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Safety and Efficacy of Stereotactic Magnetic Resonance-Guided Adaptive Radiation Therapy (SMART) for Ultracentral Metastases in Non-Small Cell Lung Cancer

Abstract:
PurposeStereotactic ablative radiation therapy (SABR) is a standard of care for early-stage lung cancer and thoracic oligometastatic or oligoprogressive disease. However, ultracentral lesions remain challenging because of their proximity to critical mediastinal structures and the associated risk of severe toxicity. Stereotactic magnetic resonance-guided adaptive radiation therapy (SMART) allows for daily plan adaptation and real-time tracking in breath-hold, enhancing target coverage while improving sparing of adjacent organs compared to conventional SABR.Methods and materialsThis retrospective study analyzed outcomes of SMART-based SABR for ultracentral metastatic lesions in patients with histologically confirmed non-small cell lung cancer (NSCLC). Ultracentral lesions were defined by planning target volume overlapping with the proximal bronchial tree, esophagus, or pulmonary vessels. Endpoints included grade ≥ 3 SMART-related toxicity, freedom from local progression, progression-free survival, and overall survival.ResultsBetween 2020 and 2023, 11 patients with 18 ultracentral NSCLC lesions underwent SMART. All treatments were delivered in breath-hold. The median dose was 40 Gy (range, 30-60 Gy) in 5 to 8 fractions. Online plan adaptation was performed for 100% of the 78 delivered fractions. No grade ≥ 3 toxicities were observed. Rates of grade 1 to 2 acute and late toxicities were 54% and 18%, respectively. At a median follow-up of 28 months (range, 5-41 months), 66.7% of patients were alive. One-year freedom from local progression was 93%. Median progression-free survival was 5.8 months (range, 1-39 months), and median overall survival was 20 months (range, 5-41 months).ConclusionsSMART with daily online adaptation achieved excellent local control and a favorable safety profile in ultracentral NSCLC, comparable to conventional non-adaptive SABR, but without severe toxicity.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.adro.2025.101906

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Institution:
University of Oxford
Role:
Author


Publisher:
Elsevier
Journal:
Advances in Radiation Oncology More from this journal
Volume:
10
Issue:
12
Pages:
101906
Publication date:
2025-09-18
DOI:
EISSN:
2452-1094
ISSN:
2452-1094
Pmid:
41211609


Language:
English
Pubs id:
2295884
UUID:
uuid_93e21d52-9476-4dae-848d-5eaba04c1288
Local pid:
pubs:2295884
Source identifiers:
3479570
Deposit date:
2025-11-18
ARK identifier:
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