Department of Surgery, University of Pittsburgh, Pittsburgh, PA 15232, USA.
J Natl Cancer Inst. 2011 Apr 20;103(8):689-97. doi: 10.1093/jnci/djr078. Epub 2011 Mar 18.
BACKGROUND: The American Joint Committee on Cancer (AJCC) has proposed the inclusion of pretreatment serum carcinoembryonic antigen (CEA) level (C-stage) into the conventional TNM staging system of colon cancer. We assessed the prognosis of various stages of colon cancer after such an inclusion. METHODS: Data for all patients (N = 17 910) diagnosed with colonic adenocarcinoma (AJCC stages I, IIA, IIB, IIC, IIIA, IIIB, IIIC, and IV, based on TNM staging system) between January 1, 2004, and December 31, 2004, with a median follow-up of 27 months (range 0-35 months), were collected from the Surveillance, Epidemiology, and End Results database. C-stage (C0-stage = normal CEA level; C1-stage = elevated CEA level) was assigned to all patients with available CEA information (n = 9083). Multivariable analyses using Cox proportional hazards models were used to identify independent factors associated with prognosis. Prognosis of overall stages (AJCC stages I-IV and C0 or C1) was analyzed using Kaplan-Meier survival curves. All statistical tests were two-sided. RESULTS: C1-stage was independently associated with a 60% increased risk of overall mortality (hazard ratio of death = 1.60, 95% confidence interval = 1.46 to 1.76, P < .001). Overall survival was decreased in patients with C1-stage cancer compared with C0-stage cancer of the respective overall stages (P < .05). Similarly, decreased overall survival was noted in patients with stage I C1 cancer compared with stage IIA C0 or stage IIIA C0 cancer (P < .001), in patients with stage IIA C1 cancer compared with stage IIIA C0 (P < .001), and in patients with stage IIB C1 or stage IIC C1 cancer compared with stage IIIB C0 cancer (P < .001). CONCLUSIONS: C-stage was an independent prognostic factor for colon cancer. The results support routine preoperative CEA testing and C-staging upon diagnosis of colon cancer and the inclusion of C-stage in the conventional TNM staging of colon cancer.
背景:美国癌症联合委员会(AJCC)提出将预处理血清癌胚抗原(CEA)水平(C 期)纳入结肠癌的常规 TNM 分期系统。我们评估了纳入该标准后不同分期结肠癌的预后。
方法:收集了 2004 年 1 月 1 日至 2004 年 12 月 31 日期间诊断为结肠腺癌(AJCC 分期 I、IIA、IIB、IIC、IIIA、IIIB、IIIC 和 IV,基于 TNM 分期系统)的所有患者(N=17910)的数据,中位随访时间为 27 个月(范围 0-35 个月),这些数据来自监测、流行病学和最终结果数据库。对所有有 CEA 信息的患者(n=9083)进行 C 期(C0 期=正常 CEA 水平;C1 期=升高的 CEA 水平)分期。使用 Cox 比例风险模型进行多变量分析,以确定与预后相关的独立因素。使用 Kaplan-Meier 生存曲线分析总体分期(AJCC 分期 I-IV 和 C0 或 C1)的预后。所有统计检验均为双侧检验。
结果:C1 期与总死亡率增加 60%独立相关(死亡风险比=1.60,95%置信区间=1.46-1.76,P<0.001)。与相应总体分期的 C0 期相比,C1 期癌症患者的总体生存率降低(P<0.05)。同样,与 IIA 期 C0 期或 IIIA 期 C0 期相比,I 期 C1 期癌症患者的总体生存率降低(P<0.001),与 IIIA 期 C0 期相比,IIA 期 C1 期癌症患者的总体生存率降低(P<0.001),与 IIIB 期 C0 期相比,IIB 期 C1 期或 IIC 期 C1 期癌症患者的总体生存率降低(P<0.001)。
结论:C 期是结肠癌的独立预后因素。结果支持常规术前 CEA 检测和结肠癌诊断时的 C 分期,并将 C 期纳入结肠癌的常规 TNM 分期。
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