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SMARCA4 缺陷型未分化尿路上皮癌患者对纳武利尤单抗的显著应答:病例报告

Marked Response to Nivolumab by a Patient With SMARCA4-Deficient Undifferentiated Urothelial Carcinoma Showing High PD-L1 Expression: A Case Report.

机构信息

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

Cancer Rep (Hoboken). 2024 Jun;7(6):e2127. doi: 10.1002/cnr2.2127.

Abstract

BACKGROUND

SMARCA4 is a component gene of the SWI/SNF (SWItch/Sucrose NonFermentable) chromatin remodeling complex; undifferentiated tumors associated with its functional deletion have been described in several organs. However, no established treatment for these tumors currently exists.

CASE

In this study, we report a case of a SMARCA4-deficient undifferentiated urothelial carcinoma with high PD-L1 expression that was effectively treated with nivolumab after early relapse following treatment for non-invasive bladder cancer. The histological morphology of the rhabdoid-like undifferentiated tumor of unknown primary led us to suspect a SWI/SNF-deficient tumor, and subsequent immunostaining led to the diagnosis of a SMARCA4-deficient undifferentiated tumor. This effort also led to the identification of the developmental origin of this SMARCA4-deficient undifferentiated tumor as a non-invasive bladder cancer. We also carried out a detailed immune phenotypic assay on peripheral T cells. In brief, a phenotypic change of CD8+T cells from naive to terminally differentiated effector memory cells was observed.

CONCLUSION

Regardless of the organ of cancer origin or cancer type, SWI/SNF-deficient tumors should be suspected in undifferentiated and dedifferentiated tumors, and immune checkpoint inhibitors may be considered as a promising treatment option for this type of tumor. The pathogenesis of SMARCA4-deficient anaplastic tumors awaits further elucidation for therapeutic development.

摘要

背景

SMARCA4 是 SWI/SNF(Switch/Sucrose NonFermentable)染色质重塑复合物的一个组成基因;其功能缺失与多个器官的未分化肿瘤有关。然而,目前这些肿瘤尚无既定的治疗方法。

病例报告

本研究报道了一例 SMARCA4 缺陷型未分化尿路上皮癌,该肿瘤 PD-L1 表达高,在非浸润性膀胱癌治疗后早期复发,用纳武利尤单抗治疗后效果显著。横纹肌样未分化肿瘤的组织形态学表现为未知原发灶的 SWI/SNF 缺陷型肿瘤,随后的免疫组化染色导致诊断为 SMARCA4 缺陷型未分化肿瘤。这一努力还确定了这种 SMARCA4 缺陷型未分化肿瘤的发育起源是非浸润性膀胱癌。我们还对外周 T 细胞进行了详细的免疫表型分析。简而言之,观察到 CD8+T 细胞从幼稚到终末分化效应记忆细胞的表型变化。

结论

无论癌症起源的器官或癌症类型如何,在未分化和去分化肿瘤中都应怀疑存在 SWI/SNF 缺陷型肿瘤,免疫检查点抑制剂可能是这种肿瘤的一种有前途的治疗选择。SMARCA4 缺陷性间变性肿瘤的发病机制有待进一步阐明,以进行治疗开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/11194675/bd4e5bbf38ec/CNR2-7-e2127-g002.jpg

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