作者: A. Radhakrishnan , J.D. Bitran , D.T. Milton , K. Tolzien , S. Hallmeyer
DOI: 10.1179/JOC.2009.21.4.439
关键词:
摘要: AbstractWe sought to evaluate the safety and efficacy of docetaxel oxaliplatin combination as first-line therapy for patients with stage IV or wet IIIB non small cell lung cancer. Patients received at 85 mg/m2 intravenously over 2 hours on days 1 15 along 30 8; both given every 28 days. Cycles were repeated 4 weeks a maximum 6. Fifteen enrolled an overall response rate 50% (95% CI 21-74%). Median progression-free survival was 2.4 months 1-year progression free 10%. 7.9 49% alive year. Most common toxicities nausea, vomiting, dehydration. This has notable activity in advanced non-small cancer favorable toxicity profile.