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Criteria-based curation of a therapy-focused compendium to support treatment recommendations in precision oncology

机译:基于标准的治疗契约培养,以支持精密肿瘤学中的治疗建议

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While several resources exist that interpret therapeutic significance of genomic alterations in cancer, many regional real-world issues limit access to drugs. There is a need for a pragmatic, evidence-based, context-adapted tool to guide clinical management based on molecular biomarkers. To this end, we have structured a compendium of approved and experimental therapies with associated biomarkers following a survey of drug regulatory databases, existing knowledge bases, and published literature. Each biomarker-disease-therapy triplet was categorised using a tiering system reflective of key therapeutic considerations: approved and reimbursed therapies with respect to a jurisdiction (Tier 1), evidence of efficacy or approval in another jurisdiction (Tier 2), evidence of antitumour activity (Tier 3), and plausible biological rationale (Tier 4). Two resistance categories were defined: lack of efficacy (Tier R1) or antitumor activity (Tier R2). Based on this framework, we curated a digital resource focused on drugs relevant in the Australian healthcare system (TOPOGRAPH: Therapy Oriented Precision Oncology Guidelines for Recommending Anticancer Pharmaceuticals). As of November 2020, TOPOGRAPH comprised 2810 biomarker-disease-therapy triplets in 989 expert-appraised entries, including 373 therapies, 199 biomarkers, and 106 cancer types. In the 345 therapies catalogued, 84 (24%) and 65 (19%) were designated Tiers 1 and 2, respectively, while 271 (79%) therapies were supported by preclinical studies, early clinical trials, retrospective studies, or case series (Tiers 3 and 4). A companion algorithm was also developed to support rational, context-appropriate treatment selection informed by molecular biomarkers. This framework can be readily adapted to build similar resources in other jurisdictions to support therapeutic decision-making.
机译:虽然存在解释癌症基因组改变的治疗意义的几个资源,但许多区域现实世界问题限制了药物的访问。需要基于分子生物标志物指导临床管理的务实,循证的上下文适应的工具。为此,我们在对药物监管数据库,现有知识库和公开文献的调查后,构成了与相关生物标志物的批准和实验疗法。每种生物标志物 - 治疗三联体使用反映关键治疗考虑的分层系统进行分类:批准和报销关于管辖权(第1级)的疗法,另一个管辖权(第2级)的有效性或批准的证据,抗肿瘤活动的证据(第3层)和合理的生物理由(第4层)。定义了两个抵抗类别:缺乏疗效(T1)或抗肿瘤活动(Tier R2)。基于这一框架,我们策划了一个专注于澳大利亚医疗系统相关的药物的数字资源(拓扑仪:治疗导向的精密肿瘤学,用于推荐抗癌药物)。截至2020年11月,Topograph在989个专家评估的条目中包含2810个生物标志性 - 疾病治疗三胞胎,其中包括373个疗法,199个生物标志物和106种癌症类型。在编目的345个疗法中,分别指定了84(24%)和65(19%),分别指定了Tiers 1和2,而临床前研究,早期临床试验,回顾性研究或案例系列支持271(79%)疗法(三和4)。还开发了一种伴随算法,以支持分子生物标志物通知的理性,上下文的治疗选择。该框架可以很容易地适应在其他司法管辖区内构建类似的资源,以支持治疗决策。

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