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程序性死亡受体配体1(PD-L1)的表达作为晚期胆管癌患者对免疫检查点抑制剂敏感性的预测标志物。

Expression of PD-L1 as a predictive marker of sensitivity to immune checkpoint inhibitors in patients with advanced biliary tract cancer.

作者信息

Kim Hongsik, Kim Ryul, Jo Hyunji, Kim Hye Ryeon, Hong Joohyun, Ha Sang Yun, Park Joon Oh, Kim Seung Tae

机构信息

Division of Hematology-Oncology, Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Republic of Korea.

Division of Hematology-Oncology, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

出版信息

Therap Adv Gastroenterol. 2022 Aug 16;15:17562848221117638. doi: 10.1177/17562848221117638. eCollection 2022.

Abstract

BACKGROUND

Expression of programmed death-ligand 1 (PD-L1) has been reported to correlate with response to immune checkpoint inhibitors (ICIs) in various tumor types. However, there are few data on the role of PD-L1 expression as a predictive and prognostic biomarker of sensitivity to ICIs in patients with advanced biliary tract cancer (BTC).

OBJECTIVES

We evaluated the role of PD-L1 expression as a predictive and prognostic biomarker of response to ICIs in patients with advanced BTC.

DESIGN

We retrospectively analyzed data from 83 advanced BTC patients who received ICIs as second- or third-line treatment between February 2018 and April 2021.

METHODS

All patient data analysis included evaluation of PD-L1 expression by the combined positive score (CPS).

RESULTS

Among 83 patients, 56 (67.5%) had PD-L1 positivity (CPS ⩾ 1). The objective response rate (ORR) to ICIs was significantly higher in advanced BTC patients with PD-L1 expression compared to those without PD-L1 expression (17.8% 0%,  = 0.026). However, there were no significant differences in median progression-free survival (PFS; 2.9 2.6 months,  = 0.330) and median overall survival (OS; 8.1 6.3 months,  = 0.289) as a response to ICIs between patients with and without PD-L1 expression. Also, there were no significant differences in ORR, PFS, and OS as a response to ICIs in conjunction with a response to a prior gemcitabine plus cisplatin regimen ( = 0.654,  = 0.278, and  = 0.302, respectively).

CONCLUSIONS

The present study suggests that the expression of PD-L1 alone was not sufficient as a novel marker to select advanced BTC patients who might benefit from ICIs. Additional comprehensive studies of biomarkers that can assist in predicting BTC patient responses to pembrolizumab and/or nivolumab therapy are required.

摘要

背景

据报道,程序性死亡配体1(PD-L1)的表达与多种肿瘤类型中免疫检查点抑制剂(ICI)的反应相关。然而,关于PD-L1表达作为晚期胆管癌(BTC)患者对ICI敏感性的预测和预后生物标志物的作用的数据很少。

目的

我们评估了PD-L1表达作为晚期BTC患者对ICI反应的预测和预后生物标志物的作用。

设计

我们回顾性分析了2018年2月至2021年4月期间接受ICI作为二线或三线治疗的83例晚期BTC患者的数据。

方法

所有患者数据分析包括通过联合阳性评分(CPS)评估PD-L1表达。

结果

83例患者中,56例(67.5%)PD-L1呈阳性(CPS⩾1)。与无PD-L1表达的晚期BTC患者相比,有PD-L1表达的患者对ICI的客观缓解率(ORR)显著更高(17.8%对0%,P=0.026)。然而,有和无PD-L1表达的患者作为对ICI反应的中位无进展生存期(PFS;2.9个月对2.6个月,P=0.330)和中位总生存期(OS;8.1个月对6.3个月,P=0.289)没有显著差异。此外,与先前吉西他滨加顺铂方案的反应相结合,作为对ICI反应的ORR、PFS和OS也没有显著差异(分别为P=0.654、P=0.278和P=0.302)。

结论

本研究表明,单独的PD-L1表达不足以作为选择可能从ICI中获益的晚期BTC患者的新标志物。需要对有助于预测BTC患者对派姆单抗和/或纳武单抗治疗反应的生物标志物进行更多综合研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ec7/9386848/36691f5be55b/10.1177_17562848221117638-fig1.jpg

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