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细胞周期蛋白依赖性激酶4/6(Cdk4/6)抑制剂与总生存期:转移性乳腺癌一线试验的效能

Cdk4/6 inhibitors and overall survival: power of first-line trials in metastatic breast cancer.

作者信息

Tanguy Marie-Laure, Cabel Luc, Berger Fréderique, Pierga Jean-Yves, Savignoni Alexia, Bidard Francois-Clement

机构信息

1Department of Biometry, Institut Curie, PSL Research University, Saint Cloud, France.

2Department of Medical Oncology, Institut Curie, PSL Research University, Paris, France.

出版信息

NPJ Breast Cancer. 2018 Jun 26;4:14. doi: 10.1038/s41523-018-0068-4. eCollection 2018.

Abstract

Palbociclib, ribociclib, and abemaciclib have been investigated in combination with aromatase inhibitors as first-line therapy for metastatic hormone receptor-positive breast cancer (PALOMA-2, MONALEESA-2 and MONALEESA-7, MONARCH-3 trials, respectively); pivotal trials led to absolute median progression-free survival (PFS) gain of about 15 months. We aimed to estimate, for each trial, the statistical power to demonstrate a significant gain in overall survival (OS). Power was calculated with Freedman's formula. Given the allocation ratio and the number of events, power was computed as a function of hazard ratio. We focused on four specific hazard ratio values (0.94, 0.89, 0.81, and 0.77), which are estimated to correspond to absolute 3, 6, 12, and 15 months gain in OS, respectively. For these calculations, the type I error rate was stated at 5% with a two-sided test, and we assumed that the risk of death was constant over time. PALOMA-2 and MONALEESA trials have an almost similar power despite different allocation ratios, while MONARCH-3 has a more limited power. Overall, the power of the four trials to demonstrate a statistically significant improvement in OS is less than 70% if the prolongation in median OS is ≤12 months, whatever the OS data maturity. This analysis shows that OS results are jeopardized by limited powers, and a meta-analysis might be required to demonstrate OS benefit. Conversely, if a significant OS improvement is observed in some but not at all trials, this discrepancy might be more attributable to chance than to a truly different drug efficacy.

摘要

帕博西尼、瑞博西尼和阿贝西利已分别与芳香化酶抑制剂联合用于转移性激素受体阳性乳腺癌的一线治疗(分别为PALOMA - 2、MONALEESA - 2和MONALEESA - 7、MONARCH - 3试验);关键试验使绝对中位无进展生存期(PFS)延长了约15个月。我们旨在估算每项试验中证明总生存期(OS)有显著改善的统计效能。效能采用弗里德曼公式计算。根据分配比例和事件数,效能作为风险比的函数进行计算。我们关注四个特定的风险比值(0.94、0.89、0.81和0.77),据估计它们分别对应OS绝对延长3、6、12和15个月。对于这些计算,I型错误率设定为双侧检验的5%,并且我们假设死亡风险随时间恒定。尽管分配比例不同,PALOMA - 2和MONALEESA试验的效能几乎相似,而MONARCH - 3的效能则较为有限。总体而言,如果中位OS延长≤12个月,无论OS数据成熟度如何,这四项试验证明OS有统计学显著改善的效能均小于70%。该分析表明,OS结果因效能有限而受到影响,可能需要进行荟萃分析来证明OS获益。相反,如果在部分而非所有试验中观察到OS有显著改善,这种差异可能更多归因于偶然性而非真正不同的药物疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ba3/6018749/f022ca3eb16f/41523_2018_68_Fig1_HTML.jpg

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