在高级非小细胞肺癌中,每6周服用布罗利祖马布,而每3周服用布罗利祖马布
Maude Dubé-Pelletier1, Catherine Labbé1, Jimmy Côté1
1Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval, Québec, Canada.
The oncologist
|June 26, 2023
概括
与每3周一次 (Q3W) 治疗方案相比,每6周一次 (Q6W) 布洛利祖马布的整体存活率,无进展存活率和毒性与晚期非小细胞肺癌 (NSCLC) 患者相似.
科学领域:
- 在瘤学瘤学.
- 药理学 药理学是指药理学的学科.
- 临床试验 临床试验
背景情况:
- 布罗利祖马布是高级非小细胞肺癌 (NSCLC) 的关键免疫疗法.
- 已确定的剂量包括每3周 (Q3W) 服用2mg/kg.
- 另一个4mg/kg每6周 (Q6W) 方案被批准,但缺乏NSCLC的直接比较数据.
研究的目的:
- 直接比较pembrolizumab Q6W与Q3W在高级NSCLC中的疗效和安全性.
- 评估总生存 (OS) 和无进展生存 (PFS) 的差异.
- 评估免疫媒介不良事件 (AE) 的发生和严重程度.
主要方法:
- 在IUCPQ对160名晚期NSCLC患者的回顾性分析.
- 80名患者接受了潘布罗利祖马布4毫克/公斤Q6W; 80名患者接受了2毫克/公斤Q3W.
- 主要结局:OS,PFS和等级≥3的免疫媒介性AE. 数据截止日期:2022年12月15日.
主要成果:
- 平均PFS:6.9个月 (Q6W) 与8.9个月 (Q3W) (aHR为1.27,P=.25) 相比.
- 中位 OS:未达到 (Q6W) 与20.5个月 (Q3W) (aHR 0.80,P=.36) 相比.
- 免疫介导的AEs等级≥3:18% (Q6W) 与19% (Q3W) 相比.
结论:
- 潘布罗利祖马布Q6W剂量方案与晚期NSCLC中的Q3W方案相似.
- 两种剂量表之间没有观察到OS,PFS或毒性的显著差异.
- 这项回顾性研究支持Q6W疗法作为先进NSCLC治疗的可行替代方案.
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