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一名35岁患有肺炎和巨细胞病毒血症患者接受嵌合抗原受体T细胞疗法后的细胞因子释放综合征

Cytokine Release Syndrome After CAR T-Cell Therapy in a 35-Year-Old Patient With Pneumonia and Cytomegalovirus Viremia.

作者信息

Helms Kristina A

机构信息

BMT/Hematology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Case Rep Med. 2024 Dec 16;2024:6751047. doi: 10.1155/carm/6751047. eCollection 2024.

DOI:10.1155/carm/6751047
PMID:39717043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11666310/
Abstract

The risk of cytokine release syndrome (CRS) in patients with infections prior to chimeric antigen receptor T-cell (CAR T-cell) therapy represents an important and underreported event. Patients with active infections needing prompt CAR T-cell therapy to treat aggressive hematologic malignancies remain a clinical challenge. This case describes the clinical course of a 35-year-old male patient with relapsed/refractory T-cell/histiocyte-rich large B-cell lymphoma who received axicabtagene ciloleucel. The patient developed ASTCT Grade II CRS on day +5, necessitating hospital admission and intravenous antibiotics, dexamethasone and tocilizumab. The patient was found to have a pneumonia (PJP) infection 3 days prior to CAR T-cell infusion and cytomegalovirus (CMV) viremia 3 days after CAR T-cell infusion. He received TMP-SMX for 21 days to treat PJP and valganciclovir to treat CMV viremia. PET/CT on day +26 demonstrated near resolution of pulmonary nodules and significant partial response of disease according to Deauville criteria. This case highlights the risk of CRS in immunocompromised patients with infections, and presents a unique case of CRS associated with PJP and CMV infections. Although the patient's clinical course was fraught with complications, he achieved a significant partial response to CAR T-cell therapy with the help of a multidisciplinary medical team.

摘要

嵌合抗原受体T细胞(CAR T细胞)治疗前感染患者发生细胞因子释放综合征(CRS)的风险是一个重要但报道不足的事件。对于患有需要及时进行CAR T细胞治疗以治疗侵袭性血液系统恶性肿瘤的活动性感染患者,仍然是一项临床挑战。本病例描述了一名35岁复发/难治性富含T细胞/组织细胞的大B细胞淋巴瘤男性患者接受axi-cabtagene ciloleucel治疗的临床过程。患者在第+5天出现美国血液与骨髓移植学会(ASTCT)II级CRS,需要住院并静脉使用抗生素、地塞米松和托珠单抗。发现该患者在CAR T细胞输注前3天患有肺孢子菌肺炎(PJP)感染,在CAR T细胞输注后3天出现巨细胞病毒(CMV)病毒血症。他接受了21天的复方新诺明治疗PJP,并接受缬更昔洛韦治疗CMV病毒血症。第+26天的PET/CT显示肺结节几乎消退,根据多维尔标准疾病有显著部分缓解。本病例突出了感染的免疫受损患者发生CRS的风险,并呈现了一例与PJP和CMV感染相关的CRS独特病例。尽管患者的临床过程充满并发症,但在多学科医疗团队的帮助下,他对CAR T细胞治疗取得了显著部分缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/227b357e84cc/CRIM2024-6751047.006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/227b357e84cc/CRIM2024-6751047.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/16c1a2ad4880/CRIM2024-6751047.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/0393d92ae4aa/CRIM2024-6751047.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/58c93d9311b3/CRIM2024-6751047.003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f2/11666310/227b357e84cc/CRIM2024-6751047.006.jpg

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本文引用的文献

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