Dongiovanni Diego, Fissore Camilla, Berruti Alfredo, Buffoni Lucio, Addeo Alfredo, Barone Carla, Polimeni Maria Antonia, Ottaviani Davide, Bertetto Oscar, Dongiovanni Vincenzo
Oncologia Medica, Centro Oncologico Ematologico Subalpino, Azienda Ospedaliera Molinette, Via Cherasco 15, 10126 Torino, Italy.
Lung Cancer. 2005 Feb;47(2):269-75. doi: 10.1016/j.lungcan.2004.06.019.
To determine the activity and safety of a sequential regimen of cisplatin and vinorelbine followed by paclitaxel and gemcitabine in patients with advanced non-small-cell lung cancer (NSCLC).
Treatment was two cycles of cisplatin 80 mg/m(2) on day 1 and vinorelbine 30 mg/m(2) on days 1 and 8 every 3 weeks followed by two cycles of paclitaxel 175 mg/m(2) on day 1 and gemcitabine 1250 mg/m(2) on days 1 and 8 every 3 weeks.
Fifty-five patients with inoperable NSCLC, performance status 2 or less were enrolled, including 19 patients with brain lesions. There were 23 partial responses (42%; 95% confidence interval 29-55). The median time to progression and overall survival were 5.8 and 10.3 months, respectively (6.5 and 12.8 in the patient subset without brain metastases). One-year survival rate was 47.5%. Grade III/IV neutropenia was the major side effect; it occurred in 56% of patients and was mainly limited to the first two chemotherapy cycles with cisplatin and vinorelbine.
Sequential combination of cisplatin and vinorelbine followed by paclitaxel and gemcitabine is a manageable and active regimen for patients with NSCLC. It deserves to be tested against a standard two-drug scheme in a phase III trial.
确定顺铂和长春瑞滨序贯方案后接紫杉醇和吉西他滨治疗晚期非小细胞肺癌(NSCLC)患者的有效性和安全性。
治疗方案为每3周进行两个周期的治疗,第1天给予顺铂80mg/m²,第1天和第8天给予长春瑞滨30mg/m²,随后每3周进行两个周期的治疗,第1天给予紫杉醇175mg/m²,第1天和第8天给予吉西他滨1250mg/m²。
纳入55例无法手术的NSCLC患者,其体能状态评分为2分或更低,其中19例有脑转移灶。有23例部分缓解(42%;95%置信区间为29%-55%)。中位疾病进展时间和总生存期分别为5.8个月和10.3个月(无脑转移的患者亚组分别为6.5个月和12.8个月)。1年生存率为47.5%。Ⅲ/Ⅳ级中性粒细胞减少是主要副作用;56%的患者出现该副作用,且主要局限于顺铂和长春瑞滨的前两个化疗周期。
顺铂和长春瑞滨序贯联合紫杉醇和吉西他滨对NSCLC患者是一种可行且有效的方案。值得在Ⅲ期试验中与标准两药方案进行对比测试。