CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neuropsychological outcomes of patients with haematological malignancies undergoing chimeric antigen receptor T-cell therapy: protocol for a prospective study.
Neuropsychological outcomes of patients with haematological malignancies undergoing chimeric antigen receptor T-cell therapy: protocol for a prospective study.
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免疫效应细胞相关神经毒性综合征(ICANS)是CAR-T 细胞治疗的常见副作用,症状从轻微到偶尔危及生命不等。ICANS 的神经、认知、精神和心理社会后遗症多样且尚未明确,给诊断和管理带来挑战。该综合征的恢复轨迹尚不确定。该人群在治疗前很少接受检查,这增加了确定仅与 CAR-T 治疗相关症状的复杂性。我们提出一项前瞻性纵向研究方案,研究对象为澳大利亚单一血液学服务机构中接受 CAR-T 治疗的成年患者。该研究将描述 ICANS 特有的神经认知特征,刻画其潜在综合征,捕捉恢复情况,识别输注后差异结局的预测因素,并确定一组急性期监测患者所需的认知工具。方法与分析:这是一项前瞻性纵向研究,包括在 CAR-T 治疗前、治疗后急性期、输注后 28 天、6 个月和 12 个月进行的神经心理和神经系统检查。数据将来源于客观心理测量指标、临床检查、精神病理学自评问卷以及主观认知主诉的描述。伦理与传播:本研究旨在指导 CAR-T 细胞治疗神经认知特征的诊断、管理和监测。本研究结果将通过同行评审期刊发表和科学会议报告进行传播。所有涉及人类受试者/患者的程序均已获得Peter MacCallum癌症中心人类研究伦理委员会批准(21/145)。
INTRODUCTION: Immune effector cell-associated neurotoxicity syndrome (ICANS) is a common side-effect of chimeric antigen receptor T-cell (CAR-T) therapy, with symptoms ranging from mild to occasionally life-threatening.
The neurological, cognitive, psychiatric and psychosocial sequelae of ICANS are diverse and not well defined, posing a challenge for diagnosis and management. The recovery trajectory of the syndrome is uncertain. Patients are rarely examined in this population pretherapy, adding a layer of complexity to specifying symptoms pertinent solely to CAR-T treatment.
We present a protocol of a prospective longitudinal research study of adult patients in a single Australian haematology service undergoing CAR-T therapy. The study will describe neurocognitive features specific to ICANS, characterise the underlying syndrome, capture recovery, identify predictors of differential postinfusion outcomes and determine a set of cognitive instruments necessary to monitor patients acutely. METHODS AND ANALYSIS: This is a prospective longitudinal study that comprises neuropsychological and neurological examinations occurring prior to CAR-T, during the acute post-treatment period, 28 days, 6 months and 12 months post infusion.
Data will be sourced from objective psychometric measures, clinical examinations, self-report questionnaires of psychopathology and accounts of subjective cognitive complaint. ETHICS AND DISSEMINATION: This study aims to guide diagnosis, management and monitoring of neurocognitive features of CAR-T cell therapy.
Results of this study will be disseminated through publication in peer-reviewed journals and presentations at scientific conferences. All procedures involving human subjects/patients were approved by the Peter MacCallum Cancer Centre Human Research Ethics Committee (21/145).
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