本帖最后由 老马 于 2013-3-13 13:43 编辑
9 A. M' C3 G- o# f( N
, x% w$ s' u6 N+ u/ K, u5 K健择(吉西他滨)+顺铂+阿瓦斯汀
1 p/ g/ x2 Q9 I) I4 D Gemzar +Cisplatin + Avastin
. ^& L8 E, r U* L& fhttp://annonc.oxfordjournals.org/content/21/9/1804.full* @+ G" c# Q1 ~; G6 `( O1 g! m$ C
Overall survival with cisplatin–gemcitabine and bevacizumab or placebo as first-line therapy for nonsquamous non-small-cell lung cancer: results from a randomised phase III trial (AVAiL) . e8 G& H! y- G# |+ \6 e( F1 b
Patients and methods: Patients (n = 1043) received cisplatin 80 mg/m2 and gemcitabine 1250 mg/m2 for up to six cycles plus bevacizumab 7.5 mg/kg (n = 345), bevacizumab 15 mg/kg (n = 351) or placebo (n = 347) every 3 weeks until progression. Primary end point was progression-free survival (PFS); OS was a secondary end point.
1 V: d. `$ ]- t: D+ [- R+ E5 |Results: Significant PFS prolongation with bevacizumab compared with placebo was maintained with longer follow-up {hazard ratio (HR) [95% confidence interval (CI)] 0.75 (0.64–0.87), P = 0.0003 and 0.85 (0.73–1.00), P = 0.0456} for the 7.5 and 15 mg/kg groups, respectively. Median OS was >13 months in all treatment groups; nevertheless, OS was not significantly increased with bevacizumab [HR (95% CI) 0.93 (0.78–1.11), P = 0.420 and 1.03 (0.86–1.23), P = 0.761] for the 7.5 and 15 mg/kg groups, respectively, versus placebo. Most patients (62%) received multiple lines of poststudy treatment. Updated safety results are consistent with those previously reported.
% s( J! [" Q# W& u
Cisplatin Gemzar Avastin.PDF
(329.84 KB, 下载次数: 930)
8 J2 l9 s% L& \0 D7 w5 w
华为网盘附件:
) ?" ~" z% U W& o6 K$ |【华为网盘】ava.JPG* P8 o- J" H1 v
|