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Table 2 Pathological outcomes of the ALK-positive and ALK-negative groups

From: Clinicopathological and computed tomography features of patients with early-stage non-small-cell lung cancer harboring ALK rearrangement

Variables

ALK+ (n = 65)

ALK- (n = 629)

Χ2(t)

P-value

Pathological type

  

3.240

0.101

 SCC

0 (0)

30 (4.8)

  

 ADC

65 (100)

599 (95.2)

  

Cell differentiation

 Well

16 (24.6)

123 (19.5)

0.942

0.332

 Moderate

30 (46.2)

376 (59.8)

4.504

0.034a

 Poor

19 (29.2)

130 (20.7)

2.562

0.109

Mucinous

9 (13.8)

34 (5.4)

7.222

0.007a

≥5% Micropapillary/solid subtype

16 (24.6)

124 (19.7)

0.879

0.348

 VPI

24 (36.9)

300 (47.7)

2.746

0.097

Lymphovascular invasion

0 (0)

11 (1.7%)

1.155

0.282

 STAS

3 (4.6)

10 (1.6)

2.934

0.114

 Ki-67 (IQR)

5 (5, 10)

7 (3, 15)

0.277

0.782

 PD-1 (IQR)

8 (1, 10)

5 (2, 10)

0.844

0.399

 PD-L1 (IQR)

0 (0, 2)

0 (0, 2)

0.020

0.984

 EGFR

9/65 (13.8)

242/347 (69.7)

71.842

< 0.001a

 KRAS

1/65 (1.5)

29/336 (8.6)

3.000

0.083

 TP53

2/20 (10.0)

51/239 (21.3)

1.458

0.385

pTNM stage

  

–

1

 IA/IB

34 (52.3)/30 (46.2)

275 (43.7)/343 (54.5)

  

 IIA/IIB

0 (0)/1 (1.5)

11 (1.8)/0 (0)

  
  1. Unless otherwise indicated, data are shown as numbers with percentages in parentheses. aindicates significant difference
  2. Abbreviations: SCC Squamous cell carcinoma, ADC Adenocarcinoma, VPI Visceral pleural invasion, STAS Spread through air space, IQR Interquartile range, PD-1 Programmed death-1, PD-L1 Programmed death ligand-1, EGFR Epidermal growth factor receptor, KRAS Kirsten rat sarcoma, TP53 Tumor protein 53