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The human tumour cloning assay in the management of breast cancer patients.

A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectiv...

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Autores principales: Dittrich, C., Jakesz, R., Wrba, F., Havelec, L., Haas, O., Spona, J., Holzner, H., Kolb, R., Moser, K.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977099/
https://www.ncbi.nlm.nih.gov/pubmed/4027163
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author Dittrich, C.
Jakesz, R.
Wrba, F.
Havelec, L.
Haas, O.
Spona, J.
Holzner, H.
Kolb, R.
Moser, K.
author_facet Dittrich, C.
Jakesz, R.
Wrba, F.
Havelec, L.
Haas, O.
Spona, J.
Holzner, H.
Kolb, R.
Moser, K.
author_sort Dittrich, C.
collection PubMed
description A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectively. An attempt was made to examine whether there was any association between parameters accepted as prognostic factors for breast cancer and clonal growth in vitro. No correlation was found between preoperative tumour burden, histopathologic grading, menopausal status or overall survival and clonal growth in vitro, whereas we observed an inverse trend between progesterone receptor content of the tumours and their growth potential (P less than 0.01). In those few cases where in vitro and in vivo data could be compared, a high accuracy of the predicted sensitivities was found with respect to chemotherapy, but not in relation to hormonal treatment. A statistically significant higher overall chemosensitivity was associated with the absence of oestrogen receptors (P less than 0.01).
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spelling pubmed-19770992009-09-10 The human tumour cloning assay in the management of breast cancer patients. Dittrich, C. Jakesz, R. Wrba, F. Havelec, L. Haas, O. Spona, J. Holzner, H. Kolb, R. Moser, K. Br J Cancer Research Article A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectively. An attempt was made to examine whether there was any association between parameters accepted as prognostic factors for breast cancer and clonal growth in vitro. No correlation was found between preoperative tumour burden, histopathologic grading, menopausal status or overall survival and clonal growth in vitro, whereas we observed an inverse trend between progesterone receptor content of the tumours and their growth potential (P less than 0.01). In those few cases where in vitro and in vivo data could be compared, a high accuracy of the predicted sensitivities was found with respect to chemotherapy, but not in relation to hormonal treatment. A statistically significant higher overall chemosensitivity was associated with the absence of oestrogen receptors (P less than 0.01). Nature Publishing Group 1985-08 /pmc/articles/PMC1977099/ /pubmed/4027163 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
Dittrich, C.
Jakesz, R.
Wrba, F.
Havelec, L.
Haas, O.
Spona, J.
Holzner, H.
Kolb, R.
Moser, K.
The human tumour cloning assay in the management of breast cancer patients.
title The human tumour cloning assay in the management of breast cancer patients.
title_full The human tumour cloning assay in the management of breast cancer patients.
title_fullStr The human tumour cloning assay in the management of breast cancer patients.
title_full_unstemmed The human tumour cloning assay in the management of breast cancer patients.
title_short The human tumour cloning assay in the management of breast cancer patients.
title_sort human tumour cloning assay in the management of breast cancer patients.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977099/
https://www.ncbi.nlm.nih.gov/pubmed/4027163
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