Vinh-Hung Vincent, Bourgain Claire, Vlastos Georges, Cserni Gábor, De Ridder Mark, Storme Guy, Vlastos Anne-Thérèse
Oncologisch Centrum, Universitair Ziekenhuis Brussel, 101 Laarbeeklaan, 1090 Jette, Brussels, Belgium.
BMC Cancer. 2007 Aug 23;7:164. doi: 10.1186/1471-2407-7-164.
Histopathology is a cornerstone in the diagnosis of cervical cancer but the prognostic value is controversial.
Women under active follow-up for histologically confirmed primary invasive cervical cancer were selected from the United States Surveillance, Epidemiology, and End Results (SEER) 9-registries public use data 1973-2002. Only histologies with at least 100 cases were retained. Registry area, age, marital status, race, year of diagnosis, tumor histology, grade, stage, tumor size, number of positive nodes, number of examined nodes, odds of nodal involvement, extent of surgery, and radiotherapy were evaluated in Cox models by stepwise selection using the Akaike Information Criteria.
There were 30,989 records evaluable. From 1973 to 2002, number of cases dropped from 1,100 new cases/year to 900/year, but adenocarcinomas and adenosquamous carcinoma increased from 100/year to 235/year. Median age was 48 years. Statistically significant variables for both overall and cause-specific mortality were: age, year of diagnosis, race, stage, histology, grade, hysterectomy, radiotherapy, tumor size and nodal ratio. The histological types were jointly significant, P < 0.001. Cause-specific mortality hazard ratios by histological type relatively to non-microinvasive squamous cell carcinoma were: microinvasive squamous cell carcinoma 0.28 (95% confidence interval: 0.20-0.39), carcinoma not otherwise specified 0.91 (0.79-1.04), non-mucinous adenocarcinoma 1.06 (0.98-1.15), adenosquamous carcinoma 1.35 (1.20-1.51), mucinous adenocarcinoma 1.52 (1.23-1.88), small cell carcinoma 1.94 (1.58-2.39).
Small cell carcinoma and adenocarcinomas were associated with poorer survival. The incidental observation of increasing numbers of adenocarcinomas despite a general decline suggests the inefficiency of conventional screening for these tumors. Increased incidence of adenocarcinomas, their adverse prognosis, and the young age at diagnosis indicate the need to identify women who are at risk.
组织病理学是宫颈癌诊断的基石,但其预后价值存在争议。
从美国监测、流行病学和最终结果(SEER)9登记处1973 - 2002年的公开使用数据中选取经组织学确诊为原发性浸润性宫颈癌且正在接受积极随访的女性。仅保留至少有100例病例的组织学类型。在Cox模型中,通过使用赤池信息准则进行逐步选择,对登记地区、年龄、婚姻状况、种族、诊断年份、肿瘤组织学类型、分级、分期、肿瘤大小、阳性淋巴结数量、检查的淋巴结数量、淋巴结受累几率、手术范围和放疗情况进行评估。
有30989条记录可评估。从1973年到2002年,病例数从每年1100例新发病例降至每年900例,但腺癌和腺鳞癌从每年100例增至每年235例。中位年龄为48岁。总体死亡率和特定病因死亡率的统计学显著变量为:年龄、诊断年份、种族、分期、组织学类型、分级、子宫切除术、放疗、肿瘤大小和淋巴结比例。组织学类型联合起来具有显著性,P < 0.001。相对于非微浸润性鳞状细胞癌,各组织学类型的特定病因死亡率风险比为:微浸润性鳞状细胞癌0.28(95%置信区间:0.20 - 0.39),未另行规定的癌0.91(0.79 - 1.04),非黏液腺癌1.06(0.98 - 1.15),腺鳞癌1.35(1.20 - 1.51),黏液腺癌1.52(1.23 - 1.88),小细胞癌1.94(1.58 - 2.39)。
小细胞癌和腺癌与较差的生存率相关。尽管总体病例数下降,但腺癌数量增加这一偶然观察结果表明对这些肿瘤进行常规筛查效率不高。腺癌发病率增加、其不良预后以及诊断时的年轻年龄表明有必要识别出有风险的女性。