Endoscopic surveillance of Barrett’s esophagus has become a foundation of the management of esophageal adenocarcinoma (EAC). Surveillance for Barrett’s esophagus commonly involves periodic upper endoscopy with biopsies of suspicious areas and random four-quadrant biopsies. However, targeted biopsies using narrow-band imaging can detect more dysplastic areas and thus reduce the number of biopsies required. Several specific mucosal and vascular patterns characteristic of Barrett’s esophagus have been described, but the proposed criteria are complex and diverse. Simpler classifications have recently been developed focusing on the differentiation between dysplasia and non-dysplasia. These include the Japan Esophageal Society classification, which defines regular and irregular patterns in terms of mucosal and vascular shapes. Cancer invasion depth is diagnosed by endoscopic ultrasonography (EUS); however, a meta-analysis of EUS staging of superficial EAC showed favorable pooled values for mucosal cancer staging, but unsatisfactory diagnostic results for EAC at the esophagogastric junction. Endoscopic resection has recently been suggested as a more accurate staging modality for superficial gastrointestinal cancers than EUS. Following endoscopic resection for gastrointestinal cancers, the risk of metastasis can be evaluated based on the histology of the resected specimen. European guidelines describe endoscopic resection as curative for well- or moderately differentiated mucosal cancers without lymphovascular invasion, and these criteria might be extended to lesions invading the submucosa (≤ 500 μm), i.e., to low-risk, well- or moderately differentiated tumors without lymphovascular involvement, and < 3 cm. These criteria were confirmed by a recent study in Japan.
Introduction
Esophageal adenocarcinoma (EAC) is an aggressive disease with an increasing incidence in the Western world [1‐3]. Although no equivalent data are available for Eastern countries, the rate of EAC is expected to increase in Asia because of the decreasing prevalence of Helicobacter pylori infection and Westernization of the diet [4, 5]. Survival of patients with EAC correlates with disease stage, with a 5-year-survival rate of about 20% in patients with locally advanced disease [6]. The poor survival of patients with advanced EAC indicates the need for its early detection [7, 8]. Endoscopic surveillance of Barrett’s esophagus (BE) has become a foundation of the management of EAC, especially in Western countries [9‐11], and this trend has accelerated in line with recent developments in advanced imaging and endoscopic resection technologies.
Surveillance and classification of lesions in patients with BE
Surveillance for EAC in patients with BE commonly involves periodic upper endoscopy, with biopsies of suspicious areas and random four-quadrant biopsies [12]. However, this biopsy protocol is time consuming, carries a risk of sampling error, and is hampered by low patient compliance [13]. New endoscopic techniques have, therefore, been developed to improve the recognition of specialized intestinal metaplasia (SIM), dysplasia, and cancer, by enhancing mucosal morphology. The most widely used such modality is narrow-band imaging (NBI) [14], and targeted biopsies sampled by this method allowed the detection of more dysplastic areas, therefore, reducing the number of biopsies required [15].
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Several groups have described specific mucosal and vascular patterns characteristic for the diagnosis of lesions in BE using NBI [16‐22]. These classification systems suggested that irregular mucosal pattern and vessels are predictive of dysplasia, while a ridged/villous pattern is predictive of SIM; however, despite promising initial findings, subsequent validation studies of these classification systems have reported unfavorable results [23‐27]. Furthermore, the proposed criteria were complex and diverse, thus limiting their use in daily clinical practice, with the complexity associated with the concept of differentiating between SIM and non-SIM and between dysplasia and non-dysplasia within the same classification.
Simpler classifications have recently been developed focusing on differentiating between dysplasia and non-dysplasia, with the aim of improving the clinical utility of the classification [28, 29]. The new classifications classify most mucosal or vascular descriptors as “regular” for non-dysplastic and “irregular” for dysplastic BE (Table 1). These simple descriptors make the classifications easy to apply in clinical practice, with acceptable sensitivity, specificity, and inter-observer agreement for the diagnosis of dysplasia in BE (Table 1).
Table 1
New endoscopic classifications for the diagnosis of lesions in patients with Barrett’s esophagus
BING classification
JES classification for Barrett’s esophagus
Non-dysplasia
Mucosal pattern: regular
Mucosal pattern: regular
Vascular pattern: regular
Vascular pattern: regular flat pattern
Dysplasia
Mucosal pattern: absent or irregular
Mucosal pattern: irregular
Vascular pattern: irregular
Vascular pattern: irregular
Diagnostic accuracy
Sensitivity 80%
Sensitivity 87%
Specificity 88%
Specificity 97%
Reproducibility
κ = 0.68
κ = 0.77
BING Barrett’s International NBI Group, JES Japan Esophageal Society
These new classifications include the Japan Esophageal Society classification of BE [29], in which the mucosal and vascular patterns are described as either regular or irregular (Table 2), based on detailed definitions of regular and irregular in terms of mucosal and vascular shape or arrangement (Figs. 1, 2) (Table 3), thus making the findings easy to interpret. This classification also includes a flat pattern (Fig. 3) as a regular pattern corresponding to non-dysplastic histology [30]. A validation study conducted by 10 endoscopic image reviewers using 156 still images showed promising accuracy and inter-observer agreement (Table 1).
Table 2
Japan Esophageal Society classification of Barrett’s esophagus
Pattern
Visibility
Morphologic features
Regularity
Mucosal
Visible
Pit
Regular or irregular
Non-pit
Invisiblea
Vascular
Visible
Net
Regular or irregular
Non-netb
Invisible
aIncluding a flat pattern
bIncluding normal-appearing long branching vessels and thick greenish vessels suggestive of a flat pattern
Fig. 1
Barrett’s esophageal cancer showing irregular vascular pattern (net type)
Fig. 2
Barrett’s esophageal cancer showing irregular mucosal pattern (non-pit type)
Table 3
Definition of regularity in Japan Esophageal Society classification of Barrett’s esophagus
Pattern
Regular
Irregular
Mucosal
Form/size
Similar
Various
Arrangement
Regular
Irregular
Density
Low or same as surrounding area
High
White zone
Clearly visible and/or with homogeneous width
Obscure/invisible or heterogeneous width
Vascular
Form
Similar or bending and branching gently or regularly
Various or bending and branching steeply or irregularly
Caliber change
Gradual
Abrupt
Location
Between or in mucosal patterns
Beyond of regardless of mucosal patterns
Flat pattern
Completely flat surface without a clear demarcation line. Greenish thick vessels and/or long branching vessels
Fig. 3
Flat-type mucosa: completely flat surface without a clear demarcation line and greenish thick vessels
×
×
×
Diagnosis of cancer invasion depth
Correct preoperative staging is crucial, given that the patient’s treatment strategy is determined largely on the basis of cancer invasion depth. Non-magnified endoscopy is the primary modality for diagnosing gastrointestinal cancer, and is also helpful for diagnosing cancer invasion depth. Correlations between endoscopic macroscopic type and invasion depth of superficial EAC have been reported [31, 32], and previous studies showed that non-magnified endoscopy could accurately diagnose invasion depth in gastrointestinal cancers [33‐36]. One study found that the overall correct diagnostic assessment of early esophageal cancers was high using either non-magnified endoscopy or endoscopic ultrasonography (EUS) with a 20-MHz mini-probe, with no significant differences between the two techniques (Table 4) [37]. Although its relative simplicity means that non-magnified endoscopy may be a good modality for diagnosing EAC invasion depth, the diagnosis is subjective, and more objective criteria are, therefore, needed.
Table 4
Diagnostic performances of non-magnified endoscopy and endoscopic ultrasonography for superficial esophageal adenocarcinoma (sensitivity and specificity for mucosal cancer)
EUS can also be used to diagnose cancer invasion depth. Conventional EUS (7.5 MHz) can differentiate between advanced T3/T4 carcinomas and T1/T2 carcinomas in more than 80% of cases; however, accurate differentiation between mucosal and submucosal (SM) invasion is difficult [38‐41]. However, EUS using a mini-probe (20 MHz) enables the esophageal wall to be imaged in nine layers, thus permitting the muscularis mucosa to be seen in greater detail. Mini-probe EUS can, therefore, be used to distinguish between mucosal and SM cancers, thereby improving staging accuracy.
A previous meta-analyses of EUS staging of superficial esophageal cancers showed favorable pooled values for mucosal cancer staging, with a sensitivity of 0.85 [95% confidence interval (CI) 0.82–0.88], specificity of 0.87 (95% CI 0.84–0.90), positive likelihood ratio of 6.62 (95%CI 3.6–12.12), and negative likelihood ratio of 0.20 (95%CI 0.14–0.30). The equivalent values for SM cancer staging were 0.86 for sensitivity (95%CI 0.82–0.89), 0.86 for specificity (95%CI 0.83–0.89), 5.13 for positive likelihood ratio (95%CI 3.36–7.82), and 0.17 for negative likelihood ratio (95%CI 0.09–0.30) [42].
However, when the results were limited to the diagnosis of EAC, the performance of EUS was not satisfactory (Table 5) [43‐46] compared with its ability to diagnose esophageal squamous cell carcinoma and gastric cancer. Meta-analyses of the diagnostic accuracy of EUS for mucosal or SM micro-invasive esophageal squamous cell carcinoma showed a sensitivity of 0.87 (95%CI 0.81–0.92), specificity 0.94 (95%CI 0.88–0.98), positive likelihood ratio 11.6 (95%CI 5.4–24.7), and negative likelihood ratio 0.15 (95%CI 0.10–0.23) [47], with equivalent results for mucosal gastric cancer of sensitivity 0.87 (95%CI 0.81–0.92), specificity 0.75 (95%CI 0.62–0.84), positive likelihood ratio 3.4 (95%CI 2.3–5.0), and negative likelihood ratio 0.17 (95%CI 0.12–0.24) [48].
Table 5
Diagnostic performance of endoscopic ultrasonography for superficial esophageal adenocarcinoma (sensitivity and specificity for mucosal cancer)
The poor diagnostic yield was probably caused by difficulties in diagnosing EAC in the distal part of the esophagus, given that the diagnostic accuracy for EAC in the distal part of the esophagus was significantly worse than that for EAC in the mid- and proximal parts of the esophagus (Table 6) [37, 49]. This emphasizes the fact that it is particularly difficult to achieve adequate water preparation in the distal esophagus by instilling fluid through the endoscopic channel, in addition to substantial motility that prevents dilatation of the distal esophagus from being maintained for longer periods.
Table 6
Diagnostic performance of endoscopic ultrasonography for superficial esophageal adenocarcinoma (sensitivity and specificity for mucosal cancer) with regard to imaging modality and lesion location
Endoscopic resection has recently been suggested as a staging modality for superficial gastrointestinal cancers, based on the limited accuracies of EUS and non-magnified endoscopy. Endoscopic resection, in the form of endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD), allows for removal of visible lesions and histologic assessment of the resected tissue, thus facilitating accurate diagnostic staging of the disease (Figs. 4, 5, 6, 7) [50, 51].
Fig. 4
IIa type esophagogastric junctional cancer
Fig. 5
IIa type esophagogastric junctional cancer with indigo carmine staining
Fig. 6
Histology of resected specimen showed deep muscularis mucosa invasion of cancer. SMM superficial muscularis mucosa, LPM lamina propria, DMM deep muscularis mucosa
Fig. 7
Mapping of the cancer. SMM superficial muscularis mucosa, LPM lamina propria, DMM deep muscularis mucosa, MM muscularis mucosa
×
×
×
×
The various modalities of EMR include the use of a transparent cap, two-channel endoscope, and ligation. However, these modalities are limited with respect to resection size, and large lesions must be resected in several fragments. Histological assessment of cancer invasion depth can be inaccurate if lesions are resected in small fragments, and histologic evaluation of several specimens does not allow the outer margins of the neoplastic area to be identified, and complete resection, therefore, cannot be confirmed. In addition, piecemeal resection of early neoplasia in BE is associated with a high local recurrence rate, probably because of small remnants of neoplastic tissue left in situ [52‐55]. ESD provides larger specimens than EMR, thus allowing more precise histological analysis and higher en bloc and curative resection rates, and potentially reducing the incidence of recurrence. A recent meta-analysis of non-randomized studies showed that ESD of early gastrointestinal tumors was superior to EMR in terms of en bloc and curative resection rates, but was more time consuming and associated with higher rates of bleeding and perforation [56].
Several studies have reported on the use of ESD for EAC and esophagogastric junction cancer [57‐66]. In general, ESD is associated with favorable outcomes with acceptable en bloc resection and complication rates. However, the curative resection rate, defined as en bloc resection with cancer-free margins and minimal risk of metastasis, limited to EAC at the esophagogastric junction, was significantly lower than those for cardia and non-cardia gastric cancers (Table 7) [57, 66]. One cause of incomplete resection of esophagogastric junction EAC was positive lateral margins caused by sub-epithelial progression of the tumor proximally, which were hard to recognize before treatment, while the low accuracy of diagnosing cancer invasion depth before treatment and high lymphovascular involvement, confirmed in resected specimens, were also contributory factors.
Table 7
Outcomes of endoscopic submucosal dissection for esophagogastric junctional cancer with regard to location
aComplete resection: en bloc resection with cancer-free margins
bCurative resection: complete resection with low risk of metastasis
Risk of metastasis
The risk of metastasis after endoscopic resection for gastrointestinal cancers is evaluated based on histologic findings of the resected specimen. Studies of esophagectomy specimens have indicated a low risk of 0.0–1.3% for mucosal EAC [67‐69], thus providing the rationale for endoscopic treatment of mucosal EAC with curative intent.
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The frequency of metastasis in EAC is known to increase with increasing depth of tumor invasion into the SM [70‐72]. SM1 cancer, i.e., cancer invading the shallow part of the SM, remains the most controversial, with some studies reporting a relevant incidence of lymph node metastasis even in SM1 cancers [73‐75]. However, when the rate of metastasis is stratified by pathologic findings, SM1 cancers without risk factors such as lymphovascular involvement and a poorly differentiated component have very low rates [76‐78]. Some studies [79, 80] have accordingly suggested that a subgroup of SM cancers could be adequately treated by endoscopic resection.
European guidelines [80] indicate that endoscopic resection appears to be curative for well- or moderately differentiated mucosal cancers without lymphatic or vascular invasion, and that these criteria might be extended to lesions with invasion into the SM (≤ 500 μm), namely to low-risk tumors (well or moderately differentiated, without lymphovascular involvement, < 3 cm) (Table 8). A recent study in Japan [81] validated these criteria, showing no metastases (0/186 lesions) in patients with mucosal cancer without lymphovascular involvement and a poorly differentiated component, or in patients with SM cancer (≤ 500 μm) without lymphovascular involvement, a poorly differentiated component, and ≤ 30 mm (0/32 lesions).
Table 8
Assessment of metastasis risk based on histology of endoscopically resected specimen
Recent advances in endoscopic technologies have provided various tools for the management of gastrointestinal cancers. Previous studies showed the utility of such tools for the early detection and accurate staging of cancers. However, most of these studies were retrospective and limited by small sample sizes. Prospective, multicenter studies are, therefore, needed to provide more reliable evidence and facilitate the use of these tools in clinical practice.
Acknowledgements
We thank Susan Furness, PhD, from Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript.
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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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