Quality Indicators for the Detection of Helicobacter pylori-Negative Early Gastric Cancer: A Retrospective Observational Study

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Clin Endosc. 2020;53(6):698-704

Publication date (electronic) : 2020 March 13

doi : https://doi.org/10.5946/ce.2019.203

Fumiaki Ishibashi^,1,2, Konomi Kobayashi^1,3, Keita Fukushima^2,3, Ryu Tanaka², Tomohiro Kawakami¹, Junko Kato², Kazuaki Sugihara²

¹Koganei Tsurukame Clinic, Endoscopy Center, Tokyo, Japan

²Shinjuku Tsurukame Clinic, Digestive Disease Center, Tokyo, Japan

³Mirraza Shinjuku Tsurukame Clinic, Tokyo, Japan

Correspondence: Fumiaki Ishibashi Koganei Tsurukame Clinic, Endoscopy Center, 6-14-28-3F, Honcho, Koganei-shi, Tokyo, 184-0004, Japan Tel: +81-42-386-3757, Fax: +81-42-386-7390, E-mail: ishibashi@tsurukamekai.jp

Received 2019 October 21; Revised 2019 November 13; Accepted 2019 December 10.

Abstract

Introduction

Helicobacter pylori (HP) is a major cause of carcinogenesis in the gastric mucosa, and the majority of intestinal-type early gastric cancers (I-EGCs) develop in the HP-positive gastric mucosa [1-3]. Moreover, diffuse-type EGCs (D-EGCs) can be detected in the HP-positive gastric mucosa. While current HP infection is a risk factor for both I-EGC and D-EGC, successful therapy and HP eradication decreases the prevalence [4-6]. Since eradication therapy of HP has been performed and public hygiene has improved worldwide, the proportion of people carrying HP has gradually decreased, and subsequently the likelihood for encountering HP-negative EGCs, including HP-naïve EGCs, has increased [7,8]. Close follow-up after successful HP-eradication therapy revealed the possibility that EGCs could be detected in uninflamed gastric mucosa [9]. Additionally, various types of HP-naïve gastric cancers, including gastric adenocarcinoma of the fundic gland type (GA-FG) and pure signet ring cell carcinoma, have been reported [7,10-12]. However, it is fairly difficult to detect HP-negative gastric cancers, including HP-naïve EGCs, compared to HP-associated EGCs because the characteristics of such cancer are unclear and atypical [7,13]. In addition, physicians tend to pay less attention to lesions during screening HP-naïve gastric mucosa.

In Japan, gastric cancer screening has been widely performed. Recently, it was suggested that screening by endoscopy is more effective than the barium swallow test with respect to detecting gastric cancer and reducing mortality rates due to gastric cancers [14-16]. Based on this evidence, screening by endoscopy has been willingly chosen for the municipality based civilian medical checkup. In addition, a number of private companies promote the medical checkup of their employees, including an examination by upper endoscopy. Consequently, endoscopy centers for gastric cancer screening are required to perform a number of endoscopic examinations a day in a relatively short time; thus, missing EGC generated in HP-eradicated or -naïve mucosa is considered likely. Moreover, the examination time of an upper endoscopy was reported to be a quality indicator for upper endoscopy [17-19]. However, it is unknown whether the shortness of the examination time influences the detection rate of EGCs, especially in the HP-negative stomach. Furthermore, the detection rate of EGCs depends on the frequency of biopsy and the physician’s experience of endoscopy [20]. In this study, we aimed to find quality indicators for detecting EGCs generated in the HP-negative stomach.

Materials and Methods

Results

Physician and patient characteristics

A total of 13,477 cases of upper endoscopy, including examinations for both outpatients and medical checkup, were performed by nine physicians. The characteristics of the patients, as well as the physicians who performed the endoscopies are shown in Table 1. The mean number of cases that physicians performed a day was 24.0. The patients’ mean age was 47.2 years old, and the ratio of male to female was 1.24:1. On the basis of the existence of atrophic gastritis and examinations for determining HP infection, the status of HP infection was current among 427 cases (3.2%), past infection among 2,309 cases (17.1%), and uninfected among 10,740 cases (79.7%). There were no significant differences in patient background among the examining physicians. Notably, there were no significant differences in baseline characteristics for each group; HP-positive, -eradicated, and -naïve.

Table 1.

Physician and Patient Characteristics

Observation time for stomach screening was shorter in the HP-eradicated and -naïve patients compared to the HP-positive patients

To address whether the observation time varies according to the status of HP infection, we compared the observation time of the HP-positive and -negative patients for all physicians. We found that the observation time in the HP-eradicated and -naïve patients was significantly shorter for all physicians (p<0.05, one-way ANOVA) (Table 2).

Table 2.

Examination Summary

Observation time and experience of endoscopy correlate with the detection rate of high-risk lesions in HP-eradicated and -naïve patients

We explored the relationship between various physician factors and the detection rate of HRLs found in our registry. Among the 13,477 cases of our registry, 23 cases of HRLs, including EGCs, were found (Table 2). The detection rate of HRLs in the HP-positive patients was 2.41% (12 cases; 3 cases of D-EGC, 6 cases of I-EGC, and 3 cases of intestinal adenoma). In contrast, the detection rate of HRLs in the HP-eradicated and -naïve patients was much lower at 0.63% (14 cases; 3 cases of D-EGC, 7 cases of I-EGC, and 4 cases of intestinal adenoma) and 0.095%, respectively (10 cases; 3 cases of GA-FG, 1 case of raspberry like tumor, 1 case of neuroendocrine tumor, 2 cases of mucosa-associated lymphoid tissue lymphoma, 2 cases of D-EGC, and 1 case of gastric-type I-EGC) compared to HP-positive patients. There was no significant difference in the pathological characteristics of the cancers in the three groups. Correlation analysis revealed that experience of endoscopy correlated with the detection rate of HRLs in the HP-naïve patients (r=0.7273; Table 3). The observation time in the HP-positive, -eradicated, and -naïve patients only correlated with the detection rate of HP-eradicated HRLs (r=0.713, 0.7827, and 0.7323, respectively). These results suggest that observation time and experience of endoscopy are quality indicators for the detection of HRLs in HP-eradicated and -naïve patients.

Table 3.

Results of Correlation Analysis between Explanatory Variables and the High-Risk Lesion Detection Rate

Observation time and experience of endoscopy are quality indicators for detecting high-risk lesions in HP-negative patients

To confirm the possibility that observation time and experience of endoscopy are predictors for the detection rate of HRLs in HP-eradicated and -naïve patients, we employed regression analysis for each explanatory variable (Table 4). Single regression analysis revealed that observation time during screening HP-positive, -eradicated, and -naïve stomach was an independent predictors for detecting HRLs in the HP -eradicated patients (p=0.03106, 0.01263, and 0.02485, respectively). In addition, experience of endoscopy was an independent predictor for detecting HRLs in the HP-naïve patients (p=0.02638). Subsequently, we employed the same dataset for the multiple regression analysis to estimate the most efficient combinations of explanatory variables. As a result, the combination of observation time and experience of endoscopy improved the prediction of HRLs in HP-naïve patients (Table 4). By using the equation on the basis of the result of Table 4, we estimated the detection rate of HRLs according to experience of endoscopy and observation time in the HP-naïve stomach (Table 5). This result suggested that less-experienced physicians could improve their detection rate of HRLs by taking sufficient time for screening. Furthermore, we validated this established model through the observed-predicted plot, and subsequently proved that the actual detection rates of HP-negative HRLs by physicians were well predicted (Fig. 1).

Table 4.

Results of Regression Analysis for Determining the Factors for Predicting the High-Risk Lesion Detection Rate

Table 5.

Estimated Detection Rate of High-Risk Lesions in Helicobacter pylori-Naïve Patients by Using the Established Model

Fig. 1.

Observed-predicted plot of the detection rate of Helicobacter pylori (HP)-naïve high-risk lesions (HRLs). On the basis of the equation calculated by multivariate analysis, a black line was drawn for the prediction of the physicians’ detection rate of HP-naïve HRLs. The grey area indicates the 95% confidence interval. Each dot plot indicates the actual physicians’ detection rate of HP-naïve HRLs.

Discussion

In contrast to the knowledge of the quality indicators for colonoscopy, little is known about the quality indicators for detecting EGCs [23]. A few studies have revealed that several factors, including observation time and frequency of biopsy, are quality indicators for detecting EGCs. In this study, we aimed to validate previously reported quality indicators for detecting HRLs, including EGCs, on the HP-positive and HP-negative stomach. As previous reports have indicated, we found that longer observation time during screening of the stomach was a predictor for detecting HRLs. Notably, we analyzed our dataset according to the status of HP infection, defined as current infection, past infection, and HP-naïve.

EGCs generated in the atrophic mucosa after successful HP eradication therapy are difficult to detect because these EGCs usually manifest as diminutive and atypical lesions [13]. Physicians recognize that HP-positive patients are at high risk for generating EGCs compared to HP-negative patients. In addition, the stomach of HP-positive patients is more difficult to screen than that of HP-negative patients due to increased mucus and active inflammation. The time required for screening the stomach is affected by such conditions. In contrast, it has been suggested that stomach with reduced inflammation post successful eradication therapy of HP tends to be screened for a shorter time compared to the HP-positive stomach. In fact, we revealed in this study that the observation time of the HP-eradicated stomach was significantly shorter than the HP-positive stomach.

Longer observation time during upper endoscopy is known to be a reliable quality indicator for detecting HRLs [17-19]. As we indicated above, the observation time was affected by the status of HP infection. Nevertheless, it has yet to be determined whether a shortened observation time lowers the detection rate of EGCs in HP-negative patients. In addition, it is not yet known whether other factors, including frequency of biopsy, are reliable quality indicators for detecting HRLs in HP-negative patients. In this study, we revealed that the observation time was a predictor for the detection of HRLs found in the HP-eradicated stomach. Thus, a shortened observation time may result in an increased risk of missing HRLs in the HP-eradicated stomach.

HP is a well-known and potent causative agent of stomach cancer. Endoscopic findings enable endoscopists to estimate the presence of HP; therefore, it is expected that detection of HP-positive HRLs might be easier than HP-negative HRLs. However, no significant predictor for detecting HP-positive HRLs was found in our study setting. In contrast, HP-naïve gastric mucosa merely generates malignant lesions, with the exception of recently reported GA-FG and other rare lesions, thus physicians have less experience of detecting HP-naïve lesions. In this study, experience of endoscopy was found to be a predictor for detecting HRLs in the HP-naïve stomach, while observation time during screening the HP-naïve stomach was not. Less experienced physicians, such as trainees, should be intensively trained for detecting these rare lesions according to the training program, and screen the HP-naïve stomach carefully. Notably, the multiple regression model we established indicated that longer observation time on the HP-naïve stomach might complement less experience of the physician.

This study has several limitations. First, this study was a retrospective observation study that involved selection bias for subjects. The average age of subjects was 47.2 years old, thus this study did not cover the general population in Japan. Our cohort enclosed younger age people than the general population because most patients in our institution were healthy employees of private companies. Second, we only analyzed 37 cases of HRLs in the small cohort (a total of 13,477 cases) and only nine endoscopists were enrolled in this study; thus, the statistical power and reliability for the analyses might be weak. Third, the actual observation time of the stomach might be underestimated because we calculated the observation time retrospectively by using recorded pictures, and the time needed for the elimination of mucus, especially in the HP-positive stomach, was included in the calculation of the observation time. Fourth, judgement on the degree of atrophy of the stomach lacked inter-observer agreement in the study. Finally, it was difficult to address whether the experience of endoscopy had a continuous effect on the detection of HRL because we did not follow the performance of the same endoscopist over the years. To overcome these limitations, a large scaled-prospective study should be conducted.

In conclusion, we revealed that experience of endoscopy was a quality indicator for detecting HRLs in HP-naïve patients, whereas observation time during screening endoscopy was a quality indicator for detecting HRLs in HP-eradicated patients.

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