Development and Optimisation of Tumour Treating Fields (TTFields) Delivery within 3D Primary Glioma Stem Cell-like Models of Spatial Heterogeneity.
Callum G JonesAurelie VanderlindenOla RominiyiSpencer James CollisPublished in: Cancers (2024)
Glioblastoma is an aggressive, incurable brain cancer with poor five-year survival rates of around 13% despite multimodal treatment with surgery, DNA-damaging chemoradiotherapy and the recent addition of Tumour Treating Fields (TTFields). As such, there is an urgent need to improve our current understanding of cellular responses to TTFields using more clinically and surgically relevant models, which reflect the profound spatial heterogeneity within glioblastoma, and leverage these biological insights to inform the rational design of more effective therapeutic strategies incorporating TTFields. We have recently reported the use of preclinical TTFields using the inovitro TM system within 2D glioma stem-like cell (GSC) models and demonstrated significant cytotoxicity enhancement when co-applied with a range of therapeutically approved and preclinical DNA damage response inhibitors (DDRi) and chemoradiotherapy. Here we report the development and optimisation of preclinical TTFields delivery within more clinically relevant 3D scaffold-based primary GSC models of spatial heterogeneity, and highlight some initial enhancement of TTFields potency with temozolomide and clinically approved PARP inhibitors (PARPi). These studies, therefore, represent an important platform for further preclinical assessment of TTFields-based therapeutic strategies within clinically relevant 3D GSC models, aimed towards accelerating clinical trial implementation and the ultimate goal of improving the persistently dire survival rates for these patients.
Keyphrases
- single cell
- cell therapy
- stem cells
- clinical trial
- dna damage response
- rectal cancer
- end stage renal disease
- healthcare
- ejection fraction
- newly diagnosed
- dna repair
- primary care
- minimally invasive
- randomized controlled trial
- dna damage
- prognostic factors
- squamous cell carcinoma
- locally advanced
- multiple sclerosis
- peritoneal dialysis
- papillary thyroid
- single molecule
- oxidative stress
- white matter
- drug administration
- phase ii
- patient reported outcomes
- combination therapy
- double blind
- chronic pain
- lymph node metastasis
- patient reported
- percutaneous coronary intervention
- smoking cessation