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嵌合抗原受体 T 细胞治疗后长期生存者的患者报告神经精神结局。

Patient-Reported Neuropsychiatric Outcomes of Long-Term Survivors after Chimeric Antigen Receptor T Cell Therapy.

机构信息

Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.

Clinical Research division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

出版信息

Biol Blood Marrow Transplant. 2020 Jan;26(1):34-43. doi: 10.1016/j.bbmt.2019.09.037. Epub 2019 Oct 9.

Abstract

CD19-targeted chimeric antigen receptor (CAR) modified T cell immunotherapy is a novel treatment with promising results in patients with relapsed/refractory lymphoid malignancies. CAR T cell therapy has known early toxicities of cytokine release syndrome and neurotoxicity, but little is known about long-term neuropsychiatric adverse effects. We have used patient-reported outcomes, including Patient-Reported Outcomes Measurement Information System (PROMIS) measures, to assess neuropsychiatric and other patient-reported outcomes of 40 patients with relapse/refractory chronic lymphocytic leukemia, non-Hodgkin lymphoma, and acute lymphoblastic leukemia 1 to 5 years after treatment with CD19-targeted CAR T cells. Mean T scores of PROMIS domains of global mental health, global physical health, social function, anxiety, depression, fatigue, pain, and sleep disturbance were not clinically meaningfully different from the mean in the general US population. However, 19 patients (47.5%) reported at least 1 cognitive difficulty and/or clinically meaningful depression and/or anxiety, and 7 patients (17.5%) scored ≤40 in global mental health, indicating at least 1 standard deviation worse than the general population mean. Younger age was associated with worse long-term global mental health (P = .02), anxiety (P = .001), and depression (P= .01). Anxiety before CAR T cell therapy was associated with increased likelihood of anxiety after CAR T cell therapy (P = .001). Fifteen patients (37.5%) reported cognitive difficulties after CAR T cell therapy. Depression before CAR T cell therapy was statistically significantly associated with higher likelihood of self-reported post-CAR T cognitive difficulties (P = .02), and there was a trend for an association between acute neurotoxicity and self-reported post-CAR T cognitive difficulties (P = .08). Having more post-CAR T cognitive difficulties was associated with worse global mental health and global physical health. Our study demonstrates overall good neuropsychiatric outcomes in 40 long-term survivors after CAR T cell therapy. However, nearly 50% of patients in the cohort reported at least 1 clinically meaningful negative neuropsychiatric outcome (anxiety, depression, or cognitive difficulty), indicating that a significant number of patients would likely benefit from mental health services following CAR T cell therapy. Younger age, pre-CAR T anxiety or depression, and acute neurotoxicity may be risk factors for long-term neuropsychiatric problems in this patient population. Larger studies are needed to confirm these findings.

摘要

CD19 靶向嵌合抗原受体 (CAR) 修饰的 T 细胞免疫疗法是一种新型治疗方法,在复发/难治性淋巴恶性肿瘤患者中显示出良好的疗效。CAR T 细胞治疗具有细胞因子释放综合征和神经毒性等早期毒性,但对长期神经精神不良影响知之甚少。我们使用患者报告的结果,包括患者报告的结局测量信息系统 (PROMIS) 测量,评估了 40 例复发/难治性慢性淋巴细胞白血病、非霍奇金淋巴瘤和急性淋巴细胞白血病患者在接受 CD19 靶向 CAR T 细胞治疗 1 至 5 年后的神经精神和其他患者报告的结局。PROMIS 全球心理健康、全球身体健康、社会功能、焦虑、抑郁、疲劳、疼痛和睡眠障碍领域的平均 T 评分与一般美国人群的平均水平没有明显的临床差异。然而,19 名患者(47.5%)报告至少有 1 项认知困难和/或有临床意义的抑郁和/或焦虑,7 名患者(17.5%)的全球心理健康评分≤40,表明至少比一般人群的平均水平差 1 个标准差。年龄较小与长期全球心理健康状况较差相关(P=0.02)、焦虑(P=0.001)和抑郁(P=0.01)。CAR T 细胞治疗前的焦虑与 CAR T 细胞治疗后的焦虑可能性增加相关(P=0.001)。15 名患者(37.5%)在接受 CAR T 细胞治疗后出现认知困难。CAR T 细胞治疗前的抑郁与患者报告的 CAR T 后认知困难的可能性更高相关(P=0.02),急性神经毒性与患者报告的 CAR T 后认知困难之间存在关联的趋势(P=0.08)。CAR T 后认知困难越多,全球心理健康和全球身体健康状况越差。我们的研究表明,在接受 CAR T 细胞治疗后,40 名长期幸存者的神经精神结局总体良好。然而,该队列中有近 50%的患者报告至少有 1 项有临床意义的负面神经精神结局(焦虑、抑郁或认知困难),这表明相当数量的患者在接受 CAR T 细胞治疗后可能需要心理健康服务。年龄较小、CAR T 前焦虑或抑郁以及急性神经毒性可能是该患者人群长期神经精神问题的危险因素。需要更大的研究来证实这些发现。

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