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免疫组化高间皮素表达预示间皮瘤患者的胸膜生存改善。

High mesothelin expression by immunohistochemistry predicts improved survival in pleural mesothelioma.

机构信息

Gene and Stem Cell Therapy Program Centenary Institute, University of Sydney, Sydney, NSW, Australia.

Department of Clinical Immunology and Allergy, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

出版信息

Histopathology. 2023 Aug;83(2):202-210. doi: 10.1111/his.14916. Epub 2023 Apr 11.


DOI:10.1111/his.14916
PMID:37040900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10952516/
Abstract

AIMS: Mesothelin (MSLN) is a cancer-associated antigen that is overexpressed in malignancies such as mesothelioma, pancreatic and ovarian cancer. It is also a target for novel personalised therapies, including antibodies, antibody-drug conjugates and chimeric antigen receptor T cells. Immunohistochemistry may predict those who would best respond to anti-mesothelin therapies and guide decisions in therapeutic strategy. This study aimed to assess the intensity and distribution of MSLN immunostaining in mesothelioma, and to determine the prognostic value of MSLN expression by histochemical-score (H-score). METHODS AND RESULTS: The MN1 anti-MSLN antibody was used to stain a formalin-fixed paraffin-embedded tissue microarray of histologically confirmed mesothelioma from 75 consecutive patients who had undergone pleurectomy with or without decortication. MSLN positivity, the staining intensity, distribution of staining and H-score were evaluated. The correlation of H-score with prognosis was investigated. Sixty-six per cent of epithelioid tumours were MSLN-positive (with expression in > 5% tumour cells). Of MSLN-expressing epithelioid tumours, 70.4% had moderate (2+) or strong (3+) intensity MSLN immunostaining, although only 37% of samples had staining in ≥ 50% of tumour cells. In multivariate analysis, MSLN H-score as a continuous variable and an H-score ≥ 33 were independent predictors of improved survival (P = 0.04 and P < 0.001, respectively). CONCLUSIONS: MSLN expression was more heterogenous in epithelioid mesothelioma than reported previously. Therefore, it would be appropriate to perform an immunohistochemical assessment of MSLN expression to stratify and assess patient suitability for mesothelin-targeted personalised therapies, such as chimeric antigen receptor T cells.

摘要

目的:间皮素(MSLN)是一种癌相关抗原,在间皮瘤、胰腺癌和卵巢癌等恶性肿瘤中过度表达。它也是新型个体化治疗的靶点,包括抗体、抗体药物偶联物和嵌合抗原受体 T 细胞。免疫组织化学可能预测那些对抗间皮素治疗反应最佳的患者,并指导治疗策略中的决策。本研究旨在评估间皮瘤中 MSLN 免疫染色的强度和分布,并通过组织化学评分(H 评分)确定 MSLN 表达的预后价值。

方法和结果:使用 MN1 抗 MSLN 抗体对 75 例连续接受胸膜切除术加或不加剥脱术的经组织学证实的间皮瘤的福尔马林固定石蜡包埋组织微阵列进行染色。评估 MSLN 阳性、染色强度、染色分布和 H 评分。研究了 H 评分与预后的相关性。66%的上皮样肿瘤为 MSLN 阳性(>5%肿瘤细胞表达)。在 MSLN 表达的上皮样肿瘤中,70.4%的肿瘤细胞具有中度(2+)或强(3+)的 MSLN 免疫染色强度,尽管只有 37%的样本中肿瘤细胞的染色强度≥50%。在多变量分析中,MSLN H 评分作为连续变量和 H 评分≥33 是生存改善的独立预测因子(P=0.04 和 P<0.001)。

结论:上皮样间皮瘤中 MSLN 的表达比以前报道的更为异质。因此,进行 MSLN 表达的免疫组织化学评估以分层和评估患者接受间皮素靶向个体化治疗(如嵌合抗原受体 T 细胞)的适宜性是合适的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5f/10952516/dbfcb76835d3/HIS-83-202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5f/10952516/c317182f284e/HIS-83-202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5f/10952516/dbfcb76835d3/HIS-83-202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5f/10952516/c317182f284e/HIS-83-202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5f/10952516/dbfcb76835d3/HIS-83-202-g003.jpg

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High mesothelin expression by immunohistochemistry predicts improved survival in pleural mesothelioma.

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引用本文的文献

[1]
Mesothelin as a Signal Pathways and Epigenetic Target in Cancer Therapy.

Cancers (Basel). 2025-3-26

[2]
Regional and intratumoral adoptive T-cell therapy.

Immunooncol Technol. 2024-6-12

[3]
Biology of Mesothelin and Clinical Implications: A Review of Existing Literature.

World J Oncol. 2023-10

[4]
New Immunohistochemical Markers for Pleural Mesothelioma Subtyping.

Diagnostics (Basel). 2023-9-14

[5]
Malignant mesothelioma tumours: molecular pathogenesis, diagnosis, and therapies accompanying clinical studies.

Front Oncol. 2023-7-4

本文引用的文献

[1]
Anetumab ravtansine versus vinorelbine in patients with relapsed, mesothelin-positive malignant pleural mesothelioma (ARCS-M): a randomised, open-label phase 2 trial.

Lancet Oncol. 2022-4

[2]
A Phase I Trial of Regional Mesothelin-Targeted CAR T-cell Therapy in Patients with Malignant Pleural Disease, in Combination with the Anti-PD-1 Agent Pembrolizumab.

Cancer Discov. 2021-11

[3]
Mesothelin Expression in Human Tumors: A Tissue Microarray Study on 12,679 Tumors.

Biomedicines. 2021-4-7

[4]
Prognosis of patients with malignant mesothelioma by expression of programmed cell death 1 ligand 1 and mesothelin in a contemporary cohort in Finland.

Cancer Treat Res Commun. 2020

[5]
Multiple proteases are involved in mesothelin shedding by cancer cells.

Commun Biol. 2020-12-1

[6]
Mesothelin Enhances Tumor Vascularity in Newly Forming Pancreatic Peritoneal Metastases.

Mol Cancer Res. 2019-11-1

[7]
Biomarker panel predicts survival after resection in pancreatic ductal adenocarcinoma: A multi-institutional cohort study.

Eur J Surg Oncol. 2018-10-11

[8]
Integrative Molecular Characterization of Malignant Pleural Mesothelioma.

Cancer Discov. 2018-10-15

[9]
Activity of Mesothelin-Specific Chimeric Antigen Receptor T Cells Against Pancreatic Carcinoma Metastases in a Phase 1 Trial.

Gastroenterology. 2018-3-20

[10]
Cancer antigen profiling for malignant pleural mesothelioma immunotherapy: expression and coexpression of mesothelin, cancer antigen 125, and Wilms tumor 1.

Oncotarget. 2017-9-12

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