Characteristics of gastric cancer in negative test of serum anti-Helicobacter pylori antibody and pepsinogen test: a multicenter study

幽门螺杆菌 医学 内科学 胃肠病学 癌症 萎缩性胃炎 外科肿瘤学 胃炎 胃蛋白酶 血清学 快速尿素酶试验 抗体 螺旋藻科 免疫学 生物 生物化学
作者
Mariko Kiso,Masaharu Yoshihara,Masanori Ito,Kentaro Inoue,Kanefusa Kato,Shigenori Nakajima,Katsuhiro Mabe,Masao Kobayashi,Naomi Uemura,Tomoyuki Yada,Masashi Oka,Takashi Kawai,Tomoyuki Boda,Takahiro Kotachi,Kazuhiko Masuda,Shinji Tanaka,Kazuaki Chayama
出处
期刊:Gastric Cancer [Springer Science+Business Media]
卷期号:20 (5): 764-771 被引量:30
标识
DOI:10.1007/s10120-016-0682-5
摘要

The serological risk prediction system combines the pepsinogen test and anti-Helicobacter pylori (H. pylori) antibody determination. In this system, chronic atrophic gastritis (CAG) is diagnosed using the pepsinogen test. Patients who are H. pylori negative and pepsinogen negative are classified into group A, are assumed to be H. pylori uninfected, and are at an extremely low risk for gastric cancer. However, gastric cancers are detected in this group. The aim of this study is to clarify the clinicopathological status of group A patients with gastric cancer. A total of 109 gastric cancer patients classified as group A were enrolled in a multicenter study. Group A patients were divided into two subgroups: group AN (H. pylori uninfected) and group AP (H. pylori infected). They were compared to 183 H. pylori-infected gastric cancer patients who were not in group A. Of the 109 patients, only 7 were classified as group AN; the other 102 were classified as group AP. The clinicopathological features of group AP included older age, predominantly differentiated type cancer, endoscopically visualized CAG, and pepsinogen (PG) I/II ratio lower than that of group AN. In group AN, the depressed type was dominant, and the PG I/II ratio was higher than in those gastric cancer patients who were infected with H. pylori. Patients in group AP had CAG, and their gastric cancers were similar to those of H. pylori-eradicated patients. Concerning the recent ABC classification system, advanced decision criteria should be proposed to decrease the false-negative evaluation of gastric cancer risk.
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