Paclitaxel and bevacizumab as first line combined treatment in patients with metastatic breast cancer: the Hellenic Cooperative Oncology Group experience with biological marker evaluation
dc.contributor.author | Fountzilas, G. | en |
dc.contributor.author | Kourea, H. P. | en |
dc.contributor.author | Bobos, M. | en |
dc.contributor.author | Televantou, D. | en |
dc.contributor.author | Kotoula, V. | en |
dc.contributor.author | Papadimitriou, C. | en |
dc.contributor.author | Papazisis, K. T. | en |
dc.contributor.author | Timotheadou, E. | en |
dc.contributor.author | Efstratiou, I. | en |
dc.contributor.author | Koutras, A. | en |
dc.contributor.author | Pentheroudakis, G. | en |
dc.contributor.author | Christodoulou, C. | en |
dc.contributor.author | Aravantinos, G. | en |
dc.contributor.author | Miliaras, D. | en |
dc.contributor.author | Petraki, K. | en |
dc.contributor.author | Papandreou, C. N. | en |
dc.contributor.author | Papakostas, P. | en |
dc.contributor.author | Bafaloukos, D. | en |
dc.contributor.author | Repana, D. | en |
dc.contributor.author | Razis, E. | en |
dc.contributor.author | Pectasides, D. | en |
dc.contributor.author | Dimopoulos, A. M. | en |
dc.date.accessioned | 2015-11-24T19:00:12Z | |
dc.date.available | 2015-11-24T19:00:12Z | |
dc.identifier.issn | 1791-7530 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/19496 | |
dc.rights | Default Licence | - |
dc.subject | Adult | en |
dc.subject | Aged | en |
dc.subject | Aged, 80 and over | en |
dc.subject | Antibodies, Monoclonal/administration & dosage | en |
dc.subject | Antibodies, Monoclonal, Humanized | en |
dc.subject | Antineoplastic Combined Chemotherapy Protocols/administration & | en |
dc.subject | dosage/*therapeutic use | en |
dc.subject | Breast Neoplasms/*drug therapy/metabolism/pathology | en |
dc.subject | Female | en |
dc.subject | Humans | en |
dc.subject | In Situ Hybridization, Fluorescence | en |
dc.subject | Middle Aged | en |
dc.subject | Neoplasm Metastasis | en |
dc.subject | Paclitaxel/administration & dosage | en |
dc.subject | Retrospective Studies | en |
dc.subject | Tumor Markers, Biological/*metabolism | en |
dc.title | Paclitaxel and bevacizumab as first line combined treatment in patients with metastatic breast cancer: the Hellenic Cooperative Oncology Group experience with biological marker evaluation | en |
heal.abstract | BACKGROUND: Randomized studies have shown that bevacizumab combined with taxane-based regimens increases response rates and prolongs progression-free survival (PFS) of patients with metastatic breast cancer (MBC). However predictive or prognostic biological markers that identify the appropriate target population, thus improving the cost-effectiveness ratio of this treatment, are still needed. PATIENTS AND METHODS: Retrospectively, 124 patients with MBC treated either with paclitaxel 90 mg/m(2) weekly x12 plus bevacizumab 10 mug/kg every 2 weeks or 15 mug/kg every 3 weeks (85 patients) or paclitaxel 175 mg/m(2) plus bevacizumab 15 mug/kg every 3 weeks for 6 cycles (36 patients) were identified. Additionally, the prognostic significance of a panel of key biological markers was evaluated centrally by immunohistochemistry (IHC) in 88 evaluable patients. RESULTS: More than two thirds of the patients completed chemotherapy, as planned. The response rate was almost identical (55.3% vs. 55.6%) in the patients treated with weekly or 3-weekly paclitaxel, respectively. After a median follow-up time of 23 months, the median PFS of the study population was 13 months, while median survival had not yet been reached. Common severe adverse events were neutropenia (33%), neuropathy (18.6%) and metabolic disturbances (17.6%). The incidence of hypertension of all grades was 28.1%. High expression of vascular endothelial growth factor (VEGF) receptor 3 (VEGFR3) was associated with clinical response, while high expression of VEGFR1 was associated with poor survival. CONCLUSION: The safety and activity of the combination of bevacizumab with paclitaxel given either weekly or 3-weekly in patients with MBC is confirmed. | en |
heal.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/21868552 | - |
heal.journalName | Anticancer Res | en |
heal.journalType | peer-reviewed | - |
heal.language | en | - |
heal.publicationDate | 2011 | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
heal.type | journalArticle | - |
heal.type.el | Άρθρο Περιοδικού | el |
heal.type.en | Journal article | en |
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