Relapse-free survival in a pediatric patient with recurrent EZH2-mutant melanoma treated with adjuvant tazemetostat.

IF 6.8 1区 医学 Q1 ONCOLOGY NPJ Precision Oncology Pub Date : 2025-02-21 DOI:10.1038/s41698-025-00826-8
Erin E Resch, Stavriani C Makri, Paola Ghanem, Ezra G Baraban, Kenneth J Cohen, Alan R Cohen, Evan J Lipson, Christine A Pratilas
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Abstract

Enhancer of zeste homolog 2 (EZH2) is an essential epigenetic regulator of H3K27 histone methylation and is mutated or overexpressed in a wide variety of cancers. In melanoma, EZH2 overexpression contributes to excessive trimethylation of H3K27 on tumor suppressor genes and has been proposed to be a mechanism of tumor progression and metastasis. EZH2-targeted therapies have been successfully used to treat patients with follicular lymphoma and epithelioid sarcoma, but their clinical use in melanoma has not been described. Here, we describe a pediatric patient with multiply relapsed melanoma harboring an EZH2 A692V missense mutation, treated adjuvantly with the EZH2 inhibitor tazemetostat, who experienced a prolonged relapse-free survival.

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一名接受他昔莫司他辅助治疗的复发性EZH2突变黑色素瘤儿科患者的无复发生存率。
zeste同源物2增强子(Enhancer of zeste homolog 2, EZH2)是H3K27组蛋白甲基化的重要表观遗传调控因子,在多种癌症中发生突变或过表达。在黑色素瘤中,EZH2过表达导致肿瘤抑制基因H3K27过度三甲基化,并被认为是肿瘤进展和转移的机制之一。ezh2靶向疗法已成功用于治疗滤泡性淋巴瘤和上皮样肉瘤,但其在黑色素瘤中的临床应用尚未被描述。在这里,我们描述了一名患有多重复发黑色素瘤的儿童患者,该患者携带EZH2 A692V错义突变,用EZH2抑制剂他zemetostat辅助治疗,他经历了延长的无复发生存期。
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来源期刊
CiteScore
9.90
自引率
1.30%
发文量
87
审稿时长
18 weeks
期刊介绍: Online-only and open access, npj Precision Oncology is an international, peer-reviewed journal dedicated to showcasing cutting-edge scientific research in all facets of precision oncology, spanning from fundamental science to translational applications and clinical medicine.
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