首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Sequential therapy with Vinorelbine followed by Gemcitabine in patients with metastatic non small cell lung cancer (NSCLC), performance status (PS) 2, or elderly with comorbidities--a multicenter phase II trial.
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Sequential therapy with Vinorelbine followed by Gemcitabine in patients with metastatic non small cell lung cancer (NSCLC), performance status (PS) 2, or elderly with comorbidities--a multicenter phase II trial.

机译:多中心II期临床试验对患有转移性非小细胞肺癌(NSCLC),表现状态(PS)2或老年合并症的患者采用长春瑞滨联合吉西他滨序贯治疗

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BACKGROUND: High risk patients with metastatic non small cell lung cancer (NSCLC) including patients with performance status (PS) 2 or elderly with comorbidities do poorly on combination chemotherapy regimens. We evaluated a sequential treatment with Vinorelbine followed by Gemcitabine to determine its effect on survival and the toxicity in this patient population. METHODS: Forty-two evaluable patients, median age 75, 21 patients with PS 2 and 21 patients with PS 0 or 1, 37 patients with stage IV and five patients with stage III B NSCLC entered the trial. They received Vinorelbine 30 mg/m2, i.v., on days 1+8 every 3 weeks followed by Gemcitabine 1000 mg/m2, i.v., on days 1+8 every 3 weeks, each for two cycles for stable disease or one cycle after best response. Then stable patients continued until progressive disease on Vinorelbine or Gemcitabine according to the patient's preference. RESULTS: A total of 126 cycles of Vinorelbine were administered to 42 patients, median of three cycles per patient and 74 cycles of Gemcitabine, median of 1.0 cycle per patient. Sixteen patients (38%) achieved PR, 11 patients on Vinorelbine, 5 patients on Gemcitabine; 12 patients (26%) had stable disease, 7 patients on Vinorelbine, 5 patients on Gemcitabine. Of 24 patients with progressive disease on Vinorelbine, 3 patients (12.5%) responded to Gemcitabine. Median time-to-first progression was 3.5 months, median survival was 8 months, 1-year survival was 12 patients (28.5%). No grade 3 or 4 toxicities were reported. CONCLUSION: This sequential treatment offers excellent palliative treatment with minimal toxicity for high-risk patients with metastatic NSCLC.
机译:背景:转移性非小细胞肺癌(NSCLC)的高危患者,包括表现状态(PS)2的患者或合并症的老年人,在联合化疗方案上的表现较差。我们评估了长春瑞滨先加吉西他滨的序贯治疗,以确定其对该患者人群生存率和毒性的影响。方法:42位可评估患者,中位年龄75岁,21例PS 2患者和21例PS 0或1患者,37例IV期患者和5例III B B期非小细胞肺癌患者进入研究。他们每3周第1 + 8天静脉输注长春瑞滨30 mg / m2,然后每3周第1 + 8天静脉输注吉西他滨1000 mg / m2,为稳定病情每两个周期或最佳反应后一个周期。然后,稳定的患者继续治疗,直到根据患者的喜好使用长春瑞滨或吉西他滨进行治疗。结果:共向42例患者施用了126个周期的长春瑞滨,每例中位数为3个周期,吉西他滨为74个周期,中位数为1.0个周期。 16例(38%)达到PR,长春瑞滨11例,吉西他滨5例; 12例(26%)病情稳定,长春瑞滨7例,吉西他滨5例。在长春瑞滨上进行性疾病的24例患者中,有3例(12.5%)对吉西他滨有反应。首次进展时间中位数为3.5个月,中位生存期为8个月,一年生存期为12例患者(28.5%)。没有3级或4级毒性的报道。结论:这种顺序治疗为转移性非小细胞肺癌高危患者提供了优异的姑息治疗,且毒性最小。

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