Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montréal, Québec, Canada.
Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montréal, Québec, Canada.
Oncologist. 2022 Sep 2;27(9):e731-e738. doi: 10.1093/oncolo/oyac114.
Randomized controlled trials (RCTs) continue to be the basis for essential evidence regarding the efficacy of interventions such as cancer therapies. Limitations associated with RCT designs, including selective study populations, strict treatment regimens, and being time-limited, mean they do not provide complete information about an intervention's safety or the applicability of the trial's results to a wider range of patients seen in real-world clinical practice. For example, recent data from Alberta showed that almost 40% of patients in the province's cancer registry would be trial-ineligible per common exclusion criteria. Real-world evidence (RWE) offers an opportunity to complement the RCT evidence base with this kind of information about safety and about use in wider patient populations. It is also increasingly recognized for being able to provide information about an intervention's effectiveness and is considered by regulators as an important component of the evidence base in drug approvals. Here, we examine the limitations of RCTs in oncology research, review the different types of RWE available in this area, and discuss the strengths and limitations of RWE for complementing RCT oncology data.
随机对照试验(RCT)仍然是癌症治疗等干预措施疗效的重要证据基础。RCT 设计存在局限性,包括选择性研究人群、严格的治疗方案和限时性,这意味着它们不能提供有关干预措施安全性或试验结果在更广泛的实际临床实践中患者适用性的完整信息。例如,艾伯塔省最近的数据显示,该省癌症登记处近 40%的患者根据常见排除标准不符合试验条件。真实世界证据 (RWE) 为补充 RCT 证据基础提供了机会,提供了有关安全性和更广泛患者人群使用情况的信息。它也越来越被认为能够提供有关干预措施有效性的信息,并被监管机构视为药物批准证据基础的重要组成部分。在这里,我们检查了 RCT 在肿瘤学研究中的局限性,回顾了该领域可用的不同类型的 RWE,并讨论了 RWE 补充 RCT 肿瘤学数据的优势和局限性。