Suppr超能文献

在 III 期随机临床试验中,brigatinib 对比crizotinib 治疗初治晚期 ALK 阳性非小细胞肺癌(ALTA-1L)患者的健康相关生活质量。

Health-related quality of life in the randomized phase III trial of brigatinib vs crizotinib in advanced ALK inhibitor-naive ALK + non-small cell lung cancer (ALTA-1L).

机构信息

Medical Oncology Service, University Hospital A Coruña (XXIAC-SERGAS), Xubias de Arriba, 84, 15006, A Coruña, Spain.

Millennium Pharmaceuticals, Inc, 35 Landsdowne Street, Cambridge, MA, 02139, USA(3).

出版信息

Lung Cancer. 2021 May;155:68-77. doi: 10.1016/j.lungcan.2021.03.005. Epub 2021 Mar 9.

Abstract

OBJECTIVE

In ALTA-1 L, first-line brigatinib versus crizotinib significantly prolonged progression-free survival in advanced ALK-positive (ALK+) non-small cell lung cancer (NSCLC). We report health-related quality of life (HRQOL) outcomes from ALTA-1 L.

MATERIALS AND METHODS

HRQOL was assessed using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) and lung cancer-specific module (QLQ-LC13). HRQOL time to worsening, change from baseline, and duration of improvement were analyzed.

RESULTS

EORTC QLQ-C30 and QLQ-LC13 compliance was >90 % for both groups (n = 131 each). Brigatinib versus crizotinib significantly delayed time to worsening in the EORTC QLQ-C30 global health status (GHS)/QOL (median: 26.74 vs 8.31 months; hazard ratio [HR]: 0.70; 95 % CI: 0.49, 1.00; log-rank P = 0.0485); emotional functioning, social functioning, fatigue, nausea and vomiting, appetite loss, and constipation scales (log-rank P < 0.05); delays in time to worsening for the physical, role, and cognitive functioning scales were not statistically significant. Mean change from baseline showed greater improvement in GHS/QOL and most EORTC QLQ-C30 functional and symptom scales with brigatinib versus crizotinib. Among patients with GHS/QOL improvement, brigatinib had longer duration of improvement versus crizotinib (median: not reached vs 11.99 months); similar results were seen in the physical, role, emotional, and social functioning; fatigue; nausea and vomiting; and appetite loss scales. Median time to worsening in dyspnea (QLQ-LC13) was 23.98 versus 8.25 months (brigatinib vs crizotinib; HR: 0.64; 95 % CI: 0.39, 1.05).

CONCLUSION

Brigatinib significantly delayed time to worsening and prolonged duration of improvement in GHS/QOL versus crizotinib, supported by improvement in functional and symptom scores. These preliminary analyses suggest brigatinib is the first ALK inhibitor with better HRQOL versus another ALK inhibitor in ALK inhibitor-naive advanced ALK + NSCLC.

摘要

目的

在 ALTA-1L 研究中,一线布加替尼对比克唑替尼显著延长了晚期 ALK 阳性(ALK+)非小细胞肺癌(NSCLC)患者的无进展生存期。我们报告了来自 ALTA-1L 的健康相关生活质量(HRQOL)结果。

材料和方法

使用欧洲癌症研究和治疗组织生活质量问卷核心 30 项(EORTC QLQ-C30)和肺癌专用模块(QLQ-LC13)评估 HRQOL。分析 HRQOL 恶化时间、自基线变化和改善持续时间。

结果

两组 EORTC QLQ-C30 和 QLQ-LC13 的依从性均>90%(n=131 例)。与克唑替尼相比,布加替尼显著延迟了 EORTC QLQ-C30 全球健康状况/生活质量(GHS/QOL)恶化时间(中位数:26.74 个月 vs 8.31 个月;风险比[HR]:0.70;95%置信区间[CI]:0.49,1.00;对数秩 P=0.0485);情绪功能、社会功能、疲劳、恶心和呕吐、食欲丧失和便秘量表(对数秩 P<0.05);身体功能、角色功能和认知功能量表的恶化时间延迟无统计学意义。与克唑替尼相比,布加替尼的 GHS/QOL 和大多数 EORTC QLQ-C30 功能和症状量表的自基线变化显示出更大的改善。在 GHS/QOL 改善的患者中,与克唑替尼相比,布加替尼的改善持续时间更长(中位数:未达到 vs 11.99 个月);在身体功能、角色功能、情绪功能和社会功能、疲劳、恶心和呕吐以及食欲丧失方面也观察到了相似的结果。呼吸困难(QLQ-LC13)恶化的中位时间为 23.98 个月 vs 8.25 个月(布加替尼 vs 克唑替尼;HR:0.64;95%CI:0.39,1.05)。

结论

与克唑替尼相比,布加替尼显著延迟了 GHS/QOL 恶化时间,并延长了 GHS/QOL 改善的持续时间,这得益于功能和症状评分的改善。这些初步分析表明,在ALK 抑制剂初治的晚期ALK+NSCLC 患者中,布加替尼是首个在 HRQOL 方面优于其他 ALK 抑制剂的 ALK 抑制剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验