CHU Liège and University of Liège, Liège, Belgium.
Policy Analysis Inc (PAI), Brookline, Massachusetts.
Clin Breast Cancer. 2022 Jun;22(4):326-335. doi: 10.1016/j.clbc.2021.12.008. Epub 2021 Dec 20.
MONALEESA-3 demonstrated an overall survival (OS) benefit for ribociclib plus fulvestrant (R+F) in postmenopausal women with hormone receptor (HR) positive, HER2 negative advanced breast cancer (ABC). This study estimated quality-adjusted (QA) survival outcomes for patients receiving R+F vs. placebo (P)+F in MONALEESA-3.
Kaplan-Meier OS was partitioned into health states: (1) toxicity (TOX)=time spent with grade 3 -4 adverse events before progression (DP); (2) progression (PROG)=time between DP and death; and (3) time without symptoms or toxicity (TWiST)=time not in TOX or PROG. QA time was calculated by combining estimated mean time in each health state with treatment-group specific health-state utility values estimated using EQ-5D-5L questionnaire. Outcomes included QA progression-free survival (QAPFS), QAOS, and QA TWiST (Q-TWiST). Q-TWiST was calculated with health-state utility values for TOX and PROG defined relative to TWiST.
Mean PFS and OS were significantly greater with R+F vs. P+F (difference 0.56 and 0.19 years). Mean time in TOX and TWiST were greater with R+F; mean time in PROG was greater with P+F. QAPFS was 0.45 years (95% CI 0.27 -0.63) greater with R+F than P+F (P <.001). QAOS was numerically greater with R+F vs. P+F (0.16 years, 95% CI 0.07 -0.45, P = .0569). Q-TWiST was 0.23 years greater with R+F (95% CI 0.07 -0.45, P = .0069). In a sensitivity analysis using an estimate of disutility for PROG, the difference in QAOS was 0.23 years (95% CI 0.08 -0.41, P = .0022).
R+F in postmenopausal women with HR+/HER2- ABC improves QAPFS, resulting in clinically important improvements in Q-TWiST and may improve QAOS.
MONALEESA-3 研究表明,对于激素受体(HR)阳性、HER2 阴性的晚期乳腺癌(ABC)患者,接受瑞博西利联合氟维司群(R+F)治疗比安慰剂联合氟维司群(P+F)能显著改善总生存(OS)。本研究旨在评估 MONALEESA-3 中 R+F 组与 P+F 组患者的质量调整生存(QA)结局。
使用 Kaplan-Meier 法将 OS 分为以下健康状态:(1)毒性(TOX)=进展前(DP)出现 3-4 级不良事件的时间;(2)进展(PROG)=DP 至死亡的时间;(3)无症状或无毒性时间(TWiST)=未处于 TOX 或 PROG 的时间。QA 时间通过将每个健康状态的估计平均时间与使用 EQ-5D-5L 问卷估计的治疗组特定健康状态效用值相结合计算得出。结果包括 QA 无进展生存期(QAPFS)、QAOS 和 QA TWiST(Q-TWiST)。Q-TWiST 根据相对于 TWiST 的 TOX 和 PROG 的健康状态效用值定义。
与 P+F 相比,R+F 组的中位 PFS 和 OS 显著延长(差异为 0.56 年和 0.19 年)。R+F 组的 TOX 和 TWiST 时间更长,P+F 组的 PROG 时间更长。R+F 组的 QAPFS 比 P+F 组延长 0.45 年(95%CI 0.27-0.63)(P<0.001)。R+F 组的 QAOS 比 P+F 组延长 0.16 年(95%CI 0.07-0.45,P=0.0569),但差异无统计学意义。R+F 组的 Q-TWiST 比 P+F 组延长 0.23 年(95%CI 0.07-0.45,P=0.0069)。在使用 PROG 失能估计值的敏感性分析中,QAOS 的差异为 0.23 年(95%CI 0.08-0.41,P=0.0022)。
对于 HR+/HER2-ABC 绝经后女性,R+F 可改善 QAPFS,从而显著改善 Q-TWiST,并可能改善 QAOS。