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:CAR T-cell therapy in relapsed/refractory diffuse large B-cell lymphoma: physician preferences trading off benefits, risks and time to infusion.
CAR T-cell therapy in relapsed/refractory diffuse large B-cell lymphoma: physician preferences trading off benefits, risks and time to infusion.
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评估医生在复发/难治性弥漫性大B细胞淋巴瘤中选择CAR-T 细胞疗法时,如何权衡获益、风险和输注等待时间。
在一项离散选择实验调查中,150名美国肿瘤科/血液科医生在两种假设CAR-T 治疗方案之间作出选择,每种方案由6项属性定义。
将输注等待时间从113天缩短至16天,对医生偏好权重的影响最大(1.91)。若24个月总生存期概率从40%提高至55%,医生愿意接受重度细胞因子释放综合征风险增加超过20%,以及重度神经系统事件风险增加15%。
医生重视缩短输注等待时间,也愿意为生存获益接受严重不良事件风险的适度增加。通俗摘要:CAR-T 是治疗至少两种既往疗法无应答的弥漫性大B细胞淋巴瘤的一种选择。CAR-T 以患者白细胞为原料,经改造后攻击淋巴瘤细胞;采集细胞后需要一定时间进行制备。CAR-T 可使淋巴瘤缩小或消失,并提高生存机会,但少数患者会出现严重副作用。一种副作用是细胞因子释放综合征(CRS),体内广泛炎症可能引起发热、心脏问题或呼吸困难;另一种是短暂但严重的神经系统问题,如意识混乱、癫痫发作和记忆障碍。为了解医生决定是否推荐CAR-T 时最看重哪些特征,研究者让医生在一系列问题中比较两种类似CAR-T 的治疗方案,并改变每题中的治疗属性。回答反映了肿瘤消退、生存机会、制备时间以及CRS或神经系统风险的重要性。医生最希望将制备时间从113天缩短至16天;为使患者2年生存概率从40%提高至55%,他们也愿意接受重度CRS风险增加超过20%、重度神经事件风险增加15%。
Aims: We evaluated physicians' willingness to trade-off benefits, risks and time to infusion for CAR T-cell therapy for relapsed or refractory diffuse large B-cell lymphoma. Materials & methods: In a discrete-choice experiment survey, 150 US oncologists/hematologists chose between two hypothetical CAR T-cell treatments defined by six attributes. Results: Decreasing time to infusion from 113 to 16 days yielded the greatest change in preference weight (1. 91). Physicians were willing to accept a >20% increase in risk of severe cytokine release syndrome and 15% increase in risk of severe neurological events in exchange for an increase in the probability of overall survival at 24 months from 40 to 55%. Conclusion: Physicians value reducing time to infusion and will accept incremental increases in serious adverse event risks to gain survival improvements. Lay abstract CAR-T therapy is a treatment option for patients with diffuse large B-cell lymphoma that has not responded to at least two other kinds of treatments. CAR-T therapies are manufactured from a patient s white blood cells, modified to attack lymphoma cells. A CAR-T therapy takes time to manufacture after these cells are collected.
CAR-T therapies can result in the reduction or disappearance of lymphoma tumors and can increase the chances of survival, but also cause serious side effects for a few patients. One of these is cytokine release syndrome (CRS), in which high levels of inflammation throughout the body may cause fever, heart problems or difficulty breathing. Another is the development of temporary but serious neurological problems such as confusion, seizures and memory problems. To understand how important physicians consider certain features of CAR-T therapies to be when deciding whether to recommend them, we asked physicians to choose between two treatment options resembling CAR-T therapies in a series of questions, with the CAR-T features varying in each question.
Their answers indicated whether disappearance of tumors, a patient s chances of survival after 1 and 2 years of treatment, manufacturing time, or the risk of CRS or neurological problems was the most important factor. Physicians most wanted to reduce manufacturing time from 113 to 16 days, but also were willing to accept a >20% increase in risk of severe CRS and a 15% increase in risk of severe neurological events to increase a patient s chance of survival from 40 to 55% at 2 years.
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