A Study Evaluating MRD Biomarker in Patients With Potentially Resectable Stage III Non-small Cell Lung Cancer

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Stratification of postoperative ctDNA status can effectively assess the risk of recurrence in patients. In addition, the multi-node dynamic monitoring of ctDNA is more effective in predicting the recurrence risk of patients. In this study, EGFR/ALK negative potentially resectable Stage III non-small cell lung cancer were enrolled. Baseline tissues, Peripheral blood samples of patients at baseline puncture tissue, after neoadjuvant therapy, after surgery (if any), after adjuvant therapy, and at multiple nodes during follow-up were collected for 1021-MRD analysis through tumor-informed personalized monitoring MRD test kit. This study aim to explore MRD biomarker in patients with potentially resectable stage III non-small cell lung cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Capable of giving signed informed consent, age ≥ 18 and ≤ 80.

• patients with stage Ⅲ non-small cell lung cancer confirmed by histology or cytology have potential surgical opportunities.

• No driving gene EGFR/ALK mutation.

• PS = 0-1.

• the treatment process cooperated with the provision of clinicopathological and imaging data needed in the research process, followed up and collected the blood of the clinical efficacy evaluation nodes, and agreed to use the test data for follow-up research and product development.

Locations
Other Locations
China
Yuyan Wang
RECRUITING
Beijing
Contact Information
Primary
Yuyan Wang
wangyuyan1219@aliyun.com
010-88196497
Backup
Han Yin
01088196084
Time Frame
Start Date: 2022-11-25
Estimated Completion Date: 2025-06-01
Participants
Target number of participants: 65
Treatments
Arms1:For stage III NSCLC patients who underwent complete resection.
Immunotherapy alone or chemotherapy combined with immunotherapy. Collect patients' baseline puncture tissues, peripheral blood samples from multiple nodes after new adjuvant treatment, surgery (if any), adjuvant treatment, and follow-up, and carry out for 1021-MRD analysis through tumor-informed personalized monitoring MRD test kit.~Assigned Interventions:1021-MRD analysis
Arms 2:For stage III NSCLC patients who underwent concurrent radio-chemotherapy.
Immunotherapy alone or chemotherapy combined with immunotherapy. Collect patients' baseline puncture tissues, peripheral blood samples from multiple nodes after new adjuvant treatment, surgery, adjuvant treatment, and follow-up, and carry out for 1021-MRD analysis through tumor-informed personalized monitoring MRD test kit.~Assigned Interventions:1021-MRD analysis
Sponsors
Collaborators: Geneplus-Beijing Co. Ltd.
Leads: Peking University Cancer Hospital & Institute

This content was sourced from clinicaltrials.gov