Tatari Nazanin, Muraro Manuele G, Hedad Hayget Mohamed Seid, Hutter Gregor
Department of Biomedicine, Brain Tumor Immunotherapy Laboratory, University Hospital of Basel and University of Basel, Basel, Switzerland.
Department of Biomedicine, Tissue Engineering Laboratory, University Hospital of Basel and University of Basel, Basel, Switzerland.
Methods Mol Biol. 2025;2944:149-161. doi: 10.1007/978-1-0716-4654-0_12.
Glioblastoma (GBM), the most common malignant primary brain tumor in adults, is resistant to Standard of Care (SOC) therapy and almost all available therapies. Clinical trials have not been successful in improving patients' survival, which underscores an urgent need for developing new effective therapies for this treatment-refractory disease. Considering the significant inter- and intratumoral heterogeneity existing in GBM, assessment of therapies in a personalized manner would allow for assigning patients to effective targeted therapies suitable for each patient's unique tumor signature.Patient-tailored ex vivo drug response platform for GBM allows for therapy planning in a personalized manner and enables the discovery of biomarkers of response. Advanced 3D methodologies have shown high efficacy in assessing the effect of therapeutics on intact tumor tissues immediately following tumor resection, allowing for studying the effect of therapies on tumor as a whole followed by detailed analysis of interactions between tumor cells and their microenvironment pre- and post-treatment.Here we describe the use of 3D perfusion bioreactors for translational assessment of therapeutics on regionally annotated patient-derived GBM explants. This model system provides the possibility of generating a 3D dynamic culture with continuous exposure and delivery of drug candidates to an intact tumor tissue material providing crucial insights on treatment-induced mechanisms and facilitating the identification of biomarkers of response, paving the way toward designing and generating more effective therapeutic interventions for GBM patients.
胶质母细胞瘤(GBM)是成人中最常见的原发性恶性脑肿瘤,对标准治疗(SOC)和几乎所有可用疗法均具有抗性。临床试验在改善患者生存率方面并未取得成功,这凸显了迫切需要为这种难治性疾病开发新的有效疗法。考虑到GBM中存在显著的肿瘤间和肿瘤内异质性,以个性化方式评估疗法将有助于为患者分配适合其独特肿瘤特征的有效靶向疗法。针对GBM的患者定制离体药物反应平台允许以个性化方式进行治疗规划,并能够发现反应生物标志物。先进的3D方法在评估肿瘤切除后立即对完整肿瘤组织的治疗效果方面显示出高效性,从而能够研究疗法对整个肿瘤的影响,随后详细分析治疗前后肿瘤细胞与其微环境之间的相互作用。在此,我们描述了使用3D灌注生物反应器对区域注释的患者来源的GBM外植体进行治疗的转化评估。该模型系统提供了生成3D动态培养的可能性,将候选药物持续暴露并递送至完整肿瘤组织材料,从而对治疗诱导机制提供关键见解,并有助于识别反应生物标志物,为设计和生成更有效的GBM患者治疗干预措施铺平道路。