Cytopathologic identification of circulating tumor cells (CTCs) in breast cancer: Application of size-based enrichment

M. Kamal, Macall Leslie, Crista E. Horton, N. Hills, Rachel Davis, R. Nguyen, M. Razaq, K. Moxley, P. Hofman, Roy Zhang, Takemi Tanaka
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引用次数: 5

Abstract

Circulating tumor cells (CTCs) are indicative of metastatic disease in multiple types of solid tumors. Technologic advances in CTC enrichment have yielded profound variability in both quantity and phenotypic characteristics of CTCs. While size-based exclusion methods have improved the sensitivity of CTC capture, their diminished specificity requires subsequent robust cytopathologic identification of CTCs. In this study, we compared CTC counts from Isolation by Size of Epithelial/Trophoblastic Tumor cells (ISET®) filters sequentially stained by May-Grünwald/Giemsa (MGG), immunocytochemistry (ICC)/hematoxylin, and ICC/hematoxylin/eosin, followed by corresponding CTC criteria. An immune and endothelial cell cocktail of CD45/CD11b/CD31 antibodies adequately ruled out immune and endothelial cells, yet a substantial number of atypical morphologies with nuclear irregularity (i.e., circulating non-hematological/endothelial cells; CNHCs) were detected in both breast cancer cases and non-cancerous controls following hematoxylin nuclear counterstain. Cytoplasmic staining with eosin, significantly diminished CNHC counts. In conclusion, detection of CTCs from ISET filters using chromogenic ICC is feasible in conjunction with identification criteria of nuclear irregularity, negative reactivity to immune and endothelial cell markers, and presentation of visible cytoplasm. *Correspondence to: Takemi Tanaka, Ph.D., Associate Professor, University of Oklahoma Health Sciences Center, School of Medicine, Dept. of Pathology, Stephenson Cancer Center at 975 NE 10th, BRC-W, Rm 1415, Oklahoma City, OK, 73104, USA, Tel: Office (405)-271-8260, E-mail: takemi-tanaka@ouhsc.edu Roy Zhang, MD., Associate Professor, University of Oklahoma Health Sciences Center, School of Medicine, Dept. of Pathology, 940 SL Young Blvd, Oklahoma City, OK 73104, USA, Tel: Office (405)-271-1794, E-mail: roy-zhang@ouhsc.edu Special Issue: Recent Advancements in Clinical and Diagnostic Pathology Rawhi Omar University of Louisville School of Medicine USA
乳腺癌循环肿瘤细胞(CTCs)的细胞病理学鉴定:基于大小的富集的应用
循环肿瘤细胞(ctc)是多种类型实体瘤转移性疾病的指示性指标。CTC富集技术的进步使CTC的数量和表型特征都发生了深刻的变化。虽然基于大小的排除方法提高了CTC捕获的敏感性,但其特异性降低需要随后对CTC进行稳健的细胞病理学鉴定。在这项研究中,我们比较了上皮/营养层肿瘤细胞(ISET®)滤光片的CTC计数,这些滤光片分别用mai - grwald /Giemsa (MGG)、免疫细胞化学(ICC)/苏木精和ICC/苏木精/伊红染色,然后进行相应的CTC标准。CD45/CD11b/CD31抗体的免疫和内皮细胞混合物充分排除了免疫和内皮细胞,但仍有相当数量的非典型形态伴核不规则(即循环非血液/内皮细胞;苏木精核反染后在乳腺癌病例和非癌对照中均检测到cnhc。胞浆伊红染色,CNHC计数明显减少。综上所述,结合核不规则性、免疫和内皮细胞标志物的阴性反应性以及可见细胞质的鉴定标准,利用显色ICC检测ISET滤过器中的ctc是可行的。*通讯:Takemi Tanaka博士,副教授,俄克拉何马大学健康科学中心,医学院,病理学系,斯蒂芬森癌症中心975 NE 10th, BRC-W, Rm 1415,俄克拉何马市,OK 73104,美国,电话:办公室(405)-271-8260,E-mail: takemi-tanaka@ouhsc.edu,俄克拉何马大学健康科学中心,医学院,病理学系,940 SL Young Blvd,俄克拉何马市,OK 73104,美国,电话:办公室(405)-271-1794,E-mail: roy-zhang@ouhsc.edu特刊:临床和诊断病理学的最新进展美国路易斯维尔医学院Rawhi Omar大学
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