Valeriya Kuznetsova, Harsh Oza, Hannah Rosenfeld, Carmela Sales, Samantha van der Linde, Izanne Roos, Stefanie Roberts, Fiore D’Aprano, Samantha M Loi, Mark Dowling, Michael Dickinson, Tomas Kalincik, Simon J Harrison, Mary Ann Anderson, Charles B Malpas
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引用次数: 0
摘要
简介:免疫效应细胞相关神经毒性综合征(ICANS)是嵌合抗原受体 T 细胞(CAR-T)疗法的一种常见副作用,症状从轻微到偶尔危及生命不等。ICANS 的神经、认知、精神和社会心理后遗症多种多样,定义不清,给诊断和管理带来了挑战。该综合征的康复轨迹尚不确定。在这一人群中,很少有患者在治疗前接受检查,这就为确定仅与 CAR-T 治疗相关的症状增加了一层复杂性。我们提出了一项前瞻性纵向研究方案,研究对象是在澳大利亚一家血液科接受 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,描述潜在综合征的特征,捕捉恢复情况,识别不同输注后结果的预测因素,并确定一套必要的认知工具,以便对患者进行急性监测。 方法与分析 这是一项前瞻性纵向研究,包括 CAR-T 治疗前、治疗后急性期、输注后 28 天、6 个月和 12 个月的神经心理学和神经学检查。数据将来自客观心理测量、临床检查、精神病理学自我报告问卷以及主观认知症状的描述。本研究的结果将通过在同行评审期刊上发表和在科学会议上演讲的方式传播。所有涉及人类受试者/患者的程序均已获得彼得-麦克卡勒姆癌症中心人类研究伦理委员会(Peter MacCallum Cancer Centre Human Research Ethics Committee)的批准(21/145)。
Neuropsychological outcomes of patients with haematological malignancies undergoing chimeric antigen receptor T-cell therapy: protocol for a prospective study
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).