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:Patient preferences for triple-class-exposed relapsed or refractory multiple myeloma treatment: a discrete-choice study.
Patient preferences for triple-class-exposed relapsed or refractory multiple myeloma treatment: a discrete-choice study.
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。
对于 TCE RRMM 患者的治疗决策,应考虑疗效、安全性和与治疗过程及初始监测相关的属性之间的权衡。
量化患者对三线暴露(TCE)复发和/或难治性多发性骨髓瘤(RRMM)新型治疗属性的偏好。
采用离散选择实验,我们引出了对7个属性的偏好:客观缓解率(ORR)、总生存期(OS)、全等级细胞因子释放综合征风险、全等级免疫效应细胞相关神经毒性综合征风险、严重感染风险(3级及以上)、治疗给药方式,以及初始住院要求。
OS 是最重要的属性(24 个月增加的条件相对重要性 [CRI] 为 32.0%),其次是严重感染风险(避免 60% 风险的 CRI 为 17.3%)、初始住院要求(避免 14 天初始住院的 CRI 为 15.0%)和 ORR(38% 增加的 CRI 为 13.7%)。基于相对偏好权重之间的差异,开始治疗时较少的初始住院天数和现成可用(相对于CAR-T [CAR-T] 细胞样)选项显著更受偏好。
Using a discrete-choice experiment, we elicited preferences for 7 attributes: objective response rate (ORR), overall survival (OS), all-grade cytokine release syndrome risk, all-grade immune effector cell-associated neurotoxicity syndrome risk, serious infection risk (grade 3+), treatment administration, and initial hospitalization requirements.
OS was the most important attribute (conditional relative importance [CRI] 32.0% for a 24-month increase), followed by serious infection risk (CRI 17.3% for avoiding a 60% risk), initial hospitalization requirements (CRI 15.0% for avoiding 14 days of initial hospitalization), and ORR (CRI 13.7% for a 38% increase). Based on differences between relative preference weights, fewer initial hospitalization days when starting treatment and off-the-shelf (vs. chimeric antigen receptor T [CAR T] cell-like) options were significantly preferred.
Therapy decisions for patients with TCE RRMM should consider tradeoffs between efficacy, safety, and attributes related to treatment process and initial monitoring.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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