A Trial of Anlotinib Combined With Docetaxel in Patients With Wild-type Advanced Non-squamous Non Small Cell Lung Cancer

This is a single arm clinical trial conducted in China. The purpose of this study is to assess the efficacy and safety of Anlotinib Hydrochloride (12mg, QD PO d1-14, 21days per cycle) combined with Docetaxel (75mg/m2 IV d1) in the treatment of wild-type advanced non-squamous non small cell lung cancer patients with progression after immunotherapy plus chemotherapy as first-line treatment. After being informed about the study and potential risks, all patients giving written informed consent will undergo a 4-week screening period to determine eligibility for study entry. The expected sample size is 42.