Vokes E E, Masters G A, Mauer A M, Hoffman P C, Watson S, Golomb H M
Department of Medicine, and Cancer Research Center, The University of Chicago, IL 60637-1470, USA.
Semin Oncol. 1998 Feb;25(1 Suppl 2):19-22.
The role of chemotherapy in the treatment of non-small cell lung cancer (NSCLC) has expanded in recent years, resulting in increased median survival and higher 5-year survival rates in some studies. Few patients with NSCLC can be cured, however, and the median survival time is still modest. Research strategies are aimed at identifying new active single agents, testing their combination in non-cisplatin- and non-carboplatin-containing regimens, and their incorporation into regimens containing more than two drugs, in efforts to improve response and survival and/or reduce toxicity. Several trials of triplet chemotherapy combinations for the treatment of NSCLC have been conducted at the University of Chicago. The three-drug regimen of vinorelbine, paclitaxel, and ifosfamide with granulocyte colony-stimulating factor was evaluated in a phase I trial. Doses of all three drugs were reduced from their standard doses so that toxicity would be manageable, although toxicity was still high. The low response rate (<20%) at the recommended phase II doses led to early closure of this trial. The University of Chicago is also assessing the three-drug combination of carboplatin, paclitaxel, and ifosfamide in patients with stage IIIB and IV NSCLC. The carboplatin and paclitaxel doses are being maintained within their active single-agent range, with the goal of identifying the maximum tolerated dose of ifosfamide when added to this combination. Additional end points include response rates, survival time, and dose-limiting toxicities. This study is ongoing.
近年来,化疗在非小细胞肺癌(NSCLC)治疗中的作用有所扩大,在一些研究中使中位生存期延长,5年生存率提高。然而,很少有NSCLC患者能够治愈,中位生存时间仍然不长。研究策略旨在确定新的活性单药,测试其在不含顺铂和卡铂的方案中的联合应用,以及将其纳入含两种以上药物的方案,以提高缓解率和生存率及/或降低毒性。芝加哥大学已经开展了多项治疗NSCLC的三联化疗联合方案试验。在一项I期试验中评估了长春瑞滨、紫杉醇和异环磷酰胺联合粒细胞集落刺激因子的三药方案。所有三种药物的剂量都从标准剂量降低,以便毒性可控,尽管毒性仍然很高。在推荐的II期剂量下缓解率较低(<20%)导致该试验提前终止。芝加哥大学还在评估卡铂、紫杉醇和异环磷酰胺的三药联合方案用于IIIB期和IV期NSCLC患者。卡铂和紫杉醇的剂量保持在其活性单药范围内,目标是确定加入该联合方案时异环磷酰胺的最大耐受剂量。其他终点包括缓解率、生存时间和剂量限制性毒性。这项研究正在进行中。