GOG Trial | N | ORR | PFS > 6mo | Median PFS (mo.) | Median OS (mo.) |
---|
229Â N [7] | 28 | 0Â % | 11Â % | 2.1 | 9.4 |
229Â K [6] | 37 | 9.4Â % | 22Â % | 3.3 | 10.1 |
229 I [8] | 45 | 18.6Â % | 30Â % | 3.3 | 10.7 |
229Â G* [5] | 53 | 24.5Â % | 47Â % | 5.6 | 16.9 |
229Â F* [4] | 49 | 8.9Â % | 40Â % | 2.9 | 14.6 |
229 E [3] | 56 | 13.5Â % | 40.4Â % | 4.2 | 10.5 |
229Â J [9] | 53 | 12.5Â % | 29Â % | 3.5 | 12.5 |
- *Significant Grade 3/4 adverse events were encountered on these studies preventing subsequent development of a phase 3 trial; GOG = gynecologic oncology group; ORR = overall response rate; PFS = progression free survival; OS = overall survival