Bozym David J, Zheng David X, Revach Or-Yam, Aref Amir, Jenkins Russell W
Mass General Cancer Center, Krantz Family Center for Cancer Research, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, 55 Fruit St., Jackson 904B, Boston, MA 02114, USA.
Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Lab Chip. 2025 Jun 24;25(13):3038-3059. doi: 10.1039/d5lc00062a.
Preclinical models capable of probing patient-specific tumor-immune interactions are particularly attractive candidates for interrogating mechanisms of resistance, developing predictors of response as well as assessing next-generation immunotherapeutics. By maintaining features of a patient's own tumor microenvironment, such patient-derived models are poised to meaningfully contribute to the functional assessment of individual tumors to provide a tailored approach to treatment. Among contemporary models, patient-derived organotypic tumor spheroids (PDOTS) have emerged as a promising microfluidic-based platform that is well positioned to become a useful tool for precision medicine efforts. The advantages and limitations of PDOTS and related state-of-the-art patient-derived tumor models, as well as ongoing challenges facing the clinical implementation of patient-derived tumor models, are reviewed.
能够探究患者特异性肿瘤-免疫相互作用的临床前模型,在探究耐药机制、开发反应预测指标以及评估新一代免疫疗法方面,是极具吸引力的候选对象。通过保留患者自身肿瘤微环境的特征,此类患者来源的模型有望为个体肿瘤的功能评估做出有意义的贡献,从而提供量身定制的治疗方法。在当代模型中,患者来源的器官型肿瘤球体(PDOTS)已成为一个有前景的基于微流控的平台,很有潜力成为精准医学领域的有用工具。本文综述了PDOTS及相关最先进的患者来源肿瘤模型的优缺点,以及患者来源肿瘤模型在临床应用中面临的持续挑战。