Esbriet Plus Anti-PD-L1 Slows Lung Cancer and Fibrosis in Mouse Study

Esbriet Plus Anti-PD-L1 Slows Lung Cancer and Fibrosis in Mouse Study
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In mouse models of lung cancer and fibrosis, a combination of Esbriet (pirfenidone) and anti-PD-L1 therapy strengthened an anti-tumor immune response and reduced tumor growth, while also easing pulmonary scarring in the animals.

This combination therapy might be useful in treating lung cancer that develops in people with idiopathic pulmonary fibrosis (IPF), and further testing is warranted, the research team wrote.

The study, “Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice,” was published in the journal OncoImmunology.

IPF, a progressive disease characterized by scarring (fibrosis) and damage to the lungs, is associated with an increased risk of lung cancer. In turn, lung cancer can worsen IPF’s course, and common lung cancer treatments such as surgery and chemotherapy can exacerbate this lung disease.

Therapies that block the programmed death-ligand 1 (PD-L1) are common lung cancer treatments, but their efficacy may be complicated by pre-existing IPF.

“An optimal therapeutic strategy for patients with both diseases is sorely needed,” the research team in Hubei, China, wrote.

Esbriet, marketed by Genentech, is an approved oral IPF treatment. Previous research by this study’s team demonstrated that the therapy lessened radiation-induced fibrosis and signaling of TGF-beta, an important fibrosis mediator.

Other studies also report that Esbriet’s use boosted immune response and attenuated the growth of fibroblasts, cells that contribute to fibrosis, in IPF patients.

Hypothesizing that anti-fibrotic Esbriet might enhance the tumor-suppressing efficacy of anti-PD-L1, the researchers investigated combining these treatments in a tumor mouse model, with and without pulmonary fibrosis. 

In mice with induced tumor growth, Esbriet’s use promoted tumor regression, suppressed TGF-beta signaling, and induced an anti-tumor immune response by increasing the density of immune defense cells and the expression of immune-associated genes.

Interestingly, in cells with lesser TGF-beta expression, Esbriet failed to slow tumor growth, indicating that the therapy’s anti-tumor response is partly mediated by TGF-beta signaling. 

In three mouse tumor models, the combination of anti-PD-L1 therapy and Esbriet induced an enhanced anti-tumor response compared to either treatment alone. The combination therapy significantly delayed tumor growth and reduced tumor size, while also prolonging mouse survival. 

An anti-PD-L1 plus Esbriet combination induced the expression (activity) of more immune-related genes than either monotherapy. The unique gene expression profile of the combo therapy included elevated expression of immune signaling proteins, and promoted an increased infiltration of immune T-cells to the tumor site. 

In the tumor-fibrosis mouse model, anti-PD-L1 plus Esbriet significantly reduced signs of pulmonary fibrosis compared to both non-treated mice and mice given an anti-PD-L1 in combination with galunisertib, an oral TGF-beta blocker with demonstrated anti-tumor effects. The Esbriet combination also induced a pronounced tumor regression effect, significantly stronger than that induced by the galunisertib combination. 

Overall, study results show that an anti-PD-L1 and Esbriet combination promotes an enhanced anti-tumor and anti-fibrotic effect. No signs of toxicity or tissue damage were observed in treated mice.

“Our results collectively demonstrated that pirfenidone facilitated antitumor immunity and enhanced the efficacy of PD-L1 blockades. It may act as an adjuvant to immunotherapy in cancer treatment, particularly, in lung cancer patients with preexisting IPF,” the researchers wrote.

These “initial findings encourage … further clinical trials to determine the efficacy of the combination,” the team added. 

Among the study’s limitations were an inability to measure other immune cell types, and the lack of a robust treatment response in immunocompromised mice (mice with a defective immune system), which should be considered if the treatment is combined with immunosuppressive therapy.

“The exact molecular mode of action of [Esbriet] on immune activation is still a question needed to be further explored,” the researchers wrote.

Aisha Abdullah received a B.S. in biology from the University of Houston and a Ph.D. in neuroscience from Weill Cornell Medical College, where she studied the role of microRNA in embryonic and early postnatal brain development. Since finishing graduate school, she has worked as a science communicator making science accessible to broad audiences.
Total Posts: 110

Patrícia holds her PhD in Medical Microbiology and Infectious Diseases from the Leiden University Medical Center in Leiden, The Netherlands. She has studied Applied Biology at Universidade do Minho and was a postdoctoral research fellow at Instituto de Medicina Molecular in Lisbon, Portugal. Her work has been focused on molecular genetic traits of infectious agents such as viruses and parasites.

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Aisha Abdullah received a B.S. in biology from the University of Houston and a Ph.D. in neuroscience from Weill Cornell Medical College, where she studied the role of microRNA in embryonic and early postnatal brain development. Since finishing graduate school, she has worked as a science communicator making science accessible to broad audiences.
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