Clinical Trial

Efficacy and Safety of Modified Si Jun Zi Tang in Perioperative NSCLC Treatment

Study acronym: MSJZT-NSCLC
Recruiting Phase 2
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Record status
This record was last updated June 6, 2024 (before its estimated December 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
Chemotherapy combined with immunotherapy is the current standard perioperative treatment for non-small cell lung cancer (NSCLC). However, this regimen has multiple side effects and shows variable efficacy among individuals. In China, adjunctive traditional Chinese medicine is widely accepted by lung cancer patients. Modified Si Jun Zi Tang, a classic formula in traditional Chinese medicine, is known for its benefits in unifying and strengthening the spleen. This study aims to evaluate whether the addition of Modified Si Jun Zi Tang to chemotherapy and immunotherapy during the neoadjuvant phase can improve the R0 resection rate, objective response rate (ORR), and safety in patients with resectable and potentially resectable NSCLC. Secondary objectives include assessing whether this combination can improve 1-year and 2-year disease-free survival (DFS) post-surgery. Additionally, we will collect relevant biological samples to identify tumor markers associated with efficacy, prognosis, and side effects, providing a theoretical basis for modernizing and standardizing traditional Chinese medicine.
Trial Details
NCT Number NCT06445881
Lead Sponsor First Affiliated Hospital of Zhejiang University
Conditions Non Small Cell Lung Cancer, Perioperative Complication
Enrollment 60 participants
Start Date 2024-06-01
Primary Completion 2025-12-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2024-06-06