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循环肿瘤细胞上的 PD-L1 表达可能对晚期黑色素瘤患者接受派姆单抗治疗的反应具有预测性:一项初步研究的结果。

PD-L1 Expression on Circulating Tumor Cells May Be Predictive of Response to Pembrolizumab in Advanced Melanoma: Results from a Pilot Study.

机构信息

Department of Medical Oncology, Fiona Stanley Hospital, Australia.

School of Medical and Health Sciences, Edith Cowan University, Perth, Australia.

出版信息

Oncologist. 2020 Mar;25(3):e520-e527. doi: 10.1634/theoncologist.2019-0557. Epub 2019 Dec 5.

Abstract

BACKGROUND

PD-1 inhibitors are routinely used for the treatment of advanced melanoma. This study sought to determine whether PD-L1 expression on circulating tumor cells (CTCs) can serve as a predictive biomarker of clinical benefit and response to treatment with the PD-1 inhibitor pembrolizumab.

METHODS

Blood samples were collected from patients with metastatic melanoma receiving pembrolizumab, prior to treatment and 6-12 weeks after initiation of therapy. Multiparametric flow cytometry was used to identify CTCs and evaluate the expression of PD-L1.

RESULTS

CTCs were detected in 25 of 40 patients (63%). Patients with detectable PD-L1 CTCs (14/25, 64%) had significantly longer progression-free survival (PFS) compared with patients with PD-L1 CTCs (26.6 months vs. 5.5 months; p = .018). The 12-month PFS rates were 76% versus 22% in the PD-L1 versus PD-L1 CTCs groups (p = .012), respectively. A multivariate linear regression analysis confirmed that PD-L1 CTC is an independent predictive biomarker of PFS (hazard ratio, 0.229; 95% confidence interval, 0.052-1.012; p = .026).

CONCLUSION

Our results reveal the potential of CTCs as a noninvasive real-time biopsy to evaluate PD-L1 expression in patients with melanoma. PD-L1 expression on CTCs may be predictive of response to pembrolizumab and longer PFS.

IMPLICATIONS FOR PRACTICE

The present data suggest that PD-L1 expression on circulating tumor cells may predict response to pembrolizumab in advanced melanoma. This needs further validation in a larger trial and, if proven, might be a useful liquid biopsy tool that could be used to stratify patients into groups more likely to respond to immunotherapy, hence leading to health cost savings.

摘要

背景

PD-1 抑制剂常用于治疗晚期黑色素瘤。本研究旨在确定循环肿瘤细胞(CTC)上的 PD-L1 表达是否可作为预测生物标志物,以预测患者对 PD-1 抑制剂 pembrolizumab 的临床获益和治疗反应。

方法

采集接受 pembrolizumab 治疗的转移性黑色素瘤患者的血液样本,在治疗前和治疗开始后 6-12 周采集。多参数流式细胞术用于鉴定 CTC 并评估 PD-L1 的表达。

结果

在 40 名患者中的 25 名(63%)中检测到 CTC。与 PD-L1 CTC 患者(26.6 个月)相比,检测到 PD-L1 CTC 的患者(14/25,64%)具有显著更长的无进展生存期(PFS)(p=0.018)。PD-L1 与 PD-L1 CTC 组的 12 个月 PFS 率分别为 76%和 22%(p=0.012)。多变量线性回归分析证实 PD-L1 CTC 是 PFS 的独立预测生物标志物(风险比,0.229;95%置信区间,0.052-1.012;p=0.026)。

结论

我们的结果揭示了 CTC 作为一种非侵入性实时活检方法,用于评估黑色素瘤患者 PD-L1 表达的潜力。CTC 上的 PD-L1 表达可能预测对 pembrolizumab 的反应和更长的 PFS。

临床意义

本数据表明,循环肿瘤细胞上的 PD-L1 表达可能预测晚期黑色素瘤对 pembrolizumab 的反应。这需要在更大的试验中进一步验证,如果得到证实,可能是一种有用的液体活检工具,可用于将患者分层为更有可能对免疫治疗有反应的组,从而节省医疗保健成本。

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