Subclassification of prostate cancer circulating tumor cells by nuclear size reveals very small nuclear circulating tumor cells in patients with visceral metastases. Issue 18 (14th May 2015)

• Record Type: Journal Article
• Authors: Chen, Jie‐Fu; Ho, Hao; Lichterman, Jake; Lu, Yi‐Tsung; Zhang, Yang; Garcia, Mitch A.; Chen, Shang‐Fu; Liang, An‐Jou; Hodara, Elisabeth; Zhau, Haiyen E.; Hou, Shuang; Ahmed, Rafi S.; Luthringer, Daniel J.; Huang, Jiaoti; Li, Ker‐Chau; Chung, Leland W. K.; Ke, Zunfu; Tseng, Hsian‐Rong; Posadas, Edwin M.
• Is Part Of: Cancer. Volume 121:Issue 18(2015)
• Page Start: 3240
• Page End: 3251
• Publication Date: 2015-05-14
• Subjects: Cancer -- Periodicals; Cancer -- Cytopathology -- Periodicals; 616.99405
• DOI: 10.1002/cncr.29455
• Languages: English
• ISSNs: 0008-543X

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr29455-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Although enumeration of circulating tumor cells (CTCs) has shown some clinical value, the pool of CTCs contains a mixture of cells that contains additional information that can be extracted. The authors subclassified CTCs by shape features focusing on nuclear size and related this with clinical information.</p> </sec> <sec id="cncr29455-sec-0002" sec-type="section"> <title>METHODS</title> <p>A total of 148 blood samples were obtained from 57 patients with prostate cancer across the spectrum of metastatic states: no metastasis, nonvisceral metastasis, and visceral metastasis. CTCs captured and enumerated on NanoVelcro Chips (CytoLumina, Los Angeles, Calif) were subjected to pathologic review including nuclear size. The distribution of nuclear size was analyzed using a Gaussian mixture model. Correlations were made between CTC subpopulations and metastatic status.</p> </sec> <sec id="cncr29455-sec-0003" sec-type="section"> <title>RESULTS</title> <p>Statistical modeling of nuclear size distribution revealed 3 distinct subpopulations: large nuclear CTCs, small nuclear CTCs, and very small nuclear CTCs (vsnCTCs). Small nuclear CTCs and vsnCTC identified those patients with metastatic disease. However, vsnCTC counts alone were found to be elevated in patients with visceral metastases when compared with those without (0.36 ± 0.69 vs 1.95 ± 3.77 cells/mL blood; <italic>P</italic><.001). Serial enumeration studies suggested the emergence of vsnCTCs occurred before the detection of visceral metastases.</p> </sec> <sec id="cncr29455-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>There are morphologic subsets of CTCs that can be identified by fundamental pathologic approaches, such as nuclear size measurement. The results of this observational study strongly suggest that CTCs contain relevant information regarding disease status. In particular, the detection of vsnCTCs was found to be correlated with the presence of visceral metastases and should be formally explored as a putative blood‐borne biomarker to identify patients at risk of developing this clinical evolution of prostate cancer. <bold><italic>Cancer</italic> 2015;121:3240–3251.</bold> © <italic>2015 American Cancer Society</italic>.</p> </sec> </abstract>