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口服拓扑替康联合静脉注射紫杉醇治疗晚期非小细胞肺癌的可行性

Feasibility of oral topotecan plus intravenous paclitaxel in advanced non-small-cell lung cancer.

作者信息

Eckardt J R

机构信息

St. John's Mercy Medical Center, St. Louis, Mo 63141, USA.

出版信息

Oncology. 2001;61 Suppl 1:30-4. doi: 10.1159/000055389.

Abstract

Standard chemotherapy regimens in non-small-cell lung cancer (NSCLC) are platinum-based (cisplatin, carboplatin), with inherent, well-known antitumor activity and toxicity. However, the availability of new agents with novel mechanisms of action and activity in a range of tumor types, coupled with suboptimal activity of single-agent therapy, have prompted the investigation of multidrug regimens in the treatment of NSCLC. One potential combination regimen, in which each agent has antitumor activity in NSCLC monotherapy, is topotecan plus paclitaxel. This article will review the feasibility and tolerability of an oral formulation of topotecan (1.0-1.5 mg/m(2)/day x 5 days) administered with intravenous paclitaxel (175 mg/m(2) as a 3-hour infusion on day 1) in advanced NSCLC patients. The maximum tolerated dose of oral topotecan will be reported, along with preliminary response and tolerability data.

摘要

非小细胞肺癌(NSCLC)的标准化疗方案是以铂类为基础(顺铂、卡铂),具有固有的、众所周知的抗肿瘤活性和毒性。然而,新型作用机制和活性的新药物在多种肿瘤类型中的出现,以及单药治疗活性欠佳,促使人们对非小细胞肺癌治疗中的多药方案进行研究。一种潜在的联合方案是拓扑替康加紫杉醇,其中每种药物在非小细胞肺癌单药治疗中均具有抗肿瘤活性。本文将回顾在晚期非小细胞肺癌患者中,口服拓扑替康(1.0 - 1.5 mg/m²/天×5天)与静脉注射紫杉醇(175 mg/m²,第1天3小时输注)联合使用的可行性和耐受性。将报告口服拓扑替康的最大耐受剂量,以及初步疗效和耐受性数据。

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