晚期胰腺癌患者临床病理特征、治疗选择和预后的种族差异的单机构分析。

Annals of Pancreatic Cancer Pub Date : 2021-10-01 Epub Date: 2021-10-30 DOI:10.21037/apc-21-5
Matthew Williams, Umut Özbek, Jung-Yi Lin, Celina Ang
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引用次数: 0

摘要

背景:调查在城市中心接受当代化疗方案治疗的不可切除/转移性胰腺导管腺癌(PDA)患者的种族差异。方法:回顾性分析2012-2017年在单一机构治疗的所有PDA患者。对连续变量和分类变量进行t检验、Mann-Whitney U检验、卡方检验或Fisher精确检验。生成Kaplan-Meier曲线,并使用Cox比例风险模型分析生存结果。结果:145例患者被确定为:白人[69],非洲裔美国人(AA, 34),亚洲人[15]和其他[27]。55.7%的患者接受了以吉西他滨为基础的治疗,36.6%的患者接受了以氟尿嘧啶(5-FU)为基础的治疗,特别是26.1%的患者接受了FOLFIRINOX, 43.7%的患者接受了吉西他滨/nab-紫杉醇。在单变量模型中,亚洲人的总生存率(OS)明显低于白人[风险比(HR) 2.74, P=0.013],但AA组与白人组(HR 1.51, P=0.297)和其他组与白人组(HR 2.05, P=0.062)之间的OS无差异。在多变量分析中,亚洲人的OS比白人差(HR 2.62, P=0.018),基于吉西他滨的治疗不如基于5- fu的治疗(HR 2.65, P=0.005)。AA组与白人组、Other组与白人组无OS差异(HR 1.12, P=0.769; HR 0.8, P=0.763)。结论:在这一系列接受当代化疗的晚期PDA患者中,AA和白人患者的预后相当,但亚洲人的OS比白人患者更差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A single-institutional analysis of racial disparities in clinicopathologic characteristics, treatment selections, and outcomes in advanced-stage pancreatic cancer patients.

A single-institutional analysis of racial disparities in clinicopathologic characteristics, treatment selections, and outcomes in advanced-stage pancreatic cancer patients.

A single-institutional analysis of racial disparities in clinicopathologic characteristics, treatment selections, and outcomes in advanced-stage pancreatic cancer patients.

Background: To investigate racial disparities among unresectable/metastatic pancreatic ductal adenocarcinoma (PDA) patients treated with contemporary chemotherapy regimens at an urban center.

Methods: Retrospective review of all PDA patients treated at a single institution between 2012-2017. Continuous and categorical variables were tested using t-test, Mann-Whitney U, chi-squared or Fisher's exact test as appropriate. Kaplan-Meier curves were generated and Cox proportional hazards models were used to analyze survival outcomes.

Results: One hundred and forty-five patients identified as: White [69], African American (AA, 34), Asian [15], and Other [27]. Fifty-five-point-seven percent of patients received gemcitabine-based therapy vs. 36.6% received fluorouracil (5-FU) based therapy, specifically 26.1% received FOLFIRINOX and 43.7% received gemcitabine/nab-paclitaxel. In a univariable model, Asians had significantly worse overall survival (OS) than Whites [hazard ratio (HR) 2.74, P=0.013], but there were no OS differences between AA vs. Whites (HR 1.51, P=0.297) nor Other vs. Whites (HR 2.05, P=0.062). On multivariable analysis, Asians had worse OS compared to Whites (HR 2.62, P=0.018), and gemcitabine-based therapy was inferior to 5-FU-based therapy (HR 2.65, P=0.005). There were no OS differences between AA vs. Whites nor Other vs. Whites (HR 1.12, P=0.769 and HR 0.8, P=0.763, respectively).

Conclusions: In this series of advanced PDA patients treated with contemporary chemotherapy, AA and White patients had comparable outcomes, but Asians had worse OS than White patients.

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