Ribociclib plus fulvestrant for advanced breast cancer: Health-related quality-of-life analyses from the MONALEESA-3 study

被引:30
作者
Fasching, Peter A. [1 ]
Beck, J. Thaddeus [2 ]
Chan, Arlene [3 ]
De Laurentiis, Michele [4 ]
Esteva, Francisco J. [5 ]
Jerusalem, Guy [6 ]
Neven, Patrick [7 ]
Pivot, Xavier [8 ]
Bianchi, Giulia V. [9 ]
Martin, Miguel [10 ]
Chandiwana, David [11 ]
Lanoue, Brad [11 ]
Ridol, Antonia [12 ]
Wang, Yingbo [13 ]
Lorenc, Karen Rodriguez [11 ]
Nusch, Arnd [14 ]
机构
[1] Friedrich Alexander Univ Erlangen Nuremberg, Univ Hosp Erlangen, Dept Gynecol & Obstet, Comprehens Canc Ctr Erlangen EMN, Erlangen, Germany
[2] Highlands Oncol Grp, Fayetteville, AR USA
[3] Breast Canc Res Ctr Western Australia, Nedlands, WA, Australia
[4] IRCCS Fdn G Pascale, Ist Nazl Tumori, Naples, Italy
[5] NYU Langone Hlth, New York, NY USA
[6] Univ Liege, CHU Liege, Liege, Belgium
[7] Univ Ziekenhuis Leuven, Multidisciplinary Breast Ctr, Leuven, Belgium
[8] Inst Reg Canc, Strasbourg, France
[9] Fdn IRCCS, Ist Nazl Tumori, Milan, Italy
[10] Univ Complutense Madrid, Inst Invest Sanitaria Gregorio Maranon, Ciberonc Geicam, Madrid, Spain
[11] Novartis Pharmaceut, E Hanover, NJ USA
[12] Novartis Pharma SAS, Rueil Malmaison, France
[13] Novartis Pharma AG, Basel, Switzerland
[14] Practice Haematol & Internal Oncol, Velbert, Germany
关键词
Breast cancer; Metastatic; Patient-reported outcomes; Quality of life;
D O I
10.1016/j.breast.2020.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: In the MONALEESA-3 Phase III trial of patients with hormone receptor-positive human epidermal growth factor receptor-negative advanced breast cancer, ribociclib plus fulvestrant significantly improved progression-free survival (PFS) and overall survival (OS). Here, we present patient-reported outcomes from the trial, including health-related quality of life (HRQOL). Methods: Patients were randomized (2:1) to receive ribociclib plus fulvestrant or placebo plus fulvestrant. Time to definitive 10% deterioration (TTD) from baseline in HRQOL (global health status [GHS] from the EORTC QLQ-C30 questionnaire) and pain (BPI-SF questionnaire) were assessed using Kaplan-Meier estimates; a stratified Cox regression model was used to estimate the hazard ratio (HR) and 95% CIs. Results: Deterioration >= 10% in the EORTC-QLQ-C30 GHS was observed in 33% of patients in the ribociclib group vs 34% of patients in the placebo (reference) group (HR for TTD >= 10% = 0.81 [95% CI, 0.62-1.1]). Similar findings were noted for TTD >= 5% (HR = 0.79 [95% CI, 0.61-1.0]) and TTD >= 15% (HR = 0.81 [95% CI, 0.60-1.08]). TTD >= 10% in emotional functioning (HR = 0.76 [95% CI, 0.57-1.01]) trended in favor of the ribociclib group, whereas results for fatigue and pain were similar between arms. TTD >= 10% in BPI-SF pain severity index score (HR = 0.77 [95% CI, 0.57-1.05]) and worst pain item score (HR = 0.81 [95% CI, 0.58-1.12]) trended in favor of ribociclib vs placebo. Conclusions: In addition to significantly prolonging PFS and OS compared with placebo plus fulvestrant, adding ribociclib to fulvestrant maintains HRQOL. (C) 2020 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:148 / 154
页数:7
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