Clinical Trial

Curatively Intended Thoracic Reirradiation

Study acronym: CureLung
Recruiting
View on ClinicalTrials.gov →
Summary
The number of long-term lung cancer (LC) survivors increases, however many patients are diagnosed with recurrent or new thoracic cancers. High-dose reirradiation (reRT) is promising but associated with high severe toxicity rates. Existing studies are small lacking high-quality data, with no clear correlation between toxicity risk and delivered radiotherapy (RT) dose. This Danish multicentre prospective cohort study aims to provide a framework for collecting radiotherapy-related toxicity data, loco-regional control, and overall survival data for patients with thoracic cancer undergoing reirradiation; with the ultimate aim of providing safe reirradiation to more patients. As a secondary aim, guidelines for dose accumulation and provisional constraints for the organs at risk will be used to establish a uniform treatment strategy for reirradiation. The CURE Lung trial will provide high-impact, globally missing data. This project will ensure full utilization of and learning from the trial, adding SDM, PROMs, and modality referral to the trial. It will model the correlation between toxicity burden and doses, enabling individualized reRT with optimized dose prescription based on toxicity risk and patient preferences, and assisting in the decision-making on the prescription dose and optimal modality. This will ensure safe reRT for the increasing number of long-term LC survivors.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-04-22.
Status change: Not Yet Recruiting → Recruiting 2026-03-02
Trial Details
NCT Number NCT06950073
Lead Sponsor University of Aarhus
Conditions Radiotherapy Side Effect, Radiation Toxicity, Oncology, Lung Cancer, Thoracic Cancer
Enrollment 500 participants
Start Date 2025-10-10
Primary Completion 2035-05-01 (estimated)
Study Completion 2035-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-03-04