Final Results from RIBBIT: A Randomized Phase III Study to Evaluate Efficacy and Quality of Life in Patients with Metastatic Hormone Receptor-Positive, HER2-Negative Breast Cancer Receiving Ribociclib in Combination with Endocrine Therapy or Chemotherapy with or without Bevacizumab in the First-Line Setting.

IF 2 4区 医学 Q2 OBSTETRICS & GYNECOLOGY
Breast Care Pub Date : 2024-02-01 Epub Date: 2023-12-20 DOI:10.1159/000535135
Thomas Decker, Matthias Zaiss, Dunja Klein, Antje Hahn, Volker Hagen, Paul La Rosée, Rüdiger Liersch, Thomas Wolff, Beate Niemeier, Larissa E Hillebrand, Carolin Lennartz, Marco Chiabudini, Fee Bengsch, Martin Indorf, Norbert Marschner
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引用次数: 0

Abstract

Background: We investigated the efficacy and health-related quality of life (HRQoL) in patients receiving either ribociclib plus endocrine therapy (ET) or chemotherapy with/without bevacizumab as first-line treatment of metastatic hormone receptor (HR)-positive, HER2-negative breast cancer (BC).

Patients and methods: In this randomized, phase III study (RIBBIT), 38 patients diagnosed with metastatic HR-positive, HER2-negative BC with presence of visceral metastases recruited between May 2018 and December 2020 were randomly assigned in a 1:1 ratio to either arm A (ribociclib + ET) or arm B (chemotherapy with/without bevacizumab) at 12 sites in Germany. The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall response rate (ORR), overall survival (OS), patient-reported HRQoL, and frequency and type of adverse events. During study conduction, the recruitment rate was persistently and considerably lower than originally expected. Therefore, the recruitment was ended prematurely. The study was initially designed to enroll and randomize 158 patients.

Results: Median [95% CI] PFS was 27.3 months [19.1 - NA, parameter not estimable] in arm A and 15.8 months [8.2 - NA] in arm B. Complete responses were achieved only in arm A (n = 2, 10.5%). The ORR [95% CI] between arm A (57.9% [33.5-79.7]) and arm B (52.6% [28.9-75.6]) was comparable. Median OS [95% CI] was not reached in arm A, while in arm B median OS was 28.4 months [25.0 - NA]. Patients in arm A reported less burden by side-effects. No new safety signals emerged.

Conclusion: Treatment of patients with visceral metastatic HR-positive, HER2-negative BC with ribociclib in combination with ET showed a tendency toward a more favorable clinical outcome. Despite small numbers of patients and sites, this head-to-head comparison with chemotherapy supports the use of ribociclib with ET in patients with visceral metastasis at risk of fast disease progression.

RIBBIT:评估转移性激素受体阳性、HER2 阴性乳腺癌患者接受 Ribociclib 联合内分泌治疗或化疗联合或不联合贝伐珠单抗一线治疗的疗效和生活质量的随机 III 期研究的最终结果。
研究背景我们研究了接受利博昔单抗联合内分泌治疗(ET)或化疗联合/不联合贝伐单抗作为转移性激素受体(HR)阳性、HER2阴性乳腺癌(BC)一线治疗的患者的疗效和健康相关生活质量(HRQoL):在这项随机III期研究(RIBBIT)中,2018年5月至2020年12月期间招募的38名确诊为转移性HR阳性、HER2阴性BC且存在内脏转移灶的患者按1:1的比例随机分配到德国12个地点的A组(ribociclib + ET)或B组(化疗联合/不联合贝伐单抗)。主要终点是无进展生存期(PFS)。次要终点包括总反应率(ORR)、总生存期(OS)、患者报告的 HRQoL 以及不良事件的频率和类型。在研究进行期间,招募率持续大幅低于最初预期。因此,招募工作提前结束。该研究最初设计招募并随机分配 158 名患者:A组的中位[95% CI]PFS为27.3个月[19.1 - NA,参数无法估计],B组为15.8个月[8.2 - NA]。A组(57.9% [33.5-79.7])和B组(52.6% [28.9-75.6])的ORR [95% CI]相当。A 组未达到中位 OS [95% CI],而 B 组的中位 OS 为 28.4 个月 [25.0 - NA]。A组患者的副作用较少。没有出现新的安全信号:结论:对于内脏转移性HR阳性、HER2阴性BC患者,使用ribociclib联合ET治疗可获得更有利的临床结果。尽管患者人数和部位较少,但这项与化疗的头对头比较结果支持在有疾病快速进展风险的内脏转移患者中使用ribociclib联合ET。
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
Breast Care
Breast Care 医学-妇产科学
CiteScore
4.40
自引率
4.80%
发文量
45
审稿时长
6-12 weeks
期刊介绍: ''Breast Care'' is a peer-reviewed scientific journal that covers all aspects of breast biology. Due to its interdisciplinary perspective, it encompasses articles on basic research, prevention, diagnosis, and treatment of malignant diseases of the breast. In addition to presenting current developments in clinical research, the scope of clinical practice is broadened by including articles on relevant legal, financial and economic issues.
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