Broes Stefanie, Lacombe Denis, Verlinden Michiel, Huys Isabelle
European Organisation for Research and Treatment of Cancer, Brussels, Belgium.
Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Front Med (Lausanne). 2018 Jan 29;5:6. doi: 10.3389/fmed.2018.00006. eCollection 2018.
The recent revolution in science and technology applied to medical research has left in its wake a trial of biomedical data and human samples; however, its opportunities remain largely unfulfilled due to a number of legal, ethical, financial, strategic, and technical barriers. Precision oncology has been at the vanguard to leverage this potential of "Big data" and samples into meaningful solutions for patients, considering the need for new drug development approaches in this area (due to high costs, late-stage failures, and the molecular diversity of cancer). To harness the potential of the vast quantities of data and samples currently fragmented across databases and biobanks, it is critical to engage all stakeholders and share data and samples across research institutes. Here, we identified two general types of sharing strategies. First, open access models, characterized by the absence of any review panel or decision maker, and second controlled access model where some form of control is exercised by either the donor (i.e., patient), the data provider (i.e., initial organization), or an independent party. Further, we theoretically describe and provide examples of nine different strategies focused on greater sharing of patient data and material. These models provide varying levels of control, access to various data and/or samples, and different types of relationship between the donor, data provider, and data requester. We propose a tiered model to share clinical data and samples that takes into account privacy issues and respects sponsors' legitimate interests. Its implementation would contribute to maximize the value of existing datasets, enabling unraveling the complexity of tumor biology, identify novel biomarkers, and re-direct treatment strategies better, ultimately to help patients with cancer.
应用于医学研究的科技革命在身后留下了生物医学数据和人类样本的试验;然而,由于一些法律、伦理、财务、战略和技术障碍,其机遇在很大程度上仍未实现。考虑到该领域新药开发方法的需求(由于成本高昂、后期失败以及癌症的分子多样性),精准肿瘤学一直处于利用“大数据”和样本的潜力为患者提供有意义解决方案的前沿。为了利用目前分散在数据库和生物样本库中的大量数据和样本的潜力,让所有利益相关者参与并在研究机构之间共享数据和样本至关重要。在此,我们确定了两种一般类型的共享策略。第一种是开放获取模式,其特点是没有任何审查小组或决策者;第二种是受控获取模式,其中某种形式的控制由捐赠者(即患者)、数据提供者(即初始组织)或独立方行使。此外,我们从理论上描述并提供了九种不同策略的示例,这些策略侧重于更广泛地共享患者数据和材料。这些模式提供了不同程度的控制、对各种数据和/或样本的访问以及捐赠者、数据提供者和数据请求者之间的不同类型关系。我们提出了一种分层模型来共享临床数据和样本,该模型考虑到隐私问题并尊重赞助商的合法利益。其实施将有助于最大限度地提高现有数据集的价值,从而能够揭示肿瘤生物学的复杂性、识别新的生物标志物并更好地重新定向治疗策略,最终帮助癌症患者。