Combined JAK inhibition and PD-1 immunotherapy for non–small cell lung cancer patients
Parker Institute for Cancer Immunotherapy · Translational Therapeutics (United States) · +5 more institutions
Abstract
Persistent inflammation driven by cytokines such as type-one interferon (IFN-I) can cause immunosuppression. We show that administration of the Janus kinase 1 (JAK1) inhibitor itacitinib after anti-PD-1 (programmed cell death protein 1) immunotherapy improves immune function and antitumor responses in mice and results in high response rates (67%) in a phase 2 clinical trial for metastatic non-small cell lung cancer. Patients who failed to respond to initial anti-PD-1 immunotherapy but responded after addition of itacitinib had multiple features of poor immune function to anti-PD-1 alone that improved after JAK inhibition. Itacitinib promoted CD8 T cell plasticity and therapeutic responses of exhausted and…
Citation impact
- FWCI
- 49.89
- Percentile
- 100%
- References
- 43
Authors
22- DMDivij MathewCorresponding
Parker Institute for Cancer Immunotherapy, Translational Therapeutics (United States), University of Pennsylvania
- MEMelina E. MarmarelisCorresponding
University of Pennsylvania
- CFCaitlin Foley
Cancer Research Institute, Foundation Center, University of Pennsylvania
- JBJoshua Bauml
University of Pennsylvania
- DYDarwin Ye
Cancer Research Institute, Foundation Center, Parker Institute for Cancer Immunotherapy, University of Pennsylvania
Topics & keywords
- Immunotherapy
- CD8
- Medicine
- Immune system
- Lung cancer
- Cancer research
- T cell
- Immunology
- Good health and well-being