Deng Ben-Yuan, Yang Min, Wen Jie-Yu, Hou Sheng-Zhong, Chen Yang, Tian Bo-Le, Liu Xu-Bao, Zhang Yi
Department of General Surgery, West China Health Hospital of Sichuan University.
Department of Pediatric Surgery.
Medicine (Baltimore). 2020 Jan;99(3):e18736. doi: 10.1097/MD.0000000000018736.
Recently, the American Joint Committee on Cancer (AJCC) 8th staging manual stipulated the World Health Organization (WHO) G3 pancreatic neuroendocrine carcinomas (p-NECs) should all be classified by the system for pancreatic exocrine adenocarcinomas, which had ignored the heterogeneity of G3 p-NECs. We focused on demonstrating whether the heterogeneous subgroups of G3 p-NECs would influence the accurate application of AJCC 8th staging systems.G3 p-NECs were divided into well-differentiated and poorly-differentiated subgroups, whose clinical features and overall survival (OS) were compared. Survival analysis by applying 2 new AJCC 8th staging systems to well-differentiated G3 p-NECs were performed to validate whether these subgroup patients should also be staged by the system proposed for all G3 p-NECs.We enrolled 172 patients who were histopathologically diagnosed as G3 p-NECs, including 64 well-differentiated G3 p-NECs and 108 poorly-differentiated ones, whose patient demographics and tumor characteristics present no notably differences (P > .05), except their Ki-67 index and mitotic rate (P = .031, P = .025; respectively). The estimated OS of well-differentiated G3 p-NECs was significantly better than those of poorly-differentiated tumors (P < .001). When applying the new AJCC system for all G3 p-NECs to well-differentiated G3 tumors, 18, 22, 12, and 12 patients were respectively distributed in the new AJCC Stage I, Stage II, Stage III, and Stage IV. Using the AJCC 8th staging system for WHO G1/G2 pancreatic neuroendocrine tumors (p-NETs) to well-differentiated G3 p-NECs, there were 5, 25, 22, and 12 patients classified from the new AJCC Stage I to Stage IV, respectively. The system for G1/G2 p-NETs could significantly differentiate the survival differences between each new stage of well-differentiated G3 p-NECs (P < .05), while comparisons of survivals between Stage II with Stage III or Stage III with Stage IV by the system for G3 p-NECs were not statistically different (P = .334, P = .073; respectively).G3 p-NECs were heterogeneous with well-differentiated and poorly-differentiated subgroups. Both AJCC 8th staging systems proposed for all G3 p-NECs and G1/G2 p-NETs were practical for well-differentiated G3 p-NECs, while the one originally applied to G1/G2 p-NETs appeared to be superior in performance due to its better prognostic stratification and more accurate predicting ability.
最近,美国癌症联合委员会(AJCC)第8版分期手册规定,世界卫生组织(WHO)G3级胰腺神经内分泌癌(p-NEC)均应按照胰腺外分泌腺癌系统进行分类,这忽视了G3级p-NEC的异质性。我们着重论证G3级p-NEC的异质性亚组是否会影响AJCC第8版分期系统的准确应用。将G3级p-NEC分为高分化和低分化亚组,比较其临床特征和总生存期(OS)。对高分化G3级p-NEC应用2种新的AJCC第8版分期系统进行生存分析,以验证这些亚组患者是否也应按照针对所有G3级p-NEC提出的系统进行分期。
我们纳入了172例经组织病理学诊断为G3级p-NEC的患者,其中包括64例高分化G3级p-NEC和108例低分化G3级p-NEC,除Ki-67指数和有丝分裂率外(分别为P = 0.031,P = 0.025),其患者人口统计学和肿瘤特征无显著差异(P>0.05)。高分化G3级p-NEC的估计总生存期显著优于低分化肿瘤(P<0.001)。对高分化G3级肿瘤应用针对所有G3级p-NEC的新AJCC系统时,新AJCCⅠ期、Ⅱ期、Ⅲ期和Ⅳ期分别有18例、22例、12例和12例患者。对高分化G3级p-NEC应用AJCC第8版针对WHO G1/G2胰腺神经内分泌肿瘤(p-NET)的分期系统时,从新AJCCⅠ期到Ⅳ期分别有5例、25例、22例和12例患者。G1/G2 p-NET的系统能够显著区分高分化G3级p-NEC各新阶段之间的生存差异(P<0.05),而G3级p-NEC系统在Ⅱ期与Ⅲ期或Ⅲ期与Ⅳ期之间的生存比较无统计学差异(分别为P = 0.334,P = 0.073)。
G3级p-NEC存在高分化和低分化亚组的异质性。针对所有G3级p-NEC和G1/G2 p-NET提出的AJCC第8版分期系统对高分化G3级p-NEC均适用,而最初应用于G1/G2 p-NET的系统由于其更好的预后分层和更准确的预测能力,在性能上似乎更优。