西罗莫司抑制mTOR与HIV相关多灶性eb病毒相关平滑肌肿瘤(EBV-SMT)的持久应答相关,并对新治疗方案进行了综述

IF 0.2 Q4 ONCOLOGY
John Kh Ang , Daniel Ry Yap , Khoon Leong Chuah , Jens Samol
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引用次数: 0

摘要

eb病毒相关的平滑肌肿瘤(EBV-SMT)是一种罕见的肿瘤,估计患病率为百万分之2。它发生在免疫功能低下和EBV再激活导致肿瘤发生的风险高的患者中。免疫功能低下状态的例子包括感染人类免疫缺陷病毒(HIV)的患者、移植后接受医源性免疫抑制的患者和原发性/先天性免疫缺陷患者。尽管EBV和EBV- smt之间的联系已经确立,但这种联系的潜在病理生理机制尚不清楚。我们报告了一例与HIV相关的EBV-SMT患者,他已接受西罗莫司治疗5年,病情持续得到控制,清楚地证明了西罗莫司在EBV-SMT治疗中的持久活性。我们仔细审查了有关用于EBV- smt管理的新疗法的文献,并将其与其他EBV相关肿瘤联系起来。据我们所知,这是首例西罗莫司治疗患者的病例报告,我们建议将西罗莫司抑制mTOR与HAART一起作为HIV相关ebv - smt患者的第一治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
mTOR inhibition with sirolimus is associated with a durable response in HIV associated multifocal Epstein-Barr Virus associated smooth muscle Tumour (EBV-SMT) and mini review of novel therapeutic options
Epstein-Barr Virus associated smooth muscle tumour (EBV-SMT) is a rare tumour with an estimated prevalence of <2 cases per million. It develops in patients who are immunocompromised and in whom the risk of EBV reactivation causing tumorigenesis is high. Examples of immunocompromised states include patients infected with human immunodeficiency virus (HIV), patients on iatrogenic immunosuppression following transplantation and patients with primary/congenital immunodeficiency. Although the association between EBV and development of EBV-SMT is well established, the underlying pathophysiology for this association is unclear.
We present a case of a patient with HIV related EBV-SMT who has been on treatment with sirolimus for >5 years with disease continuing to remain controlled, clearly demonstrating the durable activity of sirolimus in the management of EBV-SMT. We scrutinized the literature pertaining to novel therapeutics which have been used for the management of EBV-SMTs and set it into context with other EBV associated neoplasms.
To our knowledge, this is the first case report of a patient treated with sirolimus and we recommend that mTOR inhibition with sirolimus be considered as a first therapeutic option together with HAART in patients with HIV associated EBV-SMTs.
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CiteScore
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