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Front. Oncol., 07 May 2012 | https://doi.org/10.3389/fonc.2012.00042

Confocal laser endomicroscopy for diagnosis of Barrett’s esophagus

  • 1 Department of Medicine I, University of Erlangen-Nuremberg, Erlangen, Germany
  • 2 Institute of Pathology, Medical University Graz, Graz, Austria
  • 3 Institute of Pathology, Klinikum Bayreuth, Bayreuth, Germany

Barrett’s esophagus (BE) is established as a premalignant condition in the distal esophagus. Current surveillance guidelines recommend random biopsies every 1–2 cm at intervals of 3–5 years. Advanced endoscopic imaging of BE underwent several technical revolutions within the last decade including broad-field (red-flag) techniques (e.g., chromoendoscopy) and small-field techniques with confocal laser endomicroscopy (CLE) at the forefront. In this review we will focus on advanced endoscopic imaging using CLE for the diagnosis and characterization of BE and associated neoplasia. In addition, we will critically discuss the technique of CLE and provide some tricks and hints for the daily routine practice of CLE for diagnosis of BE.

Introduction

Barrett’s esophagus (BE) is a metaplastic condition which is characterized by the replacement of normal squamous epithelium into columnar (intestinal) epithelium within the distal esophagus. There is an ongoing discussion whether the diagnosis of BE needs histologically proven goblet cells as a prerequisite. At this time it is also unclear how to proceed clinically with cases without such goblet cells. The prevalence of BE still remains unknown. It is estimated that BE affects about 1–3% of the general population, although in autopsy studies the prevalence was reported to be only 0.4–0.9% (Winters et al., 1987; Cameron et al., 1990; Cameron, 1993; Ormsby et al., 2000; Vieth and Stolte, 2002). Probably these numbers are even lower according to the above mentioned discussion.

Gastroesophageal reflux disease (GERD) has been identified as the major risk factor for the development of BE, while advanced age (>60 years), obesity, male sex, and white race were additionally considered to be risk factors of BE (Gaddam and Sharma, 2010).

By itself, BE is considered to be the key risk factor for the development of esophageal adenocarcinoma (EAC). Compared to the general population, patients with BE are at a 30- to 50-fold increased risk for the development of EAC (Tytgat, 1995; Vieth et al., 2004). In this context it has been suggested that specialized intestinal metaplasia with goblet cells is the predominant preneoplastic condition which progressively develops to low-grade intraepithelial neoplasia (LGIEN), to high-grade intraepithelial neoplasia (HGIEN), and than to EAC (Reid et al., 1993; Vieth, 2007). Nevertheless, recent data indicate that even patients without goblet cells in the columnar lining at the distal esophagus show the same chromosomal and DNA content abnormalities and genetic instabilities compared to goblet cell containing esophageal metaplasia (Liu et al., 2009; Vieth and Barr, 2009). Moreover, one recent multicenter study including 210 patients with BE and LGIEN with a mean follow-up of 6.2 years demonstrated that patients with BE and LGIEN have a low annual incidence of about 0.44%/year of EAC which is similar to patients with non-dysplastic BE. In addition, no “convincing” risk factors for the progression of LGIEN to EAC could be found other than LGIEN itself preferably confirmed by a second opinion (Wani et al., 2011).

Therefore, all metaplasia in the columnar lined esophagus may already be on the path to cancer and need distinct examination by the exploiting team of an endoscopist and histopathologist.

Hence, current guidelines from most gastroenterological societies worldwide recommend endoscopic screening for the detection of BE for patients with chronic GERD. If a BE-segment is identified four-quadrant random biopsies at 2-cm intervals are recommended in patients without suspicion of HGIEN or at 1-cm intervals in patients with suspected HGIEN of metaplastic tissue supplemented with targeted biopsies of grossly suspicious areas according to the Seattle protocol (Peters et al., 2008).

While the presence of intraepithelial neoplasia or early adenocarcinoma within a BE-segment may occur patchy, standard white light endoscopy with random biopsy may miss a certain quantum of lesions. Moreover, the random biopsy protocol has several limitations, as it is time-consuming, expensive, and prone to sampling error because less than 10% of the surface area is sampled (Hwang, 2009).

Taken into account the tremendous increasing incidence of BE (about 350% over the past 20 years), the need for improved imaging techniques for diagnosis and characterization of BE becomes obvious.

Indeed, endoscopic imaging of BE has seen several technical revolutions within the last two decades. These new imaging techniques can be subdivided into broad-field techniques (“red-flag”) which allow the examination of the whole luminal surface area and small-field imaging techniques which provide an optical biopsy of the tissue. Red-flag techniques include both, dye-based (e.g., methylene blue) and dye-less chromoendoscopy (narrow band imaging, NBI; FICE; i-scan) (Figure 1) and magnification endoscopy while small-field imaging techniques include endocytoscopy and confocal laser endomicroscopy (CLE; Neumann et al., 2012).

FIGURE 1
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Figure 1. Typical endoscopic appearance of Barrett’s esophagus imaged using narrow band imaging (NBI) with single mucosal tears proximal to the esophagogastric junction.

Here, we will focus on advanced endoscopic imaging using CLE for the diagnosis and characterization of BE and associated neoplasia. In addition, we will critically discuss the technique of CLE and provide some tricks and hints for the daily routine practice of CLE for diagnosis of BE.

Technical Background

Confocal laser endomicroscopy is based on the principle of tissue illumination with a blue laser light (488 nm wave length) after application of fluorescence agents which can either be applied topically (e.g., acriflavine hydrochloride, cresyl violet) or systemically (fluorescein sodium; Neumann et al., 2010).

Up to now, only the topical applied fluorescence agents enabled imaging of cell nuclei which is essential to differentiate between LGIEN and HGIEN according to the Vienna classification of gastrointestinal neoplasia (Schlemper et al., 2000). While acriflavine accumulates in nuclei a potential mutagenic risk of this drug is discussed. Cresyl violet was recently introduced as an alternative fluorescence agent for confocal imaging which provides cytoplasmic enrichment and thereby negative visualization of nuclear morphology (Goetz et al., 2009).

Nevertheless, the most widely used fluorescent agent to date is intravenous fluorescein (mostly 3–5 ml of a 10% solution). Fluorescein is a non-toxic agent and FDA-cleared for diagnostic angiography of the retina for years. Importantly, as fluorescein is a non-selective vascular contrast agent, only architectural details could be imaged. The safety of intravenous fluorescein for confocal imaging was recently demonstrated in a large multicenter study, including 16 centers and nearly 2300 gastrointestinal endomicroscopy procedures (Wallace et al., 2010a). In this study no serious adverse events were reported. Mild adverse events occurred in 1.4% of individuals, including transient hypotension without shock (0.5%), nausea (0.39%), injection site erythema (0.35%), self-limited diffuse rash (0.04%), and mild epigastric pain (0.09%).

Currently, two different endomicroscopy systems are commercially available (Neumann et al., 2010). One is integrated into the distal tip of a standard, high-resolution endoscope (iCLE; Pentax, Tokyo, Japan) (Figure 2) and one is probe-based (pCLE; Cellvizio, Mauna Kea Technologies, Paris, France) (Figure 3) capable of passage through the accessory channel of nearly any endoscope. Both systems use an incident 488 nm wavelength laser and allow both, real-time observation and post hoc analysis of the tissue at about 1000-fold magnification.

FIGURE 2
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Figure 2. (A) Confocal laser endomicroscopy using the integrated device (iCLE). Regular shaped columnar lined epithelium with goblet cells (arrows) is clearly visible. (B) Histological image of Barrett’s epithelium with numerous typical goblet cells that replaced the regular squamous epithelium in the distal esophagus (H&E 200×).

FIGURE 3
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Figure 3. (A) pCLE image of high-grade intraepithelial neoplasia in patient with BE. Confocal imaging demonstrated dark, irregularly thickened epithelial cells, and dilated irregular vessels. (B) Histological image of Barrett’s esophagus with high-grade intraepithelial neoplasia. Cytological and architectural atypia is visible. The nuclei are larger in size with increased chromaticity, and loss of cell polarity. Architectural distortion is characterized by a back-to-back crypt pattern and focal cribriform areas.

The iCLE-system has an imaging plane depth ranging from 0 to 250 μm. The optical slice thickness is 7 μm, with lateral and axial resolutions of 0.7 μm. The observer can manually adjust the laser power output at the tissue surface ranging from 0 to 1000 μW. Confocal images are captured at a manually adjustable frame rate of 1.6 images/s at a resolution of 1024 × 512 pixels, or at 0.8 images/s at a resolution of 1024 × 1024 pixels with a confocal image field of view of 475 × 475 μm.

The pCLE-system offers different endomicroscopy-probes for luminal and non-luminal confocal exploration. Probes for endomicroscopy during esophagogastroduodenoscopy require accessory channels of 2.8 mm and have a working length of 3 m. Lateral resolution is 1 μm which constitutes to a 43% decrease in resolution compared to the iCLE-system (Bisschops and Bergman, 2010). Confocal images are streamed at a video frame rate of 12 frames/s. The system has a fixed laser power and a fixed image plane depth of 55–65 μm.

In order to achieve complete agreement between confocal diagnosis and biopsy acquisition for subsequent histopathological diagnosis one has to keep in mind that the working channel of the iCLE-system is located 5 mm to the right of the confocal lens. Therefore, when suction is applied to the mucosa, the resulting intramucosal hemorrhage is located 5 mm to the right from the area which has been evaluated using iCLE. For pCLE mild pressure is performed with the confocal probe to the tissue and the resulting reddish mucosa can guide subsequent biopsy acquisition. Moreover, we recommend attaching a clear cap at the distal tip of the endoscope for pCLE-imaging as motion artifacts substantially impede confocal imaging at the squamocolumnar junction. Even administration of antispasmodic agents (e.g., Buscopan) may help to stabilize the confocal probe for subsequent high-magnification imaging of the mucosa.

Endomicroscopy of Barrett’s Esophagus

The first study of confocal imaging for diagnosis of BE was introduced in 2006 and included 63 patients (Kiesslich et al., 2006). In this pioneer study by Kiesslich and coworkers iCLE was proven to reliable identify different epithelial cell types at the squamocolumnar junction, including squamous epithelium, gastric epithelium, and specialized intestinal epithelium containing goblet cells. Goblet cells could easily be identified as CLE displayed the mucin of goblet cells as very dark oval to round appearing structures within the columnar lined epithelium. In patients with BE-associated neoplasia CLE imaged large, irregular sheets of black cells which showed a marked dark abrupt contrast to the surrounding tissue and loss of regular architecture with irregular lumina of different diameter. The dark contrast is probably due to the lower pH within neoplastic cells. Additionally, the brightness of the lamina propria became heterogeneous according to an increased and irregular vasculature with fluorescein leakage. Based on these parameters the authors proposed a Confocal BE-classification to predict histopathology in the distal esophagus. In vivo imaging could predict BE and associated neoplasia with a sensitivity of 98 and 93%, specificity of 94 and 98%, and accuracy of 97%, respectively. Of note, most of the patients with neoplasia (80%) had mucosal irregularities or focal lesions that could be detected by high-resolution white light endoscopy.

This is of particular importance when taken into account the data of Bajbouj et al. (2010) where pCLE was compared with a standard four-quadrant biopsy protocol for the evaluation of neoplasia in BE. In this multicenter study a total of 670 pCLE-matched biopsies were obtained from 68 patients. The authors studied the diagnostic accuracy of pCLE for real-time diagnosis during ongoing endoscopy and in a blinded fashion by scoring the confocal images without having the endoscopic image available. The study demonstrates that correct image interpretation depends on simultaneous elucidation of endoscopic and confocal images, as on a per-patient basis, a significant decrease in specificity from 95 to 59% was observed when investigators were blinded to the endoscopic findings.

Therefore, simultaneous interpretation of macroscopic and microscopic images is essential as “The eye sees only what the mind is prepared to comprehend” (Henri Bergson 1859–1941, French philosopher).

In another prospective two-center trial 38 consecutive patients with BE were examined with standard high-resolution white light endoscopy and pCLE (Pohl et al., 2008). In a per-biopsy analysis, sensitivity and specificity for two independent investigators were 75 and 89%, and 75 and 91%, respectively, translating at best into a positive predictive value of 44% and a negative predictive value of 99% (Pohl et al., 2008).

One prospective, randomized, double-blind, controlled, crossover trial at a tertiary referral center evaluated whether iCLE with targeted mucosal biopsy improves the diagnostic yield of endoscopically inapparent, BE-associated neoplasia compared to standard endoscopy with a four-quadrant, random biopsy protocol (Dunbar et al., 2009). Overall, 39 patients completed the study protocol. It was found that iCLE with targeted biopsy almost doubled the diagnostic yield for neoplasia (34 vs. 17%) and was equivalent to the standard protocol for the final diagnosis of neoplasia. Moreover, two thirds of patients in the surveillance group did not need any mucosal biopsies at all. Another important lesson from the study is that there were two patients with HGIEN only identified using iCLE, whereas another two patients with HGIEN were only identified by standard white light endoscopy with random biopsies. This illustrates the limitation of CLE, which is a small-field imaging technique, therefore prone to sampling error.

Wallace et al. (2010b) determined the preliminary accuracy and interobserver agreement of pCLE in BE using a prospective, double-blind review of confocal images of BE after a training set of 20 images with known histology was reviewed to standardize image interpretation. The sensitivity for the diagnosis of neoplasia for the 11 attending endoscopists from different international centers was 88%, and the specificity was 96% with a substantial agreement on the pCLE diagnosis (86%, κ 0.72; 95% confidence interval, 0.58–0.86). These results suggest that pCLE for the diagnosis of neoplasia in BE has a very high accuracy and reliability and can relatively easy be learned and used (Figure 4).

FIGURE 4
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Figure 4. (A) In vivo endomicroscopy of advanced esophageal adenocarcinoma in patient with long-segment Barrett’s esophagus using the probe-based device (pCLE). Note the clear cap at the distal tip of the endoscope to avoid motion artifacts. (B) Corresponding endomicroscopic appearance of adenocarcinoma in a patient with Barrett’s esophagus. Irregular, dark cells with high contrast to the surrounding tissue indicate advanced neoplasia. (C) Histological image of moderately differentiated adenocarcinoma in a patient with Barrett’s esophagus with loss of regular architecture and superficial erosion.

Very recently the results of a large prospective international multicenter study on BE including five tertiary referral centers were presented (Sharma et al., 2011). In this study, 101 consecutive patients with BE were examined by high-definition white light endoscopy (HD-WLE), NBI, and pCLE, and the findings were recorded before biopsy samples were obtained. The sensitivity and specificity for HD-WLE were 34 and 93%, respectively, compared with 68 and 88%, respectively, for HD-WLE or pCLE which was statistically significant different. The sensitivity and specificity for HD-WLE or NBI were 45 and 88%, respectively, compared with 76 and 84%, respectively, for HD-WLE, NBI, or pCLE which again was statistically significant. Therefore, pCLE combined with HD-WLE significantly improved the ability to detect neoplasia in BE patients compared to HD-WLE alone.

In order to discriminate new diagnostic criteria for dysplastic BE-tissue again the group from Kansas City evaluated multiple pCLE criteria including the epithelial surface, epithelial cell, and gland morphology (Gaddam et al., 2011). By using these criteria the overall accuracy in diagnosing dysplasia was 82%. Interestingly, no differences in image interpretation were observed between experts and non-experts in confocal imaging. More importantly, after a structured teaching session, accuracy, and agreement between experienced and non-experienced observers was not different, suggesting a short learning curve of image interpretation.

Recently, a consensus of pCLE users for standardization of image criteria was introduced. The so called “Miami classification” described substantial parameters to differentiate between normal squamous epithelium, non-dysplastic Barrett’s epithelium, HGIEN, and adenocarcinoma in BE (Wallace et al., 2011). Following this classification, normal squamous epithelium is characterized by flat cells without crypts or villi and bright vessels within papillae, representing the intra papillary capillary loops. Non-dysplastic BE showed uniform villiform architecture with columnar cells and dark appearing goblet cells. In contrast, pCLE images demonstrating villiform structures and dark, irregularly thickened epithelial borders and dilated irregular vessels were specific for BE with HGIEN. Adenocarcinoma in BE was characterized by disorganized or a completely loss of villiform structures and crypts, dark columnar cells, and dilated irregular vessels.

Summary

Barrett’s esophagus is a premalignant condition as a sequel of long standing GERD. Therefore, surveillance is of paramount importance. Nevertheless, the patchy and inhomogeneous distribution of intraepithelial neoplasia within a Barrett’s segment makes a correct diagnosis often difficult. Columnar lined epithelium is often a mosaic of different cell types consisting of junctional and cardiac epithelium, specialized intestinal metaplasia with or without intraepithelial neoplasia. Random biopsies are prone to sampling error and may miss a quantum of lesions. Besides, they are cost expensive and may even result in severe complications (Vieth and Stolte, 2000; Mannath et al., 2010). Enhanced endoscopic imaging techniques seem to have overcome these limitations and are therefore highly recommended to improve diagnostic outcome of BE patients. CLE allows real-time in vivo assessment of architectural details at a comparable quality to standard histopathology. This is the base for saving time and thus money due to possible immediate further interventional steps such as local endoscopic resection in case of any suspicious lesions. Various large and multicenter studies have shown a substantial accuracy of CLE for diagnosis of BE and associated neoplasia. Therefore, this new imaging technique offers the potential of enhanced endoscopic imaging of BE for better surveillance and even to guide further endoscopic management (Leung et al., 2009). Moreover, CLE has great future potential in the assessment of BE as far as further improvement of the technique, which allows visualization of submucosal structures and new dye agents which allow specific visualization of cellular features, become available. This will allow a more precise risk stratification and triage of the patients: surgery vs. local endoscopic resection. Even more, molecular imaging with specific fluorescence-labeled probes against Barrett’s epithelium may enhance current concepts of Barrett’s management. Nevertheless, despite these exiting ongoing developments and even from a medical-legal point of view more data are needed to justify this approach in the clinical setting. In many countries a diagnosis made on base of tissue (virtual or histologically) is limited to board-certified pathologists also for legal reasons. Regulations may need revision according to these newly available techniques. Up to now, four-quadrant random biopsies according to the Seattle protocol still remained the gold standard for diagnosis and characterization of BE. More relevant and thus localized so called smarter biopsies due to the new imaging techniques may simplify and improve surveillance and planning of interventions.

Conflict of Interest Statement

Helmut Neumann: Speaker for Pentax, Mauna Kea Technologies, Essex Pharma, Abbott; research grants from Pentax, Siemens, Olympus, Nycomed, AstraZeneca, Pfizer. Cord Langner: none. Markus F. Neurath: Speaker, consultant, and advisory board member for Essex Pharma, MSD, Abbott, Giuliani, and Pentax. Research funding from the Deutsche Forschungsgemeinschaft. Michael Vieth: Speaker for Pentax, Mauna Kea Technologies, Altana, Falk, Astra Zeneca, Abbott, Olympus, Nycomed.

Abbreviations

EAC, esophageal adenocarcinoma; FICE, Fujinon intelligent color enhancement; HD-WLE, high-definition white light endoscopy; HGIEN, high-grade intraepithelial neoplasia; iCLE, integrated confocal laser endomicroscopy; LGIEN, low-grade intraepithelial neoplasia; NBI, narrow band imaging; pCLE, probe-based confocal laser endomicroscopy.

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Keywords: endomicroscopy, Barrett, cancer, CLE, advanced imgaging, fluorescein, dysplasia

Citation: Neumann H, Langner C, Neurath MF and Vieth M (2012) Confocal laser endomicroscopy for diagnosis of Barrett’s esophagus. Front. Oncol. 2:42. doi: 10.3389/fonc.2012.00042

Received: 13 January 2012; Paper pending published: 20 February 2012;
Accepted: 12 April 2012; Published online: 07 May 2012.

Edited by:

Alessandro Repici, Istituto Clinico Humanitas, Italy

Reviewed by:

Mirko Omejc, University Medical Centre Ljubljana, Slovenia
Parham Minoo, University of California San Diego, USA

Copyright: © 2012 Neumann, Langner, Neurath and Vieth. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

*Correspondence: Michael Vieth, Institut für Pathologie, Klinikum Bayreuth GmbH, Preuschwitzer Str. 101, 95445 Bayreuth, Germany. e-mail: pathologie@klinikum bayreuth.de