5.
凡德他尼二线治疗晚期非小细胞肺癌的已完成的Ⅱ期试验结果
Results of completed phase Ⅱ trials of vandetanib as second-line therapy for advanced non–small-cell lung cancer
| 中位PFS (周) | 中位OS (月) | ORR (%) | |
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aStudy met its primary endpoint significance criteria. bHR is compared with placebo + docetaxel. Abbreviations: D=docetaxel; G=gefitinib; HR=hazard ratio; NS=not significant; NSCLC=non–small-cell lung cancer; OS=overall survival; ORR=overall response rate; PFS=progression-free survival; V=vandetanib. Note: Reprinted with permission from the copyright holder ©CIG Media Group, LP a研究达到主要终点的意义标准。bHR与安慰剂+多西紫杉醇组比较。缩写:D:多西紫杉醇;G:吉非替尼;HR:危险比;NS:无意义;NSCLC:非小细胞肺癌;OS:总生存期;ORR:总有效率;PFS:无进展生存期;V:凡德他尼。 注:本图得到版权所有者©CIG Media Group, LP复制许可 | |||
| 试验3 V (300 mg) Versus G (250 mg)[60]; n=168 |
V:11 | V: 6.1 | V:8 G:1 |
| G:8.1 | G:7.4 | ||
| HR=0.69;P=0.025a | HR=1.19;P=0.34 | ||
| 试验6 V (100 mg)+D (75 mg/m2) Versus V (300 mg)+D (75 mg/m2) Versus Placebo+D (75 mg/m2)[62]; n=127 |
V (100)+D: 18.7; bHR (V100)=0.64; P=0.074a V (300)+D: 17.0; bHR (V300)=0.83; P=0.416 D: 12.0 |
V(100)+D:13.1 | V(100)+D:26 |
| V (300)+D: 7.9 | V(300)+D:18 | ||
| D:13.4 | D:12 | ||
| P=NS | |||