Efficacy and Safety of Docetaxel as a Second–Line Treatment of Patients with Advanced Non-Small Cell Lung Cancer

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ขวัญจิต ด่านวิไล
อารียา มาคุณ
วิทวัส จิตต์ผิวงาม
สาลินี ชัยวีระไทย

Abstract

Objective: To evaluate efficacy and safety of docetaxel as a second-line treatment of patients with advanced non-small-cell lung cancer (NSCLC) at Naresuan University Hospital. Methods: The study was a survey study with retrospective data collection from medical records and electronic databases in patients with advanced NSCLC treated with first-line chemotherapy and receiving docetaxel as a second-line treatment during October 1, 2010 to June 30, 2016. Treatment outcomes were median–overall survival, progression–free survival, response rate and any grade toxicity. Results: From the total of 34 patients, efficacy was derived from that data of 27 patients. Median-overall survival after treatment with docetaxel was 10.13 months (95%CI 7.71-12.55). Progression-free survival was 3.47 months (95%CI 2.13-4.81). Two patients showed overall response, 10 with stable disease and 12 with progressive disease. Analysis of docetaxel safety in all patients revealed hematologic toxicities i.e., anemia in 31 patients, neutropenia in 20 patients, febrile neutropenia in 2 patients with one patient dead from this condition and thrombocytopenia in 1 patient. Common non-hematologic toxicities included fatigue (17 patients), mucositis (12 patients), nausea (10 patients) and vomiting (7 patients). Conclusion: Patients with advanced NSCLC and receiving docetaxel as a second line treatment had a comparable median-overall survival, progression-free survival and response rate to those reported in previous studies. Incidences of docetaxel toxicities, both hematologic and non–hematologic, were higher than those reported in previous studies.

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Research Articles

References

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