Prospective analysis of the impact of VEGF-A gene polymorphisms on the pharmacodynamics of bevacizumab-based therapy in metastatic breast cancer patients |
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Authors: | Etienne-Grimaldi Marie-Christine Formento Patricia Degeorges Armelle Pierga Jean-Yves Delva Rémi Pivot Xavier Dalenc Florence Espié Marc Veyret Corinne Formento Jean-Louis Francoual Mireille Piutti Magali de Crémoux Patricia Milano Gérard |
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Affiliation: | 1Centre Antoine Lacassagne, Nice;2Institut Curie, Paris;3Centre Paul Papin, Angers;4Centre Hospitalier Universitaire Jean Minjoz, Besançon;5Institut Claudius Regaud, Toulouse;6Hôpital Saint Louis, Paris;7Centre Henri Becquerel, Rouen;8Roche, Neuilly-sur-Seine, France |
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Abstract: | AIMSTo test prospectively the impact of VEGF-A gene polymorphisms on the pharmacodynamics of bevacizumab-chemotherapy in breast cancer patients.METHODSAs part of the single-arm MO19391 trial, 137 women with locally recurrent or metastatic breast cancer receiving first-line bevacizumab-containing therapy were analysed. Patients received bevacizumab associated (76%) or not (24%) with taxane-based chemotherapy. Clinical evaluation included clinical response, time to progression (TTP) and a toxicity score corresponding to the sum of each maximum observed toxicity grade (hypertension, haemorrhage, arterial and venous thrombo-embolism). Functional VEGF-A polymorphisms at position −2578 C > A, −1498 T > C, −1154 G > A, −634 G > C and 936 C > T were analysed by PCR-RFLP (blood DNA).RESULTSOverall response rate (complete response (CR) + partial response (PR)) was 61%. Median TTP was 11 months. None of the VEGF-A polymorphisms was significantly linked to clinical response. Analysis of the 936C > T polymorphism revealed that the 96 patients homozygous for the 936C allele exhibited a marked tendency for a shorter TTP (median 9.7 months) than the 32 patients bearing the 936T allele (median 11.5 months, P = 0.022) of which 30 were CT and two were homozygous TT. Other polymorphisms did not influence TTP. VEGF-A−634 G > C was significantly related to the toxicity score with 39%, 49% and 81% of patients with score >1 in GG, GC and CC patients, respectively (P = 0.01).CONCLUSIONSThe role for VEGF-A 936C > T polymorphism as a potential marker of TTP in breast cancer patients receiving bevacizumab-containing therapy concords with the known impact of VEGF-A 936C > T polymorphism on VEGF-A expression. |
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Keywords: | bevacizumab breast cancer gene polymorphisms pharmacogenetics VEGF-A |
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