ctDNA Analysis to Monitor the Risk of Progression After First-line Immunotherapy in Patients With Advanced NSCLC

NCT05198154 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-04-23

No results posted yet for this study

Summary

This study aims to explore the correlation of circulating tumor DNA(ctDNA) and the risk of progression in patients with advanced NSCLC who have long-term benefit from first-line immunotherapy (PFS 12 months)

Conditions

  • Advanced Lung Non-Small Cell Carcinoma

Interventions

DIAGNOSTIC_TEST

ctDNA detection

High-depth sequencing method is used to detecting ctDNA.

Sponsors & Collaborators

  • Sun Yat-sen University

    collaborator OTHER
  • First Affiliated Hospital Xi'an Jiaotong University

    collaborator OTHER
  • Fujian Cancer Hospital

    collaborator OTHER_GOV
  • Third Affiliated Hospital of Third Military Medical University

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Qinghai Province Tumor Hospital

    collaborator UNKNOWN
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Zhejiang Provincial People's Hospital

    collaborator OTHER
  • Hunan Province Tumor Hospital

    collaborator OTHER
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Inner Mongolia People's Hospital

    collaborator OTHER
  • Guizhou Provincial People's Hospital

    collaborator OTHER
  • The Third Xiangya Hospital of Central South University

    collaborator OTHER
  • Yueyang Central Hospital

    collaborator OTHER
  • ZhuZhou Central Hospital

    collaborator OTHER
  • Zhangjiajie Affiliated Hospital of Hunan Normal University

    collaborator UNKNOWN
  • Loudi Central Hospital

    collaborator OTHER
  • Chang Sha First Hospital

    collaborator UNKNOWN
  • Fang Wu

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-24
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05198154 on ClinicalTrials.gov