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The edition · Pulmonology

Immune-related pneumonitis: a three-week steroid taper fell short of six

The first randomised trial of steroid duration for checkpoint-inhibitor pneumonitis backs the guideline course; an emulated trial questions immunosuppression in some fibrotic ILDs.

The edition in brief

In a randomised trial of 106 patients with grade 1–2 immune checkpoint inhibitor pneumonitis, a 3-week corticosteroid taper failed to show non-inferiority to the guideline 6-week taper: treatment success at 8 weeks was 66.7% against 85.2%, and an exploratory analysis favoured 6 weeks. Grade 3 or worse adverse events were commoner with the longer course (24% vs 12%) but manageable, and survival was similar. An international working group has revised the definition of acute exacerbation to cover all fibrotic interstitial lung disease, distinguishing exacerbation with diffuse alveolar damage from other causes of acute respiratory worsening such as oedema or pneumonia. A target trial emulation in 2270 patients with non-IPF fibrotic ILD found no survival or lung function benefit from starting mycophenolate or azathioprine, and an association with worse survival in non-IPF idiopathic interstitial pneumonia and fibrotic hypersensitivity pneumonitis; this is observational and does not override current practice. A crossover trial of 40 patients with COPD or ILD and exertional desaturation found walk distance identical on portable oxygen and air, though breathlessness was lower with oxygen. The pearl covers antigen avoidance in hypersensitivity pneumonitis.

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