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Clinical Trial Summary

Stage III non-small-cell lung cancer (NSCLC) is seen in a relatively heterogeneous group of patients with ipsilateral mediastinal (N2) lymph node involvement. The relative roles of different treatment modalities are not clear. The purpose of this study is to evaluate the efficacy and safety of neoadjuvant double-drug chemotherapy containing platinum plus anlotinib hydrochloride in patients with stage III(N2) non-small-cell lung cancer.


Clinical Trial Description

This is a prospective, open-label, multi-institutional, positive medicine control of equal rank comparative study of neoadjuvant double-drug chemotherapy with platinum plus anlotinib hydrochloride in stage III(N2) non-small-cell lung cancer.The main purpose of this study was to compare the difference in N2 downgrade rate of lymph node and resectability rate between the experimental and control groups, to evaluate the efficacy of anlotinib hydrochloride, and to observe and evaluate its objective response rate(ORR),Disease-free Survival (DFS)and overall survival(OS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04181372
Study type Interventional
Source The First Affiliated Hospital of Guangzhou Medical University
Contact Jiexia Zhang, prof.
Phone +8613903056432
Email drzjxcn@126.com
Status Not yet recruiting
Phase Phase 2
Start date December 2019
Completion date August 1, 2022

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