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. 2022 Jun 17;13:3500. doi: 10.1038/s41467-022-30908-1

Table 3.

Baseline characteristics of the 1 L ARROW trial participants given pralsetinib and Flatiron EDM cohort given 1 L pembrolizumab, and 1 L pembrolizumab with chemotherapy after IPTW-adjustment; balanced variables are those with SMD < 0.1.

Level Pembrolizumab Pralsetinib SMD Pembrolizumab with chemotherapy Pralsetinib SMD Adjusted
ESS/n 115/683 109/109 217/1270 109/109
Age (%) <65 48.3 59.6 0.23 58.9 59.6 0.015 Y
>=65 51.7 40.4 41.1 40.4
Sex (%) F 50.6 54.1 0.072 54.5 54.1 0.007 Y
M 49.4 45.9 45.5 45.9
Smoking history at baseline (%) History of smoking 48.9 39.4 0.192 40.3 39.4 0.017 Y
No history of smoking 51.1 60.6 59.7 60.6
ECOG (%) 0 27.8 31.2 0.075 32.9 31.2 0.037 Y
72.2 68.8 67.1 68.8
Time from initial diagnosis to first dose (months) (median [IQR]) 1 1.45 [0.92, 2.45] 1.74 [1.25, 2.30] 0.078 1.32 [0.92, 2.24] 1.74 [1.25, 2.30] 0.042 Y
Stage at initial diagnosis (%) STAGE I, II, or III 17 15.6 0.038 16.6 15.6 0.028 Y
STAGE IV 83 84.4 83.4 84.4
Race (%) White 56.7 49.5 0.199 52.3 49.5 0.061 Y
Other 35.6 45 41.9 45
Unknown 7.7 5.5 5.8 5.5
CNS metastases only (%) 0 82.5 72.5 0.241 87.5 72.5 0.383 N
1 17.5 27.5 12.5 27.5

ESS Effective sample size; the sample size of an unweighted sample which incorporates the precision of the given weighted sample, n number of patients in remaining in IPTW-trimmed sample.