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. Author manuscript; available in PMC: 2019 Feb 15.
Published in final edited form as: Cancer. 2017 Dec 6;124(4):688–697. doi: 10.1002/cncr.30967

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