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将3D肿瘤模型引入临床——对个性化医疗的预测价值。

Bringing 3D tumor models to the clinic - predictive value for personalized medicine.

作者信息

Halfter Kathrin, Mayer Barbara

机构信息

SpheroTec GmbH, Martinsried, Germany.

Department of General, Visceral, and Transplantation Surgery, Hospital of the LMU Munich, Munich, Germany.

出版信息

Biotechnol J. 2017 Feb;12(2). doi: 10.1002/biot.201600295. Epub 2017 Jan 18.

Abstract

Current decision-guiding algorithms in cancer drug treatment are based on decades of research and numerous clinical trials. For the majority of patients, this data is successfully applied for a systemic disease management. For a number of patients however, treatment stratification according to clinically based risk criteria will not be sufficient. The most effective treatment options are ideally identified prior to the start of clinical drug therapy. This review will discuss the implementation of three-dimensional (3D) cell culture models as a preclinical testing paradigm for the efficacy of clinical cancer treatment. Patient tumor-derived cells in 3D cultures duplicate the individual tumor microenvironment with a minimum of confounding factors. Clinical implementation of such personalized tumor models requires a high quality of methodological and clinical validation comparable to other biomarkers. A non-systematic literature search demonstrated the small number of prospective studies that have been conducted in this area of research. This may explain the current reluctance of many physicians and insurance providers in implementing this type of assay into the clinical diagnostic routine despite potential benefit for patients. Achieving valid and reproducible results with a high level of evidence is central in improving the acceptance of preclinical 3D tumor models.

摘要

目前癌症药物治疗中的决策指导算法基于数十年的研究和大量临床试验。对于大多数患者而言,这些数据已成功应用于全身性疾病管理。然而,对于一些患者来说,根据基于临床的风险标准进行治疗分层并不足够。最有效的治疗方案理想情况下应在临床药物治疗开始前确定。本综述将讨论三维(3D)细胞培养模型作为临床癌症治疗疗效的临床前测试范例的实施情况。3D培养中源自患者肿瘤的细胞以最少的混杂因素复制个体肿瘤微环境。这种个性化肿瘤模型的临床应用需要与其他生物标志物相当的高质量方法学和临床验证。一项非系统性文献检索表明,该研究领域开展的前瞻性研究数量较少。这或许可以解释为何尽管对患者可能有益,但目前许多医生和保险机构仍不愿将此类检测纳入临床诊断常规。获得具有高度证据水平的有效且可重复的结果对于提高临床前3D肿瘤模型的接受度至关重要。

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