A recent study found promise in a new drug that treats cachexia, a progressive wasting syndrome. The trial is currently in canine patients, with hopes to move to human patients in the future.
A new pilot study is showing promising results in the treatment of cachexia, a progressive wasting syndrome often seen in patients with cancer, according to researchers from the University of Missouri.
Patients experiencing cachexia may suffer from weakness and progressive loss of body weight, fat and muscle. The American Cancer Society estimates that cachexia is the immediate cause of death in 20 to 40 percent of patients with cancer.
This condition often occurs in patients in advanced stages of the disease. Although cachexia is commonly seen in patients with pancreatic and gastric cancer, it can also be seen in those with lung, esophageal, colorectal and head and neck cancer.
Researchers in partnership with Tensive Controls, Inc. developed a drug that has been tested in three canine patients, so far, and are actively recruiting more dogs.
“Our goal is to prove that this therapy works in improving the lives of dogs with naturally occurring cachexia and then hopefully move this on into people with cachexia, which is very devastating in people with cancer,” Sandra Bechtel, associate professor of medical oncology and principal investigator, said in an interview with CURE.
Cachexia causes an increase in immunological activity and that reduces substances in the body called cytokines, or small secreted proteins released by cells that have a specific effect on the interactions and communications between cells. The cytokines increase melanocortin activity in the brain, which increases metabolic rate and decreases appetite.
The drug that Kenneth Gruber, Ph.D., adjunct professor in the Department of Medical Pharmacology and Physiology and president and founder of Tensive Controls, Inc., and his team created can cross the blood brain barrier, which prevents materials from the blood from entering the brain, and inhibits overstimulation of the melanocortin system.
“Our drug addresses the increase in melanocortin activity by being a melanocortin system antagonist,” said Gruber. “It gets into the brain and normalizes melanocortin system activity so that the body can not only decrease the burning effect of high metabolic rate on lean body mass, but also increases appetite, so we can restore the normal condition of the animal even though the animal still has the underlying disease.”
In this study, none of the three dogs have cancer, but they all have diseases that caused wasting, lethargy and decrease in appetite. After receiving the drug, researchers reported seeing an increase in appetite, weight gain and body condition scores. In addition, the dogs started doing things their owners had reported they hadn’t done in a long time. For instance, one dog started to chase horses again and another seemed brighter and more active around the home.
Currently, the only side effect seen was coat changes: two dogs had a fluffier, darker tone coat than they did prior to treatment. Gruber noted that dogs are a great model for humans.
“They have evolved with us over 10,000 years. They develop many of the same diseases as humans because they live with us and diseases that we have acquired in the last 10,000 years usually show up in dogs,” he said. “A lot of drugs for cancer or other diseases are not often tested in large animals because you need to have a disease state. A lot of times you get small animal disease states to validate your efficacy, and then jump into a human trial and the success rate in that is not very good.”
The plan is to now continue enrolling dogs with naturally occurring cachexia to get data on safety and efficacy of the drug. If it continues to show promising results that can be provided to the Food and Drug Administration, Gruber said there could likely be testing of this drug in humans within the next two to three years.
“My focus in cancer therapy is always quality of life, even if I am using chemotherapy or radiation therapy, I want my canine patients to feel good through the duration of treatment,” Bechtel said. “So, this trial lines up nicely with what my goals are because it’s a trial with emphasis on quality of life.”
This article orginally appeared on curetoday.com.
Dr. Niccole Bruno, DVM, CEO and Founder of blendVET®, has built a pioneering career as a clinician, hospital leader, and advocate, dedicated to empowering underrepresented minorities in veterinary medicine through mentorship, authenticity, and community building.
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