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早期结直肠癌的生物标志物:是否已准备好进入黄金时期?

Biomarkers in early-stage colorectal cancer: ready for prime time?

机构信息

Oxford Cancer Centre, University of Oxford, Oxford, UK.

出版信息

Dig Dis. 2012;30 Suppl 2:27-33. doi: 10.1159/000341890. Epub 2012 Nov 23.

Abstract

BACKGROUND/AIMS: During the last two decades, hundreds of reports have detailed putative prognostic and predictive biomarkers for colorectal cancer (CRC). However, the majority of these studies have been small and retrospective, reporting results that are highly likely to represent false positives. Consequently, their relevance to clinical practice requires definition.

METHODS

Review of published literature on CRC biomarkers, focusing on early-stage disease.

RESULTS

Although most putative biomarkers have failed to be validated in subsequent studies, level I evidence now indicates that tumour microsatellite instability can be used to identify a cohort of patients with stage IIA disease at low risk of relapse who can be spared adjuvant chemotherapy. Emerging data suggest that gene expression arrays may have a role in selecting patients with stage IIA disease and mismatch repair-proficient tumours for chemotherapy following tumour resection.

CONCLUSION

Despite the profusion of biomarker literature, only mismatch repair status can be recommended as routine in current clinical practice. High-quality, adequately powered studies are essential to accurately define the utility of existing and putative biomarkers, and to support their rational application in the clinic.

摘要

背景/目的:在过去的二十年中,已有数百份报告详细描述了结直肠癌(CRC)的潜在预后和预测生物标志物。然而,这些研究大多规模较小且为回顾性研究,报告的结果极有可能是假阳性的。因此,它们与临床实践的相关性需要进一步明确。

方法

对已发表的 CRC 生物标志物文献进行综述,重点关注早期疾病。

结果

尽管大多数潜在的生物标志物在后续研究中未能得到验证,但目前已经有一级证据表明肿瘤微卫星不稳定性可用于识别 IIA 期疾病中复发风险较低的患者亚群,这些患者可以避免辅助化疗。新出现的数据表明,基因表达谱可能在选择 IIA 期疾病和错配修复功能正常的肿瘤患者进行肿瘤切除后的化疗方面具有一定作用。

结论

尽管生物标志物文献大量涌现,但只有错配修复状态可以被推荐作为目前临床实践中的常规检测。高质量、充分有效的研究对于准确确定现有和潜在生物标志物的效用,以及支持其在临床中的合理应用至关重要。

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