Outcomes and toxicity of stereotactic radiotherapy in non-small cell lung cancer patients with interstitial lung disease: a multicentre cohort study
Sherlock, Alexander J Tanaka, Annalise M Daniels, Harry E Carver, Antony Watkins, Steven Yahya, Sundus
Sherlock, Alexander J
Tanaka, Annalise M
Daniels, Harry E
Carver, Antony
Watkins, Steven
Yahya, Sundus
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Publication date
2025-12-26
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Abstract
Background
Lung cancer remains a major cause of cancer-related mortality, with non-small cell lung cancer (NSCLC) comprising most cases. For early-stage NSCLC (ES-NSCLC), surgery is curative but often unsuitable. Stereotactic ablative radiotherapy (SABR) offers curative intent, achieving high local control with generally acceptable toxicity. Yet, patients with interstitial lung disease (ILD) face increased risks, including high-grade and fatal toxicity. ILD-adapted dose and fractionation have been introduced, as evaluated in studies such as ASPIRE-ILD. We evaluated real-world outcomes of SABR using modified fractionation in ES-NSCLC patients with ILD. Methods A multicentre retrospective cohort study was conducted across four UK hospitals (February 2020-May 2025). Consecutive patients with stages I-II NSCLC, confirmed ILD on high-resolution computed tomography (HRCT) or pathology, and treated with ILD-adapted SABR were included. Clinical, radiologic, pulmonary function, and dosimetric data were extracted. The primary outcome was treatment-related toxicity; secondary outcomes included overall survival (OS), progression-free survival (PFS), time to progression, and local control. Kaplan-Meier analysis estimated survival. Subgroup analyses explored associations with pulmonary function, ILD subtype, Eastern Cooperative Oncology Group (ECOG) performance status, biologically effective dose (BED), and fractionation schedule.
Results
Eleven patients (median age 79.9, 54.5% male) were included. ILD subtypes were idiopathic interstitial pneumonia (45.5%), ILD with known cause (36.4%), and unclassifiable ILD (18.2%). ECOG was 0-1 in 27.3%, 2 in 45.5%, and 3 in 27.3%. Median diffusing capacity for carbon monoxide (DLCO) was 70% predicted; one patient had DLCO <40%. Most received five-fraction SABR (72.7%). All patients experienced toxicity (median onset three months); grades 1-2 affected 81.8% of patients, and grade ≥3 events occurred in 36.4%. This included three treatment-related deaths (27.3%): pneumonitis, pneumonia, or progressive fibrosis. Median follow-up was 21.9 months. Median PFS was 8.6 months, and median OS was 16.3 months, with one-year OS of 60.6%. Local control was achieved in 90% of first planned imaging. Progression included regional nodal relapse (n = 3) and distant metastasis (n = 1). Subgroup analyses showed no significant associations between DLCO, ECOG, ILD subtype, BED, or fractionation and grade ≥3 toxicity or survival, though toxicity rates varied: 40% in idiopathic interstitial pneumonia, 25% in ILD with known cause, and 50% in unclassifiable ILD. Discussion and conclusion In this real-world cohort of patients with ES-NSCLC and ILD treated with modified SABR, treatment was feasible and achieved encouraging local control and median OS. However, toxicity was substantial, with grade ≥3 events in over one-third and three treatment-related deaths. No significant associations were identified between severe toxicity and DLCO, ILD subtype, BED, or performance status, though the small sample limited statistical power. This study provides real-world evidence supporting SABR as a potential option in selected ILD patients but emphasises the need for careful risk stratification and early monitoring. Outcomes highlight the challenges of applying trial protocols to physiologically impaired, heterogeneous ILD populations. Larger prospective studies are required to validate these findings and develop refined, ILD-specific SABR frameworks.
Citation
Sherlock AJ, Tanaka AM, Daniels HE, Carver A, Watkins S, Yahya S. Outcomes and Toxicity of Stereotactic Radiotherapy in Non-small Cell Lung Cancer Patients With Interstitial Lung Disease: A Multicentre Cohort Study. Cureus. 2025 Dec 26;17(12):e100124. doi: 10.7759/cureus.100124.
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Journal Article