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福美坦,一种在非甾体类芳香化酶抑制剂(阿那曲唑和来曲唑)治疗失败后使用的甾体类芳香化酶抑制剂:仍能实现临床获益吗?

Formestane, a steroidal aromatase inhibitor after failure of non-steroidal aromatase inhibitors (anastrozole and letrozole): is a clinical benefit still achievable?

作者信息

Carlini P, Frassoldati A, De Marco S, Casali A, Ruggeri E M, Nardi M, Papaldo P, Fabi A, Paoloni F, Cognetti F

机构信息

Department of Medical Oncology, Regina Elena National Cancer Institute, Rome, Italy.

出版信息

Ann Oncol. 2001 Nov;12(11):1539-43. doi: 10.1023/a:1013180214359.

Abstract

BACKGROUND

There are few clinical data on the sequential use of aromatase inhibitors (AI). This paper focuses on the relevance of clinical benefit CB (CR + PR + SD > or = 6 months) in postmenopausal metastatic breast cancer (MBC) patients treated with the steroidal aromatase inhibitor (SAI) formestane (FOR). who had already received non-steroidal aromatase inhibitor (nSAI): letrozole (LTZ) or anastrozole (ANZ).

PATIENTS AND METHODS

Twenty postmenopausal women with MBC were analysed in this retrospective two-centre study with the sequence nSAI-FOR. When receiving ANZ, 1 of 11 achieved a complete response and 9 of 11 a stable disease > or = 6 months, and receiving LTZ 1 of 9 achieved a partial response and 4 of 9 a stable disease > or = 6 months. The analysis of the entire population treated with FOR showed an overall CB of 55% (11 of 20) with a median duration of 15 months and median time to progression (TTP) of 6 months.

CONCLUSIONS

Formestane 250 mg once bi-weekly seems to be an attractive alternative third-line hormonal therapy for the treatment of patients with MBC, previously treated with nSAI.

摘要

背景

关于芳香化酶抑制剂(AI)序贯使用的临床数据较少。本文重点关注甾体类芳香化酶抑制剂(SAI)福美坦(FOR)治疗绝经后转移性乳腺癌(MBC)患者的临床获益(CB,完全缓解+部分缓解+疾病稳定≥6个月)的相关性,这些患者之前已接受非甾体类芳香化酶抑制剂(nSAI)来曲唑(LTZ)或阿那曲唑(ANZ)治疗。

患者与方法

在这项回顾性双中心研究中,对20例接受nSAI-FOR序贯治疗的绝经后MBC女性患者进行了分析。接受阿那曲唑治疗时,11例中有1例达到完全缓解,11例中有9例疾病稳定≥6个月;接受来曲唑治疗时,9例中有1例达到部分缓解,9例中有4例疾病稳定≥6个月。对接受福美坦治疗的全部患者的分析显示,总体临床获益率为55%(20例中的11例),中位持续时间为15个月,中位疾病进展时间(TTP)为6个月。

结论

对于之前接受过nSAI治疗的MBC患者,每两周一次250mg福美坦似乎是一种有吸引力的三线激素替代疗法。

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