Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma.
Nicola FerrariGeorge A WardChristina GewinnerMatthew P DavisSimone JueligerHarpreet SainiJoanne MunckTomoko SmythRoberta FerraldeschiHarold KeerJohn LyonsMartin J SimsPublished in: Blood advances (2021)
Tolinapant (ASTX660) is a potent, nonpeptidomimetic antagonist of cellular inhibitor of apoptosis proteins 1 and 2 (cIAP1/2) and X-linked IAP, which is currently being evaluated in a phase 2 study in T-cell lymphoma (TCL) patients. Tolinapant has demonstrated evidence of single-agent clinical activity in relapsed/refractory peripheral TCL and cutaneous TCL. To investigate the mechanism of action underlying the single-agent activity observed in the clinic, we have used a comprehensive translational approach integrating in vitro and in vivo models of TCL confirmed by data from human tumor biopsies. Here, we show that tolinapant acts as an efficacious immunomodulatory molecule capable of inducing complete tumor regression in a syngeneic model of TCL exclusively in the presence of an intact immune system. These findings were confirmed in samples from our ongoing clinical study showing that tolinapant treatment can induce changes in gene expression and cytokine profile consistent with immune modulation. Mechanistically, we show that tolinapant can activate both the adaptive and the innate arms of the immune system through the induction of immunogenic forms of cell death. In summary, we describe a novel role for IAP antagonists as immunomodulatory molecules capable of promoting a robust antitumor immune response in TCL.
Keyphrases
- immune response
- cell death
- gene expression
- cell cycle arrest
- oxidative stress
- end stage renal disease
- endoplasmic reticulum stress
- endothelial cells
- chronic kidney disease
- dendritic cells
- newly diagnosed
- dna methylation
- acute lymphoblastic leukemia
- ejection fraction
- acute myeloid leukemia
- prognostic factors
- primary care
- diffuse large b cell lymphoma
- clinical trial
- big data
- open label
- randomized controlled trial
- double blind
- patient reported outcomes
- cell proliferation
- pi k akt
- multiple myeloma
- patient reported