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. Author manuscript; available in PMC: 2020 Apr 15.
Published in final edited form as: Clin Cancer Res. 2019 Jul 23;25(20):6160–6169. doi: 10.1158/1078-0432.CCR-18-3603

Table 1.

Patient and disease characteristics.

n (% of total 161 patients)
Age
 Median (range) 62 (23–88)
 Patients <65 years 94 (58%)
Sex
 Male 124 (77%)
 Female 37 (23%)
ECOG performance status
 0–1 123 (76.4%)
 ≥2 38 (23.6%)
Primary site
 Esophagus/gastroesophageal junction 85 (53%)
 Gastric 76 (47%)
Grade
 Moderately differentiated 51 (31.7%)
 Poorly differentiated 106 (65.8%)
 Unknown 4 (2.5%)
HER-2 status
 Positive 18 (11.2%)
 Negative 139 (86.3%)
 Unknown 4 (2.5%)
MMR/MSI status
 MMR-deficient/MSI 15 (9.3%)
 MMR intact/MSS 106 (65.8%)
 Unknown 40 (24.8%)
PD-L1 status
 PD-L1 positive 45 (28%)
 PD-L1 negative 24 (14.9%)
 Unknown 92 (57.1%)
Number of prior regimens
 0–2 112 (69.6%)
 ≥3 (range 3–6) 49 (30.4%)
Previous therapies
 Fluoropyrimidine 137 (85%)
 Platinum 135 (84%)
 Taxane 96 (60%)
 Ramucirumab 65 (40%)
 Irinotecan 51 (32%)
 Trastuzumab 21 (13%)
 Gemcitabine 9 (6%)
 Anthracycline 5 (3%)
 Other 14 (9%)
Number of sites of disease at start of ICI
 1–2 105 (65.2%)
 ≥3 56 (34.8%)
Type of ICI
Single-agent anti-PD-1/PD-L1 110 (68.3%)
Combination anti-CTLA-4 plus anti-PD-1/PD-L1 51 (31.7%)

MMR, mismatch repair; MSI, microsatellite instability; MSS, microsatellite stable; PD-L1, programmed death-ligand-1; ICI, immune checkpoint inhibitors; anti-PD-1, anti-programmed cell death protein-1; anti-CTLA-4, anti-cytotoxic T-lymphocyte-associated protein-4.