The effect of CDK4/6 inhibitors on the overall survival in patients with advanced HR+/HER2- BC in the entire population and in special clinical subgroups of unfavorable prognosis: A review

Q4 Medicine
K. Grechukhina, M. V. Kalugin, A. A. Prosvirnov, Margarita V. Sukhova, L. G. Zhukova
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引用次数: 0

Abstract

An increase in the median progression-free survival when using cyclin-dependent kinase 4/6 inhibitors in combination with aromatase inhibitors led to high expectations from the analysis of the overall survival of patients with HR+/HER2- metastatic breast cancer. Of the three drugs in the group, the final data were obtained in the MONALEESA-2 and PALOMA-2 studies, while a statistically significant difference in median overall survival was achieved only with the use of ribociclib. The review discusses possible factors that could affect the final results of the presented studies. The effect of ribociclib on the value of OS in clinically unfavorable prognostic subgroups (for example, patients with visceral metastases) and on progression-free survival depending on the expression of molecular genetic factors that worsen patient survival (such as Rb, p16, Ki-67, CDKN2A, CCND1, ESR1) was analyzed.The combination of ribociclib and aromatase inhibitors has proven to be an advantage in the treatment of patients with HR+/HER2- metastatic breast cancer in terms of increasing both progression-free survival and overall survival. Efficacy has been proven in subgroups with clinical and molecular adverse prognostic factors.
CDK4/6抑制剂对整个人群和预后不良的特殊临床亚组中晚期HR+/HER2- BC患者总生存率的影响:综述
当使用周期蛋白依赖性激酶4/6抑制剂与芳香化酶抑制剂联合使用时,中位无进展生存期的增加使人们对HR+/HER2-转移性乳腺癌患者的总生存期分析产生了很高的期望。在该组的三种药物中,最终数据是在MONALEESA-2和PALOMA-2研究中获得的,而中位总生存期只有在使用ribociclib时才有统计学意义的差异。本综述讨论了可能影响本研究最终结果的因素。分析了ribociclib对临床预后不良亚组(如内脏转移患者)的OS值以及依赖于恶化患者生存的分子遗传因子(如Rb、p16、Ki-67、CDKN2A、CCND1、ESR1)表达的无进展生存期的影响。在提高无进展生存期和总生存期方面,核糖环尼和芳香酶抑制剂的联合治疗已被证明是治疗HR+/HER2-转移性乳腺癌患者的优势。在具有临床和分子不良预后因素的亚组中,疗效已得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Modern Oncology
Journal of Modern Oncology Medicine-Oncology
CiteScore
0.50
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0.00%
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审稿时长
5 weeks
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