Tumor-Treating Fields in Glioblastomas: Past, Present, and Future.
Xiaopeng GuoXin YangJiaming WuHuiyu YangYilin LiJunlin LiQianshu LiuChen WuHao XingPenghao LiuYu WangChunhua HuWenbin MaPublished in: Cancers (2022)
Tumor-treating fields (TTFields), a noninvasive and innovative therapeutic approach, has emerged as the fourth most effective treatment option for the management of glioblastomas (GBMs), the most deadly primary brain cancer. According to on recent milestone randomized trials and subsequent observational data, TTFields therapy leads to substantially prolonged patient survival and acceptable adverse events. Clinical trials are ongoing to further evaluate the safety and efficacy of TTFields in treating GBMs and its biological and radiological correlations. TTFields is administered by delivering low-intensity, intermediate-frequency, alternating electric fields to human GBM function through different mechanisms of action, including by disturbing cell mitosis, delaying DNA repair, enhancing autophagy, inhibiting cell metabolism and angiogenesis, and limiting cancer cell migration. The abilities of TTFields to strengthen intratumoral antitumor immunity, increase the permeability of the cell membrane and the blood-brain barrier, and disrupt DNA-damage-repair processes make it a promising therapy when combined with conventional treatment modalities. However, the overall acceptance of TTFields in real-world clinical practice is still low. Given that increasing studies on this promising topic have been published recently, we conducted this updated review on the past, present, and future of TTFields in GBMs.
Keyphrases
- dna repair
- dna damage
- endothelial cells
- cell migration
- clinical trial
- papillary thyroid
- single cell
- clinical practice
- cell therapy
- oxidative stress
- signaling pathway
- cell death
- squamous cell
- systematic review
- big data
- dna damage response
- multiple sclerosis
- randomized controlled trial
- electronic health record
- machine learning
- case report
- bone marrow
- lymph node metastasis
- cross sectional
- case control
- open label
- phase ii