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. 2023 Apr 25;149(11):8557–8571. doi: 10.1007/s00432-023-04745-8

Table 3.

Pathological subtype performance of RASSF1A, SHOX2 methylation, EGFR mutation, and combined assay panels using FFPE samples from patients with suspected malignant lung nodules

Methylation positivity (%) Pathological subtypes Total P for chi-square P for linear correlation
Group 1 (AAH + AIS) Group 2A (MIA) Group 2B (IA)
N 125 59 74 258
RASSF1A 20a (16.0) 24b (40.7) 35b (47.3) 79 (30.6)  < 0.001  < 0.001
SHOX2 +  15a (12.0) 14a, b (23.7) 32b (43.2) 61 (23.6)  < 0.001  < 0.001
TM +  28a (22.4) 30b (50.8) 49b (66.2) 107 (41.5)  < 0.001  < 0.001
EGFR +  34a (34.0) 25a, b (25.0) 41b (41.0) 100 (38.9)  < 0.001  < 0.001
RASSF1A + EGFR +  40a (32.0) 38b (64.4) 58b (78.4) 136 (52.7)  < 0.001  < 0.001
SHOX2 + EGFR +  43a (34.4) 33b (55.9) 59c (79.7) 135 (52.3)  < 0.001  < 0.001
TM + EGFR +  48a (38.4) 41b (69.5) 66c (89.2) 155 (60.1)  < 0.001  < 0.001

TM +  total methylation, which refers to the combined methylation detection of both the RASSF1A and SHOX2 genes

Each subscript letter denotes a subset of pathological subtype categories whose column proportions do not differ significantly from each other at the 0.05 level. The same subscript letters represent no statistically significant difference at the 0.05 level