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:High Symptom Burden Predicts Poorer Quality of Life Among Children and Adolescents Receiving Hematopoietic Stem Cell Transplantation or Chimeric Antigen Receptor T-Cell Therapy.
High Symptom Burden Predicts Poorer Quality of Life Among Children and Adolescents Receiving Hematopoietic Stem Cell Transplantation or Chimeric Antigen Receptor T-Cell Therapy.
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儿童在治疗早期感觉更差,到第+90 天时有所改善。症状负担水平在所有时间点均预测总体生活质量。对实践的启示:经历高症状负担的儿童应在整个治疗过程中接受频繁评估和加强症状管理,以减轻对生活质量的负面影响。
患有癌症和其他严重疾病的儿童在造血干细胞移植和CAR-T 细胞治疗期间会经历症状负担,但有限的研究描述了这些症状如何随时间与整体生活质量相互作用。
本研究的目的是探讨接受造血干细胞移植或 CAR-T 细胞治疗的儿童的症状与生活质量之间的纵向关系。
采用多中心研究设计,收集140例接受造血干细胞移植和CAR-T 细胞治疗的儿童在细胞输注前及+30、+60和+90天的症状和生活质量信息。采用纵向平行过程模型来描述症状与生活质量之间的关系。
儿童(平均年龄8.4岁)接受了异基因移植(57.9%)、自体移植(25.7%)或CAR-T 细胞治疗(16.4%)。基线时疼痛、疲乏、恶心、呕吐和食欲不振的症状患病率最高(>50%)。生活质量评分在基线时较差(平均值[SD],69.5[15.8]),到第+90天时改善了10分。纵向模型表明,基线时高症状患病率预测了基线和第+90天时较差的生活质量。
Children with cancer and other serious illnesses experience symptom burden during hematopoietic stem cell transplantation and chimeric antigen receptor T-cell therapy, yet limited research has characterized how these symptoms interact with overall quality of life over time.
The aim of this study was to examine the longitudinal relationship between symptoms and quality of life in children receiving hematopoietic stem cell transplantation or chimeric antigen receptor T-cell therapy.
A multisite study design was used to collect symptom and quality of life information at pre-cell infusion and days +30, +60, and +90 from children (N = 140) receiving hematopoietic stem cell transplantation and chimeric antigen receptor T-cell therapy. A longitudinal parallel process model was used to characterize the relationship between symptoms and quality of life.
Children (mean age, 8.4 years) received allogeneic transplant (57.9%), autologous transplant (25.7%), or chimeric antigen receptor T-cell therapy (16.4%). Symptom prevalence was highest at baseline (>50%) for pain, fatigue, nausea, vomiting, and low appetite. Quality of life scores were worse at baseline (mean [SD], 69.5 [15.8]) and improved by 10 points by day +90. The longitudinal model indicated high symptom prevalence at baseline predicted worse quality of life at both baseline and day +90.
Children felt worse early in the treatment trajectory and improved by day +90. The level of symptom burden predicted the overall quality of life at all time points. IMPLICATIONS FOR PRACTICE: Children experiencing high symptom burden should receive frequent assessment and enhanced symptom management throughout the treatment trajectory to mitigate negative impacts on quality of life.
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