Patients on the docetaxel arm were instructed to take dexamethasone (8 mg orally twice daily the day before, the day of, and the day after docetaxel). All patients were followed up every 2 months regularly after the treatment protocol was finished. Patients were evaluated and followed up with ORR,

disease control rate (DCR), progression-free survival (PFS), median overall survival (OS), and safety profile. Responses were assessed with the use of the Response Evaluation Criteria in Solid Tumors (RECIST, set by an international collaboration including the European Organisation for Research and Treatment of Cancer, National Cancer Institute of the United States, and the National Cancer Institute of Canada GSK2118436 nmr Clinical Trials Group), and toxic effects were assessed FG-4592 supplier according to the Common Toxicity Criteria of the National Cancer Institute (Bethesda, MD) (version 2.0). Lung tumor–related symptoms including chest pain and dyspnea before and after CT-PFNECII were observed. CT-PFNECII–related side effects including pain, cough, fever, hemoptysis, and pneumothorax and chemotherapy-related side effects including myelosuppression and gastrointestinal reaction were

observed in this study. All patients were followed up until death or until the end of the study, with a minimum of 2 months and maximum of 18 months of follow-up. All primary analyses were performed on an intention-to-treat principle. The RECIST analysis was calculated according to the ordered one-way data of Ridit analysis. The effect of two kinds of treatment

regimens was calculated using a two-sided log-rank test. Survival analysis was calculated according to the Kaplan-Meier Baf-A1 mouse method with SPSS software (IBM, Armonk, NY). Ninety-five percent confidence intervals (CIs) were calculated when appropriate. Differences were considered significant at P < .05. Between October 1, 2011 and July 1, 2013, a total of 34 patients were randomly assigned to receive either CT-PFNECII combined with second-line chemotherapy or second-line chemotherapy alone. Among them, 17 patients received CT-PFNECII combined with second-line chemotherapy, and 17 patients received standard second-line chemotherapy alone. In the combination group, 7 patients received two cycles (four times) of CT-PFNECII, and 10 patients received one cycle (two times) of CT-PFNECII. The average cycle of CT-PFNECII received by patients in the combination group was 1.41. Seven patients in the combination group and six patients in the chemotherapy group had tumor-related chest pain or dyspnea. In each group, there were five (29.41%) platinum-resistant patients (disease recurred within 3 months to previous chemotherapy).