Suppr超能文献

病例报告: Erdheim-Chester病的靶向治疗策略

Case report: Targeted treatment strategies for Erdheim-Chester disease.

作者信息

Gulyás Anita, Pinczés László Imre, Mátyus János, Végh Edit, Bedekovics Judit, Tóth Judit, Barna Sándor, Hunya Zsolt, Szabó Imre Lőrinc, Gazdag Annamária, Illés Árpád, Magyari Ferenc

机构信息

Division of Hematology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Doctoral School of Clinical Medicine, University of Debrecen, Debrecen, Hungary.

出版信息

Front Oncol. 2024 Mar 14;14:1305518. doi: 10.3389/fonc.2024.1305518. eCollection 2024.

Abstract

INTRODUCTION

Erdheim-Chester disease (ECD) is a rare disease that belongs to the group of Dendritic and histiocytic neoplasms. Only 2000 cases have been reported worldwide. It can present with a wide range of symptoms, making a differential diagnosis especially difficult. The primary and most important diagnostic tool is a biopsy of the affected organ/tissue. Nowadays the analysis of different mutations affecting the BRAF and MAPK pathways makes it possible to use targeted treatments, such as vemurafenib, dabrafenib, or cobimetinib.

OBJECTIVE

Our aim is to present the results of three male patients treated in our hematology department.

RESULTS

Our BRAF mutation-positive patient presented with retroperitoneal tissue proliferation and diabetes insipidus. The initial therapy of choice was dabrafenib. After 3 months of treatment, F-fluoro-deoxyglucose positron emission tomography (FDG-PET)/computed tomography (CT) scans showed regression, and after 2 years of treatment, no disease activity was detected. In our second patient, a recurrent febrile state (not explained by other reasons) and diabetes insipidus suggested the diagnosis. A femoral bone biopsy confirmed BRAF-negative ECD. The first-line therapy was interferon-alpha. After 3 months of treatment, no response was observed on FDG-PET/CT, and treatment with cobimetinib was started. The control FDG-PET/CT imaging was negative. Our third patient was evaluated for dyspnea, and a CT scan showed fibrosis with hilar lymphadenomegaly. A lung biopsy confirmed BRAF-negative ECD. We started treatment with interferon-alpha, but unfortunately, no improvement was observed. Second-line treatment with cobimetinib resulted in a partial metabolic response (PMR) according to control FDG-PET/CT.

CONCLUSIONS

Our results demonstrate that an appropriately chosen treatment can lead to a good therapeutic response, but dose reduction may be necessary due to side effects. With advanced targeted therapeutic treatment options, survival and quality of life are significantly improved.

摘要

引言

Erdheim-Chester病(ECD)是一种罕见病,属于树突状和组织细胞性肿瘤。全球仅报告了2000例病例。它可表现出广泛的症状,这使得鉴别诊断尤为困难。主要且最重要的诊断工具是对受影响器官/组织进行活检。如今,对影响BRAF和MAPK通路的不同突变进行分析,使得使用靶向治疗成为可能,如维莫非尼、达拉非尼或考比替尼。

目的

我们的目的是展示在我们血液科接受治疗的三名男性患者的治疗结果。

结果

我们的BRAF突变阳性患者表现为腹膜后组织增生和尿崩症。最初的首选治疗是达拉非尼。治疗3个月后,F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)/计算机断层扫描(CT)显示病情缓解,治疗2年后未检测到疾病活动。在我们的第二位患者中,反复发热状态(无其他原因可解释)和尿崩症提示了诊断。股骨活检证实为BRAF阴性ECD。一线治疗是α干扰素。治疗3个月后,FDG-PET/CT未观察到反应,随后开始使用考比替尼治疗。对照FDG-PET/CT成像为阴性。我们的第三位患者因呼吸困难接受评估,CT扫描显示纤维化伴肺门淋巴结肿大。肺活检证实为BRAF阴性ECD。我们开始使用α干扰素治疗,但遗憾的是,未观察到改善。根据对照FDG-PET/CT,考比替尼二线治疗导致部分代谢反应(PMR)。

结论

我们的结果表明,适当选择的治疗可导致良好的治疗反应,但由于副作用可能需要减少剂量。随着先进的靶向治疗选择,生存率和生活质量得到显著改善。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验