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局限期原发性食管小细胞癌的预后因素及治疗策略——一项监测、流行病学和最终结果(SEER)数据库分析

Prognostic factors and treatment strategies of limited-stage primary esophageal small-cell carcinoma-a SEER database analysis.

作者信息

Yang Yang, Guo Haizhou, Li Qianping, Huang Weipeng

机构信息

Department of Endocrinology and Metabolism, Lanzhou University Second Hospital, Lanzhou, China.

Department of Thoracic Surgery, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Transl Cancer Res. 2024 Jul 31;13(7):3242-3250. doi: 10.21037/tcr-24-311. Epub 2024 Jul 26.

Abstract

BACKGROUND

Primary esophageal small-cell carcinoma (PESC) is a rare tumor with poor efficacy, and there is currently no standardized treatment method. Our aim is to explore the prognostic factors and possible optimal treatment modalities for limited-stage PESC.

METHODS

We retrospectively searched the Surveillance, Epidemiology, and End Results (SEER) database from 1975 to 2019 for data of patients with limited-stage PESC. Kaplan-Meier method was used to plot survival curves, calculate survival rates, and Log-rank was used to test the differences among survival curves. Prognostic factors were explored through univariate and multivariate Cox regression survival analyses; Cox regression survival analysis was also conducted to analyze the risk of death among treatment groups and compare the survival differences among each treatment group. The non-single treatment (ST) group was defined as the comprehensive treatment (CT) group and it was compared against the ST group.

RESULTS

A total of 186 cases of limited-stage PESC were included in the study, there were differences in survival time among different groups due to differences in age, year, median household income, and N stage (P<0.001, P=0.041, P=0.002, P=0.001). The median overall survival (mOS) of the surgical group (19 months) was longer than that of the nonsurgical group (11 months) (P=0.01). The mOS of the chemotherapy group (16 months) was longer than that of the non-chemotherapy group (4 months) (P<0.001). The mOS of the radiotherapy group (16 months) was longer than that of the non-radiotherapy group (8 months) (P<0.001). Univariate analysis showed that age ≥80 years (P=0.006), year (1997-2007) (P=0.01), year (2008-2019) (P=0.01), N2 (P=0.003), surgery (P=0.02), radiotherapy (P<0.001), and chemotherapy (P<0.001) were prognostic factors affecting overall survival (OS) in limited-stage PESC patients. Multivariate analysis showed that SEER stage (P=0.02), age (P=0.007), radiotherapy (P<0.001), surgery (P=0.006), and chemotherapy (P<0.001) were independent prognostic factors affecting OS in patients of limited-stage PESC. Prognosis was better in the non-monotherapy group than in each monotherapy group. The CT group is superior to the ST group (P<0.001). The surgery combined with chemotherapy (SC) group had the longest mOS and the highest reduced risk of death, but there was no statistical difference.

CONCLUSIONS

SEER stage, age, radiotherapy, chemotherapy, and surgery were independent prognostic factors in limited-stage patients; CT outperformed ST; the SC group had the longest median survival, but showed no statistical difference.

摘要

背景

原发性食管小细胞癌(PESC)是一种疗效较差的罕见肿瘤,目前尚无标准化治疗方法。我们的目的是探讨局限期PESC的预后因素及可能的最佳治疗方式。

方法

我们回顾性检索了1975年至2019年的监测、流行病学和最终结果(SEER)数据库,以获取局限期PESC患者的数据。采用Kaplan-Meier法绘制生存曲线、计算生存率,并使用对数秩检验来检验生存曲线之间的差异。通过单因素和多因素Cox回归生存分析探索预后因素;还进行Cox回归生存分析以分析各治疗组的死亡风险,并比较各治疗组之间的生存差异。非单一治疗(ST)组定义为综合治疗(CT)组,并与ST组进行比较。

结果

本研究共纳入186例局限期PESC患者,不同组之间的生存时间因年龄、年份、家庭收入中位数和N分期的差异而有所不同(P<0.001,P=0.041,P=(此处原文有误,推测应为0.002),P=0.001)。手术组的中位总生存期(mOS)(19个月)长于非手术组(11个月)(P=0.01)。化疗组的mOS(16个月)长于非化疗组(4个月)(P<0.001)。放疗组的mOS(16个月)长于非放疗组(8个月)(P<0.001)。单因素分析显示,年龄≥80岁(P=0.006)、年份(1997 - 2007年)(P=0.01)、年份(2008 - 2019年)(P=0.01)、N2(P=0.003)、手术(P=0.02)、放疗(P<0.001)和化疗(P<0.001)是影响局限期PESC患者总生存期(OS)的预后因素。多因素分析显示,SEER分期(P=0.02)、年龄(P=0.007)、放疗(P<0.001)、手术(P=0.006)和化疗(P<0.001)是影响局限期PESC患者OS的独立预后因素。非单药治疗组的预后优于各单药治疗组。CT组优于ST组(P<0.001)。手术联合化疗(SC)组的mOS最长,死亡风险降低幅度最大,但无统计学差异。

结论

SEER分期、年龄、放疗、化疗和手术是局限期患者的独立预后因素;CT优于ST;SC组的中位生存期最长,但无统计学差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d085/11319949/46288ba9286c/tcr-13-07-3242-f1.jpg

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