Real-world practitioner perceptions of CARTITUDE-4 results for patients with previously treated multiple myeloma

EJHaem Pub Date : 2024-11-25 DOI:10.1002/jha2.1047
Alexandrina Balanean, Samuel Baird, Brooke Dulka, Luke Jennings-Zhang, Robert N. Bone, Yolaine Jeune-Smith, Bruce Feinberg, Muhamed Baljevic
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Abstract

Introduction

Initially approved for the fifth-line or later therapeutic setting, the chimeric antigen receptor (CAR) T-cell regimen ciltacabtagene autoleucel (cilta-cel) was recently approved for second-line (2L) treatment in relapsed/refractory multiple myeloma (RRMM). Oncology practitioners use clinical trials to inform treatment, but real-world impressions and impact on practice are lacking. We aimed to determine whether presenting CARTITUDE-4 clinical trial data would impact real-world preferences/perceptions around CAR T-cell therapy.

Methods

Recruiting from the Cardinal Health Oncology Provider Extended Network (OPEN), we surveyed hematologists/oncologists to investigate fourth-line (4L) preferences in a hypothetical patient with triple-class–refractory MM. We posed the same questions and answers before and after the trial presentation and compared pre-/post-preferences toward cilta-cel and sequencing relative to bispecific antibodies (BsAbs). Using the same methodology as described above, we also performed a secondary analysis comparing pre-/post-perceptions on the use of CAR T-cell therapy in earlier lines for patients with triple-class–refractory MM.

Results

Among 50 respondents, decision-making factors before the trial presentation included CAR T-cell center availability (58%), comorbidities (52%), and center locations (34%). Additionally, 48% of 46 respondents chose 4L cilta-cel. Among 47, 40% wanted more real-world/long-term CAR T-cell therapy outcomes in any line, 38% wanted more 2L data, and 34% favored 2L/third-line (3L) use. After the presentation, the preference for cilta-cel doubled from 48% to 88% (< 0.001) among 50 respondents and rose from 34% to 55% (= 0.001) for earlier-line CAR T-cell therapy among 49. Moreover, 55% of 49 respondents preferred CAR T-cell therapy prior to BsAbs.

Discussion

We have shown that making oncology practitioners aware of trials precipitated decision-making factors and led to notable, significant shifts in future intended practice patterns. Being aware of trial data enables practitioners to make more informed decisions, tailor therapies to individual patients, and ultimately improve outcomes.

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从业人员对曾接受过治疗的多发性骨髓瘤患者的 CARTITUDE-4 结果的真实看法。
嵌合抗原受体(CAR) t细胞方案ciltacabtagene autoeucel (cilta-cel)最初被批准用于第五线或更晚的治疗环境,最近被批准用于复发/难治性多发性骨髓瘤(RRMM)的二线(2L)治疗。肿瘤学从业者使用临床试验来告知治疗,但缺乏现实世界的印象和对实践的影响。我们的目的是确定提交CARTITUDE-4临床试验数据是否会影响现实世界对CAR - t细胞治疗的偏好/看法。方法:从红衣主教健康肿瘤提供者扩展网络(OPEN)招募,我们调查了血液学家/肿瘤学家,调查了一名假设的三级难治性MM患者的第四线(4L)偏好。我们在试验报告前后提出了相同的问题和答案,并比较了相对于双特异性抗体(BsAbs), cilta- cell和测序的前后偏好。使用与上述相同的方法,我们还进行了二次分析,比较了在早期治疗中对三级难治性mm患者使用CAR - t细胞治疗的前后看法。结果:在50名受访者中,试验提出前的决策因素包括CAR - t细胞中心可用性(58%)、合并症(52%)和中心位置(34%)。此外,46名受访者中有48%选择了4L cilta-cel。在47名患者中,40%希望在任何一线获得更多真实世界/长期CAR -t细胞治疗结果,38%希望获得更多2L数据,34%支持使用2L/三线(3L)。在报告之后,49名早期CAR - t细胞治疗中,cilta- cell的偏好从48%增加到88% (p p = 0.001)。此外,49名受访者中55%的人更倾向于在bsab之前进行CAR - t细胞治疗。讨论:我们已经表明,让肿瘤学从业者意识到试验可以促成决策因素,并导致未来预期的实践模式发生显著的重大变化。了解试验数据使从业者能够做出更明智的决定,为个体患者量身定制治疗方法,并最终改善结果。
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