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Early screening of high-risk individuals for pneumonia after combined radio-immunotherapy for lung cancer based on CT pulmonary function imaging

Early screening of high-risk individuals for pneumonia after lung cancer radiotherapy combined with immunotherapy based on CT pulmonary function imaging

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129208
Enrollment
Unknown
Registered
2026-08-01
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Radiotherapy- and Immunotherapy-Related Pneumonitis Symptoms

Interventions

Observation group:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years; 2. Pathologically or cytologically confirmed lung cancer; 3. Received thoracic radiotherapy and immunotherapy, with a clearly defined temporal relationship between the two treatments; 4. Availability of at least the following CT imaging studies: a baseline CT scan before immunotherapy; a radiotherapy planning/simulation CT scan; and a follow-up CT scan after completion of treatment or a CT scan obtained at the onset of pneumonitis.

Exclusion criteria

Exclusion criteria: 1. Active infectious pneumonia or uncontrolled lower respiratory tract infection prior to initiation of immunotherapy or radiotherapy; 2. Grade >=2 respiratory failure, requirement for long-term oxygen therapy, or severe pulmonary dysfunction prior to initiation of immunotherapy or radiotherapy that may confound the assessment of subsequent pneumonitis events; 3. Active interstitial lung disease (ILD), idiopathic pulmonary fibrosis, or other clearly diagnosed fibrotic interstitial lung diseases; 4. Missing imaging at key time points, including the absence of a baseline CT scan before immunotherapy or a radiotherapy planning/simulation CT scan (4DCT).

Design outcomes

Primary

MeasureTime frame
Incidence of early severe (Grade >=3) pneumonitis;

Secondary

MeasureTime frame
The predictive efficacy of the AUC value of the prediction model for the probability of pneumonia occurrence;

Countries

China

Contacts

Public ContactBai Xue

Southern Medical University Southern Hospital

baixue1990@i.smu.edu.cn+86 20 61642136

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026