Division of Medical Oncology & Hematology, Department of Medicine, Sunnybrook Health Sciences Centre, 2075 Bayview Avenue, Toronto, ON M4N 3M5, Canada.
Faculty of Medicine, University of Toronto, 27 King's College Circle, Toronto, ON M5S 1A1, Canada.
Future Oncol. 2024;20(36):2879-2888. doi: 10.1080/14796694.2024.2342224. Epub 2024 May 29.
Despite the demonstrated efficacy of pembrolizumab in KEYNOTE-024, effectiveness and safety in routine practice remain unclear. The authors identified first-line pembrolizumab or chemotherapy patients from April 2013 to March 2021. The primary outcome was overall survival; the secondary safety outcomes included rates of hospitalization, emergency department visits, specialist visits, and adverse events. Baseline differences were adjusted using propensity score matching (1:1). The matched cohort included 2284 pairs. Median overall survival for pembrolizumab (13.0 months) was significantly longer than for chemotherapy (9.2 months), with a hazard ratio of 0.81 (95% CI: 0.71-0.92). Pembrolizumab patients reported significantly more adverse events and specialist visits, as well as a higher 1-year cumulative incidence of direct hospitalizations. The survival benefit of first-line pembrolizumab persists in the real world, although with increased toxicity and diminished benefit.
尽管 KEYNOTE-024 已证实 pembrolizumab 的疗效,但在常规实践中的有效性和安全性仍不清楚。作者从 2013 年 4 月至 2021 年 3 月确定了一线 pembrolizumab 或化疗患者。主要结局是总生存期;次要安全性结局包括住院率、急诊就诊率、专科就诊率和不良事件发生率。使用倾向评分匹配(1:1)调整基线差异。匹配队列包括 2284 对。pembrolizumab(13.0 个月)的中位总生存期明显长于化疗(9.2 个月),风险比为 0.81(95%CI:0.71-0.92)。pembrolizumab 患者报告的不良事件和专科就诊明显更多,直接住院的 1 年累积发生率也更高。在现实世界中,一线 pembrolizumab 的生存获益仍然存在,但毒性增加,获益减少。