Table 2.
Patient characteristics and clinical outcomes to post-axitinib systemic therapy
| Factor | First post-axitinib therapy (n = 25) | Second post-axitinib therapy (n = 12) | |
|---|---|---|---|
| Interval from End of Axitinib Therapy to Start of Current Therapy Median in weeks (range) | 2.0 (0–41.7)a | 37.4 (2.6–93.0) | |
| Treatment | N ( %) | N ( %) | |
| VEGF inhibitors | 18 (72 %) | 3 (25 %) | |
| Sunitinib | 8 (32 %) | −0- | |
| Pazopanib | 6 (24 %) | 1 (8 %) | |
| Bevacizumab | 4 (16 %) | 2 (17 %) | |
| mTOR inhibitors | 7 (28 %) | 8 (67 %) | |
| Everolimus | 5 (20 %) | 5 (42 %) | |
| Temsirolimus | 2 (8 %) | 3 (25 %) | |
| Other | −0- | 1 (8 %)b | |
| ECOG PS | |||
| 0 | 3 (13 %) | 2 (17 %) | |
| 1 | 19 (79 %) | 9 (75 %) | |
| 2 | 2 (8 %)a | 1 (8 %) | |
| Heng Risk Group | |||
| Favorable | 9 (41 %) | 3 (30 %) | |
| Intermediate | 12 (55 %) | 6 (60 %) | |
| Unfavorable | 1 (5 %)c | 1 (10 %)d | |
| Best Response | |||
| PD | 2 (8 %) | −0- | |
| SD | 13 (42 %) | 6 (55 %) | |
| PD | 7 (28 %) | 4 (36 %) | |
| Not evaluable | 3 (12 %) | 1 (9 %)a | |
| Reason Treatment Stopped | |||
| PD/Death | 17 (68 %) | 6 (54 %) | |
| Toxicity | 4 (16 %) | 2 (18 %) | |
| Treatment ongoing | 4 (16 %) | 3 (27 %) | |
| Duration of Treatment (subsequent therapy) Median in months (range) | 4.4 (0.2–27.5+)a | 4.8 (0.7–19.1+)a |
amissing for one patient
bMK2206
cmissing for three patients
dmissing for two patients