PD-L1高表达的SMARCA4缺陷未分化尿路上皮癌患者对Nivolumab的明显反应:病例报告。

IF 1.5 Q4 ONCOLOGY
Cancer reports Pub Date : 2024-06-24 DOI:10.1002/cnr2.2127
Yohei Arihara, Ginji Omori, Ko Kobayashi, Shintaro Sugita, Kazuyuki Murase, Tomohiro Kubo, Masashi Idogawa, Tadashi Hasegawa, Kohichi Takada
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引用次数: 0

摘要

背景:SMARCA4是SWI/SNF(SWItch/Sucrose NonFermentable)染色质重塑复合体的一个组成基因;在多个器官中都发现了与SMARCA4功能缺失相关的未分化肿瘤。病例:在本研究中,我们报告了一例SMARCA4缺失且PD-L1高表达的未分化尿路上皮癌,该患者在接受非浸润性膀胱癌治疗后早期复发,并接受了nivolumab的有效治疗。原发不明的横纹肌样未分化肿瘤的组织学形态让我们怀疑是SWI/SNF缺陷型肿瘤,随后的免疫染色让我们确诊为SMARCA4缺陷型未分化肿瘤。这项工作还使我们确定了这种 SMARCA4 缺失型未分化肿瘤的发育起源为非浸润性膀胱癌。我们还对外周 T 细胞进行了详细的免疫表型检测。简而言之,我们观察到了 CD8+T 细胞从幼稚细胞到终末分化的效应记忆细胞的表型变化:无论癌症起源器官或癌症类型如何,在未分化和去分化肿瘤中都应怀疑SWI/SNF缺陷肿瘤,免疫检查点抑制剂可能被认为是治疗这类肿瘤的一种有前途的选择。SMARCA4缺陷型无性细胞肿瘤的发病机制有待进一步阐明,以便进行治疗开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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