Circulating tumour DNA, microRNA and metabolites in cerebrospinal fluid as biomarkers for central nervous system malignancies.
Soheil ZorofchianFatima IqbalMayank RaoLeomar Y BallesterYoshua EsquenaziLeomar Y BallesterPublished in: Journal of clinical pathology (2018)
Central nervous system (CNS) malignancies can be difficult to diagnose and many do not respond satisfactorily to existing therapies. Monitoring patients with CNS malignancies for treatment response and tumour recurrence can be challenging because of the difficulty and risks of brain biopsies, and the low specificity and sensitivity of the less invasive methodologies that are currently available. Uncertainty about tumour diagnosis or whether a tumour has responded to treatment or has recurred can cause delays in therapeutic decisions that can impact patient outcome. Therefore, there is an urgent need to develop and validate reliable and minimally invasive biomarkers for CNS tumours that can be used alone or in combination with current clinical practices. Blood-based biomarkers can be informative in the diagnosis and monitoring of various types of cancer. However, blood-based biomarkers have proven suboptimal for analysis of CNS tumours. In contrast, circulating biomarkers in cerebrospinal fluid (CSF), including circulating tumour DNA, microRNAs and metabolites, hold promise for accurate and minimally invasive assessment of CNS tumours. This review summarises the current understanding of these three types of CSF biomarkers and their potential use in neuro-oncologic clinical practice.
Keyphrases
- cerebrospinal fluid
- minimally invasive
- blood brain barrier
- clinical practice
- healthcare
- ms ms
- primary care
- prostate cancer
- single molecule
- cell free
- risk assessment
- computed tomography
- human health
- climate change
- brain injury
- big data
- smoking cessation
- combination therapy
- cerebral ischemia
- ultrasound guided
- contrast enhanced
- replacement therapy
- clinical evaluation