Department of Gastrointestinal Cancer Center Surgery, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, No. 52 Fu-Cheng Road, Hai-Dian District, Beijing, 100142, People's Republic of China.
BMC Cancer. 2019 Jan 16;19(1):80. doi: 10.1186/s12885-019-5283-3.
Pathological stage is considered as the best prognosis indicator for gastric cancer. With the increasing use of neoadjuvant chemotherapy (NACT), the latest TNM staging included a new pathological stage of ypTNM for patients with NACT. However, no study has investigated if ypTNM stage has the same prognostic implication as pTNM stage for gastric cancer.
We retrospectively selected eligible patients within a prospectively maintained database containing all patients treated with gastric cancer in Peking University Cancer Hospital from 2007 to 2015 using overall survival as the outcome. Patients using ypTNM and pTNM were 1:1 matched by propensity scores (PS) calculated from a model containing variables associated with ypTNM use or survival. Overall survival was compared by unconditional Cox regression. Conventional multivariate analysis was conducted to corroborate PS matching results.
1441 patients were included in the analysis with a median follow-up of 37 months (range = 2-106). The matched sample contained 756 patients. After PS matching, patients with specific ypTNM stage were 1.34 (95%CI = 1.05-1.72, P = 0.019) times more likely to die than patients with the same pTNM stage. Similar to the results of PS matching, multivariate Cox regression yielded a hazard ratio (HR) of 1.35 (95%CI = 1.09-1.67, P = 0.006). Subgroup analysis indicated this survival difference between ypTNM and pTNM stage varied by the specific TNM stage of patients. The HR was 3.44 (95%CI = 1.06-11.18, P = 0.040) and 1.28 (95%CI = 1.00-1.62, P = 0.048) for patients in stage I and III, respectively; whereas for stage II patients, no significant difference was observed (HR = 1.37, 95%CI = 0.78-2.38, P = 0.27).
Gastric cancer patients with specific ypTNM stage had worse prognosis compared to those at the same stage defined by pTNM.
病理分期被认为是胃癌的最佳预后指标。随着新辅助化疗(NACT)的应用越来越广泛,最新的 TNM 分期为接受 NACT 的患者纳入了新的病理分期 ypTNM。然而,尚无研究探讨 ypTNM 分期对胃癌的预后是否与 pTNM 分期具有相同的预后意义。
我们从北京大学肿瘤医院 2007 年至 2015 年期间前瞻性维护的数据库中选择符合条件的患者进行回顾性分析,以总生存为结局。通过基于与 ypTNM 使用或生存相关的变量的倾向评分(PS),对使用 ypTNM 和 pTNM 的患者进行 1:1 匹配。通过无条件 Cox 回归比较总生存。进行常规多变量分析以证实 PS 匹配结果。
共有 1441 例患者纳入分析,中位随访时间为 37 个月(范围 2-106)。匹配样本包含 756 例患者。PS 匹配后,特定 ypTNM 分期的患者死亡风险是具有相同 pTNM 分期患者的 1.34 倍(95%CI 1.05-1.72,P=0.019)。与 PS 匹配结果相似,多变量 Cox 回归得到的风险比(HR)为 1.35(95%CI 1.09-1.67,P=0.006)。亚组分析表明,ypTNM 与 pTNM 分期之间的生存差异因患者的特定 TNM 分期而异。I 期和 III 期患者的 HR 分别为 3.44(95%CI 1.06-11.18,P=0.040)和 1.28(95%CI 1.00-1.62,P=0.048);而对于 II 期患者,未观察到显著差异(HR=1.37,95%CI 0.78-2.38,P=0.27)。
与 pTNM 定义的相同分期相比,具有特定 ypTNM 分期的胃癌患者预后更差。