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多西他赛与拓扑替康每周方案治疗实体瘤的I期试验。

A Phase I trial of weekly docetaxel and topotecan for solid tumors.

作者信息

Lim Wan Teck, Baggstrom Maria Q, Read William, Fracasso Paula M, Govindan Ramaswamy

机构信息

Alvin J Siteman Cancer Center, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA.

出版信息

Acta Oncol. 2008;47(2):311-5. doi: 10.1080/02841860701560340.

Abstract

BACKGROUND/AIMS: Topotecan and docetaxel are active agents in the treatment of various malignant diseases. Both drugs cause dose-limiting hematologic toxicity. This study defines the maximum tolerated dose (MTD) and dose-limiting toxicity of weekly topotecan when administered in combination with docetaxel 25 mg/m(2) given day 1, 8,15 every 28 days.

METHODS

Thirteen patients were enrolled. Median age was 62 years. Majority of the patients had lung cancer.

RESULTS

The maximum tolerated dose was docetaxel 25 mg/m(2) and topotecan 3 mg/m(2) administered weekly. Dose-limiting toxicity was febrile neutropenia. Eight patients developed at least grade 3 neutropenia in all cycles. Non-hematologic toxicities were mild. No objective responses were noted. Two patients with non-small cell lung cancer had stable disease as a best response.

CONCLUSION

Combination docetaxel and topotecan given weekly is tolerable. The recommended phase II dose is docetaxel 25 mg/m(2) and topotecan 3 mg/m(2) day 1, 8, 15 every 28 days.

摘要

背景/目的:拓扑替康和多西他赛是治疗多种恶性疾病的有效药物。两种药物都会引起剂量限制性血液学毒性。本研究确定了每28天第1、8、15天给予25mg/m²多西他赛时,每周使用拓扑替康的最大耐受剂量(MTD)和剂量限制性毒性。

方法

纳入13例患者。中位年龄为62岁。大多数患者患有肺癌。

结果

最大耐受剂量为每周给予多西他赛25mg/m²和拓扑替康3mg/m²。剂量限制性毒性为发热性中性粒细胞减少。8例患者在所有周期中至少出现3级中性粒细胞减少。非血液学毒性较轻。未观察到客观缓解。2例非小细胞肺癌患者的最佳反应为病情稳定。

结论

每周给予多西他赛和拓扑替康联合方案是可耐受的。推荐的II期剂量为每28天第1、8、15天给予多西他赛25mg/m²和拓扑替康3mg/m²。

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