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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cost of Disease Progression in Diffuse Large B-Cell Lymphoma After Frontline Treatment With Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone.
Cost of Disease Progression in Diffuse Large B-Cell Lymphoma After Frontline Treatment With Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone.
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与未进展相比,DLBCL 进展并接受治疗使调整后的每患者每月(PPPM)费用增加超过 8000 美元。
近年来,已有多种新药用于治疗复发/难治性弥漫性大B细胞淋巴瘤(DLBCL),但这些药物对治疗费用的影响尚未得到正式研究。本文报告两项独立的真实世界回顾性队列分析,评估利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)一线治疗后疾病进展的费用。
使用IQVIA PharMetrics Plus理赔数据库以及SEER-Medicare关联数据库进行分析,纳入年龄分别为18岁及以上和66岁及以上的患者。若一线R-CHOP结束后2年内未接受二线治疗,定义为“未进展”;若在该时间内开始二线治疗,则定义为“治疗后进展”。分析对基线协变量进行校正,并比较进展与未进展患者的每患者每月(PPPM)费用。
IQVIA数据库分析(2010年1月1日至2018年6月30日)纳入871例患者,其中未进展725例、进展146例,包括10例接受CAR-T 治疗者。与未进展相比,治疗后进展患者经校正的PPPM费用显著更高(10,554美元比1,561美元,P<0.001)。SEER-Medicare分析(2010年1月1日至2017年12月31日)纳入4,099例患者,其中未进展3,389例、进展710例,包括12例接受CAR-T 治疗者。治疗后进展患者经校正的PPPM费用同样显著更高(10,928美元比2,902美元,P<0.001)。
与未进展相比,DLBCL治疗后进展使经校正的PPPM费用增加超过8,000美元。
In recent years, novel agents have become available to treat relapsed/refractory diffuse large B-cell lymphoma (DLBCL); the impact of such agents on treatment costs has not been formally studied. We present results from 2 independent, retrospective, real-world cohort analyses to determine the cost of disease progression after first-line rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP).
Analyses were conducted using the IQVIA PharMetrics Plus claims database and the Surveillance, Epidemiology, and End Results registry-Medicare-linked database (SEER-Medicare) and included patients 18 years and 66 years, respectively. "No progression" was defined as no second-line therapy for 2 years after the end of first-line R-CHOP and "treated progression" as initiating a second-line therapy within 2 years following the end of first-line R-CHOP. Analyses were adjusted for baseline covariates, and per-patient-per-month (PPPM) costs were compared between progressors and nonprogressors.
The IQVIA PharMetrics Plus analysis (January 1, 2010-June 30, 2018) included 871 patients (nonprogressors, n = 725; progressors, n = 146), including 10 patients who received chimeric antigen receptor T-cell therapy (CAR-T). Treated progression was associated with significantly higher adjusted PPPM costs than no progression ($10,554 vs. $1561, P < .001). The SEER-Medicare analysis (January 1, 2010-December 31, 2017) included 4099 patients (nonprogressors, n = 3389; progressors, n = 710), including 12 patients receiving CAR-T. Treated progression was associated with significantly higher adjusted PPPM costs than no progression ($10,928 vs. $2902, P < .001).
Treated progression of DLBCL increases adjusted PPPM costs by over $8000 compared with no progression.
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