Prognostic implications of immune classification based on PD-L1 expression and tumor-infiltrating lymphocytes in endocervical adenocarcinoma.

IF 4.5 2区 医学 Q1 ONCOLOGY
Translational Oncology Pub Date : 2025-02-01 Epub Date: 2024-12-29 DOI:10.1016/j.tranon.2024.102265
Li-Jun Wei, Zi-Yun Wu, Li-Yan Wu, Ying-Wen Wu, Hao-Yu Liang, Rong-Zhen Luo, Li-Li Liu
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引用次数: 0

Abstract

Background: Endocervical adenocarcinoma (ECA) comprises a heterogeneous group of diseases whose incidence has increased significantly in recent decades. ECA can be histologically classified into human papillomavirus-associated (HPVA) and non-HPVA (NHPVA) types. Given the variability in pathological features and clinical behavior between the subtypes, evaluating their respective immune microenvironments is essential. They can be categorized into distinct tumor microenvironment immune types (TMIT).

Methods: A total of 540 surgically resected ECA samples were classified into HPVA and NHPVA subgroups. Tumor-infiltrating immune markers were assessed using immunohistochemistry. We categorized ECA into four TMIT based on PD-L1 and CD8+ tumor-infiltrating lymphocytes (TILs) expression, and analyzed their prognostic significance.

Results: PD-L1 positivity was observed in 319 out of 464 (68.8%) HPVA and 55 out of 76 (72.4%) NHPVA. Across the entire cohort, high CD8+ TILs expression was significantly associated with improved disease-free survival (DFS, p=0.018) and overall survival (OS, p=0.031). A total of 177 samples (32.8%) were classified as TMIT I (high PD-L1 and high CD8+ TILs), exhibiting markedly denser immune cell infiltration compared to the other TMIT groups. In NHPVA subgroup, TMIT was significantly associated with both DFS (p=0.005) and OS (p=0.003). Multivariate analysis identified TMIT as an independent prognostic factor for DFS in the NHPVA group, with TMIT I indicating a more favorable prognosis (p=0.042).

Conclusions: TMIT I group within the NHPVA population is most likely to benefit from PD-L1/PD-1 blockade immunotherapies. The immune classification of ECA demonstrates significant prognostic value, suggesting its potential utility in guiding clinical stratification and therapeutic decision-making.

基于PD-L1表达和肿瘤浸润淋巴细胞的宫颈腺癌免疫分类对预后的影响。
背景:宫颈内膜腺癌(ECA)是一种异质性的疾病,其发病率在近几十年来显著增加。ECA在组织学上可分为人乳头瘤病毒相关型(HPVA)和非HPVA型(NHPVA)。鉴于亚型之间病理特征和临床行为的可变性,评估其各自的免疫微环境至关重要。它们可分为不同的肿瘤微环境免疫类型(TMIT)。方法:540例手术切除的ECA标本分为HPVA亚组和NHPVA亚组。采用免疫组织化学方法评估肿瘤浸润性免疫标志物。我们根据PD-L1和CD8+肿瘤浸润淋巴细胞(TILs)的表达将ECA分为四种TMIT,并分析其预后意义。结果:464例HPVA患者中PD-L1阳性319例(68.8%),76例NHPVA患者中PD-L1阳性55例(72.4%)。在整个队列中,高CD8+ TILs表达与改善无病生存期(DFS, p=0.018)和总生存期(OS, p=0.031)显著相关。177个样本(32.8%)被归类为TMIT I(高PD-L1和高CD8+ TILs),与其他TMIT组相比,免疫细胞浸润明显更密集。在NHPVA亚组中,TMIT与DFS (p=0.005)和OS (p=0.003)均显著相关。多因素分析发现,TMIT是NHPVA组DFS的独立预后因素,TMIT I预示着更有利的预后(p=0.042)。结论:NHPVA人群中的TMIT I组最有可能从PD-L1/PD-1阻断免疫疗法中获益。ECA的免疫分类具有重要的预后价值,提示其在指导临床分层和治疗决策方面的潜在应用价值。
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来源期刊
Translational Oncology
Translational Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
7.20
自引率
2.00%
发文量
314
审稿时长
6-12 weeks
期刊介绍: Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.
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