![]() The bevacizumab plus erlotinib group vs none of 224 patients in the bevacizumab alone group), diarrhoea (21 vs two ), and asthenia (12 vs two ). Most frequent grade 3–4 adverse events were skin rash (47 of 220 patients in Plus erlotinib group and 22♱ months (19♶–26♷) in the bevacizumab group (stratified Overall survival from maintenance was 24♹ months (95% CI 21♴–28♹) in the bevacizumab Emploi : Aide soignant de nuit h/f à Lyon Recherche parmi 843. Months (4♱–5♷) in the bevacizumab group (stratified HR 0♸1 , Months (95% CI 4♳–6♲) in the bevacizumab plus erlotinib group compared with 4♹ In the final analysis, median progression-free survival from randomisation was 5♴ Jean-Amde Roch, MD, Hpital priv Jean Mermoz, Service de radiologie, Lyon, France. Randomisation was 5♱ months (95% CI 4♱–5♹) in the bevacizumab plus erlotinib groupĬompared with 6♰ months (4♶–7♹) in the bevacizumab group (stratified hazard ratio (after 231 progression-free survival events), median progression-free survival from Choisissez l'tablissement dans lequel vous souhaitez passer vos examens Imagerie Mdicale Mermoz 55 avenue Mermoz 69008 LYON 04.72.78.54.54 Imagerie Mdicale Santy 24 avenue Paul Santy 69008 LYON 04.72.78.54.54 Cabinet de radiologie Saint-Priest 10 rue Pierre Corneille 69800 Saint-Priest 04.78.21.97. Months (31♵–61♰) in the bevacizumab plus erlotinib group. Median follow-up was 51♰ months (IQR 36♰–60♰) in the bevacizumab group and 48♳ ![]() Induction treatment, patients without disease progression were randomly assigned toīevacizumab (n=228) or bevacizumab plus erlotinib (n=224). ![]() The Lancet Regional Health – Western Pacificīetween Jan 1, 2007, and Oct 13, 2011, 700 eligible patients were enrolled following.The Lancet Regional Health – Southeast Asia.The Lancet Gastroenterology & Hepatology.
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