Last updated June 23, 2020 at 11:22 am
Encouraging results in animals have researchers hoping the novel formulation could improve the quality of life of men undergoing treatment.
Why This Matters: While early days, improving the effectiveness of drugs against the most common cancer in men is good news.
A novel formulation of the prostate cancer drug abiraterone acetate – also known as Zytiga – could dramatically improve the quality of life for people suffering from prostate cancer, say researchers.
Testing a new formulation in animals, the team from the University of South Australia have found the new form improves the drug’s effectiveness by 40 per cent.
As yet it has not been tested in humans.
Developed by a research group at UniSA’s Cancer Research Institute, the team used an oil-based oral formulation that, in animals, not only enables a smaller dose of the drug to be effective, but also has the potential to dramatically reduce possible side effects, such as joint swelling and diarrhoea.
And that, says lead researcher Hayley Schultz, will ultimately provide a better treatment for patients with prostate cancer if the results carry over into humans.
Also: Big Questions: Cancer
Many prostate cancer treatments don’t dissolve, inhibiting their effectiveness
Prostate cancer is the most commonly diagnosed cancer in men, with one in six at risk of diagnosis before the age of 85.
In 2019, more than 19,500 cases of prostate cancer were diagnosed in Australia. Globally, prostate cancer cases reached 1.28 million in 2018.
“Many drugs are poorly water soluble, so when they’re ingested, they enter the gut but don’t dissolve, which means that their therapeutic effect is limited,” says Schultz.
“This is the case for Zytiga. Here, only 10 per cent of the dose is absorbed, leaving the other 90 per cent undissolved, where it simply passes through the body as waste.
“On top of this, patients taking Zytiga must fast for two hours prior to taking the drug, and another hour after taking the drug to achieve predictable absorption. And as you can imagine, this can be painstakingly inconvenient.
“Our new formulation changes this. By using oils to mimic pharmaceutical food effects, we’re able to significantly increase the drug’s solubilisation and absorption, making it more effective and a far less invasive treatment for patients.”
New formulation could be adopted by a wide range of medicines
The new formulation uses very high levels of abiraterone acetate dissolved within a specific oil and encapsulated within porous silica microparticles to form a powder that can be made into tablets or filled into capsules.
Applied to human treatment, it could reduce the dose from 1000mg to 700mg per day, without the need for fasting.
Professor Clive Prestidge, who oversaw the work, says if the team can secure funding, clinical trials in humans could be just two years away.
“Based on our knowledge of this drug’s pharmaceutical food effect, we hypothesise its absorption in humans will be extensively improved using this technology,” Prestidge says.
“Anything we can do to contribute to the development of a commercialised product to improve the lives of patients, is invaluable.
“This novel formulation is flexible enough to be adopted by thousands of different medicines; its potential to help patients of all kinds is exponential.”