Kim Hee Jin, Hwang Sung Wook, Kim Nayoung, Yoon Hyuk, Shin Cheol Min, Park Young Soo, Lee Dong Ho, Park Do Joong, Kim Hyung Ho, Kim Joo Sung, Jung Hyun Chae, Lee Hye Seung
Departments of Internal Medicine, Seoul National University Bundang Hospital, Seongnam.
Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
J Cancer Prev. 2014 Mar;19(1):56-67. doi: 10.15430/jcp.2014.19.1.56.
The prognosis of H. pylori infection-negative gastric cancer (HPIN-GC) has been rarely investigated. Applying a strict definition of H. pylori status, the prognosis and molecular prognostic markers in HPIN-GC were evaluated.
A combination of multiple methods was carried out to strictly evaluate H. pylori infection in gastric cancer (GC) patients between June 2003 and October 2012 at Seoul National University Bundang Hospital. H. pylori infection was defined as negative if histology, a rapid urease test, culturing, serology and history of H. pylori eradication were all negative. Patients with severe gastric atrophy by the serum pepsinogen test or histology were assumed to have had a previous H. pylori infection. Epstein-Barr virus (EBV) in situ hybridization, PCR-based microsatellite instability (MSI) testing, and p53 immunohistochemistry were performed.
Compared to 509 H. pylori infection-positive gastric cancer (HPIN-PC) patients, 24 HPIN-GC patients showed a significantly higher frequency of cardia location (P=0.013), and the depth of invasion in HPIN-GC was more advanced, although there was no statistical significance (pT3-pT4, 37.5% for HPIN-GC vs. 28.5% for HPIP-GC, P=0.341). In multivariate analysis, depth of invasion and lymph node metastasis were identified as the most important prognostic factors for relapse-free survival and overall survival (P<0.001). However, the status of H. pylori infection was not an independent prognostic factor for relapse-free survival and overall survival. The positivity of EBV in both groups was low, and the survivals according to MSI and p53 status in HPIN-GC patients were not significantly different.
The status of H. pylori infection was not a prognostic factor for survival in GC patients when applying the strict definition of H. pylori infection. The prognostic implication of MSI and p53 on survival in HPIN-GC patients was not clear.
幽门螺杆菌感染阴性胃癌(HPIN-GC)的预后很少被研究。应用严格的幽门螺杆菌状态定义,评估了HPIN-GC的预后及分子预后标志物。
采用多种方法相结合,对2003年6月至2012年10月在首尔国立大学盆唐医院的胃癌(GC)患者的幽门螺杆菌感染情况进行严格评估。如果组织学、快速尿素酶试验、培养、血清学及幽门螺杆菌根除史均为阴性,则将幽门螺杆菌感染定义为阴性。血清胃蛋白酶原试验或组织学显示严重胃萎缩的患者被认为曾有幽门螺杆菌感染。进行了爱泼斯坦-巴尔病毒(EBV)原位杂交、基于聚合酶链反应的微卫星不稳定性(MSI)检测及p53免疫组织化学检测。
与509例幽门螺杆菌感染阳性胃癌(HPIN-PC)患者相比,24例HPIN-GC患者贲门部肿瘤的发生率显著更高(P=0.013),且HPIN-GC的浸润深度更深,尽管无统计学意义(pT3-pT4,HPIN-GC为37.5%,HPIP-GC为28.5%,P=0.341)。多因素分析显示,浸润深度和淋巴结转移是无复发生存期和总生存期最重要的预后因素(P<0.001)。然而,幽门螺杆菌感染状态并非无复发生存期和总生存期的独立预后因素。两组EBV阳性率均较低,HPIN-GC患者根据MSI和p53状态的生存率无显著差异。
应用严格的幽门螺杆菌感染定义时,幽门螺杆菌感染状态并非GC患者生存的预后因素。MSI和p53对HPIN-GC患者生存的预后意义尚不明确。