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帕博利珠单抗治疗程序性死亡配体高表达复发性血管周上皮样细胞瘤的持续缓解:病例报告。

Sustained response to pembrolizumab in recurrent perivascular epithelioid cell tumor with elevated expression of programmed death ligand: a case report.

机构信息

University of Arizona Cancer Center, 1515 N. Campbell Ave., Tucson, AZ, 85718, USA.

College of Pharmacy, University of Arizona, Tucson, AZ, USA.

出版信息

J Med Case Rep. 2021 Jul 24;15(1):400. doi: 10.1186/s13256-021-02997-x.

Abstract

BACKGROUND

Perivascular epithelioid cell tumors are defined by the World Health Organization as "a collection of rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells." Whereas localized perivascular epithelioid cell tumor is typically benign and treated successfully with surgical resection, prognosis for patients with advanced or metastatic perivascular epithelioid cell tumor is unfavorable, and there is no standard curative treatment.

CASE PRESENTATION

We report a Caucasian case of metastatic perivascular epithelioid cell tumor previously treated with chemotherapy and surgery with elevated surface expression of programmed cell death ligand 1. Based on this result, treatment via immune checkpoint inhibition with the monoclonal antibody pembrolizumab was pursued. After 21 cycles, the patient sustained a complete response. Therapy was stopped after the 40th cycle, and she was moved to surveillance. She remained disease free 19 months off treatment.

CONCLUSIONS

This case report of a patient with perivascular epithelioid cell tumor treated successfully with programmed cell death protein-1 targeted therapy suggests that programmed cell death ligand-1 levels should be measured in patients with perivascular epithelioid cell tumor and immunotherapy considered for recurrent or metastatic patients. Future phase II/III studies in this disease should focus on sequencing of surgery and immunotherapy with a design of curative intent.

摘要

背景

血管周上皮样细胞瘤被世界卫生组织定义为“一组罕见的间叶性肿瘤,由组织学和免疫组织化学上具有独特特征的血管周上皮样细胞组成”。局限性血管周上皮样细胞瘤通常为良性,手术切除可成功治疗,而晚期或转移性血管周上皮样细胞瘤患者的预后不佳,且无标准的治愈性治疗方法。

病例介绍

我们报告了 1 例先前接受过化疗和手术治疗、且程序性细胞死亡配体 1 表面表达升高的转移性血管周上皮样细胞瘤的白种人病例。基于这一结果,我们采用程序性细胞死亡蛋白-1 靶向单克隆抗体 pembrolizumab 进行免疫检查点抑制治疗。经过 21 个周期的治疗后,患者获得了完全缓解。在第 40 个周期后停止治疗,转为监测。停药 19 个月后患者仍无疾病进展。

结论

本病例报告显示,程序性细胞死亡配体-1 靶向治疗成功治疗了血管周上皮样细胞瘤患者,提示应在血管周上皮样细胞瘤患者中测量程序性细胞死亡配体-1 水平,并考虑对复发性或转移性患者进行免疫治疗。未来在该疾病中开展的 II/III 期研究应重点关注手术和免疫治疗的测序,并采用治愈性意图的设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d688/8305520/604f3556a19b/13256_2021_2997_Fig1_HTML.jpg

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