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新型芳香化酶抑制剂作为绝经后转移性乳腺癌患者二线内分泌治疗的随机试验汇总分析

New aromatase inhibitors as second-line endocrine therapy in postmenopausal patients with metastatic breast carcinoma: a pooled analysis of the randomized trials.

作者信息

Carlini Paolo, Bria Emilio, Giannarelli Diana, Ferretti Gianluigi, Felici Alessandra, Papaldo Paola, Fabi Alessandra, Nisticò Cecilia, Di Cosimo Serena, Ruggeri Enzo Maria, Milella Michele, Mottolese Marcella, Terzoli Edmondo, Cognetti Francesco

机构信息

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

出版信息

Cancer. 2005 Oct 1;104(7):1335-42. doi: 10.1002/cncr.21339.

Abstract

BACKGROUND

New aromatase inhibitors (AI) (second-generation: formestane and fadrozole; third-generation: letrozole, anastrozole, vorozole, and exemestane) have been tested in several controlled clinical trials after tamoxifen failure in metastatic breast carcinoma (MBC). They have resulted in better survival compared with megestrol acetate (MEG) in a number of studies. The authors performed a pooled analysis including all the Phase III trials published between 1996 and 2004 evaluating the AIs approved or not by the Food and Drug Administration (FDA) and the European Agency for the Evaluation of Medical Products (EMEA) as second-line endocrine therapy (ET) for patients with MBC.

METHODS

The overall response rate (ORR) and time to disease progression (TTP) were considered the primary end points, whereas toxicity was regarded as a secondary objective. Relative risk, 95% confidence interval, and heterogeneity were derived using 2 methods.

RESULTS

No significant differences in ORR and TTP were noted in the entire group of 9 trials comparing AI with MEG (3908 patients) and in the 6 trials comparing nonsteroidal AI and MEG (2415 patients). AI yielded significantly more hot flashes than MEG (P = 0.004) but caused significantly less toxicity than MEG in weight gain (P = 0.001), dyspnea (P = 0.008), and peripheral edema (P = 0.03). Significant heterogeneity for nausea, weight gain, dyspnea, and peripheral edema was registered. When steroidal AIs were excluded from the toxicity analysis, nausea maintained its strongly significant heterogeneity (P = 0.0002), whereas weight gain, dyspnea, and peripheral edema lost their significance.

CONCLUSIONS

This pooled analysis suggested that AIs in second-line ET for patients with MBC do not seem to add any significant benefit to MEG in terms of ORR and TTP. With regard to toxicity, the findings in the current study showed that weight gain, dyspnea, and peripheral edema are more frequent with the use of MEG, whereas hot flashes were more represented using AI.

摘要

背景

新型芳香化酶抑制剂(AI)(第二代:福美司坦和法倔唑;第三代:来曲唑、阿那曲唑、伏罗唑和依西美坦)在转移性乳腺癌(MBC)患者他莫昔芬治疗失败后的多项对照临床试验中进行了测试。在多项研究中,与醋酸甲地孕酮(MEG)相比,它们带来了更好的生存率。作者进行了一项汇总分析,纳入了1996年至2004年间发表的所有III期试验,评估美国食品药品监督管理局(FDA)和欧洲药品评估局(EMEA)批准或未批准的AI作为MBC患者二线内分泌治疗(ET)的情况。

方法

总缓解率(ORR)和疾病进展时间(TTP)被视为主要终点,而毒性被视为次要目标。相对风险、95%置信区间和异质性使用两种方法得出。

结果

在比较AI与MEG的9项试验(3908例患者)的整个组中,以及在比较非甾体AI与MEG的6项试验(2415例患者)中,未观察到ORR和TTP有显著差异。AI导致的潮热明显多于MEG(P = 0.004),但在体重增加(P = 0.001)、呼吸困难(P = 0.008)和外周水肿(P = 0.03)方面,其毒性明显低于MEG。恶心、体重增加、呼吸困难和外周水肿存在显著异质性。当甾体AI被排除在毒性分析之外时,恶心仍保持其高度显著的异质性(P = 0.0002),而体重增加、呼吸困难和外周水肿失去了其显著性。

结论

这项汇总分析表明,对于MBC患者的二线ET,AI在ORR和TTP方面似乎并未给MEG带来任何显著益处。关于毒性,当前研究结果表明,使用MEG时体重增加、呼吸困难和外周水肿更常见,而使用AI时潮热更常见。

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