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Table 2 Treatment type, outcome responses, and adverse events stratified by high vs. low inflammatory markers in those receiving anti-inflammatory therapy (N = 167)

From: Serum inflammatory markers as predictors of therapeutic response in non-idiopathic pulmonary fibrosis fibrotic interstitial lung disease: a retrospective cohort analysis

Outcomes

High inflammatory markers group

(N = 104)

Low to normal inflammatory markers group (N = 63)

p-value

Prescribed medications

   

 • Anti-inflammatory agents

   

  - Corticosteroid (%)

61 (58.7%)

41 (65.1%)

0.513

  - AZA (%)

10 (9.6%)

4 (6.4%)

0.572

  - MMF (%)

46 (44.2%)

34 (54%)

0.264

  - RTX (%)

21 (20.2%)

7 (11.1%)

0.141

  - Biologics, other than RTX (%)

7 (6.8%)

1 (1.6%)

0.261

  - HCQ (%)

15 (14.4%)

4 (6.4%)

0.136

  - IVIg (%)

3 (2.9%)

2 (3.2%)

1.000

  - MTX (%)

1 (0.96%)

1 (1.6%)

1.000

 • Concomitant antifibrotics

13 (12.5%)

6 (9.5%)

0.624

Duration of treatment at response evaluation

(months, median [IQR1 to IQR3])

8.1 [4.8 to 14.6]

6 [3.4 to 13.5]

0.401

ILD-AE

13 (12.5%)

6 (9.7%)

0.626

Death during course of treatment

13 (12.5%)

8 (12.7%)

1.000

Proceed to rescue lung transplantation

8 (7.7%)

11 (17.5%)

0.077

Response to treatment

58 (55.8%)

22 (34.9%)

0.011

Adverse events from treatment

35 (33.7%)

32 (50.8%)

0.035

 • Leukemia

7 (6.7%)

3 (4.8%)

0.744

 • Neutropenia

2 (1.9%)

3 (4.8%)

0.367

 • Anemia

22 (21.2%)

21 (33.3%)

0.101

 • Thrombocytopenia

7 (6.7%)

8 (12.7%)

0.264

 • Hepatic injury

12 (11.5%)

8 (12.7%)

0.811

 • Nausea-vomiting

4 (3.9%)

1 (1.6%)

0.651

 • Diarrhea

1 (0.96%)

2 (3.2%)

0.557

 • Pneumonia

2 (1.9%)

3 (4.8%)

0.367

 • Other infection

2 (1.9%)

2 (3.2%)

0.633

 • Osteoporosis

1 (0.96%)

1 (1.6%)

1.000

Adverse events leading to treatment discontinuation

2 (1.9%)

1 (1.6%)

1.000

Adverse events leading to death

0 (0%)

0 (0%)

-