Source: Genprex, Inc. 11/19/19
- Company’s TUSC2 gene therapy found to increase effectiveness of anti-PD1 immunotherapy and anti-PD1 immunotherapy combined with platinum chemotherapy in humanized mouse model
- TUSC2 in combination with anti-PD1 and chemotherapy resulted in complete eradication of anti-PD1 resistant lung metastases
- Company’s Oncoprex™ immunogene therapy may improve on first-line standard of care for lung cancer
Genprex, Inc. (“Genprex” or the “Company”) (NASDAQ: GNPX),
a clinical-stage gene therapy company, reported that its collaborators
from The University of Texas MD Anderson Cancer Center (“MD Anderson”)
presented positive preclinical data for the combination of TUSC2
immunogene therapy with an anti-PD1 antibody, pembrolizumab, and for the
combination of TUSC2 immunogene therapy, pembrolizumab, and
chemotherapy for the treatment of some of the most resistant metastatic
lung cancers, including the KRAS and LKB1 mutations, at the American
Association of Cancer Research Tumor Immunology and Immunotherapy
Meeting 2019. The TUSC2 gene is a tumor suppressor gene and is the
active agent in Genprex’s Oncoprex™ immunogene therapy.
The poster, entitled “Efficacy of Novel Immunogene-Combinations for KRAS
and LKB1 mutant NSCLC in a Humanized Mouse Model” shows that TUSC2
confers sensitivity to checkpoint blockade for some of the most
resistant metastatic human cancers, including the KRAS and LKB1
mutations, in mice with human immune cells (humanized mice) with lung
metastases. When TUSC2 was combined with anti-PD1 therapy,
pembrolizumab, in humanized mice with KRAS and LKB1 lung metastases,
there was significantly increased antitumor activity than when compared
to either agent alone. This combination and model also demonstrated
TUSC2-related NK (Natural Killer) cell activation. A significantly
higher percentage of CD56+ NK and CD56+CD59+
active NK cells, which are immune cells that have been activated to
kill cancer cells, were found in the mice that received TUSC2 alone and
in those that received the combination of TUSC2 and pembrolizumab than
in those that received pembrolizumab alone.
The poster also shows that TUSC2 increases the effectiveness of anti-PD1
checkpoint blockade combined with platinum chemotherapy in humanized
mice with lung metastases with KRAS and LKB1 mutations, thus
demonstrating that TUSC2 may improve on first-line standard of care for lung cancer.
The combination of TUSC2 with pembrolizumab and carboplatin, a platinum
chemotherapy, in humanized mice with KRAS and LKB1 lung metastases
resulted in metastasis regression significantly greater than either
TUSC2 alone or pembrolizumab combined with carboplatin treatments. This
model showed significantly fewer or no visible tumor nodules after
treatment with the TUSC2 combination as compared with other groups, and
it showed strong antitumor efficacy. The combination of TUSC2 with
pembrolizumab and carboplatin resulted in complete eradication of
anti-PD1 resistant lung metastases in the humanized mouse model.
“These data not only further support existing preclinical data showing
that Oncoprex immunogene therapy is synergistic with anti-PD1 therapy,
but they also offer new data demonstrating that Oncoprex improves on the
combination of anti-PD1 therapy and chemotherapy, today’s first line
standard of care for lung cancer,” said Julien L. Pham, MD, MPH,
President and Chief Operating Officer of Genprex. “In a sophisticated
humanized mouse model, the combination of TUSC2 with pembrolizumab and
carboplatin resulted in complete eradication of anti-PD1 resistant lung
metastases in some of the most resistant cancer mutations. This is
highly encouraging and provides us with a strong indication that the
combination could lead to similar results in the clinic.”
Genprex, Inc. is a clinical stage gene therapy company developing potentially life-changing technologies for cancer patients based upon a unique proprietary technology platform. Genprex’s platform technologies are designed to administer cancer-fighting genes by encapsulating them into nanoscale hollow spheres called nanovesicles, which are then administered intravenously and taken up by tumor cells where they express proteins that are missing or found in low quantities. The company’s lead product candidate, Oncoprex™ immunogene therapy for non-small cell lung cancer (NSCLC), has a multimodal mechanism of action whereby it interrupts cell signaling pathways that cause replication and proliferation of cancer cells, re-establishes pathways for apoptosis, or programmed cell death, in cancer cells, and modulates the immune response against cancer cells. Oncoprex has also been shown to block mechanisms that create drug resistance. For more information, please visit the company’s web site at www.genprex.com or follow Genprex on Twitter, Facebook and LinkedIn.
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