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The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients.
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 stud...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1988
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246384/ https://www.ncbi.nlm.nih.gov/pubmed/3395555 |
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author | Baak, J. P. Schipper, N. W. Wisse-Brekelmans, E. C. Ceelen, T. Bosman, F. T. van Geuns, H. Wils, J. |
author_facet | Baak, J. P. Schipper, N. W. Wisse-Brekelmans, E. C. Ceelen, T. Bosman, F. T. van Geuns, H. Wils, J. |
author_sort | Baak, J. P. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2246384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22463842009-09-10 The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. Baak, J. P. Schipper, N. W. Wisse-Brekelmans, E. C. Ceelen, T. Bosman, F. T. van Geuns, H. Wils, J. Br J Cancer Research Article 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. Nature Publishing Group 1988-05 /pmc/articles/PMC2246384/ /pubmed/3395555 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Baak, J. P. Schipper, N. W. Wisse-Brekelmans, E. C. Ceelen, T. Bosman, F. T. van Geuns, H. Wils, J. The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title | The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title_full | The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title_fullStr | The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title_full_unstemmed | The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title_short | The prognostic value of morphometrical features and cellular DNA content in cis-platin treated late ovarian cancer patients. |
title_sort | prognostic value of morphometrical features and cellular dna content in cis-platin treated late ovarian cancer patients. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246384/ https://www.ncbi.nlm.nih.gov/pubmed/3395555 |
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