Grossi Francesco, Belvedere Ornella, Fasola Gianpiero, Barbone Fabio, Rizzato Simona, Sibau Angela, Recchia Leonardo, Vigevani Enrico, Ceschia Tino, Morelli Angelo, Guglielmi Alessandra, Puglisi Fabio, Follador Alessandro, Talmassons Giovanni, Sobrero Alberto F
Disease Management Team-Lung Cancer, Medical Oncology A, National Institute for Cancer Research, Largo R. Benzi 10, 16132 Genoa, Italy.
Lung Cancer. 2004 Oct;46(1):99-106. doi: 10.1016/j.lungcan.2004.03.003.
Aim of this study was to determine the activity and toxicity of a sequential chemotherapy regimen in advanced non-small cell lung cancer (NSCLC). Fifty-one previously untreated stage IIIB/IV NSCLC patients were enrolled to receive two cycles of cisplatin plus paclitaxel (80/175 mg/m(2) every 21 days), followed by two cycles of vinorelbine (30 mg/m(2) on days 1 and 8 every 21 days), followed by two cycles of gemcitabine (1000 mg/m(2) on days 1, 8, and 15 every 28 days). Forty-one patients (82%) completed the planned six cycles. Grade 3-4 neutropenia was the major toxicity (41% of patients) and it was mainly associated with vinorelbine administration. Response rate after cisplatin plus paclitaxel was 18%; this percentage increased to 41% after vinorelbine, and it reached 43% upon completion of the entire six cycle treatment program. Median survival time was 14.4 months, 1-year survival rate was 53%, and 2-year survival rate was 18%. Median time to disease progression was 6.8 months. This sequential chemotherapy regimen is feasible and active in patients with advanced NSCLC. This pilot experience provides the basis for an ongoing randomized phase III trial comparing our sequential regimen versus cisplatin plus gemcitabine.
本研究的目的是确定一种序贯化疗方案在晚期非小细胞肺癌(NSCLC)中的活性和毒性。51例既往未接受过治疗的IIIB/IV期NSCLC患者入组,接受两个周期的顺铂加紫杉醇(每21天80/175mg/m²),随后两个周期的长春瑞滨(每21天第1天和第8天30mg/m²),接着两个周期的吉西他滨(每28天第1天、第8天和第15天1000mg/m²)。41例患者(82%)完成了计划的六个周期。3-4级中性粒细胞减少是主要毒性(41%的患者),主要与长春瑞滨给药有关。顺铂加紫杉醇后的缓解率为18%;长春瑞滨治疗后该百分比增至41%,在整个六个周期治疗方案完成时达到43%。中位生存时间为14.4个月,1年生存率为53%,2年生存率为18%。疾病进展的中位时间为6.8个月。这种序贯化疗方案在晚期NSCLC患者中可行且有活性。这一初步经验为正在进行的一项随机III期试验提供了基础,该试验将我们的序贯方案与顺铂加吉西他滨进行比较。