Non-squamous Non-Small Cell Lung Cancer Clinical Trial
Official title:
Prospective, Multicenter, Non-intervention Clinical Trial of Apatinib in the Treatment of Advanced Non-squamous,Non-small Cell Lung Cancer
To explore the efficacy and safety of apatinib in non-squamous non-small cell lung cancer in the real-world.
This is a multi-center, non-interventional clinical study. The number of patients that
planned to be recruited is: from May 2017 to April 2019, the actual number of cases recruited
into this study.
If the clinicians thought the patient is suitable to take apatinib treatment, and give the
patient apatinib treatment, the patient can be recruited into this study. Clinicians chose
the initial dose of apatinib according to the patient's physical condition. Besides the
clinicians adjusted the dose according to the patient's tolerance during the medication. The
dosage was demanded not higher than 750 milligram (mg) per day. The patients received
apatinib continuously, 28 days for a period, until intolerance, no longer getting benefits or
patient wanted stop.
During the course of the study, the researchers will not intervene the treatment of the
patients, but only record the efficacy and adverse reactions.
Main evaluation criteria: PFS Secondary evaluation criteria: OS,DCR and ORR (according to
RECIST1.1). Main safety indicators:AE, SAE (according to NCI CTCAE V4.0) and QOL scores
(Quality of Life Questionnaire-lung cancer).
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