Stem cell treatments flourish

Jenn Ackerman/New York Times A doctor retrieves bone marrow from a patient’s pelvic bone at the Nura Precision Pain Management clinic in Edina, Minn., for a stem cell procedure, Jan. 18. The Food and Drug Administration has taken an industry-friendly approach toward companies using unproven cell cocktails to treat people desperate for relief from aging or damaged joints.

A surgeon recommended a hip replacement, but Kenneth Cevoli said no thanks.

“They’re really quick to try to give you fake joints and make a bunch of money off you,” he said.

At 71, Cevoli, a high-school guidance counselor in Teterboro, New Jersey, coaches cross-country, teaches mogul skiing, surfs and works summers as a lifeguard on Cape Cod, Massachusetts. Despite pain in his left hip and knee, he questioned the need for major surgery, worrying it would sideline him for too long.

Instead, he tried an increasingly popular treatment, in which stem cells are extracted from a patient’s own bone marrow and injected into worn or injured joints to promote healing.

Many people have become captivated by the idea of using stem cells to fix their damaged joints, and some claim to have been helped.

But there is no clear evidence that these treatments work, and their safety has yet to be established. Most researchers, including those at the National Institutes of Health, think efforts to sell therapies involving adult stem cells, which can develop into different types of cells to replenish tissue, have gotten way ahead of the science.

Even so, hundreds of clinics have popped up around the country to meet the demand. Some of the clinics also inject joints with platelet-rich plasma, a solution of platelets extracted from the patient’s own blood. A few employers have even agreed to provide insurance coverage for the treatments.

There is almost no regulatory oversight of orthopedic procedures using bone-marrow extracts or platelets, which are regarded as low risk. While the Food and Drug Administration insists that it does have the authority to regulate stem cell treatments, it adopted an industry-friendly approach in 2017 by giving companies a three-year grace period in which to describe their products or treatments so the agency can determine whether they meet the criteria of drugs that would require agency approval. So far, few companies have submitted any information.

In the meantime, rogue clinics offering other kinds of procedures have flourished, accused of blinding people by injecting cells into their eyes, mixing stem cells with smallpox vaccine to treat cancer or causing severe infections by administering contaminated blood from umbilical cords into patients’ joints or spines. In some of the worst cases, patients had already been harmed before the agency took any action, and the patients took legal steps themselves, suing the clinics that injured them.

“We had our day job clearly cut out for us,” said Dr. Scott Gottlieb, who was FDA commissioner until April. There is, he added, a lot of “really bad stuff.”

Gottlieb spoke in an interview after leaving office. A spokeswoman for the agency said current officials declined to be interviewed. But she said the agency had taken about 45 enforcement actions against stem cell businesses in the past year, including two court cases and various types of warning letters.

Many scientists are skeptical about the treatments being offered, and have called for stricter oversight.

“I believe strongly that it isn’t ethical to charge patients for unproven therapies like these and raise what are likely to be false hopes,” said Paul S. Knoepfler, a stem cell researcher at the University of California, Davis.

He said some properly conducted studies on platelet-rich plasma suggested it might help, but others did not. As for stem cells extracted from bone marrow, Knoepfler said well-controlled studies were even scarcer, also with mixed results.

Rigorous studies are essential, because symptoms from arthritis and injuries can wax and wane, making it hard to determine whether treatments work.

In part because of the scant data, no stem cell or platelet treatments are approved by the FDA for orthopedic problems, and most insurers don’t cover them. Still, many patients pay thousands of dollars out of their own pockets.

Cevoli was treated in December by a doctor in Wayne, New Jersey, affiliated with a company called Regenexx, one of the boldest players in the growing industry. Based in Des Moines, Iowa, the company has dozens of affiliated clinics around the country, specializing in treating orthopedic problems with patients’ own platelets or stem cells from their bone marrow. And Regenexx has persuaded some large, self-insured employers to cover its treatments.

The doctor in Wayne injected stem cells and platelets into Cevoli’s knee, fitted him with a brace and sold him a vitamin supplement made by Regenexx to promote healing. The procedure cost $6,900, and was not covered by insurance.

Four months later, Cevoli said he thought the procedure was helping. He skied during the winter, and has begun running a few times a week.

Navigating the existing guidelines

Some stem cell businesses have carefully navigated FDA rules to stay just inside the lines. The agency regulates cell and tissue products, but treatments that use a patient’s own cells do not require the agency’s approval if the cells are “minimally manipulated,” meaning that they have not been cultured or multiplied in a lab, and no drugs or other substances have been added.

The agency also allows what is known as “homologous use,” deploying the cells in a way similar to their original function in the body.

Platelets taken from a patient’s blood and then reinjected are not regulated as a cell or tissue product, and procedures that use them are not considered high risk.

Bone marrow transplants for blood cancers like leukemia are an established treatment, and the FDA does not regulate them.

Among the most avid customers for stem cell and platelet treatments are people with arthritis or sports injuries, who find that mainstream medicine does not provide lasting relief. More than 30 million people in the United States suffer from osteoarthritis, including 14 million with bad knees. More than 700,000 knees are replaced in the United States each year, and more than half a million hips, according to the Arthritis Foundation.

But artificial joints can wear out, and younger patients may need repeat operations later in life. Hoping to avoid surgery or at least postpone it, many people are searching for other options.

Regenexx was started in 2005 by Dr. Christopher Centeno, a pain medicine specialist in Broomfield, Colorado, who had no background in stem cell research, but saw potential after reading about a study that hinted that stem cells could be used to treat spinal conditions in rabbits.

The company is trying to commercialize stem cells and move them into mainstream medicine, while also seeking to distance itself from outfits that have injured patients and drawn fire from regulators.

Regenexx points to a registry it keeps of its results and says it has published nearly two dozen research papers. It also cites a 2016 study concluding that its procedures led to no more serious side effects than other injection-based therapies, and fewer side effects than more invasive procedures.

Regenexx claims 40,000 patients have been treated with its techniques. Of the 90,000 procedures the company says it has performed to date, 70,000 involved only platelets. Many patients pay thousands of dollars out of their own pockets. Although nearly all insurance companies have refused to cover the treatments, citing the lack of evidence that they work, some employers are covering the injections.

The company says 6 million people are now covered, and Regenexx hopes to increase that number to 20 million over the next year, Centeno said.

The company contends that employers can save hundreds of thousands of dollars by helping workers avoid more invasive, time-consuming and expensive remedies like joint replacements or other orthopedic surgery.

Regenexx is training doctors around the country to perform its procedures, and building a nationwide network of treatment centers that carry its brand.

“We have an extreme vetting,” said Jason Hellickson, the company’s chief executive.

In addition to the 53 clinics that have joined in the United States, there are seven more in other countries, some performing procedures that involve culturing patients’ cells in a lab, which cannot be done in the United States without FDA approval.

Injecting the bone marrow or platelet extracts into the knee takes skill, even with X-rays to guide the needle. The injections can cause pain and irritation, and patients are usually sent home with leg braces that they will wear for a few weeks.

Sterile techniques are essential.

“Whenever injections are administered to the joint, there is always a risk of introducing infection,” said Dr. Kiran M. Perkins, who has investigated such illnesses at the Centers for Disease Control and Prevention. With stem cell treatments, she added, “there are a lot of steps along the way where something could go wrong and you could have the introduction of microorganisms.”

Needed: Real data

Scientists say that research on stem cells does hold tremendous promise for treating many diseases. But those goals are years away.

“There’s not a whole lot you can say definitely about whether these therapies are efficacious,” said Scott Noggle, senior vice president of research at the New York Stem Cell Foundation, a nonprofit scientific group. “Until you do well-controlled clinical trials showing it works in humans, the question is still up in the air.”

Bone marrow contains many different types of cells, and unless the extracts used to treat patients are analyzed, it is not clear which cells they are receiving, Noggle said.

But the stem cell clinics aren’t using existing techniques to identify and isolate the cells, he said. “If you don’t do that, you don’t know what’s in there and you don’t know what you’re putting into people,” Noggle said. “They don’t really know from patient to patient to patient what they’re putting in.”

The popularity of these treatments has prompted some academic centers to offer similar procedures, but those are accompanied by efforts to collect data to determine whether they work.

Dr. Scott A. Rodeo, a surgeon and researcher at the Hospital for Special Surgery in New York, said the treatments were being studied there. So far, he said, “modest data” suggested that platelets might ease pain in arthritic or inflamed knees and elbows.

“There’s great potential,” he said. “We are just not there yet. The marketing and use far outpace the science.”

Centeno argues that the vast majority of orthopedic procedures performed today by mainstream physicians do not have any evidence that they work. Indeed, studies in recent years have challenged the value of many knee surgeries performed for torn cartilage.

By persuading employers to offer Regenexx, the Des Moines clinic became a billboard for Regenexx’s potential. Its procedure volume has soared to 1,234 in 2017 from 140 in 2014, according to the company.

Hellickson, who had invested in the clinic, eventually merged it with the company in 2017. He replaced Centeno as chief executive and raised $10 million from investors and expects to rapidly expand the company.

While Centeno emphasizes that the procedures taking place in the United States do not need FDA approval, doctors and company executives tend to muddy the issue by claiming that competitors may need approval and could be operating illegally because they do not have it.

As for clinical trials, Regenexx says it is conducting them now. But only one small controlled study has been published, in December. Patients with arthritic knees got either exercise therapy, or stem cell treatment. After three months, the patients given stem cells were doing better. But all the patients in the exercise group later got stem cells, too, so the results are hard to interpret.

Most of the other studies Regenexx has listed on clinicaltrials.gov have either been abandoned or will not be completed until 2021 or later.

As a result, patients rely on testimonials and other informal evidence. But experts caution that word-of-mouth experiences are not a substitute for rigorous studies.

“The power of anecdotes is just amazing when it just catches on,” said Donna Messner, president of the Center for Medical Technology Policy, a nonprofit research group. “This is how snake oil has been sold for generations.”

New York Times

Recommended for you

(0) comments

Welcome to the discussion.

Keep it Clean. Please avoid obscene, vulgar, lewd, racist or sexually-oriented language.
PLEASE TURN OFF YOUR CAPS LOCK.
Don't Threaten. Threats of harming another person will not be tolerated.
Be Truthful. Don't knowingly lie about anyone or anything.
Be Nice. No racism, sexism or any sort of -ism that is degrading to another person.
Be Proactive. Use the 'Report' link on each comment to let us know of abusive posts.
Share with Us. We'd love to hear eyewitness accounts, the history behind an article.