + 0.1) (HR, 1.266; 95% CI, 1.174-1.366; P < 0.001) and log(CRP + 0.1) (HR, 1.134; 95% CI, 1.037-1.239; P = 0.006) were associated with mortality.</p><p><strong>Conclusions: </strong>In this biomarker-selected cohort, Hispanic/Latino patients had higher recorded CEA without a statistically significant ethnic-group mortality difference. Confirmation requires clinically characterized cohorts with stage, treatment, biomarker timing, verified assay comparability, and complete mortality ascertainment.</p>\",\"PeriodicalId\":12568,\"journal\":{\"name\":\"Future Science OA\",\"volume\":\"12 1\",\"pages\":\"2743711\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2026-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13652077/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Future Science OA\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/20565623.2026.2743711\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/10/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future Science OA","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/20565623.2026.2743711","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/8 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Index-window C-reactive protein and carcinoembryonic antigen and five-year all-cause mortality in Hispanic/Latino and non-Hispanic White patients with colorectal cancer: a retrospective biomarker cohort study.
Aims: To examine index-window carcinoembryonic antigen (CEA), C-reactive protein (CRP), and five-year recorded mortality by ethnicity in colorectal cancer.
Patients and methods: This retrospective University of California Health Data Warehouse cohort included Hispanic/Latino and non-Hispanic White adults indexed during 2012-2020 with both biomarkers measured within ±30 days and complete covariates. Linear regression modeled log(CEA + 0.1); Cox regression modeled recorded all-cause mortality.
Results: Among 345 patients, 143 deaths were recorded. Hispanic/Latino ethnicity was associated with higher log(CEA + 0.1) (β = 0.743; robust 95% confidence interval [CI], 0.202-1.285; P = 0.007). The mortality association was nonsignificant (hazard ratio [HR], 0.723; 95% CI, 0.483-1.084; P = 0.117). Higher log(CEA + 0.1) (HR, 1.266; 95% CI, 1.174-1.366; P < 0.001) and log(CRP + 0.1) (HR, 1.134; 95% CI, 1.037-1.239; P = 0.006) were associated with mortality.
Conclusions: In this biomarker-selected cohort, Hispanic/Latino patients had higher recorded CEA without a statistically significant ethnic-group mortality difference. Confirmation requires clinically characterized cohorts with stage, treatment, biomarker timing, verified assay comparability, and complete mortality ascertainment.
期刊介绍:
Future Science OA is an online, open access, peer-reviewed title from the Future Science Group. The journal covers research and discussion related to advances in biotechnology, medicine and health. The journal embraces the importance of publishing all good-quality research with the potential to further the progress of research in these fields. All original research articles will be considered that are within the journal''s scope, and have been conducted with scientific rigour and research integrity. The journal also features review articles, editorials and perspectives, providing readers with a leading source of commentary and analysis. Submissions of the following article types will be considered: -Research articles -Preliminary communications -Short communications -Methodologies -Trial design articles -Trial results (including early-phase and negative studies) -Reviews -Perspectives -Commentaries