Sutphin Jessie, LeBlanc Thomas W, Janssen Ellen, Hester Laura, Wallace Matthew J, Johnson F Reed, Reed Shelby D
Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Duke Cancer Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Cancer Med. 2025 Jul;14(14):e71072. doi: 10.1002/cam4.71072.
CAR-T therapy is approved for the treatment of relapsed refractory multiple myeloma (MM) and is being studied for newly diagnosed MM (NDMM). The use of novel therapies in early-line MM raises questions on the acceptability of upfront risks in exchange for extended relapse-free periods without the treatment burden and limitations on daily activities associated with maintenance therapy.
A discrete-choice experiment was designed to elicit adults' preferences for hypothetical NDMM treatments. Benefits included time to relapse and reduction of treatment impact on daily activities. Severe adverse events were included to better understand patient preferences for rare but significant events.
On average, extending the time to relapse from 3 years (with moderate limitations on daily activities) to 5 years (without limitations) was three times more important than avoiding a 20% risk of hospitalization due to severe ICANS/CRS. Analysis revealed three latent preference classes: a benefit-risk trading class (65%), a class (28%) unwilling to accept increases in short-term treatment-related mortality, and a class (7%) that provided statistically uninformative data. For the trading class, for two additional relapse-free years with minor limitations, all else equal, patients would accept up to a 30% risk of severe ICANS/CRS-related hospitalization along with 0% risk of treatment-related mortality. Alternatively, they would accept up to an 8% risk of treatment-related mortality with a 0% risk of severe ICANS/CRS-related hospitalization, or various combinations of lower AE risks.
These results reveal preference heterogeneity among MM patients and the importance of effective communication about the benefits and risks of novel therapies.
嵌合抗原受体T细胞(CAR-T)疗法已被批准用于治疗复发难治性多发性骨髓瘤(MM),目前正在对新诊断的MM(NDMM)进行研究。在早期MM中使用新型疗法引发了一些问题,即前期风险的可接受性,以换取更长的无复发期,同时避免维持治疗带来的治疗负担和对日常活动的限制。
设计了一项离散选择实验,以了解成年人对假设的NDMM治疗的偏好。益处包括复发时间和治疗对日常活动影响的降低。纳入严重不良事件以更好地了解患者对罕见但重大事件的偏好。
平均而言,将复发时间从3年(对日常活动有中度限制)延长至5年(无限制)比避免因严重免疫效应综合征/细胞因子释放综合征(ICANS/CRS)导致20%的住院风险重要三倍。分析揭示了三个潜在的偏好类别:一个利益-风险权衡类别(65%)、一个不愿意接受短期治疗相关死亡率增加的类别(28%)以及一个提供统计学上无信息数据的类别(7%)。对于权衡类别,在其他条件相同的情况下,为了额外两年无复发且限制较小,患者将接受高达30%的因严重ICANS/CRS相关住院的风险以及0%的治疗相关死亡率风险。或者,他们将接受高达8%的治疗相关死亡率风险以及0%的因严重ICANS/CRS相关住院的风险,或较低不良事件风险的各种组合。
这些结果揭示了MM患者之间的偏好异质性以及有效沟通新型疗法的益处和风险的重要性。