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:A Systematic Literature Review of the Economic and Healthcare Resource Utilization Burden of Relapsed/Refractory Follicular Lymphoma.
A Systematic Literature Review of the Economic and Healthcare Resource Utilization Burden of Relapsed/Refractory Follicular Lymphoma.
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R/R FL 的疾病负担沉重,并随患者疾病进展而加重。
量化复发/难治性滤泡性淋巴瘤(R/R FL)造成的经济或医疗资源利用(HCRU)负担,并考察干预措施的价值。
检索PubMed和Embase数据库,纳入2019年1月1日至2023年12月31日发表的全文及会议摘要,内容涉及R/R FL经济或HCRU负担,或评估R/R FL干预措施的卫生经济模型;另手工检索补充可能未被主要数据库收录的会议摘要,并使用数据提取表整理证据。
共纳入30篇文献,包括11项回顾性或前瞻性研究、11项成本效果评估和8种其他卫生经济模型。随着治疗线数增加,成本和HCRU通常上升,后线治疗年费用超过40万美元。近期获批的CAR-T 细胞疗法每位患者费用约45万至70多万美元。卫生经济模型估计,CAR-T、他泽司他和mosunetuzumab等新疗法通常具有成本效果,并且预算影响较小或可节约成本;但模型对治疗持续时间和停药作出了较多假设。近期获批的CAR-T 及双特异性抗体等新疗法真实世界成本和资源使用数据有限。
R/R FL负担沉重,且随疾病进展而加重。新疗法(包括CAR-T 和双特异性抗体)对真实世界经济负担的影响仍存在重要证据缺口,需进一步研究才能恰当评估其价值。
To quantify the economic or healthcare resource utilization (HCRU) burden and examine the value of interventions for relapsed or refractory (R/R) follicular lymphoma (FL).
The PubMed and Embase databases were searched for full-text studies and conference abstracts published between 1 January 2019 and 31 December 2023 that reported either the economic or HCRU burden of R/R FL or reported the results of health economic models assessing interventions for R/R FL. A supplemental manual search was also undertaken to identify conference abstracts that may not have been indexed in the primary databases. A data extraction sheet was used to develop evidence tables.
A total of 30 records were included spanning 11 retrospective or prospective studies, 11 cost-effectiveness evaluations, and 8 other economic models. Costs and HCRU generally tended to increase as the line of therapy increased, reaching over US$400,000 annually in later lines. Costs associated with recently approved chimeric antigen receptor T-cell therapy (CAR-T) ranged from US$450,000 to over US$700,000 per patient. Economic models evaluating novel therapies, such as CAR-T, tazemetostat, and mosunetuzumab, estimated they would generally be cost-effective and have minimal budget impact or cost-savings. However, these models noted considerable assumptions regarding treatment duration and discontinuation. Real-world costs and resource use for newly approved therapies including CAR-Ts and bispecifics were limited.
The burden of R/R FL is substantial and increases as patients progress. Considerable gaps exist for the real-world impact of novel therapies, including CAR-Ts and bispecifics, on the economic burden and will need to be studied to properly assess their value.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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