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系统文献回顾全球套细胞淋巴瘤的疾病负担。

Systematic literature review of the global burden of illness of mantle cell lymphoma.

机构信息

Health Economics and Reimbursement, Janssen Inc., Toronto, Canada.

EMEA HEMAR, Janssen, High Wycombe, United Kingdom.

出版信息

Curr Med Res Opin. 2020 May;36(5):843-852. doi: 10.1080/03007995.2020.1742101. Epub 2020 Mar 31.

DOI:10.1080/03007995.2020.1742101
PMID:32162977
Abstract

Mantle cell lymphoma (MCL), a rare and aggressive disease, accounts for approximately 5% of all B-cell non-Hodgkin's lymphomas. Evidence on the burden of this disease, for patients and healthcare providers, is scarce. Four systematic literature reviews were developed to identify epidemiological, real-world clinical, economic and humanistic burden data on patients with MCL. Electronic databases searched included MEDLINE and Embase, NHS EED and Econlit. Eight epidemiological studies, 19 clinical burden, 2 economic impact and 0 quality of life studies were identified. The range of standardized MCL incidence rates was 0.1-1.27/100,000. Overall survival rates of patients at 3 years differed by age at diagnosis (≤65 years: 76-81%, >65 years: 46-64%) and disease stage (stage I: 73-80%, stage IV: 48-53%). Outcomes were poorer in previously treated patients, and those with later stage or blastoid disease, and improved with more recent diagnosis/treatment. Hospitalization is a major contributor to healthcare cost and differs by therapy toxicity. We identified significant data gaps for many G20 countries for epidemiology, real-world clinical, economic and humanistic burden. These literature reviews demonstrate the ongoing unmet need for MCL patients globally. Future research to further understand the real-world impact of MCL is needed along with new therapeutic options to improve patient outcomes.

摘要

套细胞淋巴瘤(MCL)是一种罕见且侵袭性强的疾病,约占所有 B 细胞非霍奇金淋巴瘤的 5%。目前关于该疾病对患者和医疗保健提供者的负担的证据很少。本研究进行了四项系统文献综述,以确定关于 MCL 患者的流行病学、真实世界临床、经济和人文负担数据。检索的电子数据库包括 MEDLINE 和 Embase、NHS EED 和 Econlit。共确定了 8 项流行病学研究、19 项临床负担研究、2 项经济影响研究和 0 项生活质量研究。标准化 MCL 发病率的范围为 0.1-1.27/100,000。不同诊断年龄(≤65 岁:76-81%;>65 岁:46-64%)和疾病分期(I 期:73-80%;IV 期:48-53%)患者的 3 年总生存率存在差异。既往接受治疗的患者、疾病分期较晚或母细胞样的患者结局较差,而最近诊断/治疗的患者结局较好。住院是医疗保健费用的主要组成部分,且因治疗毒性而异。我们发现许多 G20 国家在流行病学、真实世界临床、经济和人文负担方面存在显著的数据空白。这些文献综述表明,全球范围内 MCL 患者存在持续未满足的需求。需要进一步研究以更好地了解 MCL 的真实世界影响,并提供新的治疗选择以改善患者结局。

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