Combination therapies utilizing neoepitope-targeted vaccines.
Karin L LeeJeffrey SchlomDuane H HamiltonPublished in: Cancer immunology, immunotherapy : CII (2020)
Clinical successes have been achieved with checkpoint blockade therapy, which facilitates the function of T cells recognizing tumor-specific mutations known as neoepitopes. It is a reasonable hypothesis that therapeutic cancer vaccines targeting neoepitopes uniquely expressed by a patient's tumor would prove to be an effective therapeutic strategy. With the advent of high-throughput next generation sequencing, it is now possible to rapidly identify these tumor-specific mutations and produce therapeutic vaccines targeting these patient-specific neoepitopes. However, initial reports suggest that when used as a monotherapy, neoepitope-targeted vaccines are not always sufficient to induce clinical responses in some patients. Therefore, research has now turned to investigating neoepitope vaccines in combination with other cancer therapies, both immune and non-immune, to improve their clinical efficacies.
Keyphrases
- cancer therapy
- high throughput
- papillary thyroid
- end stage renal disease
- ejection fraction
- dna damage
- squamous cell
- newly diagnosed
- chronic kidney disease
- stem cells
- drug delivery
- randomized controlled trial
- gene expression
- clinical trial
- emergency department
- oxidative stress
- single cell
- young adults
- prognostic factors
- copy number
- bone marrow
- genome wide
- combination therapy
- peritoneal dialysis
- electronic health record
- patient reported
- cell therapy
- circulating tumor