Centre for Medical Ethics, Institute for Health and Society, University of Oslo, Oslo, Norway.
Hybrid Technology Hub, University of Oslo, Oslo, Norway.
J Eval Clin Pract. 2022 Dec;28(6):1205-1212. doi: 10.1111/jep.13649. Epub 2022 Jan 10.
Precision medicine (PM) raises a key question: How do we know what works when the number of people with a health problem becomes small or one (n = 1)? We here present a formative case from Norway. The Norwegian Board of Health Supervision was faced with a cancer patient, who had improved after treatment with a drug in the private health sector but was refused continued treatment in the public health service due to lack of clinical trial evidence. The Board overturned this decision, arguing that the drug had been unambiguously documented to work in the individual case. We aim to provide an in-depth analysis of this case and The Board's decision and thereby to illustrate and elucidate key epistemological and ethical issues and developments in PM.
We provide our analysis and discussion using tools of critical thinking and concepts from philosophy of science and medicine, such as uncertainty, evidence, forms of inference and causation. We also examine the case in light of the history of evidence-based medicine (EBM).
The case reflects an epistemological shift in medicine where PM puts greater emphasis on evidence that arises in individual patients after the treatment is provided over pre-existing population-based evidence. PM may rely more heavily on abduction to decide what works and qualitative, rather than quantitative judgements. The case also illustrates a possible shift in the concept of causation from regularity accounts to mechanistic and process accounts. We discuss the ethical implications of a shift from more 'traditional' to 'personalised EBM'.
A framework that is more based on abductions and evidence arising in the individual case has problems in creating quantifiable, reliable and generalisable evidence, and in promoting transparency and accountability. PM currently lacks clear criteria for deciding what works in an individual, posing ethical challenges.
精准医学(PM)提出了一个关键问题:当有健康问题的人数减少或变为个体(n=1)时,我们如何知道什么有效?我们在此呈现一个来自挪威的实例。挪威卫生监督局面临一位癌症患者,该患者在私营医疗部门接受一种药物治疗后有所改善,但由于缺乏临床试验证据,在公共医疗服务中被拒绝继续治疗。该委员会推翻了这一决定,认为该药物在个体病例中已明确证明有效。我们旨在深入分析该案例和委员会的决定,从而阐明和阐明 PM 中的关键认识论和伦理问题和发展。
我们使用批判性思维工具和来自科学哲学和医学的概念,如不确定性、证据、推理和因果关系的形式,对案例进行分析和讨论。我们还根据循证医学(EBM)的历史来考察该案例。
该案例反映了医学认识论的转变,在 PM 中,更加重视在提供治疗后个体患者中出现的证据,而不是基于人群的现有证据。PM 可能更多地依赖于溯因推理来确定什么有效,并且更多地依赖于定性而不是定量判断。该案例还说明了因果关系概念从规律解释向机制和过程解释的可能转变。我们讨论了从更“传统”到“个体化” EBM 的转变的伦理含义。
一个更基于个体案例中的溯因推理和证据的框架在创建可量化、可靠和可推广的证据以及促进透明度和问责制方面存在问题。PM 目前缺乏决定个体中什么有效的明确标准,这带来了伦理挑战。