Table 2.
Clinical Outcomes among Treated and Eligible Patients (N = 186)
TS-High Stratum | TS-Low Stratum | ||
---|---|---|---|
IROX/Bev | FOLFOX/Bev | FOLFOX/Bev | |
(n=61) | (n= 66) | (n=59) | |
Stopped for PD | 45.9% | 25.8% | 39% |
Stopped for Toxicity | 13.1% | 25.8% | 13.6 |
Death on Study | 9.8% | 1.5% | 0% |
CR + PR (90% CI) |
33% (23–44) |
38% (28–49) |
49% (38–61) |
CR | 0 | 2 (3.0%) | 1 (1.7%) |
PR | 20 (32.8%) | 23 (34.8%) | 28 (47.5%) |
SD | 25 (41.0%) | 36 (54.5%) | 23 (39.0%) |
PD | 2 (3.3%) | 1 (1.5%) | 0 |
Unevaluable | 14 (23.0%) | 4 (6.1%) | 7 (11.9%) |
Subsequent Surgery | 5 (8.2%) | 7 (10.6%) | 15 (25.4%) |
TS = thymidylate synthase; IROX = irinotecan and oxaliplatin; Bev = bevacizumab; FOLFOX = folinic acid (leucovorin), 5-Fluorouracil, and oxaliplatin PD = progressive disease; CR = complete response; PR = partial response; SD = stable disease. The TS-Low cohort includes both TS-Low and TS-indeterminate expression