a Clinical Oncology department, Faculty of Medicine , Ain Shams University , Cairo , Egypt.
Expert Rev Gastroenterol Hepatol. 2018 May;12(5):525-530. doi: 10.1080/17474124.2018.1413348. Epub 2017 Dec 6.
The aim of this analysis is to validate the prognostic value of the 8 edition of the American Joint Committee on Cancer (AJCC) staging system for gastric cancer.
Through SEER*Stat program, Surveillance, epidemiology and end results database (2010-2013) was accessed and 8th AJCC stages were reconstructed. Cancer-specific survival analyses according to both 7th and 8th editions were conducted through Kaplan-Meier analysis/log-rank testing and multivariate analysis was conducted through a Cox model.
Among pathologically-staged patients, P values for pairwise comparisons among different 8th AJCC stages were significant (<0.05) for all comparisons except for stage IIIC vs. IV; while P values for pairwise comparisons among different 7th AJCC stages were significant (<0.05) for all comparisons except for stage IIIA vs. IIIB and stage IIIC vs. IV. Among clinically-staged patients and according to either the clinical 8th AJCC or the 7th AJCC, significant overlap in outcomes existed between different stages. Among pathologically-staged patients, c-statistic for the pathological 8th system was: 0.762; while for the 7th system, it was: 0.763. Among clinically-staged patients, c-statistic for the clinical 8th system was: 0.634; while for the 7th system, it was: 0.637.
Compared to the 7th system, the 8th system does not bring about significant prognostic improvement (for either clinically- or pathologically-staged patients).
本分析旨在验证第八版美国癌症联合委员会(AJCC)胃癌分期系统的预后价值。
通过 SEER*Stat 程序,访问 Surveillance,Epidemiology and End Results(2010-2013 年)数据库,并重建第八版 AJCC 分期。通过 Kaplan-Meier 分析/对数秩检验对第七版和第八版进行癌症特异性生存分析,并通过 Cox 模型进行多变量分析。
在病理分期患者中,除了 IIIC 期与 IV 期之间外,所有第八版 AJCC 分期之间的两两比较的 P 值均具有统计学意义(<0.05);而除了 IIIA 期与 IIIB 期和 IIIC 期与 IV 期之间外,所有第七版 AJCC 分期之间的两两比较的 P 值均具有统计学意义(<0.05)。在临床分期患者中,根据临床第八版 AJCC 或第七版 AJCC,不同分期之间的结果存在显著重叠。在病理分期患者中,第八版病理系统的 C 统计量为:0.762;而第七版系统的 C 统计量为:0.763。在临床分期患者中,第八版临床系统的 C 统计量为:0.634;而第七版系统的 C 统计量为:0.637。
与第七版系统相比,第八版系统并没有带来显著的预后改善(无论是临床分期还是病理分期患者)。