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恩考芬尼与比美替尼联合治疗同时存在BRAF和KRAS突变的 Erdheim-Chester病的疗效:病例报告

Efficacy of Combined Encorafenib and Binimetinib Treatment for Erdheim-Chester Disease Harboring Concurrent BRAF and KRAS Mutations: A Case Report.

作者信息

Hibino Yuto, Sakai Rika, Takahashi Hiroyuki, Takeda Takaaki, Hirose Natsuki, Tokunaga Mayumi, Washimi Kota, Yokose Tomoyuki, Kasajima Rika, Hiroshima Yukihiko, Miyagi Yohei, Nakajima Hideaki

机构信息

Department of Hematology and Medical Oncology, Kanagawa Cancer Center, Yokohama, Japan.

Department of Pathology, Kanagawa Cancer Center, Yokohama, Japan.

出版信息

Cancer Rep (Hoboken). 2024 Dec;7(12):e70093. doi: 10.1002/cnr2.70093.

Abstract

BACKGROUND

Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis with diverse clinical manifestations, often associated with mutations in the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) pathway. BRAF and KRAS mutations, which are driver mutations of oncogenes, participate in the same signaling pathway (MAPK/ERK pathway) and are usually mutually exclusive. We report a case of ECD with concurrent BRAF and KRAS mutations treated using BRAF and MEK inhibitors.

CASE

A 70-year-old man was referred to our hospital with a mesenteric nodal lesion on computed tomography scan. The patient experienced symptoms consistent with ECD, including central diabetes insipidus. Biopsy revealed histiocytes positive for CD68 and CD163, negative for S100, CD1a, and CD21. Liquid-based comprehensive genomic profiling and tissue-based cancer gene panel test identified BRAF and KRAS mutations with different variant allele fraction. Additional immunohistochemistry with an antibody specific to mutant BRAF protein stained some proliferating histiocytes, consistent with ECD. Based on the genomic profiling results, we hypothesized that there was a coexistence of a clone harboring BRAF and another clone harboring KRAS, and planned a combination therapy with BRAF and MEK inhibitors targeting each clone, respectively. The patient received oral encorafenib at 100 mg once daily and oral binimetinib at 15 mg twice daily. The combination therapy resulted in rapid resolution of symptoms and significant improvement in imaging findings.

CONCLUSION

This case represents a unique presentation of ECD with concurrent BRAF and KRAS mutations. Combination therapy with encorafenib and binimetinib targeting each clone resulted in a remarkable therapeutic effect and was well-tolerated. This is the first reported case of ECD treated with encorafenib and binimetinib. The combination therapy with BRAF and MEK inhibitors is one of the rational treatment options for cases of ECD with a suspicion of multiple clones.

摘要

背景

厄尔德海姆-切斯特病(ECD)是一种罕见的非朗格汉斯细胞组织细胞增多症,临床表现多样,常与丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)通路的突变相关。BRAF和KRAS突变是癌基因的驱动突变,参与同一信号通路(MAPK/ERK通路),且通常相互排斥。我们报告了一例使用BRAF和MEK抑制剂治疗的同时存在BRAF和KRAS突变的ECD病例。

病例

一名70岁男性因计算机断层扫描显示肠系膜淋巴结病变被转诊至我院。患者出现了与ECD相符的症状,包括中枢性尿崩症。活检显示组织细胞CD68和CD163呈阳性,S100、CD1a和CD21呈阴性。液基综合基因组分析和基于组织的癌症基因检测板检测发现BRAF和KRAS突变,其变异等位基因分数不同。使用针对突变BRAF蛋白的特异性抗体进行的额外免疫组织化学染色显示一些增殖的组织细胞呈阳性,与ECD一致。基于基因组分析结果,我们推测存在一个携带BRAF的克隆和另一个携带KRAS的克隆共存,并计划分别针对每个克隆使用BRAF和MEK抑制剂进行联合治疗。患者接受了口服恩考芬尼,每日一次,每次100毫克,以及口服比美替尼,每日两次,每次15毫克。联合治疗使症状迅速缓解,影像学表现显著改善。

结论

该病例代表了同时存在BRAF和KRAS突变的ECD的独特表现。针对每个克隆使用恩考芬尼和比美替尼的联合治疗产生了显著的治疗效果,且耐受性良好。这是第一例使用恩考芬尼和比美替尼治疗的ECD报告病例。BRAF和MEK抑制剂联合治疗是疑似多克隆ECD病例的合理治疗选择之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8389/11670472/88eb64586336/CNR2-7-e70093-g002.jpg

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