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A prognostic stratification study based on interpretable AI for immunotherapy with immune checkpoint inhibitors in non-small cell lung cancer

A prognostic stratification study based on interpretable AI for immunotherapy with immune checkpoint inhibitors in non-small cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123326
Enrollment
Unknown
Registered
2026-04-24
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

non-small cell lung cancer (NSCLC)

Interventions

Sponsors

First Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient age should be 18 years or above, and both males and females are eligible; 2. Diagnosed with non-small cell lung cancer by histological/cytological examination; 3. At least one measurable lesion that meets the RECIST 1.1 criteria; 4. Clinically evaluated as suitable for immunotherapy with immune checkpoint inhibitors; 5. Expected survival period >= 6 months; 6. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1; 7. Adequate organ and tissue functions; 8. Willing and able to follow the planned visits, research treatments, laboratory tests, and other trial procedures; 9. No history of other malignant tumors in the past.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. In the judgment of the clinical physician, complications or other diseases make the patient unsuitable to participate in this study; 3. Patients with other serious physical or mental diseases or abnormal laboratory test results, which may increase the risk of participating in the study or interfere with the research results, as well as patients that the researcher considers unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival;

Secondary

MeasureTime frame
Overall Survival;

Countries

China

Contacts

Public ContactXiujuan Qu

First Hospital of China Medical University

xjqu@cmu.edu.cn+86 24 8328 1560

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026