聚乙二醇伊立替康与医生选择的治疗方案相比,用于治疗局部复发或转移性乳腺癌患者的健康相关生活质量:III期随机BEACON试验结果
Health-related quality of life in patients with locally recurrent or metastatic breast cancer treated with etirinotecan pegol versus treatment of physician's choice: Results from the randomised phase III BEACON trial.
作者信息
Twelves Chris, Cortés Javier, O'Shaughnessy Joyce, Awada Ahmad, Perez Edith A, Im Seock-Ah, Gómez-Pardo Patricia, Schwartzberg Lee S, Diéras Véronique, Yardley Denise A, Potter David A, Mailliez Audrey, Moreno-Aspitia Alvaro, Ahn Jin-Seok, Zhao Carol, Hoch Ute, Tagliaferri Mary, Hannah Alison L, Rugo Hope S
机构信息
Leeds Institute of Cancer and Pathology and St James's Institute of Oncology, Leeds, UK.
Ramon y Cajal University Hospital, Madrid, Spain; Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
出版信息
Eur J Cancer. 2017 May;76:205-215. doi: 10.1016/j.ejca.2017.02.011. Epub 2017 Mar 27.
BACKGROUND
Health-related quality of life (HRQoL) enhances understanding of treatment effects that impact clinical decision-making. Although the primary end-point was not achieved, the BEACON (BrEAst Cancer Outcomes with NKTR-102) trial established etirinotecan pegol, a long-acting topoisomerase-1 (TOP1) inhibitor, as a promising therapeutic for patients with advanced/metastatic breast cancer (MBC) achieving clinically meaningful benefits in median overall survival (OS) for patients with stable brain metastases, with liver metastases or ≥ 2 sites of metastatic disease compared to treatment of physician's choice (TPC). Reported herein are the findings from the preplanned secondary end-point of HRQoL.
PATIENTS AND METHODS
HRQoL, assessed by European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Core 30 (QLQ-C30) (version 3.0) supplemented by the breast cancer-specific Quality of Life Questionnaire (QLQ-BR23), was evaluated post randomisation in 733 of 852 patients with either anthracycline-, taxane- and capecitabine-pretreated locally recurrent or MBC randomised to etirinotecan pegol (n = 378; 145 mg/m every 3 weeks (q3wk)) or single-agent TPC (n = 355). Patients completed assessments at screening, every 8 weeks (q8wk) during treatment, and end-of-treatment. Changes from baseline were analysed, and the proportions of patients achieving differences (≥5 points) in HRQoL scores were compared.
RESULTS
Differences were seen favouring etirinotecan pegol up to 32 weeks for global health status (GHS) and physical functioning scales (P < 0.02); numerical improvement was reported in other functional scales. The findings from HRQoL symptom scales were consistent with adverse event profiles; etirinotecan pegol was associated with worsening gastrointestinal symptoms whereas TPC was associated with worsened dyspnoea and other systemic side-effects. Analysis of GHS and physical functioning at disease progression showed a decline in HRQoL in both treatment arms, with a mean change from baseline of -9.4 and -10.8 points, respectively.
CONCLUSION
There was evidence of benefit associated with etirinotecan pegol compared with current standard of care agents in multiple HRQoL measurements, including global health status and physical functioning, despite worse gastrointestinal symptoms (e.g. diarrhoea). Patients in both arms had a decline in HRQoL at disease progression.
STUDY NUMBER
NCT01492101.
背景
健康相关生活质量(HRQoL)有助于加深对影响临床决策的治疗效果的理解。尽管未达到主要终点,但BEACON(NKTR - 102治疗乳腺癌结局)试验确立了聚乙二醇依立替康(一种长效拓扑异构酶-1(TOP1)抑制剂)作为晚期/转移性乳腺癌(MBC)患者的一种有前景的治疗方法,与医生选择的治疗方案(TPC)相比,在脑转移稳定、有肝转移或≥2个转移病灶部位的患者的中位总生存期(OS)方面具有临床意义的获益。本文报告的是HRQoL预先计划的次要终点的研究结果。
患者与方法
通过欧洲癌症研究与治疗组织(EORTC)生活质量核心问卷30(QLQ - C30)(第3.0版)并辅以乳腺癌特异性生活质量问卷(QLQ - BR23)评估HRQoL,在852例接受过蒽环类、紫杉烷类和卡培他滨预处理的局部复发或MBC患者中,随机分为聚乙二醇依立替康组(n = 378;每3周145 mg/m²(q3wk))或单药TPC组(n = 355),对其中733例患者在随机分组后进行了评估。患者在筛查时、治疗期间每8周(q8wk)以及治疗结束时完成评估。分析与基线相比的变化,并比较HRQoL评分有差异(≥5分)的患者比例。
结果
在长达32周的时间里,全球健康状况(GHS)和身体功能量表方面可见聚乙二醇依立替康更具优势(P < 0.02);其他功能量表也有数值上的改善。HRQoL症状量表的结果与不良事件情况一致;聚乙二醇依立替康与胃肠道症状加重相关,而TPC与呼吸困难加重及其他全身副作用相关。疾病进展时GHS和身体功能的分析显示,两个治疗组的HRQoL均下降,与基线相比的平均变化分别为-9.4分和-10.8分。
结论
尽管胃肠道症状(如腹泻)更严重,但在包括全球健康状况和身体功能在内的多项HRQoL测量中,有证据表明聚乙二醇依立替康与当前标准治疗药物相比具有获益。两个治疗组的患者在疾病进展时HRQoL均下降。
研究编号
NCT01492101。