Table 2.
Characteristic | N/total # pts (%) |
---|---|
Response on prior anti-EGFR therapy | |
Response or stable disease ≥6 m | 37/89 (42) |
No response or stable disease <6 m | 52/89 (58) |
Clinical benefit on anti-EGFR retreatment | |
Best response CR/PR/SD | 50/86 (58) |
Best response PD | 36/86 (42) |
Prior anti-EGFR-based regimens | |
Panitumumab monotherapy | 6/89 (7) |
Panitumumab + Chemotherapya | 9/89 (10) |
Panitumumab and AMG-102/AMG-479 | 1/89 (1) |
Cetuximab monotherapy | 2/89 (2) |
Cetuximab + Chemotherapyb | 71/89 (80) |
Anti-EGFR-based retreatment regimens | |
Cetuximab, FOLFOX, and dasatinib | 31/89 (35) |
Cetuximab, irinotecan, and bevacizumab | 12/89 (13) |
Cetuximab and erlotinib | 13/89 (15) |
Cetuximab and sirolimus | 11/89 (12) |
Cetuximab, HAIc oxaliplatin, 5-FU, bevacizumab | 20/89 (23) |
Cetuximab, HAI oxaliplatin, and bevacizumab | 2/89 (2) |
Interval length between prior and retreatment anti-EGFR therapies | Months |
Median | 4.57 |
Mean ± Standard Deviation | 7.34 ± 8.9 |
Range | 0.46 – 58.7 |
aChemotherapy regimen: irinotecan (7), FOLFIRI (1), 5-FU and irinotecan (1)
bChemotherapy regimen: Irinotecan (42), FOLFIRI (15), FOLFOX (5), irinotecan and arq197 (3), irinotecan and apomab (1), irinotecan and bevacizumab (3), FOLFOX and dasatinib (1), Xelox (1)
cHAI = Hepatic Arterial Infusion