Programmed cell death ligand 1 (PD-L1) inhibitors versus programmed cell death 1 (PD-1) inhibitors for the first-line therapy of extensive-stage small cell lung cancer: a propensity score-matched study.
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引用次数: 0
Abstract
Background: The clinical efficacy and safety differences between PD-L1 inhibitors and PD-1 inhibitors remain controversial for ES-SCLC. We conduct the retrospective study and propensity score-matched analysis to explore the potential differences between them.
Methods: This retrospective study analyzed 736 ES-SCLC patients from three centers treated with EP plus either a PD-L1 or PD-1 inhibitor. According to PD-L1 or PD-1 inhibitors, they were divided into two groups. Propensity score matching (PSM, 1:1) was performed to balance the baseline characteristics of the two groups. The primary endpoints were OS and PFS.
Results: As a result, 485 patients received PD-L1 inhibitors plus EP and 251 received PD-1 inhibitors plus EP. Before PSM, the PD-1 inhibitor group showed a significantly longer PFS (8.26 vs. 7.44 months; HR 1.252, p = 0.007), but no significant OS difference (20.30 vs. 18.85 months; p = 0.337). After PSM, both median OS (22.43 vs. 20.69 months) and PFS (8.23 months for both) were comparable, with no statistical differences (OS: HR 0.938, p = 0.613; PFS: HR 1.008, p = 0.940). Safety profiles were similar between groups.
Conclusions: In conclusion, the overall efficacy and safety profile were similar between PD-L1 inhibitors and PD-1 inhibitors for the first-line treatment of ES-SCLC.
背景:PD-L1抑制剂和PD-1抑制剂治疗ES-SCLC的临床疗效和安全性差异仍存在争议。我们通过回顾性研究和倾向评分匹配分析来探讨两者之间的潜在差异。方法:这项回顾性研究分析了来自三个中心的736例ES-SCLC患者,他们接受EP加PD-L1或PD-1抑制剂治疗。根据PD-L1或PD-1抑制剂分为两组。采用倾向评分匹配(PSM, 1:1)来平衡两组的基线特征。主要终点为OS和PFS。结果:485例患者接受PD-L1抑制剂加EP治疗,251例患者接受PD-1抑制剂加EP治疗。PSM前,PD-1抑制剂组PFS明显延长(8.26 vs. 7.44个月;HR 1.252, p = 0.007), OS差异无统计学意义(20.30 vs. 18.85个月;p = 0.337)。PSM后,中位OS(22.43个月vs. 20.69个月)和PFS(8.23个月)具有可比性,无统计学差异(OS: HR 0.938, p = 0.613; PFS: HR 1.008, p = 0.940)。两组之间的安全性相似。结论:总之,PD-L1抑制剂和PD-1抑制剂一线治疗ES-SCLC的总体疗效和安全性相似。
期刊介绍:
Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community.
The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.