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下一代测序技术为胰腺囊肿的术前诊断增添了价值。

Next-generation sequencing adds value to the preoperative diagnosis of pancreatic cysts.

机构信息

Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts.

Department of Anatomical Pathology, Concord Repatriation General Hospital, Sydney, Australia.

出版信息

Cancer Cytopathol. 2017 Jan;125(1):41-47. doi: 10.1002/cncy.21775. Epub 2016 Sep 20.

Abstract

BACKGROUND

The diagnosis of a pancreatic cyst as mucinous or high-risk dictates the need for follow-up or surgery. Molecular analysis of aspirated pancreatic cyst fluid (PCF) can provide valuable information not obtained by carcinoembryonic antigen (CEA) analysis or cytology.

METHODS

All patients who underwent molecular analysis of PCF between March 2013 and June 2015 were reviewed, including pathology, imaging, and follow-up. Molecular testing was performed using a patented, anchored multiplex polymerase chain reaction next-generation sequencing (NGS) platform, which sequenced numerous hotspots in 39 genes linked with malignancy. Performance of NGS and cytology was calculated using final outcome, as determined by clinicopathologic follow-up.

RESULTS

The study cohort included 113 PCFs from 105 patients. In total, 119 variants were detected in 67 PCFs (59%). Variants were more common in intraductal papillary mucinous neoplasms (IPMNs)/cancer than in nonmucinous cysts (P < .005). The inclusion of v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS)/guanine nucleotide-binding protein (GNAS) variants improved the classification of IPMNs as mucinous from 50% by microscopy to 100%. Seventy-five percent of cancers had high-grade atypia versus 0% of IPMNs and nonmucinous cysts (P < .002). Variants in tumor protein 53 (TP53), SMAD family member 4 (SMAD4), cyclin-dependent kinase inhibitor 2A (CDKN2A), and notch1 (NOTCH1) were detected only in malignant cysts. Cytology was similarly specific (100%) for detecting malignant cysts but was more sensitive than the identification of late mutations by NGS (75% vs 46%).

CONCLUSIONS

The detection of KRAS/GNAS variants improves the identification of mucinous neoplasms. Variants in TP53, SMAD4, CDKN2A, and NOTCH1 support the diagnosis of a high-risk cyst requiring surgery or additional sampling. Although molecular analysis is not a replacement for cytopathology, it does provide valuable information for accurate preoperative diagnosis, helping to classify mucinous neoplasms and high-risk cysts that require surgical resection. Cancer Cytopathol 2017;125:41-47. © 2016 American Cancer Society.

摘要

背景

胰腺囊肿被诊断为黏液性或高危,需要随访或手术。抽吸的胰腺囊液(PCF)的分子分析可以提供通过癌胚抗原(CEA)分析或细胞学无法获得的有价值的信息。

方法

回顾了 2013 年 3 月至 2015 年 6 月间进行 PCF 分子分析的所有患者,包括病理、影像学和随访。分子检测使用专利的、锚定的多重聚合酶链反应下一代测序(NGS)平台进行,该平台对与恶性肿瘤相关的 39 个基因中的许多热点进行了测序。使用临床病理随访确定的最终结果计算 NGS 和细胞学的性能。

结果

研究队列包括 105 例患者的 113 个 PCF。总共在 67 个 PCF(59%)中检测到 119 个变异。在导管内乳头状黏液性肿瘤(IPMN)/癌中,变异比非黏液性囊肿更常见(P<0.005)。包含 v-Ki-ras2 Kirsten 大鼠肉瘤病毒致癌基因同源物(KRAS)/鸟苷酸结合蛋白(GNAS)变异可将 IPMN 由显微镜分类为黏液性的 50%提高到 100%。75%的癌症具有高级别非典型性,而 IPMN 和非黏液性囊肿为 0%(P<0.002)。肿瘤蛋白 53(TP53)、SMAD 家族成员 4(SMAD4)、细胞周期蛋白依赖性激酶抑制剂 2A(CDKN2A)和 Notch1(NOTCH1)的变异仅在恶性囊肿中检测到。细胞学对检测恶性囊肿具有同样的特异性(100%),但比 NGS 鉴定晚期突变更敏感(75%比 46%)。

结论

KRAS/GNAS 变异的检测可提高黏液性肿瘤的识别率。TP53、SMAD4、CDKN2A 和 NOTCH1 的变异支持需要手术或进一步取样的高危囊肿的诊断。虽然分子分析不是细胞病理学的替代品,但它确实为准确的术前诊断提供了有价值的信息,有助于对需要手术切除的黏液性肿瘤和高危囊肿进行分类。癌症细胞病理学 2017;125:41-47。©2016 美国癌症协会。

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