Checkpoint Inhibitor Pneumonitis in Non-Small Cell Lung Cancer With Chronic Lung Disease: A Comparative Study of ILD, COPD, and the General Population Using a Global Federated Database.
3/5 보강
TL;DR
Evaluated differences in CIP incidence, onset, recurrence, and outcomes among patients with ILD, COPD, and those without pre‐existing lung disease among patients with ILD and those without pre‐existing lung disease.
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
환자: interstitial lung disease (ILD) or chronic obstructive pulmonary disease (COPD) may be at increased risk, but data comparing these populations is limited
I · Intervention 중재 / 시술
immune checkpoint inhibitors (ICIs) between January 2017 and January 2023
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] ILD significantly increases the risk of developing CIP and worsens associated outcomes, including recurrence and mortality. These findings support closer surveillance and risk stratification in ICI-treated patients with underlying ILD.
OpenAlex 토픽 ·
Cancer Immunotherapy and Biomarkers
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Lung Cancer Treatments and Mutations
Evaluated differences in CIP incidence, onset, recurrence, and outcomes among patients with ILD, COPD, and those without pre‐existing lung disease among patients with ILD and those without pre‐existin
- 표본수 (n) 3147
- p-value p < 0.001
- 연구 설계 cohort study
APA
Geran Maule, Mohammad Abuassi, et al. (2026). Checkpoint Inhibitor Pneumonitis in Non-Small Cell Lung Cancer With Chronic Lung Disease: A Comparative Study of ILD, COPD, and the General Population Using a Global Federated Database.. Respirology (Carlton, Vic.), 31(4), 361-368. https://doi.org/10.1002/resp.70180
MLA
Geran Maule, et al.. "Checkpoint Inhibitor Pneumonitis in Non-Small Cell Lung Cancer With Chronic Lung Disease: A Comparative Study of ILD, COPD, and the General Population Using a Global Federated Database.." Respirology (Carlton, Vic.), vol. 31, no. 4, 2026, pp. 361-368.
PMID
41371776 ↗
Abstract 한글 요약
[BACKGROUND AND OBJECTIVE] Checkpoint inhibitor pneumonitis (CIP) is a serious immune-related adverse event. Patients with interstitial lung disease (ILD) or chronic obstructive pulmonary disease (COPD) may be at increased risk, but data comparing these populations is limited. We aimed to evaluate differences in CIP incidence, onset, recurrence, and outcomes among patients with ILD, COPD, and those without pre-existing lung disease.
[METHODS] We conducted a retrospective cohort study using the TriNetX Research Network, identifying patients who received immune checkpoint inhibitors (ICIs) between January 2017 and January 2023. Patients were stratified into ILD, COPD, and control groups. CIP was identified using ICD codes. Propensity score matching (1:1:1) was used to adjust for baseline characteristics. Outcomes included CIP incidence, time to onset, recurrence, hospitalisation, and mortality.
[RESULTS] Among 184,000+ ICI recipients, 3147 had ILD, 8657 had COPD, and 47,031 had no known lung disease. After matching (n = 3147/group), CIP incidence was highest in ILD patients (4.6%) compared to COPD (1.9%) and controls (1.5%) (p < 0.001). Time to CIP onset was similar across groups. ILD patients with CIP had higher recurrence (16.4% vs. 9.1% and 8.3%) and higher all-cause hospitalisation (61% vs. 40% and 39%) compared to COPD and control groups. All-cause mortality was also higher in the ILD-CIP group (41.1%).
[CONCLUSION] ILD significantly increases the risk of developing CIP and worsens associated outcomes, including recurrence and mortality. These findings support closer surveillance and risk stratification in ICI-treated patients with underlying ILD.
[METHODS] We conducted a retrospective cohort study using the TriNetX Research Network, identifying patients who received immune checkpoint inhibitors (ICIs) between January 2017 and January 2023. Patients were stratified into ILD, COPD, and control groups. CIP was identified using ICD codes. Propensity score matching (1:1:1) was used to adjust for baseline characteristics. Outcomes included CIP incidence, time to onset, recurrence, hospitalisation, and mortality.
[RESULTS] Among 184,000+ ICI recipients, 3147 had ILD, 8657 had COPD, and 47,031 had no known lung disease. After matching (n = 3147/group), CIP incidence was highest in ILD patients (4.6%) compared to COPD (1.9%) and controls (1.5%) (p < 0.001). Time to CIP onset was similar across groups. ILD patients with CIP had higher recurrence (16.4% vs. 9.1% and 8.3%) and higher all-cause hospitalisation (61% vs. 40% and 39%) compared to COPD and control groups. All-cause mortality was also higher in the ILD-CIP group (41.1%).
[CONCLUSION] ILD significantly increases the risk of developing CIP and worsens associated outcomes, including recurrence and mortality. These findings support closer surveillance and risk stratification in ICI-treated patients with underlying ILD.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Immune Checkpoint Inhibitors
- Pulmonary Disease
- Chronic Obstructive
- Female
- Carcinoma
- Non-Small-Cell Lung
- Retrospective Studies
- Lung Diseases
- Interstitial
- Lung Neoplasms
- Aged
- Middle Aged
- Pneumonia
- Incidence
- Databases
- Factual
- checkpoint inhibitor pneumonitis
- chronic obstructive pulmonary disease
- immune checkpoint inhibitors
- immune‐related adverse events
- interstitial lung disease
- pneumonitis risk stratification
… 외 1개
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- A Phase I Study of Hydroxychloroquine and Suba-Itraconazole in Men with Biochemical Relapse of Prostate Cancer (HITMAN-PC): Dose Escalation Results.
- Self-management of male urinary symptoms: qualitative findings from a primary care trial.
- Clinical and Liquid Biomarkers of 20-Year Prostate Cancer Risk in Men Aged 45 to 70 Years.
- Diagnostic accuracy of Ga-PSMA PET/CT versus multiparametric MRI for preoperative pelvic invasion in the patients with prostate cancer.
- Comprehensive analysis of androgen receptor splice variant target gene expression in prostate cancer.
- Clinical Presentation and Outcomes of Patients Undergoing Surgery for Thyroid Cancer.