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. Author manuscript; available in PMC: 2021 Jan 1.
Published in final edited form as: Lung Cancer. 2019 Oct 18;139:1–8. doi: 10.1016/j.lungcan.2019.10.012

Table 1.

Clinical Data Table

Total Non-responder Responder P-value

52 27 (52%) 25(48%)
Immunotherapy Treatment
Nivolumab 36 (69%) 19 (70%) 17 (68%) 0.98
Pembrolizumab 14 (27%) 7 (26%) 7 (28%)
Atezolizumab 2 (4%) 1 (4%) 1 (4%)
Histology
Adenocarcinoma 33 (63%) 17 (63%) 16 (64%) 0.94
Squamous 19 (37%) 10 (37%) 9 (36%)
Driver Mutation*
Yes 9 (17%) 6 (22%) 3 (12%) 0.47
Gender
Male 23 (44%) 12 (44%) 11 (44%) 0.97
Female 29 (56%) 15 (56%) 14 (56%)
Age at Diagnosis
Median 62 62 63 0.59
Age at ICB Initiation
Median 64 64 65 0.79
Smoking History
Former/Current 44 (85%) 23 (85%) 21 (84%) 0.91
Never 8 (15% 4 (15%) 4 (16%)
Smoking (Pack Years)
Median 20 25 20 0.77
PFS (mo)
Events 42 27 15 <0.001
Median 3.3 1.7 25
OS (mo)
Events 41 25 16 <0.001
Median 9.6 6.0 25

Age at ICB: Age at time of starting immunotherapy; PFS (mo): Progression-free Survival in months; OS (mo): Overall survival in months

*

Driver mutations were defined as actionable EGFR mutations or EML4-ALK fusions

Footnote: Fisher’s exact test for categorical variables, t-test or median test for continuous variables, log-rank test for PFS and OS.