Neoadjuvant Tislelizumab and Platinum-Based Doublet Chemotherapy in Stage II-IIIB EGFR-Mutated Lung Adenocarcinoma With PD-L1 Positive Expression -- A Phase II Study (DuoVitality)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Neoadjuvant EGFR TKI therapy targeting EGFR mutation has some problems failure to fulfill clinical requirements such as low MPR rate, tissue fibrosis and other major surgical impacts and unmet clinical needs.This study hypothesized that Tisleizumab combined with chemotherapy in the neoadjuvant treatment of stage II-IIIA non-squamous NSCLC with EGFR-mutant PD-L1 expression ≥1% could significantly improve the pathological response rate after neoadjuvant therapy, improve the surgical complete resection rate, reduce perioperative complications and do not increase the surgical difficulty.In this study, biomarker analysis is going to explore the possible direction of neoadjuvant therapy population screening, and to explore a possible method for the efficacy and safety of neoadjuvant immunotherapy in clinical stage II-IIIA non-squamous non-small cell lung cancer with EGFR mutation and expression of PD-L1.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Volunteer to participate in clinical research;Fully understand and be Informed of the study and sign the Informed Consent Form (ICF);Willing to follow and able to complete all test procedures;

• Age 18-75 (boundary value included), no gender limitation;

• Histologically proven stage II-IIIB Lung Adenocarcinoma (as defined by the American Joint Commission on Cancer, 8th Edition);

• EGFR gene mutation positive (can be tested by tissue or blood samples);

• PD-L1 ≥ 1%

• ECOG PS score 0-1 (including boundary value);

• Cardiopulmonary function is good, and the requirements for surgical resection for radical treatment are confirmed;

• Meet the conditions for receiving platinum containing two-drug chemotherapy;

• The expected survival time is ≥3 months, and feasible surgery is planned;

Locations
Other Locations
China
First Affiliated Hospital, Guangzhou Medical University
RECRUITING
Guangzhou
Contact Information
Primary
Henry liang, Dr
hengrui_liang@163.com
15625064712
Time Frame
Start Date: 2022-08-01
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 28
Treatments
Experimental: Neoadjuvant ICI combined with chemotherory
intravenous injection :Tislelizumab + pemetrexed + platinum Q3W 2-4 cycles
Sponsors
Leads: Jun Liu

This content was sourced from clinicaltrials.gov

Similar Clinical Trials