Baak J P, Schipper N W, Wisse-Brekelmans E C, Ceelen T, Bosman F T, van Geuns H, Wils J
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
Br J Cancer. 1988 May;57(5):503-8. doi: 10.1038/bjc.1988.114.
In 73 CAP-1 treated stage III and IV ovarian cancers, the prognostic significance of morphometric features and cellular DNA content has been evaluated in comparison with histologic type, grade of differentiation and a number of clinical characteristics. Borderline tumours were excluded from the study. Median follow-up was 44 months, median survival time 36 months. Single features associated with prognosis were (in order of decreasing significance according to single variate analysis): FIGO stage (P = 0.0002), bulky disease (P = 0.004), standard deviation and mean of nuclear area (P = 0.0006 and P = 0.01), cellular DNA content (P = 0.01), mitotic activity index (P = 0.08) and volume percentage epithelium (P = 0.13, not quite significant). Tumours with a mean nuclear area greater than 70 micron2 (which occurred in 35% of the cases) were nearly all aneuploid. Multivariate analysis showed that the statistically most significant prognostic combination of features consisted of mean nuclear area, presence or absence of bulky disease and FIGO stage (in order of decreasing importance) (Mantel-Cox = 23.07, P less than 0.00001). A low value for the multivariate function of this combination of features was associated with a poor prognosis within 24 months, a high value with a favourable outcome. Another favourable combination of features appeared to be diploid cellular DNA content and a low mitotic activity index (11 patients, one died). However, even with the prognostically most favourable combination of these features, several patients died. Of all combinations of features investigated, only two were associated with an excellent prognosis (low mitotic activity index and low volume percentage epithelium). Cancers of 7 patients (10%) displayed such features, and none of them died during the follow-up period (minimally 20 and maximally 54 months). It is concluded that morphometric and flow cytometric analysis can provide significant and objective information to predict the prognosis of cis-platin-treated advanced ovarian cancer patients.
在73例接受CAP - 1治疗的III期和IV期卵巢癌患者中,已将形态计量学特征和细胞DNA含量的预后意义与组织学类型、分化程度及一些临床特征进行了比较评估。交界性肿瘤被排除在研究之外。中位随访时间为44个月,中位生存时间为36个月。与预后相关的单一特征依次为(按单变量分析中显著性递减顺序排列):国际妇产科联盟(FIGO)分期(P = 0.0002)、大块肿瘤(P = 0.004)、核面积标准差和均值(P = 0.0006和P = 0.01)、细胞DNA含量(P = 0.01)、有丝分裂活性指数(P = 0.08)和上皮体积百分比(P = 0.13,不太显著)。核平均面积大于70平方微米的肿瘤(占病例的35%)几乎均为非整倍体。多变量分析显示,统计学上最显著的预后特征组合包括核平均面积、有无大块肿瘤及FIGO分期(按重要性递减顺序排列)(Mantel - Cox = 23.07,P小于0.00001)。该特征组合的多变量函数值低与24个月内预后不良相关,值高则与良好结局相关。另一个有利的特征组合似乎是二倍体细胞DNA含量和低有丝分裂活性指数(11例患者,1例死亡)。然而,即使具有这些特征的预后最有利组合,仍有几名患者死亡。在所有研究的特征组合中,只有两种与极佳预后相关(低有丝分裂活性指数和低上皮体积百分比)。7例患者(10%)的癌症表现出这些特征,且在随访期间(最短20个月,最长54个月)均未死亡。结论是,形态计量学和流式细胞术分析可为预测顺铂治疗的晚期卵巢癌患者的预后提供重要且客观的信息。