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癌胚抗原升高的直肠癌中极小肿瘤的癌症特异性死亡率增加。

Increased cancer-specific mortality of very small size in carcinoembryonic antigen-elevated rectal cancer.

作者信息

Pan Haiqiang, Cui Junhui, Cai Ke, Zhou Yena

机构信息

Department of Colorectal Surgery, Tongde Hospital of Zhejiang Province, Hangzhou 310012, China.

Department of General Surgery, Tongde Hospital of Zhejiang Province, Hangzhou 310012, China.

出版信息

Ann Transl Med. 2019 Sep;7(18):447. doi: 10.21037/atm.2019.08.81.

DOI:10.21037/atm.2019.08.81
PMID:31700883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6803206/
Abstract

BACKGROUND

The present study aimed to investigate the cause-specific survival (CSS) of very small rectal cancer in the context of preoperative serum carcinoembryonic antigen (CEA) elevation.

METHODS

Patients diagnosed with node-negative rectal cancer from the Surveillance, Epidemiology, and End Results (SEER) database from January 2004 to December 2010 meeting the inclusion criteria were identified for this study. The Cox proportional hazards regression analyses were conducted to identify independent factors associated with CSS. Pearson's chi-squared tests and Kaplan-Meier methods were performed.

RESULTS

A total of 8,413 patients were included into our study. Kaplan-Meier analyses showed lower 7-year CSS rate of very small tumors (≤5 mm) compared to those larger than 40 mm (70.4% 76.0%, log-rank P=0.469). Multivariate Cox analyses showed that patients with very small tumor size (≤5 mm) was also associated with a significantly increased risk of cancer-specific mortality compared with those with large tumor size (HR =2.567, 95% CI: 1.285 to 5.130, P=0.008, using ≥41 mm, C+ as a reference).

CONCLUSIONS

Very small tumor size in the context of preoperative serum CEA elevation could be a surrogate for biological aggressiveness. Our finding would provide a better understanding of tumor biology for us and elicit more future biological researches.

摘要

背景

本研究旨在探讨术前血清癌胚抗原(CEA)升高情况下超小直肠癌的病因特异性生存率(CSS)。

方法

从监测、流行病学和最终结果(SEER)数据库中确定2004年1月至2010年12月期间诊断为淋巴结阴性直肠癌且符合纳入标准的患者进行本研究。进行Cox比例风险回归分析以确定与CSS相关的独立因素。采用Pearson卡方检验和Kaplan-Meier方法。

结果

共有8413例患者纳入我们的研究。Kaplan-Meier分析显示,超小肿瘤(≤5mm)的7年CSS率低于大于40mm的肿瘤(70.4%对76.0%,对数秩检验P=0.469)。多变量Cox分析显示,与大肿瘤患者相比,肿瘤尺寸超小(≤5mm)的患者癌症特异性死亡风险也显著增加(HR=2.567,95%CI:1.285至5.130,P=0.008,以≥41mm、C+作为对照)。

结论

术前血清CEA升高情况下的超小肿瘤尺寸可能是生物学侵袭性的一个替代指标。我们的发现将使我们更好地理解肿瘤生物学,并引发更多未来的生物学研究。

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Rectal Cancer in 2018: A Primer for the Gastroenterologist.2018 年直肠癌:胃肠病学家指南。
Am J Gastroenterol. 2018 Dec;113(12):1763-1771. doi: 10.1038/s41395-018-0180-y.
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Rectal cancer patients younger than 50 years lack a survival benefit from NCCN guideline-directed treatment for stage II and III disease.50 岁以下的直肠癌患者,在接受 NCCN 指南指导的 II 期和 III 期疾病治疗时,并未从中获得生存获益。
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Cancer statistics, 2018.癌症统计数据,2018 年。
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Rectal cancer survival in the United States by race and stage, 2001 to 2009: Findings from the CONCORD-2 study.2001年至2009年美国按种族和分期划分的直肠癌生存率:CONCORD-2研究结果
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Colorectal cancer statistics, 2017.结直肠癌统计数据,2017 年。
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Prognostic impact of tumour size in completely resected thymic epithelial tumours.肿瘤大小对完全切除的胸腺上皮肿瘤的预后影响
Eur J Cardiothorac Surg. 2016 Dec;50(6):1068-1074. doi: 10.1093/ejcts/ezw178.
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Metastasis: an early event in cancer progression.转移:癌症进展中的早期事件。
J Cancer Res Clin Oncol. 2017 May;143(5):745-757. doi: 10.1007/s00432-016-2279-0. Epub 2016 Sep 29.
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