Therapeutic ResistAnce and Clonal Evolution Assessed With Liquid Biopsy of NSCLC Patients Treated With Immune Checkpoint Inhibitors (ICIs) or Targeted Therapy

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

To evaluate the predictive value of ctDNA in response, relapse for patients treated with immune checkpoint inhibitors or targeted therapy for ALK, ROS1, MET ex14 skipping.

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

• Provision of informed consent

• Newly diagnosed and histological or cytological confirmed stage IIIB-IV lung adenocarcinoma or squamous cell carcinoma patients according to the AJCC staging system. The stage IV lung cancer and brain metastasis can be diagnosed by imaging and enhanced CT respectively

• No EGFR mutation in tissue and ctDNA

• Received immune checkpoint inhibitors as the first line therapy

• ECOG performance status 0-2 with expected more than 6 months of survival time

• Willingness to comply with required protocols and give permission to use the data for clinical research and products development

Locations
Other Locations
China
Shanghai Chest Hospital
RECRUITING
Shanghai
Contact Information
Primary
Rongrong Chen, MD, PhD
chenrr@geneplus.org.cn
86-10-53955678
Backup
Lianpeng Chang, MS
changlp@geneplus.org.cn
86-10-53955678
Time Frame
Start Date: 2020-07-01
Estimated Completion Date: 2025-06-30
Participants
Target number of participants: 250
Treatments
Immune checkpoint inhibitors
Targeted therapy
Targeting ALK, ROS1, MET ex14 skipping
Sponsors
Collaborators: Shanghai Chest Hospital
Leads: Geneplus-Beijing Co. Ltd.

This content was sourced from clinicaltrials.gov