表达程序性死亡配体1的细胞外囊泡是接受免疫检查点抑制剂治疗的口腔鳞状细胞癌患者的预后因素之一

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Oral and Maxillofacial Surgery Medicine and Pathology Pub Date : 2023-12-20 DOI:10.1016/j.ajoms.2023.12.007
Yuki Seki , Keisuke Yamana , Ryoji Yoshida , Junki Inoue , Kosuke Shinohara , Toru Oyama , Ryuta Kubo , Masashi Nagata , Kenta Kawahara , Masatoshi Hirayama , Nozomu Takahashi , Masafumi Nakamoto , Akiyuki Hirosue , Ryusho Kariya , Seiji Okada , Hideki Nakayama
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引用次数: 0

摘要

导言免疫检查点抑制剂(ICIs)已被临床用于治疗各种癌症。这导致了癌症治疗模式的转变,包括复发性/转移性口腔鳞状细胞癌(R/M OSCC);然而,ICIs治疗的反应率仅限于20%-30%,而且不同患者的疗效也各不相同。因此,开发一种分层方法来准确选择有望对治疗产生反应的患者将是有益的。细胞外囊泡(EVs)是细胞间通信的重要媒介。值得注意的是,程序性死亡配体1(PD-L1)在多种恶性肿瘤的EV表面都有表达。在此,我们重点研究了接受 ICIs 治疗的 R/M OSCC 患者血清中循环的 PD-L1 表达 EVs(PD-L1 EVs)的临床意义。方法:我们对本机构接受 ICIs 治疗的 37 例 R/M OSCC 患者进行了评估,并使用接收器操作特征分析确定了 PD-L1 EVs 的最佳临界水平。此外,我们还评估了PD-L1 EVs水平与各种临床病理特征之间的关联,以及PD-L1 EVs状态对预后的影响。此外,Kaplan-Meier曲线分析显示,PD-L1 EVs水平高与总生存率低显著相关。结论这些研究结果表明,对于接受 ICIs 治疗的 R/M OSCC 患者来说,在治疗前评估血清中的 PD-L1 EVs 水平可能是一个有价值的预后指标。
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Programmed death-ligand 1-expressing extracellular vesicles are a prognostic factor in patients with oral squamous cell carcinoma treated with immune checkpoint inhibitors

Introduction

Immune checkpoint inhibitors (ICIs) have been clinically used to treat various cancers. This has resulted in a paradigm shift in the treatment of cancers, including recurrent/metastatic oral squamous cell carcinoma (R/M OSCC); however, response rate to treatment with ICIs is limited to 20–30%, and the treatment efficacy varies among patients. Therefore, developing a stratification method to accurately select patients expected to respond to the treatment would be beneficial. Extracellular vesicles (EVs) are important mediators of intercellular communication. Notably, programmed death-ligand 1 (PD-L1) is expressed on the surface of EVs in several malignancies. Herein, we focused on the clinical significance of PD-L1-expressing EVs (PD-L1 EVs) circulating in the serum of patients with R/M OSCC treated with ICIs.

Methods

Overall, 37 patients with R/M OSCC who were treated with ICIs at our institution were evaluated, and the optimum cutoff level of PD-L1 EVs was determined using a receiver operating characteristic analysis. Furthermore, we evaluated the association between PD-L1 EV levels and various clinicopathological features as well as the effects of PD-L1 EVs status on prognosis.

Results

The optimum cutoff level of PD-L1 EVs was 2.90 ng/mL. Further, Kaplan–Meier curve analysis revealed that high PD-L1 EV level was significantly associated with poor overall survival. Moreover, multivariate analysis indicated that high PD-L1 EV level was independently correlated with poor 5-year overall survival.

Conclusion

These findings indicate that assessing levels of PD-L1 EVs in serum before treatment may be a valuable prognostic indicator for patients with R/M OSCC following ICIs treatment.

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0.00%
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129
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83 days
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