Case Report: A PD-L1-Positive Patient With Pleomorphic Rhabdomyosarcoma Achieving an Impressive Response to Immunotherapy

被引:4
作者
Liu, Jiayong [1 ]
Liu, Peijie [2 ]
Gong, Fuyu [3 ]
Tian, Youhui [3 ]
Zhao, Xiaochen [3 ]
机构
[1] Peking Univ Canc Hosp & Inst, Dept Bone & Soft Tissue Tumor, Minist Educ Beijing, Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
[2] Henan Univ, Affiliated Hosp 1, Dept Oncol, Kaifeng, Peoples R China
[3] 3D Med Inc, Med Dept, Shanghai, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
中国国家自然科学基金;
关键词
pleomorphic rhabdomyosarcoma; immunotherapy; pazopanib; PD-L1; CD8 T cell; SOFT-TISSUE SARCOMA; TUMORS; IDENTIFICATION; CLASSIFICATION; PEMBROLIZUMAB; MULTICENTER; BLOCKADE; SKIN;
D O I
10.3389/fimmu.2022.815598
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There is currently a lack of effective systemic treatment for patients with advanced pleomorphic rhabdomyosarcoma (PRMS). Although programmed death protein 1 (PD-1) inhibitors have shown efficacy in various solid tumors, their effects on PRMS have not been well established. Here, we present a case of a 12-year-old Chinese male adolescent with metastatic PRMS who benefited from the PD-1 inhibitor nivolumab. The patient initially underwent primary tumor resection but failed to respond to subsequent first-line chemotherapy and second-line pazopanib treatment. Pathological examination showed positive PD-L1 expression and tumor-infiltrating lymphocytes in the tumor tissue, and the patient was administered nivolumab as a posterior-line treatment. After attaining a clinically partial response (PR), surgical resection was performed, which was followed by adjuvant nivolumab. At the time of the submission of this manuscript, the patient achieved recurrence-free survival (RFS) lasting 45 months and counting. This is the first clinical evidence that a patient with refractory PRMS was controlled by anti-PD-1 antibody, with an RFS lasting more than 3 years. This case suggests that PD-L1 expression and T-cell infiltration could be used as potential biomarkers for PRMS immunotherapy.
引用
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页数:7
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