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. 2020 Jun 5;22(3):e379–e389. doi: 10.1016/j.cllc.2020.05.028

Supplemental Table 1.

Patient Characteristics of the Screened Population

Included Patients (N = 92) Excluded Patients (N = 58)
Clinico-pathologic characteristics
 Median age, y (range) 64.5 (37-87) 69 (33-87)
 Female gender 44 (48) 31 (53)
 Smoking status, ever 84 (91) 52 (90)
 ECOG PS
 0-1 75 (82) 27 (47)
 ≥2 17 (18) 28 (48)
 Not reported 0 (0) 3 (5)
 Histology
 Non-squamous 70 (76) 45 (78)
 Squamous 15 (16) 9 (15)
 Poorly differentiated 7 (8) 4 (7)
 Driver mutation
 KRAS 33 (36) 19 (33)
 EGFR 6 (7) 3 (5)
 Others 3 (3) 3 (5)
 None identified 40 (43) 25 (43)
 Not assessed 10 (11) 8 (14)
 PD-L1 TPS, %
 <1 24 (26) 8 (14)
 1-49 17 (18) 15 (26)
 ≥50 42 (46) 31 (53)
 Not assessed 9 (10) 4 (7)
 TMB, mut/mB
 <10 20 (22) 14 (24)
 ≥10 30 (32) 11 (19)
 Not assessed 42 (46) 33 (57)
Treatment characteristics
 Line of pembrolizumab
 First line 65 (71) 39 (67)
 ≥Second line 27 (29) 19 (33)
 Treatment
 Monotherapy 41 (45) 35 (60)
 With chemotherapy 51 (55) 22 (38)
 Not known 0 (0) 1 (2)
 Treatment center
 BIDMC 47 (51) 34 (59)
 VMC 45 (49) 24 (41)
 Median no. treatment cycles (range) 8 (4-41) 2 (1-3)
 Any grade irAE, yes 54 (59) 16 (28)
 ≥Grade 3 irAE, yes 28 (30) 12 (21)
 Systemic immunosuppression for irAE, yes 41 (45) 16 (28)

Abbreviations: BIDMC = Beth Israel Deaconess Medical Center; CR = complete response; ECOG = Eastern Cooperative Oncology Group; irAE = immune-related adverse events; PD-L1 = programmed death-ligand 1; PS = performance status; TMB = tumor mutational burden; TPS = tumor proportion score; VMC = Vidant Medical Center.

Data shown as n (%), unless specified.