Juvenile Idiopathic Arthritis May Raise Kids’ Cancer Risk

Fuse/Thinkstock(BIRMINGHAM, Ala.) — Children with juvenile idiopathic arthritis (JIA), the most common form of childhood arthritis, may be at higher risk of developing cancer than children who do not have the condition, according to a new study published in the journal Arthritis & Rheumatism.

Researchers identified 7,812 children with JIA and compared them with thousands of children not affected by JIA and found that the arthritic children developed about four times as many new growths considered likely to be cancerous as children who did not have arthritis.  They followed the children for about 18 months.

“Based on the data, it appears that being diagnosed with JIA increases the likelihood of developing malignancies,” said Dr. Timothy Beukelman, the study’s lead author and an associate professor of pediatrics at the University of Alabama at Birmingham.

But despite the statistically higher risk, Dr. Sampath Prahalad, associate professor of pediatrics and human genetics at the Emory University School of Medicine, said cancer in children with JIA is rare.

“The risk is very low, and it’s more common for children with JIA to not get cancer,” he said.  The study included only 7,812 children with JIA, and nationwide, there are about 300,000.  Prahalad was not involved with the research.

Beukelman said there are a number of possible explanations for the finding, but so far, no one knows why JIA may predispose children to cancer.  He stressed, however, that there was no association between cancer risk and any treatments for the condition, including the use of drugs known as tumor necrosis factor (TNF) inhibitors.

TNF inhibitors, including the brand-name drugs Enbrel and Humira, are considered by doctors to be revolutionizing treatments that can sometimes stop rheumatoid arthritis in its tracks.

But there have been a number of case reports linking the use of TNF inhibitors to an increased cancer risk in children, prompting the Food and Drug Administration (FDA) to add a black box warning to these drugs in 2009.  A black box warning is the strongest warning used by the FDA and indicates a drug has potentially life-threatening effects.

“The initial concern about TNF inhibitors may have been overstated, since some of the risk likely comes from the disease itself,” Beukelman said.

Beukelman explained that when the FDA made its decision to include black box warnings on TNF inhibitors, the only data available compared children with JIA who took these drugs with healthy children.

Copyright 2012 ABC News Radio