Recent data reported an association between VEGF-A genotype of tumors and median overall survival as well as grade 3 or 4 hypertension when using bevacizumab in metastatic breast cancer. In the present case we report a discordant VEGF-A genotype between tumor and normal tissue in a patient with a responsive hepatic lesion of chemoresistant breast cancer treated with bevacizumab and paclitaxel. Moreover, we show that, despite the very low VEGF-A protein expression, the neoplastic lesion was well vascularized and responded to bevacizumab therapy. The discordance of VEGF-A polymorphisms in tumor and germline DNA may suggest the importance of obtaining both information in order to predict a superior overall survival or a lower risk of hypertension in patients treated with taxanes and bevacizumab.

Recent data reported an association between VEGF-A genotype of tumors and median overall survival as well as grade 3 or 4 hypertension when using bevacizumab in metastatic breast cancer. In the present case we report a discordant VEGF-A genotype between tumor and normal tissue in a patient with a responsive hepatic lesion of chemoresistant breast cancer treated with bevacizumab and paclitaxel. Moreover, we show that, despite the very low VEGF-A protein expression, the neoplastic lesion was well vascularized and responded to bevacizumab therapy. The discordance of VEGF-A polymorphisms in tumor and germline DNA may suggest the importance of obtaining both information in order to predict a superior overall survival or a lower risk of hypertension in patients treated with taxanes and bevacizumab. © 2009 Future Medicine Ltd.

Discordant somatic and germline VEGF-A genotype in a cancer patient resistant to paclitaxel/bevacizumab with chemosensitive hepatic metastasis / C. L., A. G., P. Orlandi, G. N., A. G., A. Fioravanti, B. E., B. M. T., G. Fontanini, D.T. M., R. Danesi, A. Falcone, G. Bocci. - In: PHARMACOGENOMICS. - ISSN 1462-2416. - 10:8(2009), pp. 1225-1229. [10.2217/pgs.09.55]

Discordant somatic and germline VEGF-A genotype in a cancer patient resistant to paclitaxel/bevacizumab with chemosensitive hepatic metastasis

R. Danesi;
2009

Abstract

Recent data reported an association between VEGF-A genotype of tumors and median overall survival as well as grade 3 or 4 hypertension when using bevacizumab in metastatic breast cancer. In the present case we report a discordant VEGF-A genotype between tumor and normal tissue in a patient with a responsive hepatic lesion of chemoresistant breast cancer treated with bevacizumab and paclitaxel. Moreover, we show that, despite the very low VEGF-A protein expression, the neoplastic lesion was well vascularized and responded to bevacizumab therapy. The discordance of VEGF-A polymorphisms in tumor and germline DNA may suggest the importance of obtaining both information in order to predict a superior overall survival or a lower risk of hypertension in patients treated with taxanes and bevacizumab. © 2009 Future Medicine Ltd.
Recent data reported an association between VEGF-A genotype of tumors and median overall survival as well as grade 3 or 4 hypertension when using bevacizumab in metastatic breast cancer. In the present case we report a discordant VEGF-A genotype between tumor and normal tissue in a patient with a responsive hepatic lesion of chemoresistant breast cancer treated with bevacizumab and paclitaxel. Moreover, we show that, despite the very low VEGF-A protein expression, the neoplastic lesion was well vascularized and responded to bevacizumab therapy. The discordance of VEGF-A polymorphisms in tumor and germline DNA may suggest the importance of obtaining both information in order to predict a superior overall survival or a lower risk of hypertension in patients treated with taxanes and bevacizumab.
Antibodies; Monoclonal; Humanized; Antibodies; administration /&/ dosage/adverse effects/therapeutic use; Antineoplastic Combined Chemotherapy Protocols; administration /&/ dosage/adverse effects/therapeutic use; Breast Neoplasms; drug therapy/genetics/pathology; Carcinoma; Ductal; Breast; drug therapy/genetics/pathology; DNA; Neoplasm; genetics; DNA; genetics; Disease-Free Survival; Drug Resistance; drug effects/genetics; Female; Genotype; Humans; Hypertension; chemically induced; Liver Neoplasms; blood supply/drug therapy/genetics/secondary; Middle Aged; Neovascularization; Pathologic; drug therapy/genetics; Paclitaxel; administration /&/ dosage/adverse effects/therapeutic use; Polymorphism; Genetic; Vascular Endothelial Growth Factor A; genetics
2009
http://dx.doi.org/10.2217/pgs.09.55
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1120267
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