Long-term follow-up study of gastric adenoma; tumor-associated macrophages are associated to carcinoma development in gastric adenoma

• Published in: Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2017-11, Vol.20 (6), p.929-939
• Main Authors: Taniyama, Daiki, Taniyama, Kiyomi, Kuraoka, Kazuya, Zaitsu, Junichi, Saito, Akihisa, Nakatsuka, Hirofumi, Sakamoto, Naoya, Sentani, Kazuhiro, Oue, Naohide, Yasui, Wataru
• Format: Article
• Language: English
• Subjects: Abdominal Surgery; Adenocarcinoma; Adenocarcinoma - pathology; Adenoma; Adenoma - pathology; Aged; Aged, 80 and over; Biopsy; Cancer Research; Cell Transformation, Neoplastic - pathology; Disease Progression; Female; Follow-Up Studies; Gastric cancer; Gastroenterology; Humans; Macrophages; Macrophages - pathology; Male; Medicine; Medicine & Public Health; Middle Aged; Multivariate analysis; Oncology; Original Article; Risk factors; Stomach Neoplasms - pathology; Stroma; Surgical Oncology; Tumors
• ISSN: 1436-3291; 1436-3305
• DOI: 10.1007/s10120-017-0713-x

Background Some gastric adenomas may progress to adenocarcinoma in a short time, but others remain as adenoma for a long time. Methods Among 1138 cases diagnosed as adenoma by biopsy at Kure Medical Association Hospital between 1990 and 2010, 51 adenomas were enrolled. Of these, 28 adenomas (group A) were followed for 60 months or longer with no progression to adenocarcinoma within 60 months, and the other 23 adenomas (group B) were upgraded to carcinoma by consecutive biopsies performed within 1 year after the first biopsy. These adenomas were compared clinicopathologically and immunohistochemically. Results Macroscopically, the mean size of group B adenomas was significantly larger than that of group A adenomas (18.6 vs. 9.9 mm) at the first biopsy. The frequency of a depressed area in the adenoma was significantly higher in group B than group A. Microscopically none of group A but 7 (30.4%) of 23 group B adenomas showed severe atypia. Each of a highly proliferative gland measured by Ki-67 labeling, cellular atypical grade, gastric phenotype defined by MUC5AC and MUC6 and CD204-positive tumor-associated macrophage (TAM) was a significant risk factor for adenocarcinoma development in gastric adenoma by univariate analysis. Only moderate or severe atypia of adenoma cells and the TAM number in the stroma of adenomas were independent risk factors by multivariate analysis. Conclusions As independent risk factors, cellular atypia may reconfirm the importance of morphological analysis, and the TAM number may indicate the significance of TAM function in gastric adenoma.