Boosting treatments for metastatic melanoma
Study shows repurposing a class of anxiety meds could increase the efficacy of cancer treatments
There are times when adding something new to the mix makes it better.
Give Popeye some spinach, and you've got a fighting machine. Give Mario a mushroom, and he becomes invincible. Without drinking a potion, Alice in Wonderland would never fit through the door.
Now, University of Cincinnati clinician-scientist Soma Sengupta, MD, PhD, along with lead investigator Daniel Pomeranz Krummel, PhD, says new findings point to a treatment-boosting drug to enhance therapies for metastatic cancer and make them more effective, giving patients a fighting chance at survival.
“Melanoma is a serious skin cancer that evolves from the pigment cells of the skin and eyes,” says Sengupta, associate professor of neurology at UC, UC Health neuro-oncologist and co-director of the UC Gardner Neuroscience Institute’s Brain Tumor Center. “There are millions of people in the U.S. living with this type of cancer, and the incidence is projected to increase.
“While physicians can often quickly find and treat melanoma of the skin, metastatic melanoma, or melanoma that has spread to other parts of the body, often the brain, is a lethal cancer. Often, patients who receive immunotherapy, which uses the patient’s own immune system to treat the condition, do not have good responses. They also experience many uncomfortable side effects that impact their quality of life.”
Sengupta says that her team recently published results in the International Journal of Radiation Oncology • Biology • Physics that show by targeting a particular neurotransmitter through the use of a new class of sedatives, related to Valium or Xanax, cancer treatments like radiation and immunotherapy could be boosted to better fight cancer in patients while reducing side effects. These studies were conducted in animal models but the hope is to soon study these outcomes in patients with metastatic cancer.
Researchers found by adding this particular study drug, infiltration of immune cells to the tumor greatly improved, enhancing efficacy of the treatment and allowing the cells to combat melanoma; tumors shrunk and, in some cases, completely disappeared.
We are using a drug that has already been approved for anxiety for another serious condition that claims lives every day.
Soma Sengupta, MD, PhD
“Our long-term goal is to add this new class of drugs to a patient’s radiation and immunotherapy treatment,” says Sengupta, who is a corresponding author on the paper and the Harold C. Schott Endowed Chair of Molecular Therapeutics. They are collaborating with investigators from UC who are helping to formulate the lead compound, including Pankaj Desai, PhD, with the James L. Winkle College of Pharmacy, as well as with Mohammad Khan, PhD, of Emory University, who will test this approach via clinical trial once Sengupta has approval from the Food and Drug Administration to test this drug in humans.
“We hope this will help patients avoid side effects, and that by adding this drug to the regimens, we will reduce costs, since we think the treatments will become more effective, and in turn, doses of standard treatments can be lowered. More studies are needed, but this is a promising new approach. We are using a drug that has already been approved for anxiety for another serious condition that claims lives every day.”
When researchers were preparing this study to report their team’s findings, they asked a senior colleague and UC cancer researcher Peter Stambrook, PhD, to read it and provide feedback. Sadly, Stambrook passed away from melanoma before their work was published.
“Peter died as a result of his melanoma,” says Krummel, PhD, research associate professor of neurology. “He was an outstanding scientist and was incredibly supportive of our research. We feel more driven than ever to push forward with our research and to honor Peter in this way.”
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Other investigators on this study include Laura Kallay, PhD, Debanjan Bhattacharya, PhD, Dan Ionascu, PhD, and Mario Medvedovic, PhD, all from the University of Cincinnati; Tahseen Nasti, PhD, Milota Kaluzova, PhD, Andre Burnham, PhD, David Lawson, MD, Yichun Cao, Jeffrey Switchenko, PhD, Mohammad Khan, MD, and Andrew Jenkins, PhD, all from Emory University; Johannes Melms, MD, and Benjamin Izar, MD, of Columbia University; Maxwell Xu, Johns Hopkins University; Taukir Ahmed, PhD, Guanguan Li, PhD, and James Cook, PhD, University of Wisconsin-Milwaukee; and Jeanne Kowalski, PhD, University of Texas.
Funding and disclosures available here. Conflicts of interest for Sengupta, Cook and Pomeranz Krummel include a start-up called AMLAL, which has been developed based on this data to apply for small business technology transfer funding and other funding mechanisms to bring this compound into the clinic setting faster.