Angiogenesis as a prognostic marker in breast carcinoma with conventional adjuvant chemotherapy: a multiparametric and immunohistochemical analysis

It has now been clearly established that quantitative immunohistochemical methods applied to tumour angiogenesis under suitable quality control conditions are a powerful prognostic tool for use in the initial assessment of breast carcinomas. Appropriate parameters for predicting the aggressiveness o...

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Published inThe Journal of pathology Vol. 184; no. 2; pp. 130 - 135
Main Authors Jacquemier, Jocelyne D., Penault-Llorca, Frederique M., Bertucci, Francois, Sun, Zhen Z., Houvenaeghel, Gilles F., Geneix, Jeanine A., Puig, Brigitte D., Bardou, Valerie Jeanne H., Hassoun, Jacques A., Birnbaum, Daniel, Viens, Patrice J.
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LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.02.1998
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Abstract It has now been clearly established that quantitative immunohistochemical methods applied to tumour angiogenesis under suitable quality control conditions are a powerful prognostic tool for use in the initial assessment of breast carcinomas. Appropriate parameters for predicting the aggressiveness of tumours and their sensitivity to treatment are, however, still required. To determine whether the microvessel count (MVC) may serve to predict the chemotherapeutic response, a retrospective study was carried out on a series of 162 patients with breast carcinoma, who were all treated with the same standard adjuvant chemotherapy. Angiogenesis was assessed by performing CD31 immunostaining and MVC per mm2. Several other factors such as P53, ERBB2, BCL2, and Ki67 were also measured, and their prognostic value was compared with that of the MVC. The MVC was not found to be correlated with any of the other prognostic parameters, but turned out to be of great prognostic value whatever the threshold value chosen, which suggests that it is continuously valid at all levels. The median value of the MVC (43·5 per mm2) divided this series into two significantly different prognostic categories, in terms of both disease‐free survival (P=0·0002) and overall survival (P=0·037). Univariate analysis showed that most of the parameters analysed were of prognostic value regarding the disease‐free survival, namely grade (P=0·029), mitotic index (P=0·049), size (P=0·015), oestrogen receptors (P=0·022), progesterone receptors (P=0·018), P53 (P=0·0045), ERBB2 (P=0·046), and Ki67 (P=0·0008). As regards overall survival, grade and ERBB2 showed a loss of prognostic value. In multivariate analysis on disease‐free survival, the MVC was the most accurate prognostic factor (RR=2·64), followed by Ki67 (RR=2·06) and P53 (RR=1·69). With respect to overall survival, the MVC ranked third among the prognostic parameters analysed. Standard chemotherapy did not reduce the high prognostic value of the MVC performed on tumour angiogenesis. This suggests that the MVC may predict the degree of resistance to chemotherapy. Patients with high levels of angiogenesis, particularly node‐negative patients, might therefore be able to benefit from adjuvant therapy of another kind. © 1998 John Wiley & Sons, Ltd.
AbstractList It has now been clearly established that quantitative immunohistochemical methods applied to tumour angiogenesis under suitable quality control conditions are a powerful prognostic tool for use in the initial assessment of breast carcinomas. Appropriate parameters for predicting the aggressiveness of tumours and their sensitivity to treatment are, however, still required. To determine whether the microvessel count (MVC) may serve to predict the chemotherapeutic response, a retrospective study was carried out on a series of 162 patients with breast carcinoma, who were all treated with the same standard adjuvant chemotherapy. Angiogenesis was assessed by performing CD31 immunostaining and MVC per mm2. Several other factors such as P53, ERBB2, BCL2, and Ki67 were also measured, and their prognostic value was compared with that of the MVC. The MVC was not found to be correlated with any of the other prognostic parameters, but turned out to be of great prognostic value whatever the threshold value chosen, which suggests that it is continuously valid at all levels. The median value of the MVC (43·5 per mm2) divided this series into two significantly different prognostic categories, in terms of both disease‐free survival (P=0·0002) and overall survival (P=0·037). Univariate analysis showed that most of the parameters analysed were of prognostic value regarding the disease‐free survival, namely grade (P=0·029), mitotic index (P=0·049), size (P=0·015), oestrogen receptors (P=0·022), progesterone receptors (P=0·018), P53 (P=0·0045), ERBB2 (P=0·046), and Ki67 (P=0·0008). As regards overall survival, grade and ERBB2 showed a loss of prognostic value. In multivariate analysis on disease‐free survival, the MVC was the most accurate prognostic factor (RR=2·64), followed by Ki67 (RR=2·06) and P53 (RR=1·69). With respect to overall survival, the MVC ranked third among the prognostic parameters analysed. Standard chemotherapy did not reduce the high prognostic value of the MVC performed on tumour angiogenesis. This suggests that the MVC may predict the degree of resistance to chemotherapy. Patients with high levels of angiogenesis, particularly node‐negative patients, might therefore be able to benefit from adjuvant therapy of another kind. © 1998 John Wiley & Sons, Ltd.
It has now been clearly established that quantitative immunohistochemical methods applied to tumour angiogenesis under suitable quality control conditions are a powerful prognostic tool for use in the initial assessment of breast carcinomas. Appropriate parameters for predicting the aggressiveness of tumours and their sensitivity to treatment are, however, still required. To determine whether the microvessel count (MVC) may serve to predict the chemotherapeutic response, a retrospective study was carried out on a series of 162 patients with breast carcinoma, who were all treated with the same standard adjuvant chemotherapy. Angiogenesis was assessed by performing CD31 immunostaining and MVC per mm2. Several other factors such as P53, ERBB2, BCL2, and Ki67 were also measured, and their prognostic value was compared with that of the MVC. The MVC was not found to be correlated with any of the other prognostic parameters, but turned out to be of great prognostic value whatever the threshold value chosen, which suggests that it is continuously valid at all levels. The median value of the MVC (43.5 per mm2) divided this series into two significantly different prognostic categories, in terms of both disease-free survival (P = 0.0002) and overall survival (P = 0.037). Univariate analysis showed that most of the parameters analysed were of prognostic value regarding the disease-free survival, namely grade (P = 0.029), mitotic index (P = 0.049), size (P = 0.015), oestrogen receptors (P = 0.022), progesterone receptors (P = 0.018), P53 (P = 0.0045), ERBB2 (P = 0.046), and Ki67 (P = 0.0008). As regards overall survival, grade and ERBB2 showed a loss of prognostic value. In multivariate analysis on disease-free survival, the MVC was the most accurate prognostic factor (RR = 2.64), followed by Ki67 (RR = 2.06) and P53 (RR = 1.69). With respect to overall survival, the MVC ranked third among the prognostic parameters analysed. Standard chemotherapy did not reduce the high prognostic value of the MVC performed on tumour angiogenesis. This suggests that the MVC may predict the degree of resistance to chemotherapy. Patients with high levels of angiogenesis, particularly node-negative patients, might therefore be able to benefit from adjuvant therapy of another kind.
Author Geneix, Jeanine A.
Puig, Brigitte D.
Penault-Llorca, Frederique M.
Bardou, Valerie Jeanne H.
Viens, Patrice J.
Jacquemier, Jocelyne D.
Hassoun, Jacques A.
Birnbaum, Daniel
Sun, Zhen Z.
Houvenaeghel, Gilles F.
Bertucci, Francois
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Issue 2
Keywords Antineoplastic agent
Human
Immunohistochemistry
Cell proliferation
Carcinoma
Prognosis
Adjuvant treatment
Malignant tumor
Multivariate analysis
Response
Pathology
Mammary gland diseases
Angiogenesis
Chemotherapy
Treatment
Follow up study
C-Onc gene
Female
Mammary gland
Protooncogene
Quantitative analysis
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1995; 72
1986; 73
1992; 340
1997; 42
1995; 13
1987; 5
1989; 81
1997; 24
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1994; 69
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1995; 3
1995; 6
1994; 86
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1997; 349
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1993; 54
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1994; 14
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1995; 103
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1996; 69
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1994; 74
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1996; 88
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Snippet It has now been clearly established that quantitative immunohistochemical methods applied to tumour angiogenesis under suitable quality control conditions are...
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SubjectTerms adjuvant chemotherapy
angiogenesis
Antigens, Neoplasm - analysis
Biological and medical sciences
Biomarkers, Tumor - analysis
breast cancer
Breast Neoplasms - blood supply
Breast Neoplasms - chemistry
Breast Neoplasms - drug therapy
CD31
Chemotherapy, Adjuvant
Disease-Free Survival
Female
Gynecology. Andrology. Obstetrics
Humans
Mammary gland diseases
Medical sciences
Middle Aged
Neovascularization, Pathologic - pathology
Platelet Endothelial Cell Adhesion Molecule-1 - analysis
Prognosis
Retrospective Studies
Survival Rate
Tumors
Title Angiogenesis as a prognostic marker in breast carcinoma with conventional adjuvant chemotherapy: a multiparametric and immunohistochemical analysis
URI https://api.istex.fr/ark:/67375/WNG-JM2KBS2V-L/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2F%28SICI%291096-9896%28199802%29184%3A2%3C130%3A%3AAID-PATH19%3E3.0.CO%3B2-W
https://www.ncbi.nlm.nih.gov/pubmed/9602702
https://search.proquest.com/docview/79895684
Volume 184
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