Cancer Clinical Trial
Official title:
Advanced Non-small Cell Lung Cancer With Chinese Medicine Comprehensive Treatment Plan
The purpose of this study is to observe the efficacy of chemotherapy combined with Chinese patent drugs for patients with advanced non-small-cell lung cancer, also to evaluate the adverse reaction and the reliability.
Lung cancer is the most common malignant tumor in the world with about 80%-85% non small cell
lung cancer.
The investigators perform a multi-center, randomized, controlled, prospective study in
patients with advanced NSCLC. Patients are randomized over observational group(Chinese patent
drugs plus chemotherapy), and control group (chemotherapy). The investigators will observe 2
cycles and after that regular follow-up will be arranged.
The primary end point is: Objective response rate;
The secondary end points are:
1. progression-free survival(PFS);
2. overall survival(OS);
3. Time to Progression (TTP);
4. quality of life questionnaire(QOL);
5. other end points are: Toxicity, side effects and security of the treatments will be
assessed at the same time.
The investigators expect that integrated TCM combined with chemotherapy has a better efficacy
on enhancing Objective response rate,prolonging PFS, OS, improving QOL, reducing the adverse
reaction of patients than that of chemotherapy.Therefore our study can provide evidences for
optimizing and promoting integrated TCM combined with Western Medicine treatment.
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