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:Health Care Resource Utilization and Total Costs of Care Among Patients with Diffuse Large B Cell Lymphoma Treated with Chimeric Antigen Receptor T Cell Therapy in the United States.
Health Care Resource Utilization and Total Costs of Care Among Patients with Diffuse Large B Cell Lymphoma Treated with Chimeric Antigen Receptor T Cell Therapy in the United States.
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临床试验显示,弥漫大B细胞淋巴瘤(DLBCL)第二次复发后使用CAR-T(CAR-T)细胞治疗疗效良好;然而,真实世界接受CAR-T 治疗患者的医疗资源利用(HCRU)和费用鲜有研究。
我们利用美国3个商业理赔数据库,评估复发/难治性DLBCL患者接受CAR-T 细胞治疗后的治疗模式、HCRU、费用和安全性。通过Optum Clinformatics Data Mart、IBM MarketScan商业及Medicare数据库、IQVIA PharMetrics Plus识别接受CAR-T 治疗的DLBCL成人患者。计算平均总费用并换算为2019年美元。按关注的安全事件(包括神经系统事件[NE]和细胞因子释放综合征[CRS])对输注后3个月内的HCRU和费用分层;这些事件通过基于医学专家意见设计、但尚未验证的算法识别。
数据库共识别191例接受CAR-T 治疗患者;中位年龄为56至67岁,男性占63%至75%。大多数患者(88%至98%)在住院环境接受CAR-T 输注;30%至75%接受桥接治疗。75%至84%患者报告CRS(重度CRS占15%至32%),58%至69%报告NE(重度NE占25%至43%)。总住院天数均值为17至22天;发生重度CRS时增至19至27天,发生重度NE时增至22至29天。平均医疗总支出为38万至52.6万美元;发生重度CRS或NE时通常更高(40.6万至67.9万美元)。真实世界CAR-T 治疗相关HCRU和费用可能因多种因素而异,包括不良事件是否发生及其严重程度。
The use of chimeric antigen receptor (CAR) T-cell therapy after a second relapse of diffuse large B-cell lymphoma (DLBCL) has shown favorable efficacy in clinical trials; however, little is known about health care resource utilization (HCRU) and costs of CAR T cell therapy for patients treated in real-world settings.
We assessed treatment patterns, HCRU, costs, and safety in patients receiving CAR T cell therapy for relapsed or refractory DLBCL across 3 US commercial claims databases. Adults with DLBCL treated with CAR T cell therapy were identified in the following 3 claims databases: Optum Clinformatics Data Mart, IBM MarketScan Commercial & Medicare Database, and IQVIA PharMetrics Plus. Mean total costs were calculated and adjusted to 2019 US dollars. HCRU and costs within 3 months of infusion were stratified by safety events of interest, including neurological events (NEs) and cytokine release syndrome (CRS), identified via unvalidated algorithms designed based on expert medical opinion. A total of 191 patients receiving CAR T cell therapy were identified across the databases; their median age ranged from 56 to 67 years, and 63% to 75% were male.
Most patients (88% to 98%) received CAR T cell infusions in the inpatient setting; 30% to 75% received bridging therapy. CRS was reported in 75% to 84% of patients (severe CRS, 15% to 32%), and NEs were reported in 58% to 69% (severe NEs, 25% to 43%). Mean total inpatient hospital days ranged from 17 to 22 days and increased with severe CRS (19 to 27 days) or severe NEs (22 to 29 days).
Mean total health care expenditures ranged from $380,000 to $526,000 and were generally higher with severe CRS or NEs ( $406,000 to $679,000). HCRU and costs associated with CAR T cell therapy may vary in the real world depending on several factors, including occurrence and severity of adverse events.
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