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A New Test Could Save Arthritis Patients Time, Money, and Pain

— But will it be used?

Ƶ MedicalToday
A photo of a nurse drawing blood from a patient.

SAN DIEGO -- Erinn Maury, MD, knew infliximab (Remicade) wasn't the right drug for Patti Schulte, a rheumatoid arthritis patient the physician saw at her Millersville, Maryland, practice. Schulte's swollen, painful joints hadn't responded to etanercept (Enbrel) or adalimumab (Humira), two drugs in the same class.

But the insurer insisted, so Schulte went on infliximab. It didn't work either.

What's more, Schulte suffered a severe allergic reaction to the infusion therapy, requiring a heavy dose of prednisone, a steroid with grave side effects if used at high doses for too long.

After 18 months, her insurer finally approved Maury's drug of choice, abatacept (Orencia). By then, Schulte's vertebrae, weakened by prednisone, had started cracking. She was only 60.

Schulte's story of pain, drug-hopping, and insurance meddling is all too common among patients with rheumatoid arthritis, who often cycle agonizingly through half a dozen drugs in search of one that provides a measure of relief. It's also a story of how doctors are steered by pharmacy benefit managers -- the middlemen of the drug market -- as well as by insurers.

Once people with inflammatory conditions such as rheumatoid arthritis reach a certain stage, the first prescription offered is typically adalimumab, the best-selling drug in history, and part of a class known as tumor necrosis factor (TNF) inhibitors, which fail to significantly help about half of the patients who take it.

"We practice rheumatology without any help," said , a rheumatologist and adjunct clinical professor at Stanford. She bemoaned the lack of tools available to choose the right drug while bristling at corporate intervention in the decision. "We are told by the insurer what to prescribe to the patient. After they fail methotrexate, it's a TNF inhibitor, almost always Humira. And that's not OK."

If there's a shred of hope in this story, it's that a blood test, PrismRA, may herald an era of improved care for patients with rheumatoid arthritis and other autoimmune conditions. But first, it must be embraced by insurers.

PrismRA employs a predictive model that combines clinical factors, blood tests, and 19 gene patterns to identify the roughly 60% of patients who are very unlikely to respond to a TNF inhibitor.

Over the past 25 years, drug companies have introduced five new classes of autoimmune drugs. TNF inhibitors were the first to market, starting in the late 1990s.

Some 1.3 million Americans have rheumatoid arthritis, a disease in which a person's immune system attacks their joints, causing crippling pain and, if improperly treated, disfigurement. The newer drugs, mostly , are also used by some of the 25 million or more Americans with other autoimmune diseases, such as lupus, Crohn's disease, and psoriasis. Typically costing tens of thousands of dollars annually, the drugs are prescribed after a patient fails to respond to older, cheaper .

Until recently, rheumatologists have had few ways to predict which of the new drugs would work best on which patients. Often, "it's a coin flip whether I prescribe drug A or B," said , a rheumatology professor at the University of Alabama-Birmingham.

Yet about 90% of the patients who are given one of these advanced drugs start on a TNF inhibitor, although there's often no reason to think a TNF inhibitor will work better than another type.

Under these puzzling circumstances, it's often the insurer rather than the doctor who chooses the patient's drug. Insurers lean toward TNF inhibitors such as adalimumab in part because they get large rebates from manufacturers for using them. Although the size of such payments is a trade secret, AbbVie is said to be offering rebates to insurers of up to 60% of Humira's price. That has enabled it to control 98.5% of the U.S. adalimumab market, even though it has eight biosimilar competitors.

PrismRA's developer, Scipher Medicine, has provided more than 26,000 test results, rarely covered by insurance. But on October 15, the Centers for Medicare & Medicaid for the test, and its use is expected to rise. At least are developing drug-matching tests for rheumatoid arthritis patients.

Although critics say PrismRA is not always useful, it is likely to be the first in a series of diagnostics anticipated over the next decade that could reduce the time that autoimmune disease patients suffer on the wrong drug.

Academics, small biotechs, and large pharmaceutical companies are investing in methods to distinguish the biological pathways involved in these diseases, and the best way to treat each one. This approach, called precision medicine, has existed for years in cancer medicine, in which it's routine to test the genetics of patients' tumors to determine the appropriate drug treatment.

"You wouldn't give Herceptin [trastuzumab] to a breast cancer patient without knowing whether her tumor was HER2-positive," said , a rheumatology professor at the William Harvey Research Institute in London. He was speaking before a well-attended session at an in San Diego in November. "Why do we not use biopsies or seek molecular markers in rheumatoid arthritis?"

It's not only patients and doctors who have a stake in which drugs work best for a given person.

When infliximab failed and Schulte waited for the insurer to approve abatacept, she insisted on keeping her job as an accountant. But as her prednisone-related spinal problems worsened, Schulte was forced to retire, go on Medicaid, and seek disability, something she had always sworn to avoid.

Now taxpayers, rather than the insurer, are covering Schulte's medical bills, Maury noted.

Precision medicine hasn't seemed like a priority for large makers of autoimmune drugs, which presumably have some knowledge of which patients are most likely to benefit from their drugs, since they have tested and sold millions of doses over the years. By offering rebate incentives to insurers, companies like AbbVie, which makes Humira, can guarantee theirs are the drugs of choice with insurers.

"If you were AbbVie," Curtis said, "why would you ever want to publish data showing who's not going to do well on your drug, if, in the absence of the test, everyone will start with your drug first?"

What Testing Could Do

Medicare and commercial insurers haven't yet set a price for PrismRA, but it could save insurers thousands of dollars a year for each patient it helps, according to Krishna Patel, PharmD, Scipher's associate director of medical affairs.

"If the test cost $750, I still only need it once, and it costs less than a month of whatever drug is not going to work very well for you," said Curtis, a co-author of some studies of the test. "The economics of a biomarker that's anything but worthless is pretty favorable because our biologics and targeted drugs are so expensive."

Patients are enthusiastic about the test because so many have had to take TNF inhibitors that didn't work. Many insurers require patients to try a second TNF inhibitor, and sometimes a third.

Jen Weaver, a patient advocate and mother of three, got little benefit from hydroxychloroquine, sulfasalazine, methotrexate, and abatacept, a non-TNF-inhibitor biologic therapy, before finding some relief in another, tocilizumab (Actemra). But she was taken off that drug when her white blood cells plunged, and the next three drugs she tried -- all TNF inhibitors -- caused allergic reactions, culminating with an outbreak of pus-filled sores. Another drug, apremilast (Otezla), eventually seemed to help heal the sores, and she's been stable on it since in combination with methotrexate, Weaver said.

"What is needed is to substantially shorten this trial-and-error period for patients," said , herself a patient and the director of research operations at the Global Healthy Living Foundation. "There's a lot of anxiety and frustration, weeks in pain wondering whether a drug is going to work for you and what to do if it doesn't." A survey by her group found that 91% of patients worried their medications would stop working. And there is evidence that the longer it takes to resolve arthritis symptoms, the less chance they will ever stop.

How insurers will respond to the availability of tests isn't clear, partly because the arrival of new biosimilar drugs -- essentially generic versions -- are making TNF inhibitors cheaper for insurance plans. While Humira still dominates, AbbVie has increased rebates to insurers, in effect lowering its cost. Lower prices make the PrismRA test less appealing to insurers, since widespread use of the test could cut TNF inhibitor prescriptions by up to a third.

However, rheumatologist John Boone, MD, in Louisville, Kentucky, found to his surprise that insurers mostly accepted alternative prescriptions for 41 patients whom the test showed unlikely to respond to TNF inhibitors as . Boone receives consulting fees from Scipher.

Although the test didn't guarantee good outcomes, he said, the few patients given TNF inhibitors despite the test results almost all did poorly on that regimen.

Scientists from AbbVie, which makes several rheumatology drugs in addition to adalimumab, presented a study at the San Diego ACR conference examining biomarkers that might show which patients would respond to upadacitinib (Rinvoq), a new immune-suppressing drug in a class known as Janus kinase (JAK) inhibitors. When asked about its use of precision medicine, AbbVie declined to comment.

Over two decades, adalimumab has been a blockbuster drug for AbbVie. The company sold more than in the third quarter of 2023, 36% less than a year ago. Sales of upadacitinib, which AbbVie is marketing as a treatment for patients failed by adalimumab and its class, jumped 60% to $1.1 billion.

What Patients Want

Shannan O'Hara-Levi, a 38-year-old in Monroe, New York, has been on scores of drugs and supplements since being diagnosed with juvenile arthritis at age 3. She's been nauseated, fatigued, and short of breath and has suffered allergic reactions, but she says the worst part of it was finding a drug that worked and then losing access because of insurance. This happened shortly after she gave birth to a daughter in 2022, and then endured intense joint pain.

"If I could take a blood test that tells me not to waste months or years of my life -- absolutely," she said. "If I could have started my current drug last fall and saved many months of not being able to engage with my baby on the floor -- absolutely."

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