Generating and using real-world data: A worthwhile uphill battle

被引:5
|
作者
Verkerk, K. [1 ,2 ]
Voest, E. E. [1 ,2 ,3 ]
机构
[1] Netherlands Canc Inst, Dept Mol Oncol & Immunol, Amsterdam, Netherlands
[2] Oncode Inst, Utrecht, Netherlands
[3] Netherlands Canc Inst, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
关键词
HEALTHY POSTMENOPAUSAL WOMEN; RANDOMIZED CLINICAL-TRIALS; TECHNOLOGY-ASSESSMENT HTA; ESTROGEN PLUS PROGESTIN; PRIMARY PROPHYLAXIS; INFORMED-CONSENT; BIG DATA; CANCER; CARE; RISK;
D O I
10.1016/j.cell.2024.02.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The precision oncology paradigm challenges the feasibility and data generalizability of traditional clinical trials. Consequently, an unmet need exists for practical approaches to test many subgroups, evaluate realworld drug value, and gather comprehensive, accessible datasets to validate novel biomarkers. Real-world data (RWD) are increasingly recognized to have the potential to fill this gap in research methodology. Established applications of RWD include informing disease epidemiology, pharmacovigilance, and healthcare quality assessment. Currently, concerns regarding RWD quality and comprehensiveness, privacy, and biases hamper their broader application. Nonetheless, RWD may play a pivotal role in supplementing clinical trials, enabling conditional reimbursement and accelerated drug access, and innovating trial conduct. Moreover, purpose-built RWD repositories may support the extension or refinement of drug indications and facilitate the discovery and validation of new biomarkers. This perspective explores the potential of leveraging RWD to advance oncology, highlights its benefits and challenges, and suggests a path forward in this evolving field.
引用
收藏
页码:1636 / 1650
页数:15
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