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帕博利珠单抗抗程序性死亡受体-1(PD-1)检查点抑制剂免疫治疗期间出现转移黑色素瘤且初始病情稳定患者的长期临床结局

Long-term clinical outcome of patients with metastatic melanoma and initial stable disease during anti-PD-1 checkpoint inhibitor immunotherapy with pembrolizumab.

作者信息

Noringriis Inge Mansfield, Donia Marco, Madsen Kasper, Schmidt Henrik, Haslund Charlotte Aaquist, Bastholt Lars, Svane Inge Marie, Ellebaek Eva

机构信息

National Center for Cancer Immune Therapy (CCIT-DK), Department of Oncology, Copenhagen University Hospital, Herlev, Denmark.

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Br J Cancer. 2025 May 26. doi: 10.1038/s41416-025-03048-8.

Abstract

BACKGROUND

A substantial number of patients with metastatic melanoma (MM) treated with anti-PD-1 monotherapy have initial stable disease (SD), yet the real-world prognosis of these patients remains unclear.

METHODS

In this nationwide cohort study, we analysed real-world outcomes of patients with MM treated with pembrolizumab in Denmark. Focusing on patients with initial SD, we assessed best overall response (BOR), progression-free survival (PFS), and overall survival (OS) and identified predictors of survival in multivariable analyses.

RESULTS

Out of 1048 included patients, 233 (22.2%) had initial SD with a median PFS and OS of 14.7 and 50.1 months. Subsequent partial response (PR) or complete response (CR) was developed by 44 (18.9%) and 52 (22.3%) patients showing significantly improved PFS compared to patients with continued SD (PR: HR 0.52, 95% CI 0.34-0.81, p = 0.003; CR: HR 0.15, 95% CI 0.07-0.32, p < 0.001) and survival rates comparable to patients with initial PR and CR, respectively. Furthermore, 49 (21.0%) patients showed continued disease control (median follow-up of 82.3 months). For 51.0% of these patients, the last dose of pembrolizumab was administered during SD with a median treatment duration of 12.4 months.

CONCLUSIONS

Of patients with initial SD, 40% developed a subsequent objective response with improved long-term prognosis comparable to patients with initial response. More than 20% exhibited continued disease control.

摘要

背景

大量接受抗程序性死亡蛋白1(PD-1)单药治疗的转移性黑色素瘤(MM)患者最初病情稳定(SD),但这些患者的真实世界预后仍不清楚。

方法

在这项全国性队列研究中,我们分析了丹麦接受帕博利珠单抗治疗的MM患者的真实世界结局。聚焦于最初病情稳定的患者,我们评估了最佳总体缓解(BOR)、无进展生存期(PFS)和总生存期(OS),并在多变量分析中确定了生存预测因素。

结果

在纳入的1048例患者中,233例(22.2%)最初病情稳定,中位PFS和OS分别为14.7个月和50.1个月。44例(18.9%)患者随后出现部分缓解(PR)或完全缓解(CR),与病情持续稳定的患者相比,PFS显著改善(PR:风险比[HR]0.52,95%置信区间[CI]0.34-0.81,p = 0.003;CR:HR 0.15,95% CI 0.07-0.32,p < 0.001),生存率分别与最初PR和CR的患者相当。此外,49例(21.0%)患者病情持续得到控制(中位随访82.3个月)。在这些患者中,51.0%在病情稳定期间接受了最后一剂帕博利珠单抗,中位治疗持续时间为12.4个月。

结论

在最初病情稳定的患者中,40%随后出现客观缓解,长期预后改善,与最初缓解的患者相当。超过20%的患者病情持续得到控制。

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