血浆置换治疗检查点抑制剂引起的严重免疫相关不良事件:早期的机会窗口?

IF 4.1 Q2 IMMUNOLOGY Immunotherapy advances Pub Date : 2022-01-01 DOI:10.1093/immadv/ltac012
Tamiko R Katsumoto, Kalin L Wilson, Vinay K Giri, Han Zhu, Shuchi Anand, Kavitha J Ramchandran, Beth A Martin, Muharrem Yunce, Srikanth Muppidi
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引用次数: 8

摘要

免疫检查点抑制剂(ICIs)已经彻底改变了几种晚期恶性肿瘤的治疗,导致部分患者的持久缓解。它们的迅速扩大使用导致免疫相关不良事件(irAEs)的频率增加。irAEs的发病机制尚不清楚,但可能涉及T细胞的异常活化,导致炎症细胞因子释放或致病抗体的产生,导致器官损伤。严重的irae会使人极度虚弱,在某些情况下,甚至会危及生命。irae可能并不总是对皮质类固醇有反应,或者可能需要过高的,通常是有毒的皮质类固醇剂量。治疗性血浆置换(PLEX)是一种治疗方式,在治疗某些严重的irAEs(包括目前治疗指南中未提及的irAEs)方面显示出良好的效果。PLEX可以通过加速ICI的清除,或通过急性清除致病抗体、细胞因子和趋化因子,减弱正在进行的irae和预防延迟的irae。在这里,我们从文献中总结了PLEX成功用于治疗irAEs的例子。我们认为时机可能是一个关键因素,尽早使用PLEX治疗危及生命的irae可能会产生更有利的结果。在irae高危人群中,PLEX作为一种潜在的缓解治疗策略的可用性可能会鼓励挽救生命的ICI使用或重新挑战。未来的研究对于更好地确定哪些适应症最适合PLEX,特别是在irAE治疗序列中确定最佳位置,以及评估ICI去除对癌症结果的影响至关重要。
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Plasma exchange for severe immune-related adverse events from checkpoint inhibitors: an early window of opportunity?

Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of several advanced malignancies leading to durable remission in a subset of patients. Their rapidly expanding use has led to an increased frequency of immune-related adverse events (irAEs). The pathogenesis of irAEs is poorly understood but may involve aberrant activation of T cells leading to inflammatory cytokine release or production of pathogenic antibodies leading to organ damage. Severe irAEs can be extremely debilitating and, in some cases, life threatening. IrAEs may not always be corticosteroid responsive or may require excessively high, often toxic, corticosteroid doses. Therapeutic plasma exchange (PLEX) is a treatment modality that has shown promising results for the management of certain severe irAEs, including irAEs that are not mentioned in current treatment guidelines. PLEX may attenuate ongoing irAEs and prevent delayed irAEs by accelerating clearance of the ICI, or by acutely removing pathogenic antibodies, cytokines, and chemokines. Here, we summarize examples from the literature in which PLEX was successfully used for the treatment of irAEs. We posit that timing may be a critical factor and that earlier utilization of PLEX for life-threatening irAEs may result in more favorable outcomes. In individuals at high risk for irAEs, the availability of PLEX as a potential therapeutic mitigation strategy may encourage life-saving ICI use or rechallenge. Future research will be critical to better define which indications are most amenable to PLEX, particularly to establish the optimal place in the sequence of irAE therapies and to assess the ramifications of ICI removal on cancer outcomes.

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