免疫检查点抑制剂贫血谱:来自单中心早期临床试验病例系列经验的结果。

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2022-06-01 Epub Date: 2022-06-02 DOI:10.14740/jh1006
Blessie Elizabeth Nelson, Chinenye Lynette Ejezie, Bettzy A Stephen, Mirella Nardo, Erick Campbell, Jing Gong, David S Hong, Siqing Fu, Timothy A Yap, Mariela Blum Murphy, Sarina Piha-Paul, Naval G Daver, Cristhiam M Rojas-Hernandez, Aung Naing
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引用次数: 1

摘要

免疫检查点抑制剂贫血(ICI-A)是一种罕见的疾病,如果不及时发现,可能会危及生命。本研究的目的是描述早期临床试验中ICI治疗的表现、评估和结果,以指导未来的研究和制定标准化的护理指南。对在德克萨斯大学MD安德森癌症中心参加早期临床试验的333例患者的回顾性图表回顾显示,2016年至2020年期间有4例ci - a。我们确定了四例病例,其中包括ICI相关的自身免疫性溶血性贫血、噬血细胞淋巴组织细胞增多症和血栓性微血管病,这是ICI联合研究治疗的结果。本文回顾了患者的表现、评估、骨髓病理、干预措施和临床过程。在本回顾性研究中,血液免疫相关不良事件(血红素- iraes)发生的中位时间为3.5周(2 - 6周)。一名患者先前患有未经治疗的慢性淋巴细胞白血病。糖皮质激素在大多数患者中是有效的一线治疗,尽管大多数患者没有再挑战,但成功地完全恢复并继续进行非免疫治疗为基础的治疗。在临床试验中对ci - a的认识对于血红素- iraes的早期识别至关重要。在临床试验登记和免疫介导的血液毒性的最佳管理策略中,需要进一步的研究来确定和分层危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spectrum of Immune Checkpoint Inhibitor Anemias: Results From a Single Center, Early-Phase Clinical Trials Case Series Experience.

Spectrum of Immune Checkpoint Inhibitor Anemias: Results From a Single Center, Early-Phase Clinical Trials Case Series Experience.

Immune checkpoint inhibitor anemias (ICI-A) are a rare entity which can be potentially life-threatening without prompt identification. The goal of the study is to characterize the presentation, evaluation, and outcomes of ICI therapy in early phase clinical trial setting to guide future research and to develop standardized care guidelines. Retrospective chart review of 333 patients who participated in early phase clinical trials at the University of Texas MD Anderson Cancer Center revealed four cases with ICI-A between 2016 and 2020. We identified a spectrum of four cases which included ICI-related autoimmune hemolytic anemias, hemophagocytic lymphohistiocytosis and thrombotic microangiopathy as a result of combinatory investigational therapies involving ICI. Patient presentation, evaluation, bone marrow pathology, interventions, and clinical course were reviewed. The median time to onset of hematological immune-related adverse events (heme-irAEs) in this retrospective series was 3.5 weeks (2 - 6 weeks). One patient had pre-existing untreated chronic lymphocytic leukemia. Glucocorticoids are an effective first-line treatment in most patients although most patients were not rechallenged but successfully had complete recovery and pursued further non-immunotherapy-based therapies. Cognizance of ICI-A in clinical trial setting is paramount to early recognition of heme-irAEs. Further research is needed to identify and stratify risk factors during clinical trial enrollment and optimal management strategies for immune-mediated hematologic toxicities.

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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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