Greco F A, Hainsworth J D
Sarah Cannon-Minnie Pearl Cancer Center, Nashville, TN 37203, USA.
Semin Oncol. 1997 Aug;24(4 Suppl 12):S12-14-S12-17.
This study was performed to determine the activity and toxicity of paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) given by 1-hour infusion plus carboplatin in the treatment of patients with advanced non-small cell lung cancer when used in a multicenter, community-based setting. The study population included 100 chemotherapy-naive patientswith stage IIIB or IV non-small cell lung cancer, Karnofsky performance status 70 to 100, measurable disease, and adequate kidney, liver, and bone marrow function. All patients received paclitaxel 225 mg/m2 intravenously by 1-hour infusion followed immediately by carboplatin at a targeted area under the concentration-time curve of 6.0 (Calvert formula). Cycles were repeated every 21 days. Colony-stimulating factors were not used routinely. Thirty-eight (38%) of 100 patients had objective responses (38 [40%] of 94 evaluable patients) to treatment (three complete responses, 35 partial responses). Thirty-two other patients had stable disease at initial re-evaluation. Weight gain during treatment occurred in 47% of those patients with objective response or stable disease. The median survival among all 100 patients was 8 months, with a 1-year survival rate of 42%. Leukopenia was common, but hospitalization for treatment of neutropenia and fever occurred in only 3% of courses. Cumulative peripheral neuropathy occurred consistently, but usually after the third or fourth course; it was severe (grade 3) in only 15% of patients. Other grade 3 and 4 toxicity was uncommon. One patient died as a result of treatment due to sepsis. This large, multicenter, community-based phase II trial demonstrates the efficacy of paclitaxel/carboplatin combination chemotherapy in advanced non-small cell lung cancer. This regimen is relatively well tolerated and when paclitaxel is given by 1-hour infusion, this treatment is easily administered in the outpatient setting.
本研究旨在确定在多中心、基于社区的环境中,采用1小时输注的紫杉醇(泰素;百时美施贵宝公司,新泽西州普林斯顿)联合卡铂治疗晚期非小细胞肺癌患者时的活性和毒性。研究人群包括100例初治的IIIB期或IV期非小细胞肺癌患者,卡氏评分70至100,有可测量的病灶,且肾、肝和骨髓功能良好。所有患者均接受静脉输注1小时的225mg/m²紫杉醇,随后立即给予卡铂,目标浓度-时间曲线下面积为6.0(卡尔弗特公式)。每21天重复一个周期。未常规使用集落刺激因子。100例患者中有38例(38%)对治疗有客观反应(94例可评估患者中有38例[40%])(3例完全缓解,35例部分缓解)。另外32例患者在初次重新评估时病情稳定。47%有客观反应或病情稳定的患者在治疗期间体重增加。100例患者的中位生存期为8个月,1年生存率为42%。白细胞减少很常见,但因中性粒细胞减少和发热住院治疗仅发生在3%的疗程中。累积性周围神经病变持续出现,但通常在第三或第四个疗程后发生;仅15%的患者病情严重(3级)。其他3级和4级毒性不常见。1例患者因治疗导致的败血症死亡。这项大型、多中心、基于社区的II期试验证明了紫杉醇/卡铂联合化疗在晚期非小细胞肺癌中的疗效。该方案耐受性相对良好,当采用1小时输注紫杉醇时,这种治疗在门诊环境中易于实施。