Skip to main content
. 2021 Dec 7;5:100. doi: 10.1038/s41698-021-00239-3

Table 1.

Patient characteristics.

ALK+ NSCLC patients analyzed in this study (n = 43)
Age, median (39–80) 57 (10)
Sex, % male 53%
Smoking status (% never smokers)a 78%
ECOG PS (%) at baseline
 0 26
 1 14
 2 1
 No data 2
Histologyb
adenocarcinoma 42/43
ALK fusion variantc
 EML4-ALK V3 13
 EML4-ALK V1/V2 22
 Other 4
 No data 4
TP53 status at baseline, mutatedd 11/39
ALK TKI, patient number
 Crizotinib 25
 Ceritinib/alectinib/brigatinib 36
 Lorlatinib 4
Chemotherapy 7
Follow-up in months (median, [Q3-Q1]) 37 (52–27)
Number of samples analyzed per patient (mean [range]) 8 (4–31)
Percentage of cases with treatment-naive samples 21%
Number of samples at disease progression per patient, mean 2.8
Number of TKI lines covered with liquid biopsy per patient, mean 1.9

SD standard deviation, EML4-ALK echinoderm microtubule-associated protein-like 4 (EML4) and anaplastic lymphoma kinase (ALK) fusion, PS performance status, TKI tyrosine kinase inhibitor.

aData available for 41/43 cases.

bOne patient had an ALK+ large-cell neuroendocrine lung carcinoma responsive to ALK inhibitors.

cData available for 39/43 cases; one case with E18A20, one with E9A20, one with K9A20 (KCL1), and one with K24A20 (KIF5B).

dData available for 39 cases by NGS of tissue biopsies at diagnosis of stage IV disease.