治疗设施、种族和放化疗对食道印戒细胞癌存活的影响:国家癌症数据库的分析

J. Gootee, C. Willman, S. Aurit, P. Silberstein
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引用次数: 0

摘要

背景:食管印戒细胞癌(SRCCE)是一种侵袭性肿瘤,约占所有食管癌的3.5-5.0%。先前的研究表明,治疗设施与不同癌症的生存之间存在很强的相关性,但尚未在SRCCE中进行研究。本研究的目的是评估基于治疗设施类型的生存差异。方法:使用国家癌症数据库(NCDB)的组织学8490和地形图代码C15.0-C15.9鉴定出2,021例SRCCE患者。使用描述性分析、Kaplan-Meier曲线和多变量Cox风险回归分析来确定治疗设施类型和其他变量的显著性。结果:该队列主要在学术中心接受治疗(47.7%)。随着年龄的增加,死亡率也增加(HR=1.01;95% CI:1.01-1.02, p<0.001)。非裔美国人(HR=1.44;95% CI:1.02-2.02, p=0.036)与非西班牙裔高加索人相比,死亡风险增加。与社区项目相比,在学术机构接受治疗的患者显示出较低的死亡风险(HR=0.73;95% CI:0.64-0.84, p<0.001)和综合癌症规划(HR=0.69;95% CI:0.58-0.83, p=0.008)。与辅助放化疗相比,新辅助放化疗死亡率降低(HR=1.41;95% CI:1.21-1.63, p<0.001)和无放化疗(HR=1.84;95% CI:1.58-2.14, p<0.001)。结论:对于被诊断为SRCCE的患者,与非学术机构相比,在学术中心接受治疗的生存率更高。老年患者、非裔美国人、肿瘤分期增加、无放化疗和辅助放化疗以及Charlson-Deyo评分为1和2+的合并症均与SRCCE死亡风险增加相关。
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The Effect of Treatment Facility, Race, and Chemoradiation on Survival for Signet Ring Cell Carcinoma of the Esophagus: An Analysis of the National Cancer Database
Background: Signet ring cell carcinoma of the esophagus (SRCCE) is an aggressive tumor that represents approximately 3.5-5.0% of all esophageal cancers. Prior studies have shown a strong correlation between treating facility and survival for different cancers, but this has not been studied in SRCCE. The goal of this study is to assess differences in survival based on the type of treatment facility. Methods: There were 2,021 patients with SRCCE identified using the histology 8490 and topography codes C15.0-C15.9 in the National Cancer Database (NCDB). Descriptive analysis, Kaplan-Meier curves, and a multivariable Cox hazard regression analysis were all utilized to determine the significance of treatment facility type and other variables. Results: The cohort mostly received treatment at academic centers (47.7%). As age increased, mortality also increased (HR=1.01; 95% CI:1.01-1.02, p<0.001). Africans Americans (HR=1.44; 95% CI:1.02-2.02, p=0.036) had an increased risk of mortality when compared to Non-Hispanic Caucasians. Patients at academic facilities demonstrated a decreased risk of mortality when compared to community programmes (HR=0.73; 95% CI:0.64-0.84, p<0.001) and integrated cancer programmes (HR=0.69; 95% CI:0.58-0.83, p=0.008). Neoadjuvant chemoradiation resulted decreased mortality when compared to adjuvant chemoradiation (HR=1.41; 95% CI:1.21-1.63, p<0.001) and no chemoradiation (HR=1.84; 95% CI:1.58- 2.14, p<0.001). Conclusion: For patients diagnosed with SRCCE, receiving treatment at academic centers resulted in better survival probabilities compared to nonacademic facilities. Older patients, African Americans, increasing tumor stage, no and adjuvant chemoradiation, and comorbidities with Charlson-Deyo scores of 1 and 2+ were all associated with an increased risk of mortality from SRCCE.
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