Enumeration and molecular characterization of circulating tumor cell using an in vivo capture system in squamous cell carcinoma of head and neck

Haidong Zhang, Shanchun Gong, Yaqun Liu, Longjun Liang, Shuangba He, Qingxiang Zhang, Mingyuan Si, Zhenkun Yu

Otorhinolaryngology and Head and Neck Surgery Department, Nanjing Tongren Hospital, School of Medicine, Southeast University, Nanjing 211100, China

Enumeration and molecular characterization of circulating tumor cell using an in vivo capture system in squamous cell carcinoma of head and neck

Haidong Zhang, Shanchun Gong, Yaqun Liu, Longjun Liang, Shuangba He, Qingxiang Zhang, Mingyuan Si, Zhenkun Yu

Otorhinolaryngology and Head and Neck Surgery Department, Nanjing Tongren Hospital, School of Medicine, Southeast University, Nanjing 211100, China

Objective:Detection rate and isolation yield of circulating tumor cell (CTC) are low in squamous cell carcinoma of head and neck (SCCHN) with in vitro approaches due to limited sample volumes. In this study, we applied the CellCollector to capture CTC in vivo from peripheral blood.

Methods:In total, the study included 22 cases with 37 times of detection. All of the patients were newly diagnosed with locally advanced or metastatic SCCHN, including laryngocarcinoma (40.9%, 9/22) and hypopharyngeal carcinoma (59.1%, 13/22). All patients received CTC analysis before treatment. Three patients received induction chemotherapy. Sixteen patients received surgical therapy, of which 13 patients received postoperative detection. Two patients received both induction chemotherapy and surgery treatment. Patients underwent two successive CellCollector applications 24 h before and 7 d after surgical therapy. Nine healthy volunteers were enrolled as the control group. Epidermal growth factor receptor variant type III (EGFRVIII) expression was analyzed with fluorescent dye labeled antibody.

Results:With CellCollector isolation, 72.7% (16/22) of the patients were positive for ≥1 CTC (CTC; range, 1—17 cells) before treatments and 46.7% (7/15) of patients were CTC positive for ≥1 CTC (CTC; range, 1—29 cells) after surgical therapy. Moreover, the detection rate of CellCollector (82.4%, 14/17; CTC count range, 0—17) in advanced SCCHN (stage III—IV) was much higher than that in early stages (stage I—II, 40.0%, 2/5; CTC count range, 0—2) (P＜0.05). EGFRVIII expression of CTC was also analyzed with fluorescence staining. One CTCEGFRVIII-positive patient was detected from six CTC-positive patients, and the positive expression of EGFRVIII was also found in the tumor tissue of this patient.

Conclusions:In vivo detection of CTCs had high sensitivity in SCCHN, which might improve CTC application in clinic.

CellCollector; SCCHN; in vivo; CTC detection

View this article at:https://doi.org/10.21147/j.issn.1000-9604.2017.03.05

Introduction

Although circulating tumor cell (CTC) has been reported almost 150 years ago, efficiency detection and molecular assay have only gained attention recently. Technology improvement makes CTC isolation possible for clinical application and more and more CTC detection methods have been reported recently (1). However, it is still a great challenge to detect CTC from peripheral blood of cancerpatients. Due to rarity of CTC and high unspecific cells background, with 6×106leukocytes, 2×108platelets and 4×109erythrocytes per mL of patient-derived blood sample, isolation and downstream molecular analysis of CTC are still a challenge (2). High detection rate, sufficient amounts of CTC and downstream molecular analysis are needed to satisfy clinical utility (3-5).

Squamous cell carcinoma of head and neck (SCCHN) is one of the frequently occurring and deadly diseases. CTC is a promising blood biomarker for “liquid biopsies” to improve individual treatment regimens for cancer patients (6-8), So far, several studies have shown that the sensitivity of CTC isolation is low and insufficient to satisfy clinical requirement in SCCHN (9-13). Although molecular characterization analysis could provide more clinical information for individual treatment, CTC isolation method with little unspecific white blood cells still needs to be improved (14,15).

More than 40 different methods for CTC detection have been reported (16). Various detection strategies have been developed to increase detection sensitivity and yield of CTC (2,17). To our best knowledge, a few of those methods had qualification for clinical utility (18,19). In this study, we used a new strategy to capture CTC in vivo with CellCollector (GILUPI CellCollector, GILUPI GmbH, Germany) (20). During 30 min incubation in the arm vein of cancer patients, functional domain of CellCollector was exposed to 2—3 L of blood, which significantly improved CTC detection sensitivity. CellCollector has high detection rate in lung cancer and neuroendocrine tumor (21,22). Monitoring treatment response with changes in CTC counts detected with CellCollector shows promising potential in clinic (21). This study will support the use of in vivo CTC capture as a new diagnostic principle for future clinical study testing the relevance of “liquid biopsies” to cancer treatments.

Materials and methods

Clinical information

This prospective, CTC observer blinded, single-center clinical study investigated the detection and molecular characterization of CTC from the peripheral blood of SCCHN patients using the CellCollector. The study was conducted at the Nanjing Tongren Hospital in November 2016 to April 2017, and included 22 cases with 37 times of detection. All of them were newly diagnosed SCCHN.

Most patients were male (21/22) aged 47—82 years old, including laryngocarcinoma (40.9%, 9/22) and hypopharyngeal carcinoma (59.1%, 13/22). All patients were received CTC detection before treatment. Three patients received induction chemotherapy after the first CTC detection. One case died of cancer-related complications before further treatment. Sixteen patients received surgical therapy, 13 of whom received postoperative CTC detection. Two patients received both induction chemotherapy and surgery treatment. Patients underwent two successive CellCollector detections 24 h before and 7 d after surgical therapy. A detailed summary of all patient data, including CTC counts, is shown in Table 1. At the same time, 9 healthy volunteers with no evidence of cancer disease were included as the control group. This study is registered in ClinicalTrials.gov (No. NCT03071900), and was approved by the Ethics Committee of Nanjing Tongren Hospital.

In vivo application of CellCollector

The GILUPI CellCollector is based on a sterile stainless steel medical wire, covered with a gold layer and a hydrogel layer at its functionalized tip. Before the application of the device, a 20 G peripheral venous catheter was placed into the median cubital vein of the patient. The CellCollector was inserted into the vein through the catheter until the tip of the device was extended 2 cm into the vein. After 30 min, the CellCollector was removed from the vein, cleaned and fixed for further examination.

CTC identification and epidermal growth factor receptor variant type III (EGFRVIII) staining

This function domain of CellCollector is covalently coupled with epithelial cell adhesion molecule (EpCAM) (humanized HEA 125, GILUPI GmbH, Potsdam, Germany) (Figure 1A). After the in vivo application, the CellCollector was washed three times and fixed with acetone for 10 min at room temperature. Captured cells were stained with EpCAM (Acris, New York, USA; clone HEA125-FITC) and pan-keratins (Exbio, Vestec, Czech Republic; clone C11-Alexa488; Millipore, Massachusetts, USA; clone LP5K-FITC; Exbio, Vestec, Czech Republic; clone A53-B/A2-Alexa488). CD45 (also called leukocyte common antigen) staining was performed to identify unspecific leucocytes (Exbio, Vestec, Czech Republic; clone MEM-28-Alexa647). Nuclear staining was performed with Hoechst33342 (Invitrogen, California, USA) at aconcentration of 1 mg/mL for 2 min. A cell was counted as positive CTC when its morphological features (4 μm, intact nucleus) and staining patterns were consistent with those of an epithelial cell (Hoechst33342/pan-keratin and/or EpCAM-positive/CD45-negative; Figure 1B). Specific antibody against EGFRVIII was used in EGFRVIII staining. The EGFRVIII antibody was labeled with phycoerythrin (PE) fluorescent dye. EGFRVIII expression was analyzed by immunohistochemical (IHC) method as described in published references.

Table 1 Clinicopathological data of all patients and number of captured CTCs

Statistical analysis

Statistical analyses were performed with SPSS Statistics (Version 17.0; SPSS Inc., Chicago, IL, USA) for Windows, and figures were generated using Prism 6 (GraphPad Software, Inc., La Jolla, CA, USA). Normal distribution was analyzed. Nonparametric tests (Kolmogorov-Smirnov test) were used. CTC counts in preoperative and postoperative groups were analyzed with Wilcoxon rank sum test. P＜0.05 was considered statistically significant.

Results

Patient characteristics

We enrolled 22 SCCHN patients and 9 healthy volunteers as the control group. Table 1 shows the clinicopathological characteristics of patients with laryngocarcinoma (n=9) and hypopharyngeal carcinoma (n=13). The median age of SCCHN patients was 65.5 (range, 47—82) years, and the patients were in different stages, including stage I (n=1), stage II (n=4), stage III (n=4) and stage IV (n=13).

In this study, 16 patients underwent surgical treatment, 3 patients underwent induction chemotherapy, and 2 patients received both induction chemotherapy and surgical treatments. One case died of cancer-related complications before further treatment. Fifteen patients received CTC detection before and after surgical treatment respectively.

Figure 1 Circulating tumor cells (CTC) capture and identification in vivo. (A) Schematic overview of CellCollector and in vivo application. The CellCollector wire is coated with anti-epithelial cell adhesion molecule (anti-EpCAM) antibodies and placed into the arm vein of cancer patients for 30 min to bind EpCAM-positive cells to the CellCollector; (B) The tumor cells are stained for EpCAM and keratins. Nuclear counterstain is done using Hoechst33342. CD45 staining is necessary to classify false positive events (leukocytes). Scale bars, 10 μm; (C) Images of CTCs isolated with the CellCollector. Tumor cells were identified as EpCAM and/or pan-keratin-positive (green) and CD45-negative (red) events. Hoechst33342 (blue) was used for nuclear counterstain. Scale bars, 10 μm.

CTC counts and correlations to clinicopathologic characteristics

For analyzing clinical correlation to CTC enumeration, CTC detection rate and CTC counts were used in multivariate analysis. The repeatability and stabilization of CTC analysis method that we used in this study were verified before (21). Representative images of CTC from spiking experiments are show in Figure 1C. In total, 72.7% (16/22) of the patients were positive for ≥1 CTC (range, 1—17 cells; Figure 2A). Most of the analyzed cells were single CTC. However, CTC clusters (range, 2—8) were also detected in 8 of 37 observed CellCollector results. No CTC-like events were observed on the CellCollector used in control group (Figure 2A). CTC detection rate was higher in patients with late stage than in patients with early stage (P＜0.05). In total, 5 patients were detected with stage I and II, two of whom had CTC-positive results, while, 82.4% (14/17) of stage III and IV patients have CTC-positive detection results, indicating CellCollector has high detection rate in SCCHN, especially in late stage (Figure 2B). CTC detection rates were not different between laryngocarcinoma and hypopharyngeal carcinoma (Figure 2C).

Monitoring of CTC during surgical therapy

To evaluate CTC number changes as a marker for analyzing surgical response in six patients with surgery, CTC detection was performed with CellCollector 24 h before and 7 d after surgical therapy. The detection rate of positive CTC decreased from 72.7% (16/22) with median CTC number of 2 before surgical treatment to 46.7% (7/15) with median CTC number of 0 after surgical treatment (P＜0.05), indicating that changes of CTC counts may have potential value to show treatment effect (Figure 2D).

EGFRVIII expression assay in CTC and tissue

To analyze EGFRVIII expression, CTC from six patients were analyzed with EGFRVIII fluorescence antibody staining during CTC identification process. PE was covalently linked to EGFRVIII antibody to observe EGFRVIII at orange channel by fluorescence microscope. EGFRVIII positive and negative CTC are shown in Figure 3A. EGFRVIII expression level was calculated with peripheral blood mononuclear cell (PBMC) as a negative control. Cut-off value is a ratio that was calculated with PBMC fluorescence value divided by background(unstaining area) fluorescence value. The cut-off value is 0.8 here. Base on calculation results, two patients were found EGFRVIII-positive CTC, one case positive boundary, and three negative among those analyzed patients (Figure 3B). The expression of EGFRVIII was detected in the primary tumor and metastatic tumor of a patient with IHC staining (Figure 4).

Figure 2 Analysis of circulating tumor cells (CTCs) detection rate. (A) Detection rate of CellCollector in squamous cell carcinoma of head and neck (SCCHN) and control group. Kolmogorov-Smirnov test, P＜0.05; (B) CTC enumeration in stage I—II and III—IV patients. Kolmogorov-Smirnov test, P＜0.05; (C) CTC enumeration in laryngocarcinoma and hypopharyngeal carcinoma. Kolmogorov-Smirnov test, P＞0.05; (D) The changes of CTC counts before and after therapy. Wilcoxon rank sum test, P＞0.05.

Discussion

In vivo analysis

Here, we reported that in vivo detection of CTC is a promising method for clinical utilization. In vivo detection methods show high CTC isolation rate (11,23). CellCollector has been shown high detection rate in lung cancer and neuroendocrine tumor (21,22). Increasing of blood volumes may overcome ex vivo limitation to increase detection rate (3). Although CellCollector was used in an in vivo way, it is user-friendly for clinical application. The 30-min incubation in peripheral vein is acceptable for the most of tested patients. With immunofluorescence technique, which was proved by clinical evidence, CTC could be identified under a fluorescence microscope (20).

CTCEGFRVIIIexpression

EGFRVIII is important for growth of tumor cells and specifically expressed in tumor cells (24,25). Here, we reported EGFRVIII expression on CTC. In total, 33.3% (2/6) patients were found CTCEGFRVIIIpositive. Interestingly, we found that in this patient with EGFRVIII-positive CTC, EGFRVIII expression in both primary and metastatic tumor tissues was positive, indicating EGFRVIII expression level may be coordinated between CTC and tumor tissue. CTC-based EGFRVIII analysis may be important for SCCHN especially when tumor tissue is not available. The comparison of CTC and tumor tissue shows that EGFRVIII expression may have consistency, indicating CTC is a potential biomarker for analyzing EGFRVIII expression.

Figure 3 Analysis of epidermal growth factor receptor variant type III (EGFRVIII) expression. (A) Circulating tumor cells (CTCs) are stained for epithelial cell adhesion molecule (EpCAM) and keratins. Nuclear counterstain is done using Hoechst33342. CD45 staining is necessary to classify false positive events (leukocytes). EGFRVIII positive and negative CTCs were shown. Bar, 10 μm; (B) Relative fluorescence analysis of EGFRVIII expression. EGFRVIII expression level of CTCs from six patients was analyzed. Cut-off value is 0.8.

Figure 4 Expression of epidermal growth factor receptor variant type III (EGFRVIII) in squamous cell carcinoma of head and neck (SCCHN) by immunohistochemical (IHC) staining (400×). (A) Primary carcinoma; (B) Metastatic carcinoma; (C) Control. EGFRVIII was expressed mainly on the cell membrane (yellow staining) and blue staining was the nuclei.

Molecular analysis of CellCollector

It already has been approved that gene mutations of CTC captured by CellCollector could be detected with digital polymerase chain reaction (PCR) (21). Next generation sequencing (NGS) could provide much more genetic information compared with digital PCR or amplification refractory mutation system-quality PCR (ARMS-qPCR) (26). CTC on functional domain was easy to separate from CellCollector with little unspecific cells by using a special cutter. Isolated CTC and CellCollector fragment together were collected into one Eppendorf (EP) tube to amplify the whole CTC genomic DNA for NGS analysis. Due to this isolation process, the sensitivity of NGS was greatly increased for detecting CTC genomic mutations. Next, we will focus on the work of CTC sequencing in SCCHN.

Clinical value of CellCollector in SCCHN

Base on high detection rate and high yield of CTC, monitoring of therapy effect with the changes of CTC counts before and after treatment could give more clinical information (21,27,28). Chemotherapy response of CTC counts have been reported for years (29). Additionally, CTC number sharply decreased after surgery compared with pre-operation CTC detection (30-32). In this study, two successive CTC detections have been carried out during surgical and/or induction chemotherapy process. After treatment, many patients had no CTC observed. In 5 of 15 patients, increased CTC number was found aftertreatment. The follow-up of those patients may be important to analyze different progression-free survival or overall survival compared with patients with decreased CTC number.

Conclusions

Low detection rate is the most important limitation for CTC study in SCCHN. In this study, CellCollector showed high sensitivity to CTC isolation from SCCHN patient’s peripheral vein blood, especially in advanced SCCHN patients. Moreover, CTC was easy to separate from CellCollector after identification with immunofluorescence staining. Molecular analysis of CTC may push “liquid biopsy” to a new level to apply and study.

Acknowledgements

We thank Dr. Jiaoteng Bai from Viroad Biotechnology Co. for technical support for this study. This study was supported by Grants from the National Nature Research Program of China (No. 81541057); Science and Technology Department Research Program of Jiangsu Province (No. BK20151080); and Science and Technology Department Research Program of Nanjing (No. 201402060).

Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.

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Cite this article as:Zhang H, Gong S, Liu Y, Liang L, He S, Zhang Q, Si M, Yu Z. Enumeration and molecular characterization of circulating tumor cell using an in vivo capture system in squamous cell carcinoma of head and neck. Chin J Cancer Res 2017;29(3):196-203. doi: 10.21147/ j.issn.1000-9604.2017.03.05

Zhenkun Yu. Otorhinolaryngology and Head and Neck Surgery Department, Nanjing Tongren Hospital, School of Medicine, Southeast University, Nanjing 211100, China. Email: yuzk@njtrh.org.

10.21147/j.issn.1000-9604.2017.03.05

Submitted Apr 24, 2017. Accepted for publication Jun 14, 2017.