# Is Immunotherapy a Contraindication for Treating Lung Cancer Patients with Interstitial Lung Diseases? A Review of the Literature

## TL;DR

This review explores the challenges of using immunotherapy for lung cancer patients with interstitial lung diseases, highlighting the risks and the need for personalized treatment strategies.

## Contribution

The paper provides a comprehensive review of the safety and efficacy of immunotherapy in lung cancer patients with interstitial lung diseases.

## Key findings

- Immunotherapy-related pneumonitis is more common in patients with pre-existing interstitial lung diseases.
- Antifibrotic drugs may help reduce post-operative complications in IPF patients undergoing cancer treatments.
- Personalized treatment and close monitoring are essential for managing lung cancer patients with ILDs.

## Abstract

The management of lung cancer (LC) in patients with interstitial lung diseases (ILDs) presents significant challenges, particularly with the increasing use of immunotherapy (IT). Immunotherapy-related pneumonitis (ICIP) is a potential complication of immune checkpoint inhibitors (ICIs) that can be difficult to differentiate from pre-existing or treatment-induced ILD. The incidence of treatment-related pneumonitis is higher in patients with pre-existing ILD, which complicates the therapeutic approach. Moreover, antifibrotic drugs have shown potential in reducing the incidence of post-operative acute exacerbations in IPF patients undergoing surgery and radiotherapy. ILDs in LC patients can either develop ab initio, linked to environmental exposures, autoimmune diseases, or emerge because of cancer therapies. Although large-scale clinical trial evidence remains limited, careful therapy selection, early detection of pneumonitis, and close monitoring are crucial. Further prospective studies are needed to refine therapeutic strategies, particularly regarding the role of IT in this sensitive population and the role of combination therapies with antifibrotics and ICIs to optimize outcomes for patients with both LC and ILDs. This review summarizes the available evidence on the safety and efficacy of IT in this population, emphasizing the importance of personalized treatment approaches and vigilant monitoring.