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肿瘤免疫微环境可预测前列腺切除术后的复发情况,以及在前列腺癌中雄激素剥夺和免疫治疗的疗效。

Tumor immune contexture predicts recurrence after prostatectomy and efficacy of androgen deprivation and immunotherapy in prostate cancer.

机构信息

Department of Urology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.17 Panjiayuan Nanli, Chaoyang District, Beijing, 100021, China.

Department of Urology, Chinese PLA General Hospital, No 28 Fuxing Road, Beijing, 100853, China.

出版信息

J Transl Med. 2023 Mar 14;21(1):194. doi: 10.1186/s12967-022-03827-4.

Abstract

BACKGROUND

Prostate cancer is one of the most common cancers in men with notable interpatient heterogeneity. Implications of the immune microenvironment in predicting the biochemical recurrence-free survival (BCRFS) after radical prostatectomy and the efficacy of systemic therapies in prostate cancer remain ambiguous.

METHODS

The tumor immune contexture score (TICS) involving eight immune contexture-related signatures was developed using seven cohorts of 1120 patients treated with radical prostatectomy (training: GSE46602, GSE54460, GSE70769, and GSE94767; validation: GSE70768, DKFZ2018, and TCGA). The association between the TICS and treatment efficacy was investigated in GSE111177 (androgen deprivation therapy [ADT]) and EGAS00001004050 (ipilimumab).

RESULTS

A high TICS was associated with prolonged BCRFS after radical prostatectomy in the training (HR = 0.32, 95% CI 0.24-0.45, P < 0.001) and the validation cohorts (HR = 0.45, 95% CI 0.32-0.62, P < 0.001). The TICS showed stable prognostic power independent of tumor stage, surgical margin, pre-treatment prostatic specific antigen (PSA), and Gleason score (multivariable HR = 0.50, 95% CI 0.39-0.63, P < 0.001). Adding the TICS into the prognostic model constructed using clinicopathological features significantly improved its 1/2/3/4/5-year area under curve (P < 0.05). A low TICS was associated with high homologous recombination deficiency scores, abnormally activated pathways concerning DNA replication, cell cycle, steroid hormone biosynthesis, and drug metabolism, and fewer tumor-infiltrating immune cells (P < 0.05). The patients with a high TICS had favorable BCRFS with ADT (HR = 0.25, 95% CI 0.06-0.99, P = 0.034) or ipilimumab monotherapy (HR = 0.23, 95% CI 0.06-0.81, P = 0.012).

CONCLUSIONS

Our study delineates the associations of tumor immune contexture with molecular features, recurrence after radical prostatectomy, and the efficacy of ADT and immunotherapy. The TICS may improve the existing risk stratification systems and serve as a patient-selection tool for ADT and immunotherapy in prostate cancer.

摘要

背景

前列腺癌是男性最常见的癌症之一,患者之间存在显著的异质性。肿瘤免疫微环境在预测根治性前列腺切除术后生化无复发生存(BCRFS)和系统治疗在前列腺癌中的疗效方面的意义仍不明确。

方法

使用涉及 8 个与免疫微环境相关特征的肿瘤免疫组织学评分(TICS),对 7 个接受根治性前列腺切除术的患者队列(训练:GSE46602、GSE54460、GSE70769 和 GSE94767;验证:GSE70768、DKFZ2018 和 TCGA)进行了开发。在 GSE111177(雄激素剥夺治疗 [ADT])和 EGAS00001004050(ipilimumab)中研究了 TICS 与治疗效果之间的关联。

结果

高 TICS 与根治性前列腺切除术后的 BCRFS 延长相关(训练:HR=0.32,95%CI 0.24-0.45,P<0.001;验证:HR=0.45,95%CI 0.32-0.62,P<0.001)。TICS 在独立于肿瘤分期、手术切缘、治疗前前列腺特异性抗原(PSA)和 Gleason 评分的情况下,具有稳定的预后能力(多变量 HR=0.50,95%CI 0.39-0.63,P<0.001)。将 TICS 添加到基于临床病理特征构建的预后模型中,显著提高了其 1/2/3/4/5 年 AUC(P<0.05)。低 TICS 与同源重组缺陷评分高、涉及 DNA 复制、细胞周期、类固醇激素生物合成和药物代谢的异常激活途径以及肿瘤浸润免疫细胞较少有关(P<0.05)。TICS 高的患者接受 ADT(HR=0.25,95%CI 0.06-0.99,P=0.034)或 ipilimumab 单药治疗(HR=0.23,95%CI 0.06-0.81,P=0.012)的 BCRFS 良好。

结论

我们的研究描述了肿瘤免疫微环境与分子特征、根治性前列腺切除术后复发以及 ADT 和免疫治疗疗效之间的关联。TICS 可能改善现有的风险分层系统,并作为 ADT 和免疫治疗在前列腺癌中的患者选择工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5889/10012744/8f469dd4c3d4/12967_2022_3827_Fig1_HTML.jpg

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