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MRD monitoring of minimally invasive combined therapy for stage I NSCLC

MRD monitoring of minimally invasive combined therapy for stage I NSCLC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097483
Enrollment
Unknown
Registered
2025-02-19
Start date
2023-03-06
Completion date
Unknown
Last updated
2025-02-24

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

Observational group:None

Sponsors

Beijing Hostipal
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Signed informed consent, age > 18 years and < 90 years; (2) Pathology confirmed NSCLC, according to the 8th edition of the International Association for the study of Lung Cancer TNM staging for stage I NSCLC; (3) The patient's Eastern Cooperative Oncology Group performance status (ECoG PS) score was 0-3 points; (4) Multi disciplinary treatment (MDT) was used to evaluate patients who could not or refused surgical resection; (5) The estimated survival is more than 3 months; (6) During the treatment process, provide the clinical pathological data and imaging data required by the research process, cooperate with the follow-up and collect the blood of the clinical efficacy evaluation node, and agree to use the test data for subsequent research and product development.

Exclusion criteria

Exclusion criteria: (1) Suffering from other malignant tumors or severe multiple organ dysfunction; (2) After surgery, they received other treatments, such as chemotherapy, radiotherapy, targeted therapy, immunotherapy, etc; (3) The estimated survival time is less than 3 months; (4) Unable to accept or provide imaging and other specified efficacy evaluation methods.

Design outcomes

Primary

MeasureTime frame
The ctDNA clearance under comprehensive minimally invasive radical surgery treatment;the relationship between ctDNA monitoring and tumor recurrence;Analyzing the value of MRD technology in patients with NSCLC under comprehensive minimally invasive radical surgery treatment in conjunction with clinical data;

Secondary

MeasureTime frame
Comparative analysis of the specificity and sensitivity of ctDNA and imaging CT tests and serum tumor markers;MRD positivity predicts recurrence in advance of clinical confirmation of recurrence;2-year OS (Overall Survival);

Countries

China

Contacts

Public ContactXiaoguang Li

Beijing Hostipal

xglee88@126.com+86 156 9975 7271

Outcome results

None listed

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