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多模式治疗的间变性甲状腺癌患者中PD-1和PD-L1的表达:一项回顾性研究的结果

Expression of PD-1 and PD-L1 in Anaplastic Thyroid Cancer Patients Treated With Multimodal Therapy: Results From a Retrospective Study.

作者信息

Chintakuntlawar Ashish V, Rumilla Kandelaria M, Smith Carin Y, Jenkins Sarah M, Foote Robert L, Kasperbauer Jan L, Morris John C, Ryder Mabel, Alsidawi Samer, Hilger Crystal, Bible Keith C

机构信息

Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota 55905.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

J Clin Endocrinol Metab. 2017 Jun 1;102(6):1943-1950. doi: 10.1210/jc.2016-3756.

Abstract

CONTEXT

Anaplastic thyroid cancer (ATC) is rare and a highly fatal malignancy. The role of programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) as prognostic and/or predictive markers in ATC is unknown.

OBJECTIVE

Multimodal therapy offers the best chance at tumor control. The objective of this study was to detect potential associations of PD-1/PD-L1 axis variables with outcome data in ATC.

DESIGN

Retrospective study of a uniformly treated cohort.

SETTING

Single institution retrospective cohort study.

PATIENTS OR OTHER PARTICIPANTS

Sixteen patients who received intensity-modulated radiation therapy (15 had preceding surgery) were studied.

MAIN OUTCOME MEASURE

Patients treated with multimodal therapy were followed and assessed for overall survival (OS) and progression-free survival (PFS).

RESULTS

All samples demonstrated PD-1 expression in inflammatory cells whereas tumor cells were primarily negative. PD-L1 was expressed on ATC tumor cells in most samples and showed mainly membranous staining. High PD-1 expression (>40% staining) in inflammatory cells was associated with worse overall survival (OS; hazard ratio, 3.36; 95% confidence interval, 1.00 to 12.96; P < 0.05) and trended toward worse PFS, whereas high PD-L1 expression in tumor cells (>33% staining) trended toward worse PFS and OS.

CONCLUSION

PD-1/PD-L1 pathway proteins are highly expressed in ATC tumor samples and appear to represent predictive markers of PFS and OS in multimodality-treated ATC patients.

摘要

背景

间变性甲状腺癌(ATC)罕见且是一种高度致命的恶性肿瘤。程序性死亡蛋白1(PD-1)和程序性死亡配体1(PD-L1)作为ATC的预后和/或预测标志物的作用尚不清楚。

目的

多模式治疗提供了控制肿瘤的最佳机会。本研究的目的是检测PD-1/PD-L1轴变量与ATC结局数据之间的潜在关联。

设计

对一组接受统一治疗的队列进行回顾性研究。

设置

单机构回顾性队列研究。

患者或其他参与者

研究了16例接受调强放射治疗的患者(15例之前接受过手术)。

主要结局指标

对接受多模式治疗的患者进行随访,并评估总生存期(OS)和无进展生存期(PFS)。

结果

所有样本均显示炎症细胞中有PD-1表达,而肿瘤细胞主要为阴性。大多数样本中,PD-L1在ATC肿瘤细胞上表达,主要呈膜性染色。炎症细胞中高PD-1表达(>40%染色)与较差的总生存期(OS;风险比,3.36;95%置信区间,1.00至12.96;P<0.05)相关,且无进展生存期有变差趋势,而肿瘤细胞中高PD-L1表达(>33%染色)无进展生存期和总生存期有变差趋势。

结论

PD-1/PD-L1通路蛋白在ATC肿瘤样本中高表达,似乎代表了多模式治疗的ATC患者无进展生存期和总生存期的预测标志物。

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