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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Remission after CAR T-cell therapy: Do lymphoma patients recover a normal life?
Remission after CAR T-cell therapy: Do lymphoma patients recover a normal life?
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CAR-T 细胞(CAR-T 细胞)可使相当一部分复发/难治性淋巴瘤患者获得持久缓解。然而,患者接受 CAR-T 细胞治疗后的生活情况仍知之甚少。
我们前瞻性评估了缓解期淋巴瘤患者的多维度恢复状况,评估时间包括白细胞单采前、CAR-T 细胞输注前,以及输注后 3、6 和 12 个月。采用经验证的工具测量淋巴瘤相关及总体健康相关生活质量(HRQoL;癌症治疗功能评估量表-淋巴瘤版[FACT-Lym]和 EQ-5D-5L)、认知主诉(FACT-Cognition)、疲劳(FACIT-Fatigue 子量表)、心理状态(医院焦虑抑郁量表、创伤后应激检查表)及性健康(关系与性健康量表)。缓解超过 12 个月后,还调查身体、职业、性健康及总体生活状况。治疗后 3、6 和 12 个月分别有 53、35 和 23 例患者可评估。淋巴瘤相关 HRQoL 在 3、6 和 12 个月均有临床意义上的改善,相较基线平均变化分别为 10.9(95% 置信区间[CI]:5.8–16.1)、12.2(95% CI:4.2–20.1)和 11.72(95% CI:2.06–21.38)。总体 HRQoL、疲劳和焦虑均有临床意义上的改善,但随访期间仍有 20%–40% 的患者持续存在疲劳、心理困扰和认知主诉。CAR-T 细胞治疗 12 个月后,在 22 例可评估患者中,81.8% 对日常生活感到满意。近半数患者的身体活动、职业、性健康及整体幸福感已恢复至诊断前水平。
研究发现,CAR-T 细胞治疗后患者的 HRQoL 得到改善,包括焦虑、抑郁、性满意度及总体幸福感。然而,并非所有患者都能恢复“正常生活”。仍需进一步研究确定哪些患者有生活质量受损风险,以改善 CAR-T 细胞输注后的恢复。
Chimeric antigen receptor T cells (CAR T cells) can induce prolonged remission in a substantial subset of patients with relapse/refractory lymphoma.
However, little is known about patients' life after CAR T-cell therapy.
We prospectively assessed the multidimensional recovery of lymphoma patients in remission, before leukapheresis, before CAR T-cell infusion, and 3, 6, and 12 months thereafter. Validated tools were used to measure lymphoma-related and global health-related quality of life (HRQoL; Functional Assessment of Cancer Therapy-Lymphoma [FACT-Lym] and EQ-5D-5L), cognitive complaint (FACT-Cognition), fatigue (FACIT-Fatigue subscale), psychological status (Hospital Anxiety and Depression Scale, Post-Traumatic Check List Scale), and sexuality (Relationship and Sexuality Scale). Beyond 12 months of remission, we also surveyed physical, professional, sexual, and general life status. At 3, 6, and 12 months, 53, 35, and 23 patients were evaluable, respectively.
Improvement in lymphoma-related HRQoL was clinically relevant at 3, 6, and 12 months with a mean change from baseline of 10. 9 (95% confidence interval [CI]: 5. 8; 16. 1), 12. 2 (95% CI: 4. 2; 20. 1), and 11. 72 (95% CI: 2. 06; 21. 38), respectively.
Improvement in global HRQoL, fatigue, and anxiety was clinically relevant, but 20%-40% of patients experienced persistent fatigue, psychological distress, and cognitive complaints over time. Beyond 12 months after CAR T cells, 81. 8% of 22 evaluable patients were satisfied with their daily life. Physical activity, professional, sexual, and global well-being had returned to prediagnosis levels in nearly half of the patients.
We found an improvement in HRQoL after CAR T-cell therapy including anxiety, depression, sexual satisfaction, and general well-being.
However, not all patients recover a "normal life." Further research is needed to determine which patients are at risk of quality-of-life impairment to improve recovery after CAR T-cell infusion.
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