Mastrantoni Luca, Orlandi Armando, Palazzo Antonella, Garufi Giovanna, Fabi Alessandra, Daniele Gennaro, Giannarelli Diana, Tortora Giampaolo, Bria Emilio
Medical Oncology, Università Cattolica del Sacro Cuore, Rome, Italy.
Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
EClinicalMedicine. 2023 Jan 20;56:101824. doi: 10.1016/j.eclinm.2023.101824. eCollection 2023 Feb.
In hormone-receptor positive/HER2-negative metastatic breast cancer (mBC) no randomized comparisons are available between CDK4/6 inhibitors. We undertook this systematic review and meta-analysis to assess the reliability of the likelihood of being helped or harmed (LHH).
PubMed, CENTRAL, Embase and oncological meetings websites were searched to September 13th, 2022. We included phase III randomized controlled trials (RCTs) investigating palbociclib, ribociclib and abemaciclib in addition to endocrine therapy (ET) compared to placebo in hormone-receptor positive/HER2-negative advanced or mBC. Outcomes were progression-free survival (PFS), overall survival (OS), adverse events (AEs), dose reductions and discontinuations. Hazard ratios (HRs) and risk differences were computed with a random effect model to estimate the number needed to treat/harm (NNT/NNH). LHH was computed as (1/NNT)/(1/NNH). PROSPERO registration number: CRD42022362417.
2204 records were screened and seven RCTs (4415 patients) were included. A significant PFS benefit was observed in patients treated with a CDK4/6 inhibitor compared to placebo (HR 0.549; 0.508-0.594, = 0). Palbociclib, ribociclib and abemaciclib had similar NNTs (4.4, 5.0 and 4.4). Palbociclib and ribociclib showed lower LHHs for grade 3-4 neutropenia (0.33 and 0.35) and febrile neutropenia ([FN], 14.27 and 15.52), while abemaciclib the lowest LHH for any grade diarrhea (0.42). Abemaciclib had a lower LHH for grade 3-4 fatigue (9.92) and the highest LHH for all grade 3-4 AEs (0.62), while ribociclib the lowest LHH (1.75) for grade 3-4 hepatotoxicity. Palbociclib had the highest LHH for dose reductions and discontinuations (0.65 and 6.17). Considering OS, an overall benefit was observed (HR 0.788, 0.727-0.856, = 0%); ribociclib and abemaciclib had lower NNTs (9.7 and 10.0). Ribociclib showed the highest LHH for diarrhea (1.29), fatigue (7.37), dose reductions (0.28) and discontinuations (2.40), while abemaciclib the highest LHHs for neutropenia (0.40), FN (12.53) and hepatotoxicity (2.23).
Palbociclib and ribociclib showed lower LHHs for haematological toxicities and abemaciclib for diarrhea. Palbociclib confirmed to be a manageable drug. The LHH appears to be a reliable synthesis tool for balancing risks and benefits of experimental drugs when head-to-head comparisons are missing.
None.
在激素受体阳性/人表皮生长因子受体2阴性转移性乳腺癌(mBC)中,尚无关于细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂之间的随机对照比较。我们进行了这项系统评价和荟萃分析,以评估获益或伤害可能性(LHH)的可靠性。
检索截至2022年9月13日的PubMed、CENTRAL、Embase和肿瘤学会议网站。我们纳入了III期随机对照试验(RCT),这些试验研究了哌柏西利、瑞博西尼和阿贝西利联合内分泌治疗(ET)与激素受体阳性/HER2阴性晚期或mBC患者使用安慰剂相比的情况。结局指标为无进展生存期(PFS)、总生存期(OS)、不良事件(AE)、剂量减少和停药情况。采用随机效应模型计算风险比(HR)和风险差异,以估计治疗/伤害所需人数(NNT/NNH)。LHH计算为(1/NNT)/(1/NNH)。国际前瞻性系统评价注册库注册号:CRD42022362417。
筛选了2204条记录,纳入了7项RCT(4415例患者)。与安慰剂相比,接受CDK4/6抑制剂治疗的患者观察到显著的PFS获益(HR 0.549;0.508 - 0.594,P = 0)。哌柏西利、瑞博西尼和阿贝西利的NNT相似(4.4、5.0和4.4)。哌柏西利和瑞博西尼在3 - 4级中性粒细胞减少(0.33和0.35)和发热性中性粒细胞减少([FN],14.27和15.52)方面显示出较低的LHH,而阿贝西利在任何级别腹泻方面的LHH最低(0.42)。阿贝西利在3 - 4级疲劳方面的LHH较低(9.92),在所有3 - 4级AE方面的LHH最高(0.62),而瑞博西尼在3 - 4级肝毒性方面的LHH最低(1.75)。哌柏西利在剂量减少和停药方面的LHH最高(0.65和6.17)。考虑到OS,观察到总体获益(HR 0.788,0.727 - 0.856,P = 0%);瑞博西尼和阿贝西利的NNT较低(9.7和10.0)。瑞博西尼在腹泻(1.29)、疲劳(7.37)、剂量减少(0.28)和停药(2.40)方面显示出最高的LHH,而阿贝西利在中性粒细胞减少(0.40)、FN(12.53)和肝毒性(2.23)方面的LHH最高。
哌柏西利和瑞博西尼在血液学毒性方面显示出较低的LHH,阿贝西利在腹泻方面显示出较低LHH。哌柏西利被证实是一种可管理的药物。当缺乏直接比较时,LHH似乎是一种平衡实验药物风险和获益的可靠综合工具。
无。