PLOIDY AS A PROGNOSTIC FACTOR IN OVARIAN-CANCER
PLOIDY AS A PROGNOSTIC FACTOR IN OVARIAN-CANCER
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DOI:
10.1097/00004347-198301000-00005
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发表时间:
1983-01-01
影响因子:
2.4
通讯作者:
TATTERSALL, MHN
中科院分区:
文献类型:
--
作者:
FRIEDLANDER, ML;TAYLOR, IW;TATTERSALL, MHN
The cellular DNA content of 50 ovarian common epithelial carcinomas was determined by flow cytometry, and tumours were classified as being either diploid or aneuploid. A significant association between tumour stage and ploidy was demonstrated, with all diploid tumours being of an early stage (p< 0.001). Forty percent of early-stage tumours (FIGO stages I and II) and all late-stage tumours (FIGO stages III and IV) were aneuploid. This heterogeneity with respect to DNA content among tumours of a similar stage may allow the identification of neoplasms with a different natural history. The proportion of S-phase cells determined by flow cytometry is a measure of cellular proliferation and may also be of prognostic significance. Diploid tumours had a median S phase of 9.8%(2.4–14.1%), while aneuploid tumours had a significantly higher S phase of 19.6%(7–24.7%; p< 0.05). In this study there was no relationship between histological grading of invasive carcinomas and ploidy, but in view of the relatively small numbers and limited follow-up, it was_not possible to perform a multivariate analysis of all known prognostic factors in ovarian cancer. Our results suggest that ploidy reflects tumour behaviour, but prolonged follow-up and increased patient accrual is necessary to assess whether the flow cytometric analysis of DNA content will provide clinically important information in ovarian cancer.