Combination bezafibrate and nivolumab treatment of patients with advanced non-small cell lung cancer.
Kentaro TanakaKenji ChamotoSho SaekiRyusuke HataeYuki IkematsuKazuko SakaiNobuhisa AndoKazuhiro SonomuraShinsuke KojimaMasanori TaketsunaYoung Hak KimHironori YoshidaHiroaki OzasaYuichi SakamoriTomoko HiranoFumihiko MatsudaToyohiro HiraiKazuto NishioTakuro SakagamiMasanori FukushimaYoichi NakanishiTasuku HonjoIsamu OkamotoPublished in: Science translational medicine (2022)
Despite the success of cancer immunotherapies such as programmed cell death-1 (PD-1) and PD-1 ligand 1 (PD-L1) inhibitors, patients often develop resistance. New combination therapies with PD-1/PD-L1 inhibitors are needed to overcome this issue. Bezafibrate, a ligand of peroxisome proliferator-activated receptor-γ coactivator 1α/peroxisome proliferator-activated receptor complexes, has shown a synergistic antitumor effect with PD-1 blockade in mice that is mediated by activation of mitochondria in T cells. We have therefore now performed a phase 1 trial (UMIN000017854) of bezafibrate with nivolumab in previously treated patients with advanced non-small cell lung cancer. The primary end point was the percentage of patients who experience dose-limiting toxicity, and this combination regimen was found to be well tolerated. Preplanned comprehensive analysis of plasma metabolites and gene expression in peripheral cytotoxic T cells indicated that bezafibrate promoted T cell function through up-regulation of mitochondrial metabolism including fatty acid oxidation and may thereby have prolonged the duration of response. This combination strategy targeting T cell metabolism thus has the potential to maintain antitumor activity of immune checkpoint inhibitors and warrants further validation.
Keyphrases
- advanced non small cell lung cancer
- epidermal growth factor receptor
- gene expression
- fatty acid
- end stage renal disease
- oxidative stress
- newly diagnosed
- ejection fraction
- cancer therapy
- ms ms
- tyrosine kinase
- peritoneal dialysis
- cell death
- papillary thyroid
- squamous cell carcinoma
- adipose tissue
- reactive oxygen species
- skeletal muscle
- insulin resistance
- squamous cell
- patient reported
- chemotherapy induced
- smoking cessation