Clinical significance of interstitial lung abnormalities and immune checkpoint inhibitor‐induced interstitial lung disease in patients with non‐small cell lung cancer. Issue 1 (14th November 2022)
- Record Type:
- Journal Article
- Title:
- Clinical significance of interstitial lung abnormalities and immune checkpoint inhibitor‐induced interstitial lung disease in patients with non‐small cell lung cancer. Issue 1 (14th November 2022)
- Main Title:
- Clinical significance of interstitial lung abnormalities and immune checkpoint inhibitor‐induced interstitial lung disease in patients with non‐small cell lung cancer
- Authors:
- Murata, Daiki
Azuma, Koichi
Matama, Goushi
Zaizen, Yoshiaki
Matsuo, Norikazu
Murotani, Kenta
Tokito, Takaaki
Hoshino, Tomoaki - Abstract:
- Abstract: Background: Interstitial lung abnormalities (ILAs) are known to be a risk of drug‐induced pneumonitis. However, there are few reports on the relationship between ILAs and immune checkpoint inhibitor‐related interstitial lung disease (ICI‐ILD). We retrospectively investigated the clinical significance of ILAs in patients with non‐small cell lung cancer (NSCLC) receiving ICIs. Methods: We defined ILAs as nondependent abnormalities affecting more than 5% of any lung zone, including ground‐glass or diffuse centrilobular nodularities, traction bronchiectasis, honeycombing, and nonemphysematous cysts. Early‐onset ICI‐ILD was defined as developing within 3 months after the initiation of ICI administration. Results: Of 264 patients with advanced NSCLC, 57 patients (21.6%) had ILAs (43 fibrotic and 14 nonfibrotic ILAs). The difference between the incidence of ICI‐ILD in patients with or without ILAs was not significant. Of 193 patients treated by ICI monotherapy, 18 (9.3%) developed early‐onset ICI‐ILD. Among patients receiving ICI monotherapy, the incidence of early‐onset ICI‐ILD was significantly higher in patients with than in patients without nonfibrotic ILAs. Conclusion: The presence of nonfibrotic ILAs is a significant risk for early‐onset ICI‐ILD in patients with NSCLC undergoing ICI monotherapy. Clinicians should be aware of ILAs, especially nonfibrotic ILAs, before administering ICIs to lung cancer patients. Abstract : We retrospectively investigated the clinicalAbstract: Background: Interstitial lung abnormalities (ILAs) are known to be a risk of drug‐induced pneumonitis. However, there are few reports on the relationship between ILAs and immune checkpoint inhibitor‐related interstitial lung disease (ICI‐ILD). We retrospectively investigated the clinical significance of ILAs in patients with non‐small cell lung cancer (NSCLC) receiving ICIs. Methods: We defined ILAs as nondependent abnormalities affecting more than 5% of any lung zone, including ground‐glass or diffuse centrilobular nodularities, traction bronchiectasis, honeycombing, and nonemphysematous cysts. Early‐onset ICI‐ILD was defined as developing within 3 months after the initiation of ICI administration. Results: Of 264 patients with advanced NSCLC, 57 patients (21.6%) had ILAs (43 fibrotic and 14 nonfibrotic ILAs). The difference between the incidence of ICI‐ILD in patients with or without ILAs was not significant. Of 193 patients treated by ICI monotherapy, 18 (9.3%) developed early‐onset ICI‐ILD. Among patients receiving ICI monotherapy, the incidence of early‐onset ICI‐ILD was significantly higher in patients with than in patients without nonfibrotic ILAs. Conclusion: The presence of nonfibrotic ILAs is a significant risk for early‐onset ICI‐ILD in patients with NSCLC undergoing ICI monotherapy. Clinicians should be aware of ILAs, especially nonfibrotic ILAs, before administering ICIs to lung cancer patients. Abstract : We retrospectively investigated the clinical significance of Interstitial lung abnormalities (ILAs) in patients with NSCLC receiving immune checkpoint inhibitor (ICI). The incidence of early‐onset ICI‐ related interstitial lung disease (ICI‐ILD) was significantly higher in patients with than in patients without nonfibrotic ILAs. The presence of nonfibrotic ILAs is a significant risk for early‐onset ICI‐ILD in patients with NSCLC undergoing ICI monotherapy. … (more)
- Is Part Of:
- Thoracic cancer. Volume 14:Issue 1(2023)
- Journal:
- Thoracic cancer
- Issue:
- Volume 14:Issue 1(2023)
- Issue Display:
- Volume 14, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 14
- Issue:
- 1
- Issue Sort Value:
- 2023-0014-0001-0000
- Page Start:
- 73
- Page End:
- 80
- Publication Date:
- 2022-11-14
- Subjects:
- ICI‐ILD -- ILA -- NSCLC -- PD‐1 inhibitor
Chest -- Cancer -- Periodicals
Chest -- Cancer -- Treatment -- Periodicals
Chest -- Surgery -- Periodicals
616.99494005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/%28ISSN%291759-7714;jsessionid=9202029487E02D838DF722140677202D.d04t01 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1759-7714 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.wiley.com/bw/journal.asp?ref=1759-7706&site=1 ↗ - DOI:
- 10.1111/1759-7714.14718 ↗
- Languages:
- English
- ISSNs:
- 1759-7706
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8820.242500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 25608.xml