[Clinicopathological factors and clinical significance of No.12b lymph node metastasis in gastric antrum cancer].

Q3 Medicine
B Zhang, G L Zheng, Y Zhang, Y Zhao, H T Zhu, T Zhang, Y Liu, Z C Zheng
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引用次数: 0

Abstract

Objective: To investigate the clinicopathological factors and clinical significance of (micro)metastasis in No.12b lymph node in patients with gastric antrum cancer. Methods: This was a retrospective cohort study of data of 242 patients with gastric adenocarcinoma without distant metastasis, complete follow-up data, and no preoperative anti-tumor therapy or history of other malignancies. All study patients had undergone radical gastrectomy (at least D2 radical range) + No.12b lymph node dissection in the Department of Gastric Surgery of Liaoning Cancer Hospital from January 2007 to December 2012. Immunohistochemical staining with antibody CK8/18 was used to detect micrometastasis to lymph nodes. Patients with positive findings on hematoxylin and eosin stained specimens and/or CK8/18 positivity in No.12b lymph node were diagnosed as having No.12b (micro)metastasis and included in the No.12b positive group. All other patients were classified as 12b negative. We investigated the impact of No.12b (micro)metastasis by comparing the clinicopathological characteristics and recurrence free survival (RFS) of these two groups of patients and subjecting possible risk factors to statistical analysis. Results: Traditional hematoxylin-eosin staining showed that 15/242 patients were positive for No.12b lymph nodes and 227 were negative. A total of 241 negative No. 12b lymph nodes were detected. Immunohistochemical testing revealed that seven of these 241 No.12b lymph nodes (2.9%) were positive for micrometastasis. A further seven positive nodes were identified among the 227 nodes (3.1%) that had been evaluated as negative on hematoxylin-eosin-stained sections. Thus, 22 /242 patients' (9.1%) No.12b nodes were positive for micrometastases, the remaining 220 (90.9%) being negative. Factor analysis showed that No.12b lymph node (micro) metastasis is associated with more severe invasion of the gastric serosa (HR=3.873, 95%CI: 1.676-21.643, P=0.006), T3 stage (HR=1.615, 95%CI: 1.113-1.867, P=0.045), higher N stage (HR=1.768, 95%CI: 1.187-5.654, P=0.019), phase III of TNM stage (HR=2.129, 95%CI: 1.102-3.475, P=0.046), and lymph node metastasis in the No.1/No.8a/No.12a groups (HR=0.451, 95%CI: 0.121-0.552, P=0.035; HR=0.645, 95%CI:0.071-0.886, P=0.032; HR=1.512, 95%CI: 1.381-2.100, P=0.029, respectively). Survival analysis showed that the 5-year RFS of patients in the No.12b positive group was worse than that of those in the No.12b negative group (18.2% vs. 34.5%, P<0.001). Independent predictors of RFS were poorer differentiation of the primary tumor (HR=0.528, 95%CI:0.288-0.969, P=0.039), more severe serous invasion (HR=1.262, 95%CI:1.039-1.534, P=0.019), higher T/N/TNM stage (HR=4.880, 95%CI: 1.909-12.476, P<0.001; HR=2.332, 95%CI: 1.640-3.317, P<0.001; HR=0.139, 95%CI: 0.027-0.713, P=0.018, respectively), and lymph node metastasis in the No.12a/No.12b group(HR=0.698, 95%CI:0.518-0.941, P=0.018; HR=0.341, 95%CI:0.154-0.758,P=0.008, respectively). Conclusion: Detection of micrometastasis can improve the rate of positive lymph nodes. In patients with gastric antrum cancer, dissection of group No.12b lymph nodes may improve the prognosis of those with intraoperative evidence of tumor invasion into the serosa, more than two lymph node metastases, and suspicious lymph nodes in groups No.1 / No.8a / 12a.

[胃癌 12b 淋巴结转移的临床病理因素及临床意义]
目的探讨胃癌患者 12b 淋巴结(微)转移的临床病理因素和临床意义。方法: 这是一项回顾性队列研究:这是一项回顾性队列研究,研究对象为 242 例无远处转移、随访资料完整、术前未接受抗肿瘤治疗或无其他恶性肿瘤病史的胃腺癌患者。所有患者均于2007年1月至2012年12月在辽宁省肿瘤医院胃外科接受了根治性胃切除术(至少D2根治范围)+12b号淋巴结清扫术。采用 CK8/18 抗体免疫组化染色检测淋巴结微转移。苏木精和伊红染色标本阳性和/或12b号淋巴结CK8/18阳性的患者被诊断为12b号(微)转移,并纳入12b号阳性组。其他患者均被归为 12b 阴性组。我们通过比较两组患者的临床病理特征和无复发生存期(RFS),并对可能的风险因素进行统计分析,研究了12b(微)转移的影响。结果传统的苏木精-伊红染色显示,15/242 例患者的 12b 号淋巴结阳性,227 例阴性。共检测出 241 个阴性 12b 淋巴结。免疫组化检测显示,在这 241 个 12b 号淋巴结中,有 7 个(2.9%)微转移阳性。在苏木精-伊红染色切片上被评估为阴性的 227 个淋巴结(3.1%)中,又发现了 7 个阳性淋巴结。因此,242 名患者中有 22 个(9.1%)No.12b 结节微转移阳性,其余 220 个(90.9%)为阴性。因子分析显示,12b 号b淋巴结(微转移)与胃黏膜受侵袭更严重(HR=3.873,95%CI:1.676-21.643,P=0.006)、T3分期(HR=1.615,95%CI:1.113-1.867,P=0.045)、较高的N期(HR=1.768,95%CI:1.187-5.654,P=0.019)、TNM分期的III期(HR=2.129,95%CI:1.102-3.475,P=0.046)以及淋巴结转移在No.1/No.8a/No.12a组(HR=0.451,95%CI:0.121-0.552,P=0.035;HR=0.645,95%CI:0.071-0.886,P=0.032;HR=1.512,95%CI:1.381-2.100,P=0.029)。生存分析显示,No.12b 阳性组患者的 5 年 RFS 比 No.12b阴性组患者的5年RFS更差(18.2% vs. 34.5%,PP=0.039),浆液性浸润更严重(HR=1.262,95%CI:1.039-1.534,P=0.019),T/N/TNM分期更高(HR=4.880,95%CI:1.909-12.476,PPP=0.018),No.12a/No.12b组(HR=0.698,95%CI:0.518-0.941,P=0.018;HR=0.341,95%CI:0.154-0.758,P=0.008)。结论微转移的检测可提高淋巴结阳性率。在胃窦癌患者中,对于术中有证据表明肿瘤侵犯浆膜、有两个以上淋巴结转移、1/8a/12a 组淋巴结可疑的患者,清扫 12b 组淋巴结可改善其预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华胃肠外科杂志
中华胃肠外科杂志 Medicine-Medicine (all)
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6776
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