首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Phase I/II study of vinorelbine and exisulind as first-line treatment of advanced non-small cell lung cancer in patients at least 70 years old: a wisconsin oncology network study.
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Phase I/II study of vinorelbine and exisulind as first-line treatment of advanced non-small cell lung cancer in patients at least 70 years old: a wisconsin oncology network study.

机译:长春瑞滨和exisulind作为一线治疗至少70岁的晚期非小细胞肺癌的I / II期研究:威斯康星州肿瘤学网络研究。

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INTRODUCTION: Exisulind is an apoptotic agent with preclinical activity in non-small cell lung cancer (NSCLC). Vinorelbine is safe and effective in older patients with advanced NSCLC. We assessed these agents together as palliative treatment for older patients with advanced NSCLC. METHODS: Chemotherapy-naive patients >/=70-years-old with stage IIIB-IV NSCLC and a performance status (PS) /=3 neutropenia occurred in 14/30 patients. Two patients experienced neutropenic fever. There were no complete responses, one partial response and 12 patients with stable disease as their best response. The objective response rate was 4.0% (95% CI: 0.1-20.4%). Phase II median time-to-progression was 4.7 months (95% CI: 3.1-9.3 months) and median OS was 9.6 months (95% CI: 6.6-19.1 months). CONCLUSIONS: This combination is safe, seems to have activity in the elderly with advanced NSCLC and a PS
机译:简介:Exisulind是一种在非小细胞肺癌(NSCLC)中具有临床前活性的凋亡因子。长春瑞滨对晚期NSCLC老年患者安全有效。我们将这些药物评估为晚期NSCLC老年患者的姑息治疗。方法:年龄≥70岁,初治为IIIB-IV期NSCLC且表现状态(PS) / = 3级。 2例患者出现中性白细胞减少症。没有完全缓解,只有部分缓解,12例疾病稳定的患者为最佳缓解。客观回应率为4.0%(95%CI:0.1-20.4%)。第二阶段的平均进展时间为4.7个月(95%CI:3.1-9.3个月),中位OS​​为9.6个月(95%CI:6.6-19.1个月)。结论:这种组合是安全的,似乎在患有晚期NSCLC和PS

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