Kim Hongsik, Kim Ryul, Jo Hyunji, Kim Hye Ryeon, Hong Joohyun, Ha Sang Yun, Park Joon Oh, Kim Seung Tae
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.
Therap Adv Gastroenterol. 2022 Aug 16;15:17562848221117638. doi: 10.1177/17562848221117638. eCollection 2022.
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).
We evaluated the role of PD-L1 expression as a predictive and prognostic biomarker of response to ICIs in patients with advanced BTC.
We retrospectively analyzed data from 83 advanced BTC patients who received ICIs as second- or third-line treatment between February 2018 and April 2021.
All patient data analysis included evaluation of PD-L1 expression by the combined positive score (CPS).
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).
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.
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。
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。
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。
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。
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)。
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。