Real-world evidence in lung and hematologic oncology health technology appraisals: a review of six assessment agencies

被引:1
|
作者
Harricharan, Sharada [1 ]
Curran, Eileen [2 ]
Lin, Huamao Mark [2 ]
Walton, Laura [3 ]
Gurjar, Khushboo [1 ]
Nguyen, Khoi [1 ]
Forsythe, Anna [1 ]
机构
[1] Cytel Inc, Waltham, MA 02451 USA
[2] Takeda Dev Ctr Amer Inc, Lexington, MA 02421 USA
[3] Takeda Pharmaceut, CH-8152 Zurich, Switzerland
关键词
health technology assessment; oncology; real-world evidence; ASSESSMENT HTA;
D O I
10.2217/fon-2022-0553
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: To assess the use and acceptability of real-world evidence (RWE) in lung and hematologic cancer appraisals. Materials & methods: A review of appraisals published by National Institute for Health and Care Excellence (NICE) in the UK was conducted. A total of 20 case studies employing RWE were identified and compared across five additional health technology assessment agencies: Scottish Medicines Consortium (SMC) (Scotland), CADTH (Canada), INESSS (Quebec), HAS (France) and IQWiG (Germany). Results: Of 80 RWE references from 20 case studies from NICE, 67 were identified in the respective CADTH submissions, 46 in IQWiG, 37 in INESSS, 37 in HAS, and 33 in SMC. NICE had the highest RWE acceptance rate (90%), followed by HAS (88%), SMC (82%), INESSS (73%), IQWiG (68%), and CADTH (67%). Conclusion: RWE was generally accepted by respective committees, allowing improved access to innovative treatments. Plain language summary Use of real-world evidence for assessing the value of cancer treatmentsHealth technology assessment (HTA) is a process used to decide whether a drug works well enough to be worth paying for. Most drugs have data showing how well they work from special studies called clinical trials. Sometimes a manufacturer also has evidence of a drug or disease that is not from a clinical trial but from the real world. This review discusses how real-world evidence (RWE) is being used for HTAs of new lung and blood cancer therapies. We reviewed twenty HTA submissions for new therapies. All twenty were submitted to these agencies: National Institute for HealthCare and Excellence (NICE; UK), Scottish Medicines Consortium (SMC; Scotland), Canadian Agency for Drugs and Technologies in Health (CADTH; Canada), National Institute of Excellence in Health and Social Services (INESSS; Quebec), French National Authority for Health (HAS; France) and Institute for Quality and Efficiency in HealthCare (IQWiG; Germany). RWE was often used to describe the type of patient that needs the new therapy. RWE was also used to show the cost of the treatment and how well the treatment worked in relation to its cost. It was also used to show how well the new therapy works compared with other treatments. Most of the RWE was accepted by the agencies. High-quality RWE in relevant patients helped support access to new treatments.
引用
收藏
页码:603 / 616
页数:14
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