A drug approved for treating rheumatoid arthritis (RA) might also prevent or delay onset of the disease in high-risk individuals, two proof-of-concept trials suggest.
In a UK trial published in The Lancet, the estimated proportion of participants remaining RA-free after a year of weekly treatments with Bristol Myers Squibb’s Orencia (abatacept) was 92.8%, versus 69.2% in those who received a placebo.
A year after the treatment was stopped, RA had developed in 25% of those who received abatacept and in 37% of those in the placebo group.
The 213 study volunteers all had severe joint pain and antibodies typically found in the blood before RA is diagnosed, but they did not have full-blown disease. “The risk for developing RA within a short time is high” in such individuals, the study team said.
Orencia was also associated with improvements in pain scores, function and quality of life measurements, and early signs of joint and tendon inflammation.
In a separate trial conducted at 14 hospitals in Europe, 100 similar high-risk patients received abatacept or placebo for six months.
The proportion of participants with improved signs of inflammation at the end of the treatment period was 57% in the abatacept group and 31% for the placebo group, researchers reported in The Lancet.
A year after treatment stopped, improvement in inflammation was seen in 51% in the abatacept group versus 24% for placebo, while 35% in the drug group and 57% in the placebo group had developed RA, the researchers said.
The two papers “present the most positive data published to date in the pre-RA field,” according to an editorial published with the reports.
Longer follow-up is needed to see whether the differences between the groups persist, and whether use of abatacept to delay progression would be cost-effective, the editorial said.