Noringriis Inge Mansfield, Donia Marco, Madsen Kasper, Schmidt Henrik, Haslund Charlotte Aaquist, Bastholt Lars, Svane Inge Marie, Ellebaek Eva
National Center for Cancer Immune Therapy (CCIT-DK), Department of Oncology, Copenhagen University Hospital, Herlev, Denmark.
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Br J Cancer. 2025 May 26. doi: 10.1038/s41416-025-03048-8.
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.
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.
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.
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.
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。
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。
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。
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。