Anti-KRAS drug delivers unprecedented results in pancreatic cancer care
[Dec 9, 2022: Meagan Raeke, UPenn School of Medicine]
A small molecule inhibitor that attacks the difficult to target, cancer-causing gene mutation KRAS, found in nearly 30 percent of all human tumors. (CREDIT: Creative Commons)
A small molecule inhibitor that attacks the difficult to target, cancer-causing gene mutation KRAS, found in nearly 30 percent of all human tumors, successfully shrunk tumors or stopped cancer growth in preclinical models of pancreatic cancer, researchers from Penn Medicine’s Abramson Cancer Center showed, suggesting the drug is a strong candidate for clinical trials. The study was published in Cancer Discovery, a journal of the American Association for Cancer Research.
“The results of this study are in stark contrast to anything we’ve seen before in pancreatic cancer,” said co-corresponding senior author Ben Stanger, MD, PhD, the Hanna Wise Professor in Cancer Research in the Perelman School of Medicine at the University of Pennsylvania and director of the Penn Pancreatic Cancer Research Center. “Even in preclinical research models for this cancer type, most drugs tested within the last decade – including novel immunotherapies – have had limited impact.”
Patients with pancreatic cancer have an overall poor prognosis with a five-year survival rate of 11 percent and limited treatment options. Nearly 90 percent of pancreatic cancers are driven by a mutation in the KRAS gene, the most common oncogene across cancer types. The first targeted therapy for KRAS was approved last year for non-small cell lung cancer with KRAS G12C mutations, but only 2 percent of pancreatic cancers express that type of mutation. Around 36 percent of pancreatic cancers with a KRAS mutation are KRAS G12D-mutant.
The small molecule inhibitor used in this study, MRTX1133 (developed by Mirati Therapeutics) specifically targets KRAS G12D, as the company first reported last month in Nature Medicine.
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The Penn study now shows the KRAS-inhibitor not only directly targets cancer cells but also unexpectedly cooperates with the immune system to produce a durable response to treatment, which is important because cancer eventually finds a way to evade most targeted therapies.
“We know from KRAS G12C studies and other targeted therapy studies that resistance is going to happen,” Stanger said. “Even before we get to clinical trials, we’re thinking about how to combine drugs so that the tumors won’t come back. Our findings provide evidence to suggest immunotherapy as a partner with KRAS G12D inhibitors.”
The researchers were able to assess the impact of MRTX1133 on the immune system because the type of model used in the study allows the tumor to spontaneously evolve after implantation in otherwise healthy mice, making it possible to discern the drug’s impact on the surrounding tumor microenvironment (TME).
MRTX1133 selectively inhibits KRASG12D and downstream MAPK signaling in vitro. MRTX1133 dose response of BxPC-3 (KRASWT), AsPC-1 (KRASG12D), and MIA PaCa-2 (KRASG12C) cells after 72h of treatment. 3-fold serial dilutions were used, and cell viability was measured with CellTiter-Glo. IC50 values are listed. (CREDIT: Cancer Discovery)
The immunocompetent KPC model was developed by Penn Medicine nearly 20 years ago and is the gold standard used worldwide to assess potential therapies for pancreatic ductal adenocarcinoma (PDAC). PDAC is known for having a particularly dense TME, which contributes to resistance to therapy.
The research team found that the drug prompted an increase of T cells in the TME, which improved the depth and duration of response to MRTX1133. All complete remissions observed in the study were accompanied by T cell mediated anti-tumor immunity.
MRTX1133 selectively inhibits KRASG12D and downstream MAPK signaling in vitro. Representative western blot of cell lysates from 6419c5 (KRASG12D) cells treated with MRTX1133 or DMSO control for two hours. Representative western blot of cell lysates from BxPC-3 (KRAS-WT) cells treated with MRTX1133 or DMSO control for two hours. MRTX1133 dose response of 4662-KRASG12D and 4662-KRASG12C after 72h of treatment. 5-fold serial dilutions were used. IC50 values are listed (CREDIT: Cancer Discovery)
In mice without T cells, the effect of MRTX1133 was brief and tumors grow back much more quickly. These results suggest that MRTX1133 could be combined with immunotherapy to improve long-term response to therapy and keep the cancer from returning.
“After many years of work to find much-needed new approaches for patients with pancreatic cancer, it’s exciting to have a new class of drugs on the horizon,” said co-corresponding author Robert Vonderheide, MD, DPhil, director of the Abramson Cancer Center and the John H. Glick Abramson Cancer Center Professor in the Perelman School of Medicine, whose lab members worked with those in Stanger’s lab in a focused cooperative team on this study. “We’re optimistic that KRAS G12D inhibitors will make their way into clinical trials soon. KRAS is surrendering, and now we know the immune system can see it.”
MRTX1133 is selective for KRASG12D in immunocompetent implantation tumor models. Waterfall plot of vehicle and MRTX1133 treated tumors (6419c5, subcutaneous) showing change in tumor volume after 7d of treatment compared to baseline at day 0. Each bar represents a single tumor. n=10 mice/group. (CREDIT: Cancer Discovery)
The study was supported by the National Institutes of Health (R01-CA229803, R01-CA252225, T32-CA009140 and P30-CA016520), the Cancer Research Institute (CRI4097), the Parker Institute for Cancer
Immunotherapy, the Penn Pancreatic Cancer Research Center and The Abramson Family Cancer Research Institute.
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Note: Materials provided above by UPenn School of Medicine. Content may be edited for style and length.
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