Skip to content

Screening of markers for early diagnosis of non-small cell lung cancer and prognostic markers for PD-L1 efficacy

Screening of markers for early diagnosis of non-small cell lung cancer and prognostic markers for PD-L1 efficacy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093890
Enrollment
Unknown
Registered
2024-12-13
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-16

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

Interventions

Index test:To verify whether CSNK2B and SLC52A2 gene expression levels can be used as biomarkers for the early diagnosis of NSCLC and to predict whether NSCLC patients will respond to PD-L1 immunother

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Subjects aged 18-80 years who were newly diagnosed with NSCLC and healthy controls were recruited during the 3-year period from January 1, 2025 to January 1, 2028; 2.Subjects have been diagnosed with non-small cell lung cancer and plan to receive or have begun PD-L1 treatment; 3.The subject is willing to provide blood or tissue samples for research purposes; 4.Subjects have health conditions that allow them to receive anti-PD-L1 therapy and participate in regular follow-up; 5.Subjects have read the relevant information and agreed to participate in the study;

Exclusion criteria

Exclusion criteria: 1.The subject is under 18 years old or over 80 years old; 2.The subject has other serious health problems, such as active infections or other malignant tumors; 3.The subject is unwilling to provide the necessary biological samples; 4.Subjects have a history of allergy or other serious side effects of anti-PD-L1 treatment; 5.The subjects were unable to understand the research information or to give informed consent;

Design outcomes

Primary

MeasureTime frame
The occurrence of non-small cell lung cancer;Whether PD-L1 is effective in treating non-small cell lung cancer;Receiver operating characteristic curve (ROC Curve);The area under the AUC curve;Sensitivity;Specificity;

Secondary

MeasureTime frame
Positive predicative value;Negative predictive value;

Countries

China

Contacts

Public ContactXIONG Qiuxia

First Affiliated Hospital of Kunming Medical University

xiongqiuxia1@kmmu.edu.cn+86 13577115377

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026