肿瘤DNA与血浆和血清循环游离DNA KRAS突变评估的比较。

Q3 Medicine
Clinical Medicine Insights- Pathology Pub Date : 2012-01-01 Epub Date: 2012-05-15 DOI:10.4137/CPath.S8798
Shethah R Morgan, Jessica Whiteley, Emma Donald, John Smith, Marcia T Eisenberg, Eddie Kallam, Lauren Kam-Morgan
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引用次数: 48

摘要

转移性结直肠癌(mCRC)患者的KRAS癌基因突变检测通常使用福尔马林固定石蜡包埋肿瘤组织的DNA进行;然而,获取标本的途径有限,分析具有挑战性。本研究使用市售的KRAS聚合酶链反应(PCR)试剂盒评估了循环游离DNA (cfDNA)中KRAS突变的鉴定。匹配的血浆、血清和肿瘤样本来自71例既往接受过治疗但在治疗后病情进展的mCRC患者。血浆和血清样品的cfDNA产量相当。70/71份血浆提取标本(特异性:97%,敏感性:31%)和67/71份血清提取标本(特异性:100%,敏感性:25%)分析成功。该研究表明,使用市售的KRAS PCR试剂盒可以在cfDNA中检测到KRAS突变,这证实了cfDNA在诊断环境中作为肿瘤DNA的潜在替代来源,如果档案肿瘤标本的获取受到限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of KRAS Mutation Assessment in Tumor DNA and Circulating Free DNA in Plasma and Serum Samples.

Comparison of KRAS Mutation Assessment in Tumor DNA and Circulating Free DNA in Plasma and Serum Samples.

Comparison of KRAS Mutation Assessment in Tumor DNA and Circulating Free DNA in Plasma and Serum Samples.

Comparison of KRAS Mutation Assessment in Tumor DNA and Circulating Free DNA in Plasma and Serum Samples.

Testing for mutations in the KRAS oncogene for patients with metastatic colorectal cancer (mCRC) is generally performed using DNA from formalin-fixed paraffin-embedded tumor tissue; however, access to specimens can be limited and analysis challenging. This study assessed the identification of KRAS mutations in circulating free DNA (cfDNA) using a commercially available KRAS polymerase chain reaction (PCR) kit. Matched plasma, serum and tumor samples were available from 71 patients with mCRC who had received prior therapy but whose disease progressed following therapy. Yields of cfDNA from plasma and serum samples were comparable. Analyses were successful in 70/71 plasma-extracted samples (specificity: 97%, sensitivity: 31%) and 67/71 serum- extracted samples (specificity: 100%, sensitivity: 25%). This study demonstrates that KRAS mutations can be detected in cfDNA using a commercially available KRAS PCR kit, confirming cfDNA as a potential alternative source of tumor DNA in a diagnostic setting if access to archival tumor specimens is limited.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
0
审稿时长
4 weeks
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