Actively Recruiting
Single-Cell Sequencing Analysis of Radiation Pneumonitis Signals in Patients Treated for Cancer with Radiotherapy
Led by NHS Lothian · Updated on 2026-01-09
5
Participants Needed
3
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating radiation pneumonitis, a serious lung inflammation caused by radiotherapy in cancer treatment, particularly in lung cancer patients. This condition can lead to severe breathing problems and even death, and current treatment options are limited. The study aims to better understand the cellular mechanisms behind radiation pneumonitis using a new technique called single-cell RNA sequencing, which can identify different cell types and their activity in affected lung tissue. Participants who have received thoracic radiotherapy and show signs of radiation pneumonitis will undergo a clinical bronchoscopy as part of the ELFMAN study, where a sample of lung cells will be collected. This sample will be analyzed using single-cell sequencing to identify the cells present and their functions. The procedure involves deep bronchial brushings to safely obtain cells for analysis while minimizing risk. The study will recruit patients over a year, aiming to create a detailed dataset within a month of sample collection. During the study, participants will be assessed for lung inflammation signs and must be stable enough to tolerate bronchoscopy without oxygen support. Researchers will monitor the success of the sequencing process and look for specific signals related to radiation pneumonitis over several months. The study may help identify new targets for treatment, improving the management of this lung toxicity in cancer patients. Participation involves bronchoscopy and follow-up evaluations to understand lung cell behavior after radiotherapy.
CONDITIONS
Brief Title
Single-Cell Sequencing Analysis of Radiation Pneumonitis Signals In Patients Treated For Cancer With Radiotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Received thoracic radiotherapy with clinical or radiological signs consistent with radiation pneumonitis occurring 1 to 4 months after treatment
- Ambulatory and oxygen independent with oxygen saturation above 92% on room air
- Haemodynamically stable and able to tolerate bronchoscopy, including lying flat without breathing difficulties
- Able to consent to participate in the ELFMAN protocol and SPITFIRE trial
You will not qualify if you...
- Contraindications to bronchoscopy such as previous intolerance, inability to lie flat, or oxygen saturation below 92% on room air
- Requirement for hospital admission or oxygen support
- Tested positive for Covid-19 within 6 weeks prior to enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo a bronchoscopy procedure to collect deep bronchial brushing samples for single-cell sequencing analysis to identify cellular processes involved in radiation pneumonitis.
1 visit (in-person)
Duration - 3 to 6 months
Participants are monitored for up to 6 months to assess signals related to radiation pneumonitis from the collected samples and observe clinical outcomes.
Follow-up visits as needed
Trial Site Locations
Total: 3 locations
1
Centre for Information Research, University of Edinburgh
Edinburgh, United Kingdom, EH16 4UU
Not Yet Recruiting
2
Henderson Lab
Edinburgh, United Kingdom, EH16 4UU
Not Yet Recruiting
3
Edinburgh Cancer Centre
Edinburgh, United Kingdom, EH4 2XU
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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