Division of Cytopathology, Department of Pathology and Laboratory Medicine, New York-Presbyterian Hospital-Weill Cornell Medical College, New York, New York.
Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Cancer Cytopathol. 2020 Sep;128(9):656-672. doi: 10.1002/cncy.22270. Epub 2020 Apr 8.
Morphologic and genetic analysis of thyroid nodules may be performed from a single vial. Preanalytic variables that affect nucleic acid extracted from a single vial are evaluated.
Thyroid fine-needle aspiration (FNA) specimens collected in CytoLyt were evaluated. A ThinPrep slide was prepared. Extracted nucleic acids were analyzed using Oncomine Comprehensive Panel, version 2, after Ion AmpliSeq library preparation. A pathologist and a cytotechnologist enumerated specimen cellularity.
Fifty-six samples were collected from 55 nodules in 53 patients. Bethesda category correlated with cellularity (P = .01), and storage time (median, 43 days; range, 7-77 days) was longer for specimens in categories II and III than for those in categories IV and VI (P = .01). The mean specimen DNA concentration was 4.5 ng/µL (range, 0-23.8 ng/µL), and 25 (45%) had concentrations >3.3 ng/µL. The mean specimen RNA concentration was 4.8 ng/µL (range, 0-42.4 ng/µL), and 31 (55%) had concentrations >1.4 ng/µL. Nucleic acid quantity increased with epithelial cellularity. Storage time weakly correlated with the quantity of extracted DNA, independent of cellularity, but not extracted RNA. Greater proportions of cell-free DNA and lesser proportions of long, intact RNA fragments were extracted from a subset of samples with longer storage time. Among 15 single nucleotide variants, the median mutant allelic fraction was 15.1%. One false-negative result was identified. Five specimens subsequently determined to harbor a genetic alteration failed quality metrics.
Cellularity and storage time affect the quantity and quality of nucleic acid extracted from thyroid FNA specimens collected in CytoLyt. Further investigation will serve to quantify the magnitude of such effects and to elucidate other contributing factors.
甲状腺结节的形态学和遗传学分析可从单个小瓶中进行。评估影响从小瓶中提取的核酸的分析前变量。
评估收集在 CytoLyt 中的甲状腺细针抽吸 (FNA) 标本。准备 ThinPrep 载玻片。提取的核酸在 Ion AmpliSeq 文库制备后使用 Oncomine 综合面板,版本 2 进行分析。病理学家和细胞技术专家计数标本的细胞数量。
从 53 名患者的 55 个结节中收集了 56 个样本。贝塞斯达分类与细胞数量相关(P = 0.01),并且 II 类和 III 类标本的储存时间(中位数,43 天;范围,7-77 天)长于 IV 类和 VI 类标本(P = 0.01)。标本的平均 DNA 浓度为 4.5ng/µL(范围,0-23.8ng/µL),25 个(45%)浓度>3.3ng/µL。标本的平均 RNA 浓度为 4.8ng/µL(范围,0-42.4ng/µL),31 个(55%)浓度>1.4ng/µL。核酸数量随上皮细胞数量增加而增加。储存时间与提取 DNA 的数量呈弱相关,与细胞数量无关,但与提取的 RNA 无关。从储存时间较长的亚组样本中提取出更多的无细胞游离 DNA 和较少的长、完整的 RNA 片段。在 15 个单核苷酸变异中,中位突变等位基因分数为 15.1%。确定了一个假阴性结果。五个随后被确定含有遗传改变的标本未能达到质量指标。
细胞数量和储存时间会影响从小瓶中提取的甲状腺 FNA 标本的核酸数量和质量。进一步的研究将有助于量化这种影响的程度,并阐明其他影响因素。