01 September 2021

A blood test could determine the right drug and dosage for rheumatoid arthritis patients.

A simple blood test could determine which drug and dosage is more likely to be effective against rheumatoid arthritis, potentially saving sufferers serious side effects and Australian taxpayers millions of dollars.

New research led by the University of South Australia suggests that blood concentration levels and genetic markers need to be measured to reveal whether the common rheumatoid arthritis (RA) drug Leflunomide will work for patients.

The finding, published in Arthritis Care & Research, emerged from a study of 67 patients taking Leflunomide, which is traditionally prescribed in either 10 or 20 milligram dosages.

Lead investigator, UniSA Associate Professor Michael Wiese, says arbitrary dosages are poor predictors of how well a patient will respond because bodies metabolise the drug quite differently.

“Blood concentrations of Leflunomide are highly variable and unpredictable between patients, so we need to find the sweet spot for each person where we see a good response and minimal side effects, rather than adhere to the existing one-size-fits-all approach,” Assoc Prof Wiese says.

Researchers believe a blood test could determine the right dosage for individuals, indicating whether a higher or lower dosage is required or whether a new drug is appropriate.

“Leflunomide may not work for all patients, depending on their genetic makeup, but if we had a clear indicator whether a dosage change is necessary or if a new drug would be more appropriate, that would save patients a lot of money and some unnecessary side effects. A blood test is the key.”

Assoc Prof Wiese says an increasing number of people are being prescribed injectable biological drugs (including antibodies), but these are very expensive and often have severe side effects, including potential life-threatening infections, as well as hives and chills.

Biological drugs prescribed for rheumatoid arthritis are available on the Federal Government’s Pharmaceutical Benefits Scheme (PBS) and cost Australian taxpayers between $15,000 and $25,000 per patient per annum, or at least $383 million in total each year.

In comparison, older drugs such as Leflunomide – currently prescribed to at least 15,000 Australians – are available on the PBS for between $100-$500 a year per patient.

“People are quite excited about these expensive biological drugs, but the older drugs can be just as effective and far cheaper on the public purse, particularly if we can establish correct dosages for patients.

“Some individuals should be on the biological drugs, but we need to be smarter about who is selected for which drug. A blood test will determine who is more likely to respond to Leflunomide based on their genetic makeup.”

The researchers hope to progress with clinical trials, contingent on funding.

Notes for editors

Rheumatoid arthritis is an autoimmune condition, affecting about one per cent of the population, and causing inflammation and pain around the joints. It is commonly treated by medication which relieves symptoms and slows disease progression, but there is no cure.

Precision Medicine with Leflunomide: Consideration of the DHODH Haplotype and Plasma Teriflunomide Concentration and Modification of Outcomes in Patients with Rheumatoid Arthritis” is published in Arthritis Care & Research. For a copy of the paper please email candy.gibson@unisa.edu.au


Contact for interview:  Assoc Prof Michael Wiese T: +61 8 8302 2312 M: 0408 159 539

Media contact: Candy Gibson M: +61 434 605 142 E: candy.gibson@unisa.edu.au

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