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甲状腺细针抽吸细胞学检查中三种分子标志物对异常类别分子检测的诊断准确性。

Diagnostic accuracy of molecular testing with three molecular markers on thyroid fine-needle aspiration cytology with abnormal category.

机构信息

Department of Pathology, Goztepe Research and Training Hospital, Istanbul Medeniyet University, Istanbul, Turkey.

Department of Medical Genetics, Istanbul Medeniyet University, Istanbul, Turkey.

出版信息

Diagn Cytopathol. 2020 Jun;48(6):507-515. doi: 10.1002/dc.24394. Epub 2020 Feb 7.

Abstract

BACKGROUND

Cases with abnormal category, determined by thyroid fine-needle aspiration (FNA), frequently undergo surgical resection, despite the majority of cases being identified as benign after resection. Additional diagnostic markers are needed to guide the management of patients with abnormal thyroid nodules.

MATERIALS AND METHODS

The retrospective study enrolled 150 cases diagnosed abnormal by FNA cytology that had undergone molecular testing with three markers (BRAF V600E, NRAS, and KRAS) on the cell block. Seventy-one cases had a surgical follow-up.

RESULTS

When NIFTP is not considered as malignant, positive predictive values (PPVs) of cytology and combined cytology and molecular testing (CC-MT) were 67.6% (95% CI: 0.555-0.782) and 89.2% (95% CI: 0.746-0.970) (P = .004), respectively. The sensitivity of the CC-MT was 68.8%, specificity was 82.5%, and the false-positive rate was 17.4%. When NIFTP is considered as malignant, PPVs of cytology and CC-MT were 83.1% (95% CI: 0.743-0.918) and 94.6% (95% CI: 0.873-1.018) (P = .047), respectively. The sensitivity of the CC-MT was 59.3%, specificity was 83.3%, and the false-positive rate was 16.7%.

CONCLUSION

The addition of molecular testing with a small panel to FNA cytology may increase the PPV of cytology in abnormal categories. Small panel (BRAF V600E, KRAS, and NRAS) with high specificity and high PPVs may be used particularly for the detection of thyroid malignancy. Cell blocks can be an especially useful and straightforward method for molecular diagnostic studies.

摘要

背景

甲状腺细针抽吸(FNA)结果异常的病例常需进行手术切除,尽管大多数病例在切除后被诊断为良性。需要额外的诊断标志物来指导异常甲状腺结节患者的管理。

材料与方法

这项回顾性研究纳入了 150 例 FNA 细胞学诊断异常的病例,这些病例均进行了细胞块上三个标志物(BRAF V600E、NRAS 和 KRAS)的分子检测。71 例患者有手术随访。

结果

当不考虑非典型滤泡性肿瘤/增生(NIFTP)为恶性时,细胞学和联合细胞学与分子检测(CC-MT)的阳性预测值(PPV)分别为 67.6%(95%CI:0.555-0.782)和 89.2%(95%CI:0.746-0.970)(P=0.004)。CC-MT 的敏感性为 68.8%,特异性为 82.5%,假阳性率为 17.4%。当考虑 NIFTP 为恶性时,细胞学和 CC-MT 的 PPV 分别为 83.1%(95%CI:0.743-0.918)和 94.6%(95%CI:0.873-1.018)(P=0.047)。CC-MT 的敏感性为 59.3%,特异性为 83.3%,假阳性率为 16.7%。

结论

在 FNA 细胞学异常分类中,添加小型分子检测面板可提高细胞学的阳性预测值。具有高特异性和高 PPV 的小型面板(BRAF V600E、KRAS 和 NRAS)可特别用于检测甲状腺恶性肿瘤。细胞块是进行分子诊断研究的一种特别有用和直接的方法。

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