Adjuvant Treatment Based on MRD for EGFR Mutant NSCLC

MRD Clinical Trial

Official title: Adjuvant Treatment Based on Minimal Residual Disease for Resectable Non-squamous Non-Small-Cell-Lung-Cancer With EGFR Mutations

Status Recruiting

Clinical Trial Summary

A prospective, multicenter clinical study designed to explore the efficacy of postoperative adjuvant EGFR-TKIs therapy based on MRD status in patients with stage IB-IIIB EGFR-mutant non-squamous non-small cell lung cancer (non-squamous NSCLC). Primary endpoints include 3-year Disease-Free Survival rate (3y-DFS) and median disease-free survival (mDFS).

Clinical Trial Description

All subjects enrolled in this clinical trial will receive peripheral blood MRD status assessment within 1 week and 1 month after surgery, and will be divided into MRD positive group (+) and MRD negative group (-) according to their results , followed by MRD status assessment every 12 weeks.

The MRD positive group would receive icotinib as adjuvant treatment. When the peripheral blood MRD turned negative, the subjects entered the drug withdrawal observation period. When the MRD turned positive again, the subjects resumed icotinib treatment. If EGFR T790M mutation was found, researchers would resume medication and choose osimertinib therapy.

The MRD negative group (-) directly entered the follow-up observation period. When the MRD status of peripheral blood turned positive, the subjects received osimertinib treatment. When the MRD turned negative again, the subjects entered the drug withdrawal observation period. ;

Related Conditions & MeSH terms

• MRD

• NCT number: NCT05536505
• Study type: Interventional
• Source: Guangdong Association of Clinical Trials
• Contact: Yi-Long Wu, MD
• Phone: 020-83827812
• Email: syylwu@live.cn
• Status: Recruiting
• Phase: Phase 2
• Start date: September 13, 2022
• Completion date: October 1, 2030