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CD74 与炎症肿瘤免疫微环境相关,并可预测实体瘤患者对 PD-1/CTLA-4 双特异性抗体的反应性。

CD74 is associated with inflamed tumor immune microenvironment and predicts responsiveness to PD-1/CTLA-4 bispecific antibody in patients with solid tumors.

机构信息

Research and Development Department, Akeso Biopharma Inc, Zhongshan, Guangdong, China.

Department of Oncology, Sir Peter MacCallum, The University of Melbourne, Parkville, VIC, Australia.

出版信息

Cancer Immunol Immunother. 2024 Jan 27;73(2):36. doi: 10.1007/s00262-023-03604-2.


DOI:10.1007/s00262-023-03604-2
PMID:38280003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10822011/
Abstract

INTRODUCTION: Cadonilimab (AK104) is a first-in-class tetravalent bispecific antibody that targets both PD-1 and CTLA-4, showing a manageable safety profile and favorable clinical benefits. This study aimed to identify the biomarkers of clinical response and explore the immune response within the tumor microenvironment upon the AK104 therapy in advanced solid tumors. MATERIAL AND METHODS: Gene expression profiles of paired pre- and post-treatment tumor tissues from twenty-one patients were analyzed. The association of gene expression levels with either clinical efficacy or prognosis was evaluated and subsequently validated with published datasets using log-rank for Kaplan-Meier estimates. Comparative immune profile analyses of tumor microenvironment before and after AK104 treatment were conducted. The visualization of tumor-infiltrating lymphocytes was performed using multiplex immunohistochemistry. The predictive value of CD74 was further validated with protein expression by immunohistochemistry. RESULTS: Baseline CD74 gene expression was associated with favorable patient outcomes (overall survival [OS], HR = 0.33, 95% CI 0.11-1.03, p = 0.0463), which was further confirmed with the published datasets. Tumors with high CD74 gene expression at baseline were more likely to exhibit an immune-inflamed microenvironment. AK104 efficiently enhanced the infiltration of immune cells in the tumor microenvironment. Additionally, high CD74 protein expression (≥ 10% of the tumor area occupied by CD74 stained immune cells) at baseline was associated with better progressive-free survival (HR = 0.21, 95% CI 0.06-0.68, p = 0.0065) and OS (HR = 0.35, 95% CI 0.12-1.08, p = 0.0615). CONCLUSIONS: Our findings demonstrate that CD74 is a promising predictive biomarker for AK104 therapeutic response in advanced solid tumors. Trial registration number NCT03261011.

摘要

简介:Cadonilimab(AK104)是一种首创的四价双特异性抗体,可同时靶向 PD-1 和 CTLA-4,具有可管理的安全性和良好的临床获益。本研究旨在鉴定 AK104 治疗晚期实体瘤的临床反应生物标志物,并探索肿瘤微环境中的免疫反应。 材料与方法:分析了 21 名患者治疗前后配对的肿瘤组织的基因表达谱。评估基因表达水平与临床疗效或预后的相关性,并使用对数秩检验对 Kaplan-Meier 估计值进行了随后的验证。对 AK104 治疗前后肿瘤微环境的免疫谱进行了比较分析。使用多重免疫组化法进行肿瘤浸润淋巴细胞的可视化。通过免疫组化法验证 CD74 的蛋白表达进一步验证了 CD74 的预测价值。 结果:基线 CD74 基因表达与患者的良好预后(总生存期[OS],HR=0.33,95%CI 0.11-1.03,p=0.0463)相关,这在已发表的数据集上得到了进一步证实。基线时 CD74 基因表达较高的肿瘤更可能表现出免疫炎症的微环境。AK104 有效地增强了肿瘤微环境中免疫细胞的浸润。此外,基线时 CD74 蛋白表达(肿瘤区域内被 CD74 染色免疫细胞占据的面积≥10%)较高与更好的无进展生存期(HR=0.21,95%CI 0.06-0.68,p=0.0065)和 OS(HR=0.35,95%CI 0.12-1.08,p=0.0615)相关。 结论:我们的研究结果表明,CD74 是 AK104 治疗晚期实体瘤疗效的有前途的预测生物标志物。试验注册号 NCT03261011。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/19f4f68cdabb/262_2023_3604_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/9ab132b54f1b/262_2023_3604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/112ea591737f/262_2023_3604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/19d769d5e3b5/262_2023_3604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/62faf96b2e5d/262_2023_3604_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/19f4f68cdabb/262_2023_3604_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/9ab132b54f1b/262_2023_3604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/112ea591737f/262_2023_3604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/19d769d5e3b5/262_2023_3604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/62faf96b2e5d/262_2023_3604_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d3/10992620/19f4f68cdabb/262_2023_3604_Fig5_HTML.jpg

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本文引用的文献

[1]
A phase 1a/1b first-in-human study (COMPASSION-01) evaluating cadonilimab in patients with advanced solid tumors.

Cell Rep Med. 2023-11-21

[2]
Safety and antitumour activity of cadonilimab, an anti-PD-1/CTLA-4 bispecific antibody, for patients with advanced solid tumours (COMPASSION-03): a multicentre, open-label, phase 1b/2 trial.

Lancet Oncol. 2023-10

[3]
Cadonilimab, a tetravalent PD-1/CTLA-4 bispecific antibody with trans-binding and enhanced target binding avidity.

MAbs. 2023

[4]
Localization and density of tertiary lymphoid structures associate with molecular subtype and clinical outcome in colorectal cancer liver metastases.

J Immunother Cancer. 2023-2

[5]
Five-Year Survival Outcomes With Nivolumab Plus Ipilimumab Versus Chemotherapy as First-Line Treatment for Metastatic Non-Small-Cell Lung Cancer in CheckMate 227.

J Clin Oncol. 2023-2-20

[6]
Identification and characterization of three Siglec15-related immune and prognostic subtypes of breast-invasive cancer.

Int Immunopharmacol. 2022-5

[7]
HLA Class II Histocompatibility Antigen γ Chain (CD74) Expression Is Associated with Immune Cell Infiltration and Favorable Outcome in Breast Cancer.

Cancers (Basel). 2021-12-8

[8]
CD74 Correlated With Malignancies and Immune Microenvironment in Gliomas.

Front Mol Biosci. 2021-9-1

[9]
Identification of three immune molecular subtypes associated with immune profiles, immune checkpoints, and clinical outcome in multiple myeloma.

Cancer Med. 2021-10

[10]
CD74 macrophages are associated with favorable prognosis and immune contexture in hepatocellular carcinoma.

Cancer Immunol Immunother. 2022-1

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