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Table 1 Clinical characteristics of study patients. (N = 938)

From: Risk factors and clinical characteristics of lung cancer in idiopathic pulmonary fibrosis: a retrospective cohort study

 

Total (N = 938)

IPF with lung cancer (n = 135)

IPF without lung cancer (n = 803)

P value

Age, years

65.6 ± 8.1

65.2 ± 7.2

65.7 ± 8.2

0.479

Gender, male

744 (79.3)

128 (94.8)

616 (76.7)

< 0.001

Smoking

 Current

220 (23.5)

60 (44.4)

160 (19.9)

< 0.001

 Ex-smoker

462 (49.3)

74 (54.8)

390 (48.6)

 Never smoker

256 (27.3)

1 (0.8)

253 (31.5)

FVC, %

83.0 ± 18.6

89.5 ± 14.8

81.9 ± 19.0

< 0.001

FVC < 80%

316/818 (38.6)

24/115 (20.9)

292/703 (41.5)

< 0.001

DLco, %

71.3 ± 20.9

73.2 ± 20.3

71.0 ± 21.0

0.290

DLco < 80%

475/724 (65.6)

67/105 (63.8)

408/619 (65.9)

0.675

FEV1/FVC < 70%

101/795 (12.7)

25/111 (22.5)

76/684 (11.1)

0.001

Decline of FVC ≥ 10%/yeara

148/691 (21.4)

18/92 (19.6)

130/599 (21.7)

0.642

Decline of DLco ≥15%/yeara

132/571 (23.1)

12/81 (14.8)

120/490 (24.5)

0.056

Use of azathioprineb

96 (10.2)

11 (8.1)

85 (10.6)

0.387

Use of steroidb

123 (13.1)

13 (9.6)

110 (13.7)

0.195

Follow-up duration, years

4.5 ± 3.1

3.8 ± 2.6

4.6 ± 3.2

0.002

  1. DLco diffusing capacity for carbon monoxide, FEV1 forced expiratory volume in 1 s, FVC forced vital capacity, IPF idiopathic pulmonary fibrosis
  2. a Annual decline of FVC and DLco was calculated using the results of pulmonary function tests at the time of IPF diagnosis and at one year after the IPF diagnosis
  3. b Use of medication and duration of follow-up for patients who developed lung cancer are applicable to period from IPF diagnosis to lung cancer development