Rosell R, González-Larriba J L, Alberola V, Molina F, Monzó M, Benito D, Pérez J M, de Anta J M
Medical Oncology Service, University Hospital Germans Trias i Pujol, Barcelona, Spain.
Semin Oncol. 1995 Dec;22(6 Suppl 14):12-8.
Currently available cytotoxic drugs are only moderately active in non-small cell lung cancer (NSCLC) and prolong survival only slightly. In two published trials, single-agent paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) was reported to have significant activity in NSCLC, with response rates of 21% and 24%. Treatment-limiting hypersensitivity reactions, however, were noted in a phase I trial of paclitaxel given as a 3-hour infusion at doses > or = 190 mg/m2. We report the results of a phase II trial of paclitaxel given by 3-hour intravenous infusion at 210 mg/m2 every 3 weeks in an outpatient setting. The study was conducted simultaneously at three centers and included chemotherapy-naive patients with unresectable locoregional or metastatic NSCLC. The study objectives were to evaluate response rate, the potential link between p53 and K-ras gene mutations and increased paclitaxel resistance, and toxicity. Sixty-two patients were eligible for this study. All patients were premedicated with dexamethasone 20 mg given orally or intravenously 12 and 6 hours before paclitaxel infusion and cimetidine 300 mg and diphenhydramine 50 mg, both given 60 minutes prior to initiation of paclitaxel infusion. Of the 62 patients who were initially enrolled, 50 (44 men and six women) were evaluable for toxicity at interim analysis; 47 of these patients were evaluable for response. Twenty-four had squamous cell carcinoma, 20 had adenocarcinoma, and six had undifferentiated large cell carcinoma. The median age was 61 years (age range, 36 to 75 years). The median Zubrod performance status was 1 (range, 0 to 2). Seventeen (36%) patients achieved either partial or complete response. Among 24 patients with squamous cell carcinoma, eight (33%; 95% confidence interval, 15% to 61%) had a partial response. Seven (41%; 95% confidence interval, 18% to 64%) of 17 patients with adenocarcinoma had a partial or complete response. Tissue blocks were obtained for analysis of K-ras and p53 gene mutations by means of polymerase chain reaction followed by single-strand conformation polymorphism assay. Our findings indicate that mutations are associated with a poor clinical course and may be prognostic of paclitaxel resistance. Paclitaxel was well tolerated. None of the patients experienced allergic reactions. Granulocytopenia was generally mild. Therapy was interrupted in only two patients because of the development of grade 3 neuropathy. In our experience, paclitaxel is one of the most active cytotoxic drugs targeting NSCLC.
目前可用的细胞毒性药物在非小细胞肺癌(NSCLC)中的活性仅为中等,对延长生存期的作用也很有限。在两项已发表的试验中,据报道单药紫杉醇(泰素;百时美施贵宝公司,新泽西州普林斯顿)在NSCLC中具有显著活性,缓解率分别为21%和24%。然而,在一项I期试验中,当紫杉醇以3小时输注方式给药且剂量≥190mg/m²时,观察到了限制治疗的超敏反应。我们报告了一项II期试验的结果,该试验在门诊环境中每3周以210mg/m²的剂量通过3小时静脉输注给予紫杉醇。该研究在三个中心同时进行,纳入了未接受过化疗的不可切除的局部区域或转移性NSCLC患者。研究目的是评估缓解率、p53和K-ras基因突变与紫杉醇耐药性增加之间的潜在联系以及毒性。62名患者符合本研究条件。所有患者在紫杉醇输注前12小时和6小时口服或静脉给予20mg地塞米松进行预处理,并在紫杉醇输注开始前60分钟给予300mg西咪替丁和50mg苯海拉明。在最初入组的62名患者中,50名(44名男性和6名女性)在中期分析时可评估毒性;其中47名患者可评估缓解情况。24例为鳞状细胞癌,20例为腺癌,6例为未分化大细胞癌。中位年龄为61岁(年龄范围36至75岁)。Zubrod体能状态中位数为1(范围0至2)。17名(36%)患者达到部分缓解或完全缓解。在24例鳞状细胞癌患者中,8例(33%;95%置信区间,15%至61%)有部分缓解。17例腺癌患者中有7例(41%;95%置信区间,18%至64%)达到部分缓解或完全缓解。通过聚合酶链反应随后进行单链构象多态性分析获取组织块,以分析K-ras和p53基因突变。我们的研究结果表明,基因突变与不良临床病程相关,可能预示着对紫杉醇耐药。紫杉醇耐受性良好。没有患者发生过敏反应。粒细胞减少症一般较轻。仅两名患者因3级神经病变的发生而中断治疗。根据我们的经验,紫杉醇是针对NSCLC最具活性的细胞毒性药物之一。