Skip to main content
. Author manuscript; available in PMC: 2016 Jun 1.
Published in final edited form as: Invest New Drugs. 2015 Mar 31;33(3):621–631. doi: 10.1007/s10637-015-0226-6

Table 5.

Characteristics of patients included in the study

Subject ID Gender Race Age
(years)
Anti-EGFR
Pretreatment
Response
Assessment
Method
ECOG
PS
Best
Response
EGFR
Mutation
Status
KRAS
Mutation
Status
Comments
CA-01-0006 Female Black 75 Yes RECIST 1 SD Not done KRAS −ve 15 weeks on trial with mixed
tumor response, 8% decrease
target lesions
CA-01-0015 Female White 83 Yes RECIST 0 SD EGFR −ve KRAS −ve 45 weeks on trial, cavitation of
lesions on PET scan, 3%
decrease target lesions
CA-01-0017 Female White 60 Yes RECIST 0 PD EGFR −ve KRAS +ve
CA-01-0063 Male White 34 Yes RECIST 1 PD EGFR −ve KRAS +ve
CA-01-0068 Female Asian 49 Yes RECIST 1 PD EGFR −ve Not done
CA-01-0069 Male White 71 Yes irRC 1 PD EGFR −ve KRAS +ve
CA-01-0070 Male Hispanic 54 Yes irRC 2 PD EGFR +ve KRAS −ve
CA-01-0072 Female White 76 Yes irRC 1 PD Not done Not done
CA-01-0074 Female Hispanic 50 Yes irRC 1 SD EGFR −ve KRAS +ve 16 weeks SD
CA-01-0075 Female Asian 37 Yes irRC 0 PD EGFR −ve KRAS −ve
CA-01-0056 Female White 52 No RECIST 0 SD EGFR −ve KRAS +ve 12 weeks,6% decrease target
lesions after 2 doses/6 weeks
CA-01-0066 Female White 70 No RECIST 1 PD EGFR −ve Not done
CA-01-0073 Male White 63 No irRC 0 PD EGFR −ve KRAS +ve
CA-01-0076 Male White 57 No irRC 1 SD EGFR −ve KRAS −ve 18 weeks SD, 8.6% decrease
target lesions
CA-01-0077 Female White 64 No irRC 0 PD EGFR −ve Not done
CA-01-0079 Male White 53 No irRC 1 PD EGFR −ve KRAS +ve