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KRAS 基因突变检测在胆管刷检细胞学标本中的意义:一项 10 年回顾性研究。

Significance of KRAS mutation testing in biliary brushing cytology specimens: A 10-year retrospective review.

机构信息

Department of Pathology, Yale University School of Medicine, New Haven, Connecticut.

Department of Pathology & Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts.

出版信息

Cancer Cytopathol. 2022 Jul;130(7):558-565. doi: 10.1002/cncy.22579. Epub 2022 Apr 13.

Abstract

BACKGROUND

Biliary strictures can be caused by benign and malignant conditions. A biliary duct brushing diagnosis can be challenging because of low cellularity and overlapping morphology among different entities, leading to a variable reported sensitivity. This study aimed to assess the value of KRAS mutation testing in adding cytological diagnosis of biliary duct brushings.

METHODS

With institutional review board approval, biliary duct brushing cytology specimens were collected from 269 patients with extrahepatic biliary stenosis between August 2011 and July 2021. The results of cytology and KRAS mutational analyses were evaluated in view of corresponding cytology examination and histopathological/clinical follow-up.

RESULTS

KRAS mutations were identified in 50 of 269 biliary stricture brushing cases (19%). Among the cases with available follow-up, 72% (34 of 47) of biliary brushings had confirmed malignancy when there were KRAS mutations. The overall specificity and sensitivity of KRAS mutation testing was 92% and 36%, respectively. KRAS mutation was significantly more enriched in pancreatic duct adenocarcinoma than in cholangiocarcinoma (66% vs 5%, P < .001). The absolute risk of malignancy was 3%, 28%, and 71%, respectively, in negative, atypical, and suspicious cytological diagnostic categories and the risks increased to 14%, 68%, and 95% in corresponding categories with KRAS mutation.

CONCLUSIONS

Our results suggested that KRAS mutational analysis can be considered supplementary to cytology diagnosis of biliary duct brushing for patients with extrahepatic biliary stenosis in clinical practice.

摘要

背景

胆道狭窄可由良性和恶性病变引起。由于胆管刷检的细胞数量少,且不同病变实体之间形态学重叠,胆管刷检的细胞学诊断具有挑战性,导致其报道的敏感性存在差异。本研究旨在评估 KRAS 基因突变检测在胆管刷检细胞学诊断中的价值。

方法

经机构审查委员会批准,收集了 2011 年 8 月至 2021 年 7 月期间 269 例肝外胆管狭窄患者的胆管刷检细胞学标本。根据相应的细胞学检查和组织病理学/临床随访结果,评估细胞学和 KRAS 基因突变分析的结果。

结果

在 269 例胆管狭窄刷检病例中,有 50 例(19%)检测到 KRAS 突变。在有随访结果的病例中,当 KRAS 突变时,胆管刷检中 72%(34/47)的病例被证实为恶性肿瘤。KRAS 基因突变检测的总体特异性和敏感性分别为 92%和 36%。KRAS 突变在胰腺导管腺癌中明显比胆管癌更丰富(66%比 5%,P<.001)。在阴性、非典型和可疑细胞学诊断类别中,恶性肿瘤的绝对风险分别为 3%、28%和 71%,而在相应的 KRAS 突变类别中,风险分别增加至 14%、68%和 95%。

结论

我们的研究结果表明,KRAS 基因突变分析可作为胆管刷检细胞学诊断的补充方法,用于临床实践中肝外胆管狭窄患者的诊断。

相似文献

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Significance of KRAS mutation testing in biliary brushing cytology specimens: A 10-year retrospective review.
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