Stinchcombe Thomas E, Mauer Ann M, Hodgson Lydia D, Herndon James E, Lynch Thomas J, Green Mark R, Vokes Everett E
Multidisciplinary Thoracic Oncology Program, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599-7305, USA.
J Thorac Oncol. 2008 Nov;3(11):1301-7. doi: 10.1097/JTO.0b013e318187494a.
Cancer and Leukemia Group B trial 9430 was a randomized phase II trial which investigated the safety and activity of four novel doublets in untreated extensive stage small cell lung cancer. The results of the paclitaxel and cisplatin arm have not been reported.
Patients received paclitaxel 230 mg/m followed by cisplatin 75 mg/m on day 1 every 21 days. All patients received granulocyte colony stimulating factor 5 microg/kg/d beginning on day 3 of each cycle.
The patient characteristics of the 34 patients assigned to this treatment arm were: median age 61.5 years (range 41-82), male (76%), performance status 0 (41%), 1 (32%), and 2 (26%). An objective response was observed in 23 patients (68%; 95% confidence interval (CI): 49-83%); 2 complete responses (6%) and 21 partial responses (62%). Median progression-free survival time was 5.6 months (95% CI: 4.8-7.1 month), and median overall survival time was 7.7 months (95% CI: 7.2-12.6 months). The 1-year survival rate observed was 29% (95% CI: 15-45%). Grade 3/4 neutropenia and thrombocytopenia was observed in 5 (15%) and 4 (12%) patients, respectively. Two patients developed febrile neutropenia including one patient who died of neutropenic sepsis. Grade 3/4 nonhematologic observed were: sensory neuropathy in eight patients (24%); and hyperglycemia, malaise and nausea were all observed in four patients (12%).
Cancer and Leukemia Group B will not pursue further investigation of paclitaxel and cisplatin due to the modest activity and the toxicity observed on this trial.
癌症与白血病B组试验9430是一项随机II期试验,研究了四种新型联合方案在未经治疗的广泛期小细胞肺癌中的安全性和活性。紫杉醇和顺铂治疗组的结果尚未报告。
患者接受紫杉醇230mg/m²,随后在第1天接受顺铂75mg/m²,每21天为一周期。所有患者从每个周期的第3天开始接受粒细胞集落刺激因子5μg/kg/天。
分配至该治疗组的34例患者的特征如下:中位年龄61.5岁(范围41 - 82岁),男性(76%),体能状态为0(41%)、1(32%)和2(26%)。23例患者观察到客观缓解(68%;95%置信区间(CI):49 - 83%);2例完全缓解(6%)和21例部分缓解(62%)。中位无进展生存期为5.6个月(95%CI:4.8 - 7.1个月),中位总生存期为7.7个月(95%CI:7.2 - 12.6个月)。观察到的1年生存率为29%(95%CI:15 - 45%)。分别有5例(15%)和4例(12%)患者发生3/4级中性粒细胞减少和血小板减少。2例患者发生发热性中性粒细胞减少,其中1例死于中性粒细胞减少性败血症。观察到的3/4级非血液学不良反应有:8例患者出现感觉神经病变(24%);4例患者出现高血糖、不适和恶心(均为12%)。
由于该试验中观察到的活性一般且毒性较大,癌症与白血病B组将不再对紫杉醇和顺铂进行进一步研究。