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FDA Challenges Stem Cell Companies As Patients Run Out Of Time

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FDA Challenges Stem Cell Companies As Patients Run Out Of Time

Medical Treatments

FDA Challenges Stem Cell Companies As Patients Run Out Of Time

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LAURA SULLIVAN, HOST:

It's WEEKENDS on ALL THINGS CONSIDERED from NPR News. I'm Laura Sullivan.

GOV. RICK PERRY: Adult stem cells and regenerative medicine hold the promise of miracles.

SULLIVAN: That's no preacher selling snake oil. That's Texas Gov. Rick Perry, touting the benefits of a controversial therapy called adult stem cell replacement. In 2011, Perry underwent back surgery, and he says the treatment aided his recovery. He's been a convert ever since, and he's not the only one. Many Americans are hoping this process can heal them of a host of diseases. And it's estimated the industry could be a $16 billion business by 2020.

But the FDA has expressed concerns. They've shut down one company in Colorado already, and they've closed the lab of another company in Texas. And that's our cover story today. Eighteen years ago, SammyJo Wilkinson was a young, ambitious computer programmer launching an Internet startup when suddenly, she collapsed. Her doctor told her it was secondary progressive multiple sclerosis.

SAMMYJO WILKINSON: And it was just devastating. It's a very scary diagnosis 'cause you know that the long-term outlook is that you might end up, you know, in a wheelchair.

SULLIVAN: Now, at 48, Wilkinson is in a wheelchair. She has tried every available, FDA-approved drug and two experimental therapies, including a two-year course of chemotherapy.

WILKINSON: You know, it left tracks on my arms - like a junkie - and decreased my heart function. I had to actually go off it a year early because of the heart damage.

SULLIVAN: Here's what you need to know about SammyJo Wilkinson: She's read every word of published literature on MS. She even talks in the language of medical researchers. She wanted to try stem cells, but she didn't want to go abroad. So she waited; she and her husband, Doug, biding their time, saving their money.

And then two years ago, a U.S. company opened its doors, a Houston company called Celltex. She called them up. They told her she would need a doctor's approval. And then they gave her a recommendation of who she should see.

WILKINSON: I flew to Houston. I wouldn't know where to go find a doctor from out of town.

SULLIVAN: So who was the doctor that prescribed the treatment for you?

WILKINSON: Dr. Jones.

SULLIVAN: As I'm sure you know, Dr. Stanley Jones is one of the founders of Celltex.

WILKINSON: Yes. And he's also a personal investor in this.

SULLIVAN: Did that raise any red flags for you?

WILKINSON: You know, the commercial side of this is just a fact of life. And thank God for it because, you know, if there's a financial incentive that is going to encourage doctors to bring a lifesaving therapy to this country and make it available, then I'm all for it.

SULLIVAN: Wilkinson paid $28,000 for her stem cell treatment. In a nutshell, the company promises to remove good, healthy stem cells; store them; make more; and put them back into her body. Wilkinson says she believes that she got better immediately. She says 11 of her 25 MS-related symptoms have either improved or disappeared completely. She was all set to go back and do it again, and then the FDA shut down the Celltex lab.

Susan Berfield is a writer for Bloomberg Businessweek. And she wrote an article for the magazine last month, investigating the FDA's case against Celltex.

SUSAN BERFIELD: What the FDA said is what Celltex does to the stem cells, it's more than minimally manipulated - which means when they put the stem cells in that medium, they're doing something to it; and that process needs to be regulated. What Celltex argues is that we're not doing anything more than mixing it with some stuff and putting it right back in the patients; and that that should just be considered a medical procedure, not a product, not a drug. But the FDA wasn't satisfied that what Celltex was promising patients is what the patients were getting.

SULLIVAN: Is there any way for them to know exactly what they're getting? I mean, is there a chance that without their knowledge, they could possibly be getting a bag of sugar?

BERFIELD: There is a chance, and the FDA's report on inspection of Celltex's lab raised those kinds of questions. Celltex has since opened up discussions with the FDA. But at the same time, they've said that they will begin to comply with FDA regulations, and that they will begin an early-stage clinical trial. So they've acknowledged the FDA's - you know, sovereignty, if you will, over them and what they are doing in Texas.

SULLIVAN: So what are they going to do in the meantime?

BERFIELD: This week, they sent an email to their patients, and let them know that Celltex was going to start working with doctors in Mexico. They will also open another lab in Houston, where the company is based. And though they weren't clear about it, it seems that they will use that lab to conduct the FDA trials and research. And at the same time, they'll be offering treatments in Mexico.

SULLIVAN: We reached out to Celltex to see if we could talk to co-founder Dr. Stanley Jones, or someone else at the company, about the work that they do. They put us in touch with their lawyer, Andrea Ferrenz. She represents Celltex before the FDA. Ferrenz says Celltex is not selling a cure to sick people. She says the company only provides treatment when independent doctors request the company's services for their patients.

ANDREA FERRENZ: We actually don't employ physicians that provide treatments. We're really a laboratory, a laboratory service provider. We're providing a therapeutic product.

SULLIVAN: So Dr. Jones never treated patients?

FERRENZ: You're talking about Stan Jones?

SULLIVAN: Yeah.

FERRENZ: He is an independent physician. He does not have a clinic here at Celltex. He is on our board of directors, but he does not operate out of Celltex. He has his own, spinal surgery practice.

SULLIVAN: Does Dr. Jones send his patients to Celltex?

FERRENZ: He has had patients that come to Celltex that he ordered products for, but we have other physicians as well, that order products through Celltex.

SULLIVAN: Ferrenz says this is not a conflict. Dr. Jones is only one of many doctors who want their patients to undergo adult stem cell replacement. And she says Dr. Jones is a patient himself. He has said that stem cell replacement cured him of arthritis. Ferrenz says the move to Mexico is about expanding their growing business.

FERRENZ: We're bringing this technology to Mexico. It would be through physicians in Mexico.

SULLIVAN: You know, a lot of people might hear that and think of, you know, a guy behind a door on a street in Mexico, you know, who says he's a doctor. And if you want to get the Celltex process, you just knock on his door, and he'll send you over to Celltex. I mean, there's something that sounds like there's less regulation, perhaps, in that process than there might have been in the United States.

FERRENZ: It's unfortunate that that might be the impression people have. We have met with very highly credible physicians - and will be working with very highly credible physicians and excellent hospitals - that are in Mexico. And COFEPRIS, Mexico's equivalent of the FDA, is as concerned with safety for the people in its country as the U.S. FDA.

SULLIVAN: Celltex's Andrea Ferrenz cites studies the company has done, and some independent research, that suggests the treatments are effective. But Dr. George Daley, one of the founders of the Harvard Stem Cell Institute, disagrees.

DR. GEORGE DALEY: There's a lot of promise, but we are still in the earliest experimental stages. Certainly, we don't have convincing, compelling evidence that these cells work in humans; certainly not for the vast array of diseases that seem to be being treated, at this time.

SULLIVAN: So what's your take on these companies that are selling this treatment as a way to cure disease?

DALEY: Oh, I'm deeply concerned - deeply, deeply concerned because I think they are getting way ahead of what we understand. We are not even yet completely comfortable that these cells can be delivered safely in many, many different circumstances. We know that cell preparations like the ones that are being infused, have resulted in things like clots that have led to patients dying.

When they're injected in spaces of the body where they don't typically exist - like the central nervous system - we know that they can cause all kinds of damage. We're starting to see reports in the medical literature of some of the complications. So I think that the patients who are otherwise desperate - you know, they're willing to bear any risk, pay any price - they have to realize that these are experimental and in fact, the treatments could make their disease, or their condition, worse.

SULLIVAN: What do you say to people who say, look - you know, I think that this is working for me; you know, it's my money. I don't think that this is hurting me. I just really think the FDA needs to get out of the way.

DALEY: You know, I wish that we could make medical advances by anecdote alone. We can't. The fact is that when people have a financial stake in the outcomes of clinical trials, it's very hard to see them objectively assessing the outcomes. When patients are driven and feel so inclined to pay tens of thousands of dollars for a treatment, they're bound to think that they're going to get some benefits, something we've appreciated in medicine for many, many years - a placebo effect.

SULLIVAN: Do you think that it's going to be a treatment that we're going to see used normally on lots of patients, in the future?

DALEY: Well, I'm hugely optimistic. I mean, I direct our stem cell transplantation program at the Children's Hospital. We use primarily hematopoietic, or blood, stem cells. We do it from bone marrow; we do it from cord blood; and we use it to treat leukemias and some solid cancers, like neuroblastoma, and a variety of genetic diseases, like immune deficiency and sickle-cell anemia. We know it works there. And it's really the only established, accepted standard of care using adult stem cells. Everything else is the realm of experimentation today. I believe, truly, if we look into the future - maybe 20, 30, 40 years - cells are going to be delivered as medicines, and they will be part of our everyday practice. But it takes decades.

SULLIVAN: For SammyJo Wilkinson, that may be a bit too long.

WILKINSON: I don't have time. I'm completely out of time.

SULLIVAN: Wilkinson says she knows the FDA has to do its job, and she knows Celltex is in the business to make money. But she just wants to live.

WILKINSON: We've decided, you know, through endless hours of discussion, that this is the best investment we can make to improve both our lives, you know, because it's no fun being a caretaker of a disabled wife. I mean, he has to do all the housework, all the cleaning, all the cooking, all the shopping. And I can't do anything. So it just, you know, creates an unfortunate, unbalanced lifestyle. And we're always just waiting, in hope.

SULLIVAN: And that's exactly what critics of these companies are worried about.

(SOUNDBITE OF MUSIC)

SULLIVAN: You're listening to ALL THINGS CONSIDERED, from NPR News.

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