Clinicopathological features of early gastric cancers arising in Helicobacter pylori uninfected patients

Chiko Sato, Kingo Hirasawa, Yoko Tateishi, Yuichiro Ozeki, Atsushi Sawada, Ryosuke Ikeda,Takehide Fukuchi, Masafumi Nishio, Ryosuke Kobayashi, Makomo Makazu, Hiroaki Kaneko, Yoshiaki Inayama,Shin Maeda

Abstract

Key words: Early gastric cancer; Helicobacter pylori; Un-infection; Negative;

INTRODUCTION

Most gastric cancers involveHelicobacter pylori(H. pylori) infection in their development, and in 1994H. pyloriwas certified as a “definite carcinogen” for gastric cancer development[1,2].H. pyloriinfection results in inflammation, atrophy of the gastric mucosa, and intestinal metaplasia; whenH. pyloriinfection becomes chronic there is a high-risk gastric cancer[3].

In recent years, awareness of eradication therapy has increased in Japan, thus reducing the rate ofH. pyloriinfection, especially in the young people due to the improvement of sanitary environment and expanding the indication of eradication[4].AsH. pyloriinfections decrease, the proportion of gastric cancers arising fromH. pyloriuninfected gastric mucosa will increase[5]. However, at the moment,H. pyloriuninfected gastric cancer (HpUIGC) is very rare as compared toH. pylori-positive gastric cancer (HpPGC). The definition is not yet well established, and its frequency is reported to differ from 0.4 to 5.4%[6-11]. Previous studies have reported that the undifferentiated-type of HpUIGC is more frequently observed than differentiatedtype[7-9]. However, in recent years, differentiated-type gastric cancers such as oxyntic glands adenoma/adenocarcinoma and foveolar type adenoma/adenocarcinoma, even including HpUIGC, were reported[12,13]. Few studies have investigated HpUIGC and its clinicopathological features have not been sufficiently documented. Therefore,elucidation of characteristics of early-stage HpUIGC is essential. We evaluated the characteristics of HpUIGC treated with endoscopic submucosal dissection (ESD)focusing on pathological and endoscopic features.

MATERIALS AND METHODS

Determination of H. pylori-uninfection status

Three criteria were used to determine whether a patient wasH. pylori-uninfected: (1)No medical history ofH. pylorieradication therapy, which was determined by investigating the patients’ medical records and conducting patient interviews; (2)Lack of endoscopic atrophy, patients with C-0 atrophy were selected as HpUIGC[14].As a supplementary finding, we referenced the endoscopic findings of the Kyoto classification score, including RAC (regular arrangement of collecting venule)[15,16]. The endoscopic findings were subsequently verified by three skilled endoscopists (KH,CS, and SM). And (3) laboratory examination that included serum anti-H. pylori-IgG antibody, Urease breath test (UBT), Rapid urease test (RUT), and microscopic examination[17]. If a test was negative forH. pyloriby two or more examinations this was consideredH. pyloriuninfected[18,19]. Among the HpUIGC patients, the presence or absence of pathological atrophy was evaluated using the updated Sydney system in the background mucosa of ESD specimens[20]. Tumors satisfying all the three conditions described above were identified as HpUIGC.

Patients

Between May 2000 and September 2019, a total of 2569 patients with 3477 gastric cancers were treated by endoscopic submucosal dissection (ESD) at Yokohama City University Medical Center. Of these patients, 2462 consecutive patients with 3370 gastric cancers were assessed forH. pyloristatus and enrolled in this study. The remaining 107 patients included 87 patients with cancer in their gastric remnants, 16 with cancer in their gastric tubes, 4 with neuroendocrine tumors, were excluded. Of the 3370 gastric cancers, 30 gastric cancers satisfied the three criteria outlined above and were classified as HpUIGCs.

Characterization of clinicopathological features of the HpUIGCs

We investigated the frequency and features of HpUIGC. Clinicopathological features including age, sex, location, macroscopic type, histological type, tumor size, depth of invasion, presence or absence of lymphovascular invasion, and treatment outcome were evaluated. The location of the gastric lesions was categorized based on stomach location: upper third (U), middle third (M), and lower third (L). The histological type was identified as differentiated or undifferentiated according to the 15thedition of the Japanese classification of gastric cancer[21]. The differentiated type was further classified into well-differentiated (tub1), moderately differentiated (tub2), or,papillary (pap) adenocarcinoma. The undifferentiated type was classified as poorly differentiated (por) or signet-ring cell (sig) adenocarcinoma. HpUIGC was further categorized into four types based on their histopathological features (1) Fundic gland adenocarcinoma, (2) Foveolar-type adenocarcinoma, (3) Intestinal phenotype adenocarcinoma, and (4) Pure signet-ring cell carcinoma. Finally, the 30 cases of HpUIGC were evaluated for their mucin phenotypes and endoscopic features.

Indications of ESD

Indications of gastric ESD were determined according to the gastric cancer treatment guidelines of the Japanese Gastric Cancer Association (JGCA). Briefly, the indication criteria were defined as differentiated-type mucosal gastric cancer lesions without ulcers [UL (-)] regardless of size, differentiated-type mucosal gastric cancer lesions ≤ 3 cm in size with ulcers [UL (+)], undifferentiated-type mucosal gastric cancer lesions ≤2 cm in size without ulceration [UL (-)], and confirming no evidence of lymph node metastasis (LNM), and distant metastasis by preoperative computed tomography[22].

Endoscopic submucosal dissection

All lesions were treated by ESD. The gastric ESDs were performed as previously described[23,24]. Briefly, after marking approximately 5 mm around the borders of the lesion, circumferential incision and submucosal dissection were made using an ITknife2 (Olympus Medical Systems Corporation, Tokyo, Japan) or Dual knife(Olympus Medical Systems Corporation, Tokyo, Japan). Hyaluronic acid and/or glycerol were used as the submucosal injecting solution.

Histopathological investigation

The resected specimens were fixed with 10% buffered formalin immediately after the procedure. To reliably evaluate the deepest part of the lesion and the horizontal margin, it was cut into thin sections (2-3 mm) parallel to the oral side to the anal side[21]. The resected specimens were embedded in paraffin and mounted on slides then subjected to hematoxylin and eosin staining and immunohistochemistry.Specimen size, tumor size, macroscopic type, and the depth of invasion were measured in accordance with the Japanese Gastric Cancer Treatment Guideline 2014(Ver. 4)[22], describing the. Treatment was deemed curative when all of the following conditions were fulfilled: en bloc resection, negative horizontal margin (HM0),negative vertical margin (VM0), and no lymphovascular infiltration [ly(-), v(-)]. In histologically differentiated-type tumors with pT1a UL(-) regardless of tumor size,pT1a UL(+) with tumor size ≤ 3 cm, histologically of differentiated type, and pT1b(SM1, 500 microns from the muscularis mucosae) with tumor size ≤ 3 cm were judged curative. In histologically undifferentiated-type, pT1a, UL(-) with tumor size ≤ 2 cm was also considered as curative. Resections that does not satisfy any of the above criteria were considered non-curative.

Immunohistochemistry and histological classification

Immunohistochemical staining of the 30 HpUIGCs was performed in representative sections taken from the tumor at its largest diameter. Mucin phenotype was evaluated using MUC2, MUC5AC, MUC6, CD10, CDX2, PG-I, and H+/K+ -ATPase markers.We used monoclonal antibodies against the following markers: Mucin 5AC(MUC5AC) as a marker for gastric foveolar cells, MUC6 as a marker for gastric mucous neck cells and pyloric glands, MUC2 as a marker for intestinal goblet cells,CD10 as a marker for small intestinal brush border, CDX2 as a marker for epithelial intestinal differentiation. The tumors that showed differentiation to the fundus gland were immunochemically stained for definitive diagnosis of the oxyntic tumor; PG-I was used as a marker for chief cells, and proton pump/H+/K+-ATPase alpha subunit as a marker for parietal cells. MUC2, MUC5AC, MUC6, CD10, PG-I, H+/K+-ATPase reactivity was considered significantly positive when > 10% of tumor cells were stained. Cases with ＜ 10% positive cells were regarded as unaffected. The mucin phenotype was divided into (1) gastric phenotype, (2) intestinal phenotype, and (3)gastric and mixed intestinal phenotype. The gastric and mixed intestinal phenotype was subdivided into gastric phenotype dominant or intestinal phenotype dominant[25,26].

RESULTS

A total of 2462 consecutive patients with 3370 c gastric cancers (3132 early gastric cancer lesions and 238 adenomas) were enrolled. In total, 30 lesions form 30 patients(1.2%) were classified HpUIGC. The clinicopathological features of HpUIGC are shown in Table 1. The study included 19 males and 11 females with a mean age of 59 years. Of the 30 lesions, 15 were U, one was M and 14 were L. Morphologically, 17 lesions were protruded and flat elevated type (0-I, 0-IIa, 0-IIa+IIc), and 13 lesions were flat and depressed type (0-IIb, 0-IIc). Tumor diameter ranged from 2 mm to 98 mm,with a median diameter of 8 mm. Histopathologically, 22 lesions (73.3%) were identified as differentiated-type and eight lesions (26.7%) as undifferentiated-type. All of the undifferentiated lesions tested were signet-ring cell carcinomas. Tumor invasion in 24 lesions (80%) was limited to the mucosa, while the remaining 6 lesions showed submucosal invasion. One of the lesions invaded the submucosal layer to a depth of 500 μm (SM2). Outcomes for the HpUIGC patients were positive, all received successful en bloc resections, free from tumor margin. The curative resection rate was 96.3%. Details of 30 HpUNGCs are shown in Table 2.

Histological and endoscopic features of HpUINGC

Histologically the HpUIGC lesions were classified into fundic gland type adenocarcinoma (7 cases), foveolar type well-differentiated adenocarcinoma (8 cases),intestinal phenotype adenocarcinoma (7 cases), and pure signet-ring cell carcinoma (8 cases). The histological and endoscopic findings of different types of lesions areexplained below.

Table 1 Clinicopathological features of Helicobacter pylori uninfected early gastric cancers

Fundic gland type adenocarcinoma (Figure 1): Histopathological finding: HE staining showed the presence of tumor cells mimicking fundic glands at the bottom of the mucosa, and the surface of the tumor was covered with non-cancerous epithelium.Immunohistologically, the fundic gland cancer cells were positive for PG-I and MUC6, and part of the tumor expressed H+/K+-ATPase. Six of the seven lesions showed submucosal invasion, while one of them showed SM2 invasion (distance from muscularis mucosae was 780 μm). None of the lesions revealed lymphovascular invasion. Endoscopic finding: All seven lesions were located in the upper part of the stomach and were recognized as small protrusions. With white light imaging, a yellowish-white tumor covered with non-cancerous epithelium was observed in submucosal tumors (SMTs). Magnified narrow-band imaging (ME-NBI) revealed dilated branched vessels and intervening part on the lesion’s surface.

Foveolar type well-differentiated adenocarcinoma (Figure 2): Histopathological finding: Seven of the foveolar type gastric cancers were composed of dysplastic columnar cells with clear cytoplasm and showed villous or papillary structures mimicking foveolar epithelium. On the surface of the mucosa, the expanded glands composed of non-tumor cells pushed up the cancerous epithelium. Tumor existed only on the surface, and atypia was recognized as low-grade well-differentiated adenocarcinoma. None of the lesions showed submucosal invasion, although thetumor size was large (mean diameter 37.3 ± 18.3 mm). All foveolar type gastric cancers were positive for MUC5AC, but negative for PG-I, MUC2, and CD10 were negative. MUC6 was positive for expanded non-cancerous glands in the middle to the bottom layer of the mucosa. No lymphovascular invasion was observed in any of the eight gastric cancers.Endoscopic finding: All lesions were located in the upper part of the stomach. Seven of eight foveolar-type well-differentiated adenocarcinomas were observed as laterally spreading elevated lesions with whitish color such as an intestinal-type adenoma, and one lesion showed raspberry-like appearance[13]. MENBI showed a papillary or villous shaped fine mucosal pattern with intra-structural irregular vessels in all lesions. One of the foveolar type well-differentiated adenocarcinomas was recognized as a small protrusion with a raspberry-like appearance in the greater curvature of the upper part of the stomach. Although this lesion resembled a hyperplastic polyp, tumor cell atypia revealed well-differentiated adenocarcinoma.

Intestinal phenotype adenocarcinoma (Figure 3): Histopathological finding: All tumors showed well-differentiated adenocarcinoma characterized by tubular structures lined by tall columnar cells with hyperchromatic, pencillate, and pseudostratified nuclei. Luminal borders were sharp with a brush border. Goblet cells were positive for MUC2 and the brush border of intestinal absorptive epithelial cells was positive for CD10. The surface epithelium was focally positive for MUC5AC, and deeper glands were focally positive for MUC6. These lesions were classified as the intestinal-type dominant mucin phenotype. Endoscopic finding: The white light image revealed a 0-IIa+IIc-type lesion mimicking verrucosa with a red tone,approximately 5 mm in size, and all the lesions were found in the gastric antrum.Unlike conventional verrucosa, which frequently occurs in the antrum, it was characterized by only one or two humps. An irregular microvascular pattern and irregular microsurface pattern with a demarcation line were observed in the recessed area with ME-NBI.

Figure 1 Fundic gland type adenocarcinoma. A: Cancer cells with enlarged nuclei formed irregular glands. The surface of the tumor was covered with noncancerous epithelium, hematoxylin and eosin, original magnification 4 ×; B: The tumor invaded into the submucosal layer in a state that kept the muscularis mucosa.The distance from muscularis mucosa was 75 μm, hematoxylin and eosin, original magnification 40 ×; C: PG-I stains showed focal positive for cancer cells; D: The submucosal tumor like a small protrusion on the greater curvature of the upper gastric body, white light endoscopy; E: The surface of the tumor was covered with normal epithelium, magnifying endoscopy with narrow-band imaging.

Pure signet-ring cell carcinoma (Figure 4): Histopathological finding: Pure signetring cell carcinoma existed in the proliferative zone to the surface layer of mucosa.Most of the lesions, cancer cells were limited to the proliferative zone, and the surface layer of mucosa was found to be covered with non-cancerous epithelium. Endoscopic finding: In the lower part of the stomach, mainly in the antrum, discolored and slightly depressed lesions were observed with a white light image. In six of these, the tumor size was less than 10 mm. Typical features such as corkscrew-like vessels[27],could not be observed.

Mucin phenotype of H. pylori-uninfected gastric cancers

All HpUIGC lesions were evaluated for their mucin phenotype (Table 3). The fundic gland adenocarcinoma, foveolar type well-differentiated adenocarcinoma, and pure signet-ring cell adenocarcinoma revealed gastric phenotype or gastric phenotype dominant, whereas intestinal phenotype adenocarcinoma showed intestinal phenotype dominant.

Long-term outcomes

We investigated long-term outcomes of 30 HpUIGC cases with a median 30-mo(ranged 10-138 mo) observation period. Neither gastric cancer mortality nor death from other diseases was observed; therefore, both overall survival and disease-free survival were 100%. Metachronous gastric cancer was not observed during patient follow-up.

DISCUSSION

H. pyloriinfection causes chronic inflammation and atrophy of the gastric mucosa and often results in gastric cancer. Since 1994,H. pylorihas been recognized as a “definite carcinogen”, contributing to the development of gastric cancer[1-2]. A prospective study reported thatH. pylorieradication therapy suppressed two-thirds of metachronous gastric cancer[28]. As a result, since 2010, the Japanese insurance system has allowed patients who have undergone endoscopic resection to receiveH.pylorieradication therapy[17], and in the current Japan eradication therapy forH. pyloriis insurance adaptation to allH. pyloriinfection patients. Improved sanitation has significantly reduced the rate of newH. pyloriinfections andH. pyloriinfection rate among young adults is reported to be decreasing yearly[4,5].

Figure 2 Foveolar type adenocarcinoma. A: The villous structure composed of dysplastic columnar cells with clear cytoplasm. Hematoxylin and eosin, original magnification 4 ×; B: MUC5AC was positive for cancer; C: MUC6 was negative for cancer but positive for expanded noncancerous glands in the middle layer of mucosa; D: Whitish laterally spreading elevated lesion was seen at the greater curvature of the upper gastric body, white light endoscopy; E: A papillary or villous like fine mucosal pattern with intra-structural irregular vessels in all lesions, one lesion showed raspberry-like appearance magnifying endoscopy with narrow-band imaging; F: One lesion showed raspberry-like appearance.

The frequency ofH. pylori-negative gastric cancers is low[6-11]; however, this number is expected to increase, and the frequency of HpUIGC may increase proportionately.Currently, HpUIGC is still rarely reported so far, and the frequency varies considerably from 0.66% - 14% of gastric cancers[6-11,29-31]. The variation in this range may be owing to differences in the definition ofH. pyloriuninfected status in previous reports.

H. pyloridetection methods possess high sensitivity and specificity and are usually divided into invasive (endoscopic based) and noninvasive methods. Invasive diagnostic tests include endoscopic imaging, histology, RUT, culture, and molecular methods. Non-invasive diagnostic tests include UBT, stool antigen test, serological,and molecular examinations. The accuracy ofH. pyloriinfection diagnosis varies depending on the test. The sensitivity and specificity of UBT, serum anti-HP-IgG antibody, and RUT are 95% and 95%, 91%-100%, and 50%-91%, and 85%-95% and 95%-100%, respectively. However, some tests may produce false negatives owing to Proton Pomp Inhibitor (PPI) or patient factors, including past antibiotic use. To confirmH. pyloriun-infected status, it is necessary to prove multiple tests[17,32-34]. In Japan, combination diagnostic testing showed the occurrence of gastric cancer ranged from 0.42% to 0.66% in patients withoutH. pyloriinfection[6,7,9]. Even if a patient is currently negative forH. pyloritests, there is a possibility of past infection; therefore,assessment of gastric atrophy is necessary to distinguish determine if there was a past infection. We emphasized endoscopic findings revealing C-0 atrophy The ESD specimen was confirmed to have no evidence of histological atrophy and inflammation in the background mucosa using the updated Sydney system[20]. In this study, the combination of two or moreH. pyloritests (serum antibody, UBT, RUT,etc.)based on the Japanese society forH. pyloriresearch guidelines in combination with no history ofH. pylorieradication therapy were used to confirmH. pyloriun-infection. As a result, HpUIGC was diagnosed in 30 of 2462 cases (1.2%). This was similar to previous reports. The average age of patients in our study was 59 years old; however,the males were, on average, older than the females[6-11].

Undifferentiated-type adenocarcinomas were more common than differentiatedtype adenocarcinoma, and pure signet-ring cell carcinomas appeared at a rate similar to previous reports[5,7]. Unlike previous reports, most of the lesions (22/30 lesions)were the differentiated type. The eight undifferentiated-type adenocarcinomas were tiny pure signet-ring cell carcinomas that were confined to the proliferative zone and did not contain poorly differentiated type components. Signet-ring HpUIGCs were easily recognized owing to their lack of atrophy as minute discolored depressed lesions.

Figure 3 lntestinal-type adenocarcinoma. A: The tubular structures lined by tall columnar cells with hyperchromatic, pencillate, and pseudostratified nuclei,hematoxylin and eosin, original magnification 4 ×; B: MUC2 was weakly positive for cancer cells; C: CD10 was positive for cancer cells; D: 0-IIa+IIc type tumor mimicking verrucosa on the gastric antrum, white light endoscopy; E: An irregular microvascular pattern and irregular microsurface pattern with a demarcation line were observed just in the recessed area, magnifying endoscopy with narrow-band imaging.

Unusual neoplastic changes in ME-NBI were owing to tumor cells only existing in the proliferative zone of the mucosa, and the surface layer being covered with noncancerous epithelium. This is the reason why pathological findings do not show the typical corkscrew pattern[35]. Immunochemically, tumor cells showed a gastric phenotype. Reportedly, signet-ring cell carcinoma of the intestinal phenotype infiltrate from the proliferative zone of the mucosa into the deep mucosal layer, and infiltrate into the submucosa individually while maintaining the muscularis mucosa,and sometimes progressing to scirrhous gastric cancer. Gastric phenotype signet-ring cell carcinomas that progress from the proliferative zone to the surface layer of the mucosa, have a lower potential of being malignant potential than the intestinal phenotype[36,37].

Previous reports on the differentiated type of HpUIGC have mostly identified fundic gland type adenocarcinomas and gastric phenotype gastric cancer with lowgrade atypia. However, with the small number of reports, it is difficult to identify the consistent clinicopathological features of HpUIGC. To the best of our knowledge, the present study reports the largest number of HpUIGC cases, 30, that had been evaluated for both endoscopic and pathological findings. It is notable that, in addition to pure signet-ring cell carcinoma and fundic gland type adenocarcinomas, which were often seen in previous reports, our study also included gastric phenotype lowgrade adenocarcinoma, foveolar type adenocarcinoma, and intestinal-type adenocarcinoma. Additionally, our endoscopic findings and histopathological observations varied from those typically found in HpPGC.

The occurrence of fundic gland type adenocarcinomas has been reported next to the undifferentiated type in previous reports of HpUIGC[38,39]. This tumor has a gastric phenotype and low-grade adenocarcinoma occurring in the fundic gland on the middle layer of mucosa or just above the muscularis mucosae. The tumor is covered with non-cancerous epithelium; therefore, it demonstrates a submucosal tumor-like(SMT-like) morphology and sometimes infiltrates the submucosa. Similar to previous research, all cases in the present study showed SMT-like morphology, of which six cases (85.7%) showed frequent submucosal invasion (SM1: 5, SM2: 1) without lymphovascular invasion[12,39,40]. The only case where a tumor invaded into SM2 received additional surgical treatment as per the guidelines[22]. Proximal gastrectomy was selected, and no lymph node metastasis was observed in the resected specimen.

Figure 4 Pure signet-ring cell carcinoma. A, B: Pure signet ring cell carcinoma were observed proliferative zone to the surface layer of mucosa, hematoxylin and eosin, A: Original magnification 4 ×; B: High magnification 40 ×; C:Discolored slightly depressed lesion on the gastric antrum, white light endoscopy; D: The surface of the tumor was covered with normal mucosa, magnifying endoscopy with narrow-band imaging

The foveolar type adenocarcinoma mainly showed low-grade atypia adenocarcinoma with a tendency to differentiate into the foveolar epithelium. Since there are few reports on HpUIGC differentiated cancer other than fundic gland type adenocarcinoma[11], the characteristics have not been clarified. This tumor has been classified as dysplasia/adenoma in the West[41]; however, in Japan, only the typical pyloric gland adenoma is classified as adenoma, and other fundic gland types and foveolar type are often treated as an adenocarcinoma even if it is non-invasive.Therefore, we classified them as foveolar-type adenocarcinomas. This type of tumor had unique histological findings such as MUC6 positive cell proliferation beneath the superficial dysplasia/well-differentiated adenocarcinomain situcomponents[42]. We found MUC5AC positive tumor cells derived from the foveolar epithelium and a MUC6 positive cystic expanded gland in the middle layer of the mucosa, so flat or protruded macroscopic type was defined as a characteristic.

Whether this MUC6-positive cell was cancerous or noncancerous is still controversial. However, we determined that MUC6 positive cells were non-cancerous since the junction between MUC5AC positive cancer cells and MUC6 positive cells was clear, and no cell atypia was found in MUC6 positive cells with low KI-67 index.This tumor showed discolored flat elevation with a granular structure similar to intestinal adenoma as a colonic lateral spreading tumor (LST)[43]. However, this tumor was seen in the greater curvature of the fornix in the upper third of the stomach, not in the lower part of the stomach where intestinal-type adenomas occur frequently.

Although the intestinal phenotype of HpUIGC is rare and only a few cases were seen in case reports[44-47], it is essential to recognize that there are not a few intestinal phenotype adenocarcinomas among HpUIGCs. In this study, 7 verrucous-like tumors found in the antrum predominantly showed the intestinal phenotype, and to the best of our knowledge, this is the first report that revealed the endoscopic and the pathological features of this kind of tumor. In intestinal phenotype cancers, as the tumor grows, the gastric phenotype of the background mucosa gradually changes to the intestinal phenotype of the tumor and is eventually replaced or considered to be null. In this study, the tumor showed mixed gastrointestinal phenotype as the intestinal phenotype adenocarcinoma was very small, and the gastric phenotype in the background remained. Intestinal phenotype adenocarcinoma is characterized by a macroscopic type resembling a single verrucous found in the antrum. It is desirable to perform the endoscopy screening with ME-NBI inH. pyloriuninfected patients to identify this tumor. It is reported that gastric epithelial cells might be generated by stem cells and progenitor cells located in the isthmus[48]. The types of stem cells in the isthmus are different between corpus and antrum, and the only antrum contains intestinal stem cells. Considering these observations, the intestinal-type adenocarcinoma we observed in the current study could be generated from the intestinal stem cells and, thus, detected only in the antrum.

Research motivation

Previously,H. pylori-uninfected gastric cancer including case report such as undifferentiated gastric cancer or fundic gland-type gastric cancer was reported. However, due to the rare frequency, there was very few reports. In the future,H.pylori-uninfected gastric cancer may increase relatively; therefore, importance of clarifying the clinicopathological features of those is desired. In this study, we experienced 30 cases ofH. pylori-uninfected early gastric cancer and could classify histopathological features of these.

Research objectives

To clarify clinicopathological feature ofH. pylori-uninfected gastric cancer (HpUNGC) treated by endoscopic submucosal dissection (ESD).

Research methods

This study is retrospective study. A total of 2462 patients with 3375 instances of early gastric cancers that were treated by ESD were enrolled in our study between May 2000 and September 2019. We defined a patient asH. pylori-uninfected using the following three criteria; i) the patient did not receive treatment forH. pylori, which was determined by investigating medical records and conducting patient interviews, ii) lack of endoscopic atrophy, and iii) the patient was negative forH. pyloriafter being tested at least twice using various diagnostic methods,including serum anti-H. pylori-IgG antibody, urease breath test, rapid urease test, and microscopic examination.

Research results

Of these, 30 lesions in 30 patients were diagnosed as HpUIGC. Histologically 30 HpUIGC lesions were classified into 4 types (fundic gland type adenocarcinoma, foveolar type well-differentiated adenocarcinoma, intestinal phenotype adenocarcinoma, and pure signet-ring cell carcinoma).Unlike previous reports, most of the lesions (22/30 lesions) were the differentiated type.

Research conclusions

In this study, we classified 30 HpUIGCs into 4 types histologically. Unlike previous reports,there were more differentiated cancers than undifferentiated cancers. Although the most of HpUIGC showed gastric phenotype, it is essential to recognize that there are not a few intestinal phenotype adenocarcinomas among HpUIGCs. HpUIGC is very rare, among which,histologically high incidence of undifferentiated adenocarcinoma. Besides undifferentiated adenocarcinoma and gastric fundic gland type adenocarcinoma, there is another HpUIGC having different histopathological features. HpUIGC may show various type of histopathological features. Histologically, HpUIGC is classified into at least 4 types (fundic gland type adenocarcinoma, foveolar type well-differentiated adenocarcinoma, intestinal phenotype adenocarcinoma, and pure signet-ring cell carcinoma). To the best of our knowledge, the present study reports the largest number of HpUIGC cases that had been evaluated for both endoscopic and pathological findings. To recognize clinicopathological feature of HpUIGC will be helpful for early detection of HpUIGC in the future clinical practice.

Research perspectives

To recognize the various clinicopathological features of HpUIGC is useful for clinical diagnosis in the future. Because HpUIGC is rare frequency, we consider multicenter clinical trial for case collection to elucidate more detail of the clinicopathological characteristics of HpUIGC.Multicenter observational trial is the best method for the future research.