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The role of cetuximab as first-line treatment of colorectal liver metastases.西妥昔单抗作为结直肠癌肝转移一线治疗的作用。
HPB (Oxford). 2013 Jan;15(1):11-7. doi: 10.1111/j.1477-2574.2012.00591.x. Epub 2012 Oct 17.
2
A survival analysis of the liver-first reversed management of advanced simultaneous colorectal liver metastases: a LiverMetSurvey-based study.基于 LiverMetSurvey 的研究:对晚期结直肠癌肝转移同期序贯肝优先反转管理的生存分析。
Ann Surg. 2012 Nov;256(5):772-8; discussion 778-9. doi: 10.1097/SLA.0b013e3182734423.
3
Staged hepatectomy for bilobar colorectal hepatic metastases.两叶肝切除术治疗结直肠肝转移瘤。
HPB (Oxford). 2012 Nov;14(11):782-9. doi: 10.1111/j.1477-2574.2012.00543.x. Epub 2012 Aug 26.
4
Folate receptor-α expression in resectable hepatic colorectal cancer metastases: patterns and significance.可切除肝转移性结直肠癌中叶酸受体-α的表达:模式与意义。
Mod Pathol. 2011 Sep;24(9):1221-8. doi: 10.1038/modpathol.2011.82. Epub 2011 May 13.
5
Is perioperative chemotherapy useful for solitary, metachronous, colorectal liver metastases?围手术期化疗对单发、异时性结直肠癌肝转移是否有效?
Ann Surg. 2010 Nov;252(5):774-87. doi: 10.1097/SLA.0b013e3181fcf3e3.
6
What defines 'cure' after liver resection for colorectal metastases? Results after 10 years of follow-up.结直肠转移瘤肝切除术后“治愈”的定义是什么?10 年随访结果。
HPB (Oxford). 2010 May;12(4):244-9. doi: 10.1111/j.1477-2574.2010.00155.x.
7
The validity of clinical risk score for patients undergoing liver resection for colorectal metastases.用于结直肠癌肝转移患者肝切除的临床风险评分的有效性
Hepatogastroenterology. 2009 Sep-Oct;56(94-95):1452-8.
8
KRAS mutation correlates with accelerated metastatic progression in patients with colorectal liver metastases.KRAS 突变与结直肠癌肝转移患者的转移性进展加速相关。
Ann Surg Oncol. 2010 Feb;17(2):572-8. doi: 10.1245/s10434-009-0605-3. Epub 2009 Sep 1.
9
Validation of prognostic scoring systems for patients undergoing resection of colorectal cancer liver metastases.结直肠癌肝转移患者切除术预后评分系统的验证。
Ann Surg Oncol. 2009 Dec;16(12):3279-88. doi: 10.1245/s10434-009-0654-7.
10
Slow proliferation as a biological feature of colorectal cancer metastasis.缓慢增殖作为结直肠癌转移的生物学特征。
Br J Cancer. 2009 Sep 1;101(5):822-8. doi: 10.1038/sj.bjc.6605229. Epub 2009 Aug 4.

能否改进临床风险评分?p53、Ki-67 和胸苷酸合成酶在结直肠肝转移患者根治性切除术中的预后价值。

Can we improve the clinical risk score? The prognostic value of p53, Ki-67 and thymidylate synthase in patients undergoing radical resection of colorectal liver metastases.

机构信息

Department of Abdominal and General Surgery, University Medical Centre Maribor, Maribor, Slovenia.

出版信息

HPB (Oxford). 2014 Mar;16(3):235-42. doi: 10.1111/hpb.12089. Epub 2013 Mar 19.

DOI:10.1111/hpb.12089
PMID:23509992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3945849/
Abstract

OBJECTIVES

The aim of this study was to assess whether biological markers can provide prognostic information additional to that supplied by the clinical risk score (CRS) in patients with colorectal liver metastases.

METHODS

A retrospective review of a prospectively maintained database was conducted. Patients selected for this study were treated between 1996 and 2011 with potentially curative liver surgery. Expressions of p53, Ki-67 and thymidylate synthase were assayed using immunohistochemical techniques on tissue microarrays.

RESULTS

A total of 98 (24%) of 406 patients met the inclusion criteria. The median follow-up was 103 months. Analysis revealed a correlation between p53 protein overexpression and high CRS (P = 0.058). Following multivariate analysis, only high CRS remained as an independent negative prognostic predictor of survival (P = 0.018), as well as an indicator of early recurrence of disease (P = 0.010). Of the biological markers investigated, only Ki-67 overexpression was identified as a positive predictor of survival on multivariate analysis (P = 0.038).

CONCLUSIONS

Ki-67 overexpression was a positive predictor of survival. Only high CRS remained an independent negative prognostic predictor.

摘要

目的

本研究旨在评估生物标志物是否可以提供除临床风险评分(CRS)以外的预后信息,这些信息适用于结直肠癌肝转移患者。

方法

对前瞻性维护的数据库进行了回顾性分析。本研究选择的患者于 1996 年至 2011 年间接受了潜在可治愈的肝切除术治疗。使用组织微阵列上的免疫组织化学技术检测 p53、Ki-67 和胸苷酸合成酶的表达。

结果

在 406 名患者中,共有 98 名(24%)符合纳入标准。中位随访时间为 103 个月。分析显示,p53 蛋白过表达与高 CRS 之间存在相关性(P = 0.058)。多变量分析后,仅高 CRS 仍然是生存的独立负预后预测因子(P = 0.018),也是疾病早期复发的指标(P = 0.010)。在所研究的生物标志物中,只有 Ki-67 过表达在多变量分析中被确定为生存的阳性预测因子(P = 0.038)。

结论

Ki-67 过表达是生存的阳性预测因子。只有高 CRS 仍然是独立的负预后预测因子。