Slowing inflammation may boost immunotherapy’s effectiveness against advanced lung cancer

Newswise — PHILADELPHIA – Adding an anti-inflammatory drug to anti-PD1 checkpoint inhibitor immunotherapy has shown great promise as a new strategy against advanced lung cancer, based on results from a small clinical trial led by investigators at the Abramson Family Cancer Center at the University of Pennsylvania Perelman School of Medicine. 

The results were published today in Science, based the strategy on an accumulating body of evidence for the dual nature of inflammation—it can be beneficial against infectious pathogens and cancers in the short term, but can also lead to a weakened immune system when it becomes chronic. Signs of this chronic inflammatory response, particularly involving a cytokine called interferon, are often seen in patients taking anticancer immunotherapies and are linked to worse outcomes. 

In the study, the researchers used a drug called a JAK1 inhibitor to specifically reduce persistent inflammatory signaling while not interfering with the initial inflammatory signaling required to generate antitumor activity. The JAK1 inhibitor was given for six weeks in 21 patients with advanced non-small cell lung cancer (NSCLC), but only after they had received two doses of anti-PD1 immunotherapy. The result was an overall response rate of 67 percent and median progression-free survival of almost 24 months both of which are very high for advanced NSCLC. 

“Many oncologists might find it surprising to combine a JAK inhibitor with immunotherapy since the focus has typically been on creating a strong inflammatory response for effective anti-PD1 treatment. However, there's a growing understanding that chronic inflammation, especially chronic interferon, can be harmful. Our study's high response rate and the improvements in immune cells suggest that our approach could help control inflammation and interferon levels before they become detrimental,” said co-senior author Andy Minn, MD, PhD, professor of Radiation Oncology and director of the Mark Foundation Center for Immunotherapy, Immune Signaling, and Radiation. 

“It’s also encouraging that the best responders in this trial were those who had either low baseline inflammation or high baseline inflammation that responded to the JAK1 inhibitor treatment,” said co-senior author E. John Wherry, MD, the Richard and Barbara Schiffrin President's Distinguished Professor, Chair of the Department of Systems Pharmacology & Translational Therapeutics, and Director of the Institute for Immunology and Immune Health. 

The study’s co-first authors were Divij Mathew, PhD, a postdoctoral researcher in the Wherry Lab, and Melina Marmarelis, MD, an assistant professor of Medicine (Hematology-Oncology) at the University of Pennsylvania Perelman School of Medicine and principal investigator of the clinical trial. Other study co-authors include Caitlin Foley, MD, PhD, a former medicine fellow in the Minn Lab, and Joshua Bauml, MD, former assistant professor of Medicine and co-principal investigator of the clinical trial. 

Although the trial did not include a comparison group, the results suggested a striking effectiveness for the combination. The response rates for pembrolizumab alone in large clinical trials in stage 4 NSCLC patients usually has been approximately 45 percent. In this case, the overall response rate was 67 percent—and even now, a significant proportion of the patients remain alive, suggesting many of these responses are durable. 

Analyses of the patients, and earlier tests in NSCLC mouse models, supported the treatment rationale: Lower levels of interferon-driven inflammation at baseline or following itacitinib treatment were associated with signs of a more effective CD8 T cell response—and better overall outcomes. 

The researchers now plan to follow up with a larger confirmatory clinical trial as well as additional investigations into the role of JAK1 inhibition in patients with disease progression on immunotherapy, an area of great clinical need. 

“Combined JAK Inhibition and PD-1 Immunotherapy for Non-Small Cell Lung Cancer Patients” was co-authored by Divij Mathew, Melina Marmarelis, Caitlin Foley, Joshua Bauml, Darwin Ye, Reem Ghinnagow, Shin Foong Ngiow, Max Klapholz, Soyeong Jun, Zhaojun Zhang, Robert Zorc, Christiana Davis, Maximillian Diehn, Josephine R. Giles, Alexander Huang, Wei-Ting Hwang, Nancy Zhang, Adam Schoenfeld, Corey Langer, E. John Wherry, and Andy Minn. 

Funding was provided by the Mark Foundation for Cancer Research, the Parker Institute for Cancer Immunotherapy, the LUNGevity Foundation, Incyte Corporation, the National Institute of Health (AI155577, AI115712, AI117950, AI108545, AI082630, CA210944, P30 CA008748), and the American Association of Immunologists Intersect Fellowship Program for Computational Scientists and Immunologists. 

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