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对双重免疫检查点阻断有反应的CIC::DUX4融合阳性肉瘤中的免疫相关因素

Immunologic correlates in a CIC::DUX4 fusion-positive sarcoma responsive to dual immune checkpoint blockade.

作者信息

Babatunde Olayode O, Coca Membribes Sara, Anthonescu Cristina, Bradic Martina, O'Malley Bernard, Linkov Irina, Bartlett Edmund, Momtaz Parisa, Alektiar Kaled, Gounder Mrinal M, Rosenbaum Evan, Tap William D, D'Angelo Sandra P, Kelly Ciara M

机构信息

Medical Oncology/Hematology Fellowship Program, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Barts Cancer Institute Biomedical Research Centre, London, UK.

出版信息

NPJ Precis Oncol. 2025 Mar 25;9(1):85. doi: 10.1038/s41698-025-00878-w.

Abstract

CIC

:DUX4 sarcoma (CDS) is a rare and aggressive subtype of soft tissue sarcoma with poor prognosis and limited treatment options. Immunotherapy has not been studied in this disease. To our knowledge, response to immune checkpoint blockade (ICB) has not been previously reported. Here, we present the first case of a patient with CDS responding to dual ICB with nivolumab and relatlimab. Immunohistochemical (IHC) analysis of pre-treatment samples revealed minimal immune cell infiltration, with scarce CD3+, CD8+, and FOXP3+ T-cells and negligible expression of PD-L1 and PD-1 markers. Post-treatment tumor samples revealed a significant shift in the immune microenvironment, with increased CD8 + T-cell infiltration and co-expression of exhaustion markers PD-1 and LAG-3 following treatment. These findings suggest that doublet ICB can activate an antitumor immune response in CDS, overcoming the immune cold phenotype typically associated with this sarcoma. This case provides the first evidence of dual PD-1/LAG-3 blockade inducing an immune response in CDS. The favorable response and tolerability observed in this patient highlight the potential of dual ICB as a therapeutic option in CDS that merits further investigation.

摘要

CIC

:DUX4肉瘤(CDS)是一种罕见且侵袭性强的软组织肉瘤亚型,预后较差且治疗选择有限。免疫疗法尚未在该疾病中进行研究。据我们所知,此前尚未报道过对免疫检查点阻断(ICB)的反应。在此,我们报告首例CDS患者对纳武单抗和瑞弗利单抗双重ICB产生反应的病例。治疗前样本的免疫组织化学(IHC)分析显示免疫细胞浸润极少,CD3 +、CD8 +和FOXP3 + T细胞稀少,PD-L1和PD-1标志物表达可忽略不计。治疗后的肿瘤样本显示免疫微环境发生显著变化,治疗后CD8 + T细胞浸润增加,且耗竭标志物PD-1和LAG-3共表达。这些发现表明双重ICB可在CDS中激活抗肿瘤免疫反应,克服通常与此类肉瘤相关的免疫冷表型。该病例提供了双重PD-1/LAG-3阻断在CDS中诱导免疫反应的首个证据。该患者观察到的良好反应和耐受性凸显了双重ICB作为CDS治疗选择的潜力,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e6/11933392/dc38a0ebefaf/41698_2025_878_Fig1_HTML.jpg

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