Harbeck Nadia, Brufsky Adam, Rose Chloe Grace, Korytowsky Beata, Chen Connie, Tantakoun Krista, Jazexhi Endri, Nguyen Do Hoang Vien, Bartlett Meaghan, Samjoo Imtiaz A, Pluard Timothy
Breast Center, Department of Gynecology and Obstetrics and Comprehensive Cancer Center Munich, LMU University Hospital, Munich, Germany.
UPMC Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Front Oncol. 2025 Mar 10;15:1530391. doi: 10.3389/fonc.2025.1530391. eCollection 2025.
Since 2021, additional real-world evidence (RWE) has emerged on the effectiveness of cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) as first-line treatment of HR-positive/HER2-negative (HR+/HER2-) advanced/metastatic breast cancer (A/MBC), necessitating this updated review.
MEDLINE, Embase, and Cochrane Databases (07/06/2019-01/09/2024), and key congresses (2020-2024) were searched. Studies reporting first-line CDK4/6i use, over 100 participants, and progression-free survival (PFS) and/or overall survival (OS) data were included.
This update included 82 unique studies, 42.7% for palbociclib, 7.3% for ribociclib, and 3.7% for abemaciclib; 46.3% assessed multiple CDK4/6i. In studies including multiple CDK4/6is, median PFS was 23.4-31.0 months for palbociclib, 19.8-44.0 for ribociclib, and 14.0-39.5 for abemaciclib. When reached, median OS was 38.0-58.0 months, 40.4-52.0 months, and 34.4 months, respectively. These real-world PFS and OS results were within the range of single-arm and CDK4/6i versus endocrine therapy (ET) studies, where CDK4/6i demonstrated greater benefits than ET alone.
First-line CDK4/6i RWE demonstrates significant clinical benefits in HR+/HER2- A/MBC. These data are important to guide clinical decision-making, as they include patients who are not adequately represented in clinical trials. Studies with longer follow-up are needed to assess long-term benefits of all three CDK4/6i therapies in HR+/HER2- A/MBC.
自2021年以来,关于细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)作为激素受体阳性/人表皮生长因子受体2阴性(HR+/HER2-)晚期/转移性乳腺癌(A/MBC)一线治疗有效性的更多真实世界证据(RWE)已出现,因此需要进行此次更新综述。
检索了MEDLINE、Embase和Cochrane数据库(2019年6月7日至2024年9月1日)以及主要会议(2020 - 2024年)。纳入了报告一线使用CDK4/6i、超过100名参与者以及无进展生存期(PFS)和/或总生存期(OS)数据的研究。
本次更新纳入了82项独特研究,其中42.7%涉及哌柏西利,7.3%涉及瑞博西利,3.7%涉及阿贝西利;46.3%评估了多种CDK4/6i。在包括多种CDK4/6i的研究中,哌柏西利的中位PFS为23.4 - 31.0个月,瑞博西利为19.8 - 44.0个月,阿贝西利为14.0 - 39.5个月。达到中位OS时,分别为38.0 - 58.0个月、40.4 - 52.0个月和34.4个月。这些真实世界的PFS和OS结果在单臂研究以及CDK4/6i与内分泌治疗(ET)研究的范围内,其中CDK4/6i显示出比单独ET更大的益处。
一线CDK4/6i的RWE表明在HR+/HER2- A/MBC中具有显著的临床益处。这些数据对于指导临床决策很重要,因为它们纳入了临床试验中未充分代表的患者。需要进行更长随访时间的研究,以评估所有三种CDK4/6i疗法在HR+/HER2- A/MBC中的长期益处。