Clinicopathological features and risk analysis of lymph node metastasis in type 3 gastric neuroendocrine tumor
-
摘要:
目的 分析无远处转移的3型胃神经内分泌肿瘤(neuroendocrine tumor,NET)的临床病理特征,并探索影响淋巴结转移的危险因素。 方法 回顾性分析2016年3月至2019年5月就诊于中日友好医院的36例无远处转移的3型胃NET患者临床病理资料,构建逻辑回归模型分析淋巴结转移的危险因素。 结果 研究纳入36例无远处转移的3型患者,8例(22.2%)出现淋巴结转移。淋巴结转移的患者具有较大的肿瘤直径和较高的Ki-67指数,内镜下溃疡型病灶也更多见(50%),肿瘤T分期以T4为主(50%)。单因素结果显示,肿瘤≥2 cm、溃疡型病灶、病理分级G2/3、T2/4是淋巴结转移的高危因素。而多因素分析发现仅肿瘤直径≥2 cm(OR=8.54,95%CI:1.16~62.96)和溃疡型病灶(OR=10.97,95%CI:1.16~103.52)是影响淋巴结转移的独立因子。 结论 具备淋巴结转移高危因素的3型胃NET需要在术前全面评估区域淋巴结状态,以选择最佳的治疗方式。 -
关键词:
- 3型胃神经内分泌肿瘤 /
- 临床病理特征 /
- 淋巴结转移
Abstract:Objective To analyze clinicopathological features of type 3 gastric neuroendocrine tumor (NET) without distant metastasis and identify risk factors of lymph node metastasis. Methods Data of 36 patients with type 3 gastric NET without metastasis from March 2016 to May 2019 in China-Japan Friendship Hospital were retrospectively analyzed. A Logistic regression model was used to identify risk factors of lymph node metastasis. Results This study included 36 patients, and eight patients (22.2%) had lymph node metastasis. Patients with lymph node metastasis had a larger tumor diameter and higher Ki-67 index than those without lymph node metastasis. In addition, endoscopic ulcerative lesions were more common (50%), and the T staging of the tumor was mainly T4 (50%). Univariate analysis revealed that tumor diameter ≥2 cm, ulcerative lesions, and pathological grade G2/3 and T2/4 were the main risk factors of lymph node metastasis. Multivariate analysis revealed that only tumor diameter ≥2 cm [odds ratio (OR)=8.54; 95%CI: 1.16-62.96] and ulcerative lesions (OR) =10.97; 95%CI: 1.16- 103.52) were independent factors affecting lymph node metastasis. Conclusions In patients with type 3 gastric NET with high risk factors for lymph node metastasis, it is necessary to comprehensively evaluate the regional lymph node status before surgery to select the best treatment. -
表 1 36例无远处转移3型胃NET患者的临床病理资料例(%)
表 2 淋巴结转移患者的单因素及多因素回归分析
表 3 12例行外科手术患者术式、淋巴结状态及清扫范围
-
[1] Rindi G, Luinetti O, Cornaggia M, et al. Three subtypes of gastric argyrophil carcinoid and the gastric neuroendocrine carcinoma: a clinicopathologic study[J]. Gastroenterology, 1993, 104(4): 994-1006. doi: 10.1016/0016-5085(93)90266-F [2] Dasari A, Shen C, Halperin D, et al. Trends in the Incidence, Prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States[J]. JAMA Oncol, 2017, 3(10): 1335-1342. doi: 10.1001/jamaoncol.2017.0589 [3] Boyce M, Thomsen L. Gastric neuroendocrine tumors: prevalence in Europe, USA, and Japan, and rationale for treatment with a gastrin/ CCK2 receptor antagonist[J]. Scand J Gastroenterol, 2015, 50(5): 550- 559. doi: 10.3109/00365521.2015.1009941 [4] WHO Classification of Tumours Editorial Board. WHO classification of tumours of digestive system tumours (5th Edition) [M]. Lyon: IARC press, 2019: 14-20. [5] 谭煌英. 胃神经内分泌肿瘤临床分型的共识和争议[J]. 中华胃肠外科杂志, 2017, (9): 977-981. doi: 10.3760/cma.j.issn.1671-0274.2017.09.004 [6] Min BH, Hong M, Lee JH, et al. Clinicopathological features and outcome of type 3 gastric neuroendocrine tumours[J]. Br J Surg, 2018, 105 (11): 1480-1486. doi: 10.1002/bjs.10901 [7] Vanoli A, La SR, Miceli E, et al. Prognostic evaluations tailored to specific gastric neuroendocrine neoplasms: analysis of 200 cases with extended follow-Up[J]. Neuroendocrinology, 2018, 107(2): 114-126. doi: 10.1159/000489902 [8] Delle Fave G, O'Toole D, Sundin A, et al. ENETS consensus guidelines update for gastroduodenal neuroendocrine neoplasms[J]. Neuroendocrinology, 2016, 103(2): 119-124. doi: 10.1159/000443168 [9] Welton ML, Steele SR, Goodman KA, et al. AJCC Cancer Staging Manual. 8th ed [M]. Chicago, IL: AJCC, 2017. [10] Waldum HL, Srdal YF, Mjnes PG. The Enterochromaffin-like (ECL) cellcentral in gastric physiology and pathology[J]. Int J Mol Sci, 2019, 20 (10): 2444. doi: 10.3390/ijms20102444 [11] Corey B, Chen H. Neuroendocrine tumors of the stomach[J]. Surg Clin North Am, 2017, 97(2): 333-343. doi: 10.1016/j.suc.2016.11.008 [12] Gilligan CJ, Lawton GP, Tang LH, et al. Gastric carcinoid tumors: the biology and therapy of an enigmatic and controversial lesion[J]. Am J Gastroenterol, 1995, 90(3): 338-352. [13] Kawasaki K, Nakamura S, Sugai T, et al. Type 3 gastric neuroendocrine tumor with unique endoscopic features[J]. Dig Liver Dis, 2016, 48(10): 1264. doi: 10.1016/j.dld.2016.07.001 [14] Lee HE, Mounajjed T, Erickson LA, et al. Sporadic gastric well-differentiated neuroendocrine tumors have a higher Ki-67 proliferative index [J]. Endocr Pathol, 2016, 27(3): 259-267. doi: 10.1007/s12022-016-9443-6 [15] Hirasawa T, Yamamoto N, Sano T. Is endoscopic resection appropriate for type 3 gastric neuroendocrine tumors? A retrospective multicenter study[J]. Dig Endosc, 2021, 33(3): 408-417. doi: 10.1111/den.13778 [16] Kwon YH, Jeon SW, Kim GH, et al. Long-term follow up of endoscopic resection for type 3 gastric NET[J]. World J Gastroenterol, 2013, 19(46): 8703-8708. doi: 10.3748/wjg.v19.i46.8703
点击查看大图
表(3)
计量
- 文章访问数: 199
- HTML全文浏览量: 44
- PDF下载量: 19
- 被引次数: 0