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:The Patient Symptom Experience After Tisagenlecleucel and Lisocabtagene Maraleucel CAR T-Cell Therapy for Lymphoma.
The Patient Symptom Experience After Tisagenlecleucel and Lisocabtagene Maraleucel CAR T-Cell Therapy for Lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
参与者持续报告症状,包括疲乏、神经病变、耐力低下、失眠、记忆问题和疼痛。大多数症状随时间改善。部分症状干扰了社交活动、工作、驾驶和体力活动,尽管参与者报告大多数症状在 CAR T-cell 治疗前就已存在,且总体而言,他们认为 CAR T-cell 治疗是可接受的。对护理实践的启示:CAR T-cell 治疗后处于缓解期的患者往往仍持续经历症状。护士应继续评估这一不断增长的患者群体,并确定患者是否需要额外的症状管理或支持。需要进一步研究以了解长期症状轨迹及其与既往治疗线和 CAR T-cell 治疗的关联。
嵌合抗原受体(CAR)T细胞治疗与几种独特毒性相关,治疗后即刻的短期症状轨迹已有充分记录。然而,患者长期症状体验知之甚少。本研究旨在引出因B细胞淋巴瘤接受CAR-T 细胞治疗后处于缓解期的成年患者的症状体验。
采用定性描述设计并进行主题分析。招募在一家三级学术医疗中心进行,纳入标准如下:入组前3至12个月因B细胞淋巴瘤接受CAR-T 细胞治疗的成年受者,且目前处于缓解状态。进行了半结构化访谈,对转录文本进行归纳编码,团队成员每周会面以确保严谨性。最终样本包括10例患者:7例接受tisagenlecleucel,3例接受lisocabtagene marleucel,输注后中位时间为169天,年龄中位数为65岁。
Chimeric Antigen Receptor (CAR) T-cell treatment is associated with several unique toxicities, and the short-term symptom trajectory in the immediately after therapy is well-documented. However, little is known about patients' long-term symptom experience. The study aimed to elicit the symptom experience of adult patients in remission after CAR T-cell therapy for B cell lymphoma. DATA SOURCES: A qualitative descriptive design with thematic analysis was utilized. Recruitment occurred at a tertiary academic medical center using the following inclusion criteria: adult recipient of CAR T-cell therapy for B-cell lymphoma between 3 and 12 months prior to enrollment, and currently in remission. Semi-structured interviews were conducted, transcripts were inductively coded, and team members met weekly to ensure rigor. The final sample included 10 patients: Seven received tisagenlecleucel and three received lisocabtagene marleucel and were a median of 169 days post-infusion and 65 years of age.
Participants continued to report symptoms, including fatigue, neuropathy, low endurance, insomnia, memory problems, and pain. Most symptoms improved over time. Some symptoms interfered with social activities, work, driving, and physical activity, though participants reported that most symptoms existed prior to CAR T-cell therapy, and overall, found CAR T-cell therapy acceptable. IMPLICATIONS FOR NURSING PRACTICE: Patients in remission after CAR T-cell therapy often continue to experience symptoms. Nurses should continue to assess this growing patient population and determine if patients require additional symptom management or support. Further research is needed to understand long-term symptom trajectory and associations with prior lines of therapy and CAR T-cell therapy.
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