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. Author manuscript; available in PMC: 2020 Feb 1.
Published in final edited form as: Invest New Drugs. 2018 Jul 28;37(1):147–158. doi: 10.1007/s10637-018-0646-1

Table 5.

Summary of subjects with an overall response of stable disease or better

Subject (Age/Sex) and Cohort (Dose) Tumor type Best response (Tumor response) Weeks on treatment (Main phase/Extension phase) VEGF-A Baseline (pg/mL) Largest VEGF-A Decrease (% Change from baseline)
55 / Female Ovarian SD (3.5%) 16.4 / No 300 −13.0%
Part 1, Cohort 2 (8 mg/kg biw) 59 / Male Colorectal SD (−3.1%) 15.1 / No 753 −22.4%
Part 1, Cohort 2 (8 mg/kg biw) 77 / Female# Non-small cell lung SD (−3.4%) 24.0 / Yes 2150 (High) −75.9%
Part 1, Cohort 4 (24 mg/kg biw) 76 / Female# Colorectal PR (−37.5%) 25.0/Yes 3620 (High) −96.9%
Part 1, Cohort 5 (24 mg/kg qw) 52 / Female Ovarian SD (2.6) 22.0 / No 982 −3.9%
Part 2 (24 mg/kg qw) 76 / Female# Ovarian SD * 23.9/Yes 18,600 (High) −45.0%
Part 2 (24 mg/kg qw) 29 / Female Ovarian SD (2.9) 24.0 / Yes 171 5.2%
Part 2 (24 mg/kg qw)

Tumor response was determined by percent change from baseline in the sum of longest diameters of the target lesions. High baseline VEGF-A levels were defined as >1500 pg/mL.

#

Indicates the three notable subjects of interest (Subjects 1, 2, and 3) with high baseline VEGF-A and clinical benefit discussed further in the text.

*

Tumor size was not assessable by RECIST for this subject. Biw = every two weeks; qw = every week