在切除的 III 期黑色素瘤(EORTC 1325-MG/KEYNOTE-054)中使用 pembrolizumab 与安慰剂的辅助治疗:一项双盲、随机对照 3 期试验的长期健康相关生活质量结果。

IF 41.6 1区 医学 Q1 ONCOLOGY
Lancet Oncology Pub Date : 2024-09-01 Epub Date: 2024-08-12 DOI:10.1016/S1470-2045(24)00338-3
Emanuel Bührer, Michal Kicinski, Mario Mandala, Madeline Pe, Georgina V Long, Victoria Atkinson, Christian U Blank, Andrew Haydon, Stéphane Dalle, Adnan Khattak, Matteo S Carlino, Andrey Meshcheryakov, Shahneen Sandhu, Susana Puig, Dirk Schadendorf, Rahima Jamal, Piotr Rutkowski, Alfonsus J M van den Eertwegh, Corneel Coens, Dmitri Grebennik, Clemens Krepler, Caroline Robert, Alexander M M Eggermont
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引用次数: 0

摘要

研究背景在欧洲癌症研究和治疗组织(EORTC)的1325-MG/KEYNOTE-054研究中,辅助治疗pembrolizumab提高了切除的III期黑色素瘤患者的无复发生存率和无远处转移生存率。早期结果显示,pembrolizumab 对健康相关生活质量(HRQOL)没有影响。人们对pembrolizumab治疗结束后的HRQOL知之甚少,而这是涉及可能成为长期幸存者的患者的一个重要研究领域。本研究报告了长期的 HRQOL 结果:这项双盲、随机、对照、3 期试验比较了 pembrolizumab 与安慰剂的辅助治疗效果,受试者年龄在 18 岁或以上,患有既往未治疗过的 IIIA、IIIB 或 IIIC 期切除皮肤黑色素瘤,且东部合作肿瘤学组表现状态评分为 1 分或 0 分,受试者来自 23 个国家的 123 个学术中心和社区医院。采用最小化技术对患者进行随机分配(1:1),根据分期和地理区域进行分层,每3周一次静脉注射200毫克pembrolizumab或安慰剂,最多18次。研究人员、患者、数据收集或分析人员均被蒙蔽,不知道分组情况。试验的主要终点是无复发生存期(在别处报告)。HRQOL是预设的探索性终点,采用EORTC生活质量问卷-核心30进行测量。所有接受过基线 HRQOL 评估且在随机分组后 108 周内存活的患者均被纳入长期 HRQOL 分析。长期 HRQOL 包括随机分组后 108 周至 48 个月期间每 6 个月进行的评估。所有 HRQOL 量表的临床相关性阈值为平均变化 5 分。试验正在进行中,招募工作已经完成,HRQOL 数据收集工作也已完成。该研究已在ClinicalTrials.gov(NCT02362594)和EudraCT(2014-004944-37)上注册:2015年8月26日至2016年11月14日期间,1019名患者被随机分配至pembrolizumab(n=514)或安慰剂(n=505)。基线HRQOL评估的完成率超过90%(pembrolizumab组有481名[94%]患者,安慰剂组有467名[92%]患者),基线后时间点的完成率在60%至90%之间。在进行了基线 HRQOL 评估的患者中,365 人(39%)为女性,583 人(61%)为男性。从基线到长期HRQOL的平均变化,pembrolizumab组为-0-56(95% CI -2-33至1-22),安慰剂组为1-63(-0-12至3-38)。两组之间的差异为-2-19(-4-65 至 0-27,P=0-081)。所有其他量表的差异均小于5,无统计学意义:与安慰剂相比,辅助治疗的pembrolizumab对切除的III期黑色素瘤患者的长期HRQOL没有显著影响。这些研究结果以及之前的疗效和HRQOL结果都支持在这种情况下使用pembrolizumab:默沙东公司。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adjuvant pembrolizumab versus placebo in resected stage III melanoma (EORTC 1325-MG/KEYNOTE-054): long-term, health-related quality-of-life results from a double-blind, randomised, controlled, phase 3 trial.

Background: In the European Organisation for Research and Treatment of Cancer (EORTC) 1325-MG/KEYNOTE-054 study, adjuvant pembrolizumab improved recurrence-free survival and distant-metastasis-free survival in patients with resected stage III melanoma. Earlier results showed no effect of pembrolizumab on health-related quality of life (HRQOL). Little is known about HRQOL after completion of treatment with pembrolizumab, an important research area concerning patients who are likely to become long-term survivors. This study reports long-term HRQOL results.

Methods: This double-blind, randomised, controlled, phase 3 trial compared adjuvant pembrolizumab with placebo in patients aged 18 years or older with previously untreated stage IIIA, IIIB, or IIIC resected cutaneous melanoma and an Eastern Cooperative Oncology Group performance status score of 1 or 0, recruited from 123 academic centres and community hospitals in 23 countries. Patients were randomly assigned (1:1) with a minimisation technique stratified for stage and geographical region to receive 200 mg of intravenous pembrolizumab or placebo every 3 weeks for up to 18 doses. Investigators, patients, and those collecting or analysing data were masked to group assignment. The primary endpoint of the trial was recurrence-free survival (reported elsewhere). HRQOL was a prespecified exploratory endpoint, measured with the EORTC Quality of Life Questionnaire-Core 30. All patients with a baseline HRQOL evaluation available who were alive 108 weeks from randomisation were included in this analysis of long-term HRQOL. Long-term HRQOL included assessments measured every 6 months between 108 weeks and 48 months after randomisation. The threshold of clinical relevance for all HRQOL scales used was an average change of 5 points. The trial is ongoing, recruitment is completed, and HRQOL data collection is finalised. This study is registered with ClinicalTrials.gov, NCT02362594, and EudraCT, 2014-004944-37.

Findings: Between Aug 26, 2015, and Nov 14, 2016, 1019 patients were randomly assigned to pembrolizumab (n=514) or placebo (n=505). Completion of the HRQOL evaluation at baseline exceeded 90% (481 [94%] patients in the pembrolizumab group and 467 [92%] in the placebo group), and ranged between 60% and 90% for post-baseline timepoints. Among patients with a baseline HRQOL evaluation, 365 (39%) were female and 583 (61%) were male. The mean change from baseline to long-term HRQOL was -0·56 (95% CI -2·33 to 1·22) in the pembrolizumab group and 1·63 (-0·12 to 3·38) in the placebo group. The difference between the two groups was -2·19 (-4·65 to 0·27, p=0·081). Differences for all other scales were smaller than 5 and not statistically significant.

Interpretation: Adjuvant pembrolizumab did not have a significant impact on long-term HRQOL compared with placebo in patients with resected stage III melanoma. These findings, together with earlier results on efficacy and HRQOL, support the use of pembrolizumab in this setting.

Funding: Merck Sharp & Dohme.

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来源期刊
Lancet Oncology
Lancet Oncology 医学-肿瘤学
CiteScore
62.10
自引率
1.00%
发文量
913
审稿时长
3-8 weeks
期刊介绍: The Lancet Oncology is a trusted international journal that addresses various topics in clinical practice, health policy, and global oncology. It covers a wide range of cancer types, including breast, endocrine system, gastrointestinal, genitourinary, gynaecological, haematological, head and neck, neurooncology, paediatric, thoracic, sarcoma, and skin cancers. Additionally, it includes articles on epidemiology, cancer prevention and control, supportive care, imaging, and health-care systems. The journal has an Impact Factor of 51.1, making it the leading clinical oncology research journal worldwide. It publishes different types of articles, such as Articles, Reviews, Policy Reviews, Personal Views, Clinical Pictures, Comments, Correspondence, News, and Perspectives. The Lancet Oncology also collaborates with societies, governments, NGOs, and academic centers to publish Series and Commissions that aim to drive positive changes in clinical practice and health policy in areas of global oncology that require attention.
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