Altomare Nicole J, Li Yutai, Neill Clayton, Hussain Maha, VanderWeele David J
Department of Medicine, Northwestern University, Chicago, IL 60611, United States.
Department of Urology, Northwestern University, Chicago, IL 60611, United States.
Oncologist. 2025 Mar 10;30(3). doi: 10.1093/oncolo/oyaf025.
Checkpoint inhibitors targeting PD-1/PD-L1, such as pembrolizumab, can be effective in a small population of biomarker-selected patients with metastatic prostate cancer (mPC), as has been demonstrated by small case series. The objective of this study is to help identify which biomarker-selected patients are most likely to benefit from pembrolizumab and estimate their likelihood of response. This is a single-center study in which we analyzed clinical data of 18 patients with mPC who were treated with pembrolizumab for a biomarker-driven indication. We found that 38.9% of patients showed a 50% or greater decline in PSA, all of whom had high microsatellite instability (MSI-H). One patient with MSI-H and high tumor mutation burden (TMB-H) had 100% decline in PSA and remained on pembrolizumab after 47 months. Neither MSI-H nor TMB-H, however, was sufficient for response. These results support biomarker testing for all patients with mPC and use of immunotherapy in select populations.
靶向PD-1/PD-L1的检查点抑制剂,如帕博利珠单抗,在一小部分经生物标志物筛选的转移性前列腺癌(mPC)患者中可能有效,小病例系列研究已证明了这一点。本研究的目的是帮助确定哪些经生物标志物筛选的患者最有可能从帕博利珠单抗中获益,并估计他们的反应可能性。这是一项单中心研究,我们分析了18例因生物标志物驱动的适应症接受帕博利珠单抗治疗的mPC患者的临床数据。我们发现,38.9%的患者PSA下降了50%或更多,所有这些患者都有高度微卫星不稳定(MSI-H)。一名MSI-H和高肿瘤突变负荷(TMB-H)的患者PSA下降了100%,并在47个月后继续使用帕博利珠单抗。然而,单独的MSI-H或TMB-H都不足以预测反应。这些结果支持对所有mPC患者进行生物标志物检测,并在特定人群中使用免疫疗法。