Radiotherapy enhances responses of lung cancer to CTLA-4 blockade.
Anna C WilkinsFiona McDonaldKevin HarringtonAlan MelcherPublished in: Journal for immunotherapy of cancer (2019)
Formenti et al. have recently reported the clinical outcomes and translational readouts of a trial of the anti-CTLA-4 inhibitor, ipilimumab, in combination with palliative radiotherapy in 39 patients with non-small cell lung cancer. A radiological response was seen in 18% of patients and 31% of patients experienced disease control. These clinical outcomes appear to be superior to historical studies using ipilimumab alone and suggest that radiation may have triggered systemic, so-called abscopal, immune responses in some patients. Induction of interferon-beta (IFN-β) and maximal expansion and contraction of distinct T cell receptor clones were the most significant factors predicting response. Importantly, established predictive biomarkers of response to immunotherapy alone, including the expression of PD-L1 in diagnostic biopsies and tumour mutational burden, did not predict response. The report provides important human qualification of pre-clinical mechanistic insights indicating that abscopal responses can be generated with optimised radiotherapy fractionation schedules and anti-CTLA-4 inhibition. Additionally, an intriguing mechanism by which radiation can be immunogenic is described, namely radiation-induced transcriptional upregulation of neo-antigens.
Keyphrases
- radiation induced
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- immune response
- radiation therapy
- early stage
- dendritic cells
- poor prognosis
- peritoneal dialysis
- clinical trial
- blood pressure
- cell proliferation
- binding protein
- long non coding rna
- body composition
- palliative care
- inflammatory response
- patient reported
- open label
- toll like receptor
- heat shock protein
- resistance training
- placebo controlled
- double blind