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比较突变分析在肺部病变评估中的应用:是否应该成为标准的治疗方法?

Comparative mutational profiling in the assessment of lung lesions: should it be the standard of care?

机构信息

Division of Cardiothoracic Surgery, Department of Surgery, Ohio State University, Columbus, OH 43210, USA.

出版信息

Ann Thorac Surg. 2010 Aug;90(2):388-96. doi: 10.1016/j.athoracsur.2010.03.059.

Abstract

BACKGROUND

Discerning primary versus metastatic lung lesions is problematic. Comparative mutational profiling (CMP) involves genetic and point mutation analysis of lesions to facilitate this. We sought to review our experience in cases of two lung lesions or head and neck cancer and lung lesions to determine whether a significantly clinical problem existed, what standard processes were in place to address it, and whether a new diagnostic standard was required.

METHODS

Between January 1, 2007, and October 31, 2008, CMP was used in 24 cases of two lung lesions or a head and neck cancer and lung lesion. Routine hematoxylin and eosin stain examination and immunohistochemistry were performed as appropriate. The CMP involved DNA sequencing for specific oncogene point mutations and a panel of allelic imbalance markers. Metastatic cancer required demonstration of concordant mutations affecting the same allele copy in different cancer deposits.

RESULTS

The patient mean age was 62 years; there were 13 men and 11 women. The cases involved two lung lesions (n = 13) or a head and neck cancer and a lung lesion (n = 11). Standard pathology examination was unable to discriminate the lesions, and they were subsequently differentiated by CMP. Fifteen discordant CMP results were interpreted as independent primaries; 9 cases were concordant, consistent with metastatic disease.

CONCLUSIONS

Discerning primary versus metastatic disease when dealing with lung lesions is a clinically significant problem. Comparative mutational profiling was found to be useful and reliable to assess the relatedness of multiple cancer lesions when routine pathology assessment was unable to.

摘要

背景

鉴别原发性与转移性肺部病变具有一定难度。比较突变分析(CMP)涉及对病变进行基因和点突变分析,以促进这一过程。我们旨在回顾我们在两个肺部病变或头颈部癌症和肺部病变的 24 例病例中的经验,以确定是否存在显著的临床问题,是否存在解决该问题的标准流程,以及是否需要新的诊断标准。

方法

在 2007 年 1 月 1 日至 2008 年 10 月 31 日期间,我们对 24 例两个肺部病变或头颈部癌症和肺部病变的患者使用了 CMP。适当进行了常规苏木精和伊红染色检查和免疫组织化学检查。CMP 涉及针对特定致癌基因突变和一组等位基因失衡标志物的 DNA 测序。转移性癌症需要证明在不同的癌灶中影响同一等位基因拷贝的一致性突变。

结果

患者的平均年龄为 62 岁;男性 13 例,女性 11 例。病例包括两个肺部病变(n=13)或头颈部癌症和肺部病变(n=11)。标准病理学检查无法区分病变,随后通过 CMP 进行了区分。15 个不一致的 CMP 结果被解释为独立的原发性病变;9 个结果一致,符合转移性疾病。

结论

在处理肺部病变时,鉴别原发性与转移性疾病是一个具有临床意义的问题。当常规病理学评估无法进行时,比较突变分析被发现是一种有用且可靠的方法,可以评估多个癌症病变之间的相关性。

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