I’m going to begin the story of Addy Joy Sooter and Clínica 0-19 at its end, because the end is so tragic. It came to public attention three weeks ago or so, when an image posted by her father to her Facebook page Hope for Addy Joy – Fighting DIPG went viral. It’s a heart-rending photo of Addy Joy’s 6-year-old brother Jackson saying goodbye and trying to comfort her as she lay on her deathbed in hospice. There were a number of stories about this image (original image here) and the story of Addy Joy and her family, from news outlets as varied as Arkansas Patch, Today, various FOX affiliates, CBS News, etc.
Addy herself died of DIPG a few hours after the photo was taken. Those of you who have read my many deconstructions of Stanislaw Burzynski‘s anecdotes and testimonials designed to show that he could cure deadly brain tumors with his “antineoplastons” might remember that DIPG stands for diffuse intrinsic pontine glioma and that DIPG is a particularly deadly brainstem cancer. Addy Joy’s story, unfortunately, began similarly to the way all too many Burzynski patient stories began and played out the same way as that of a typical Burzynski patient.
Addy Joy, however, was not a Burzynski patient.
What caught my attention in stories about this viral image were passages that mentioned an “experimental treatment” in Monterrey, Mexico that Addy had undergone. These mentions made me very, very curious, particularly given that the name of the clinic and hospital were almost never revealed in these stories, and the treatment was included in the narrative a very matter-of-fact manner, as though it were an actual legitimate experimental therapy. However, having had so much experience discussing “experimental treatments” in Mexico that were in reality cancer quackery, learning that Addy Joy Sooter had undergone treatment in Monterrey, combined with seeing no mention of what that treatment was, and topped off with reports that the parents had spent over $200,000 on the treatment all conspired to set my skeptical antennae a’twitchin’ mightily. So I did some digging. What I found was horrifying, and Addy Joy’s family was not by any means the only family victimized by doctors selling what, it turns out, is an unproven and potentially dangerous treatment.
Before I explain what I’m talking about, however, it will be necessary to go back to the beginning of this story.
Addy Joy Sooter versus DIPG
In October 2016, Addy Joy Scooter was a healthy, happy two-year-old living with her parents in Arkansas. That’s when, during a trip to the Silver Dollar theme park in Missouri, the parents noticed something very wrong:
The family’s ordeal began in October 2016, when the Sooters spent a day at the Silver Dollar City theme park in Missouri. There, Matt’s mother noticed that Adalynn — who the family calls “Addy” — was walking “funny.” Matt, who first shared his story with Love What Matters, says he noticed a “hitch” in Addy’s step as well.
“We were confused, but we thought it could be because of the growth spurt she had just gone through,” he tells PEOPLE. “As it got worse, we became more and more concerned.”
Throughout the weeks that followed, Matt and Chandra noticed that Addy was having even more trouble walking, often stumbling and falling. He says the little girl even had difficulty holding her eating utensils.
Worried, they took the then-2-year-old to the hospital where doctors found a tumor growing on the girl’s brain stem. She was diagnosed with diffuse intrinsic pontine glioma (DPIG). Doctors said the little girl would likely live for only a few more months.
Thus began an all-too-familiar (to me) story: A toddler facing almost certain death at far too young an age due to a deadly disease. Her family is devastated and desperate to save her life by any means necessary. Like most such parents in these stories, initially they utilized science-based medicine to treat their girl. Unfortunately, as is usually the case with DIPG, the treatments were only effective for a relatively short period of time after her therapy began at Arkansas Children’s Hospital in November 2016:
Over the next few weeks, Addy endured dozens of radiation treatments and, much to the family’s delight, the tumor shrank to nearly half its size.
“We were relieved and we hoped and prayed she would be one of the rare ones whose tumor would stabilize,” Matt says. “But we knew the odds were that it would come back.”
And it did. By July 2017, doctors noticed the tumor had begun to grow again. They told the devastated parents that there was nothing more they could do for the little girl.
If this were an article about Burzynski, regular readers would know what was coming next. It’s not, though. That doesn’t mean that what was coming next isn’t all too familiar:
For nearly a year, they’ve taken the little girl to Monterrey for treatment and Matt says a single trip can last up to 12 days. Travel and medical expenses have cost the family more than $200,000 — but Matt says he and Chandra would do anything for their now 4-year-old daughter.
The story thus far comes primarily from a PEOPLE Magazine story from a little over a month ago. The story is also laid out in considerably more detail on both the Sooters’ Facebook page and copious updates to her GoFundMe page. At that point, the “experimental therapy” in Monterrey had clearly failed, but the Sooters nonetheless thought it had done her daughter some good before it “ceased to work”:
Now — more than 18 months later — the Rogers, Arkansas, girl has shocked medical officials with her survival. But the girl’s parents, Matt and Chandra Sooter, say they know her days are numbered.
“The fact that she’s survived over 18 months now is purely incredible. Her doctors have grown to love her and have been amazed by how well she has done,” Matt tells PEOPLE. “While we’re doing everything we can to change the outcome we don’t expect to win this fight. We haven’t given up, but it seems we are losing the war.”
Here we see a common theme in alternative cancer cure testimonials, that of a patient far exceeding the life expectancy that doctors initially gave them and that patient’s good fortune being used as evidence that the treatment works. It’s impossible to know if it was because the doctors were too pessimistic (although any oncologist worth his salt always leavens a dire prognosis by pointing out that such estimates are medians and that half of patients will live longer, a few a lot longer) or whether the parents, as distraught parents are wont to do, latched on to the most pessimistic part of the prognosis. It doesn’t matter, really. The girl was suffering, and her parents still are. For purposes of this discussion, what does matter is that such estimates feed into the narrative used to sell unproven treatments that “treatment X kept this patient alive far longer than the doctors thought she would live.” Never mind that in this case (as in many cases) Addy Joy had received the full course of conventional therapy, with a very good response lasting seven months.
In a more detailed account of Addy Joy’s story published in Love What Matters, there’s not much more detail about this experimental treatment in Mexico:
In July of 2017 an MRI confirmed that her tumor was once again growing. During those months we searched the globe for a treatment. We spoke with doctors in New York, London, Mexico, and nearly everywhere in-between. The week before Addy’s MRI we received word that she had been accepted into an experimental program in Monterrey, Mexico. After the MRI I sent my wife, Addy, and our son to spend the weekend with family while I made preparations to travel to Mexico. The next week we were all on a plane toward a lot of unknowns. We prepared for a long trip because we didn’t know how long we would be there. Our first meeting with the doctors in Mexico and Addy’s first treatment all went well and we were able to return home after only a few days. Since then we’ve been traveling back and forth every three to six weeks to have treatment. These treatments have been expensive, totaling over $250,000 for treatments and airfare since July 2017. God has provided through many generous people who have continually partnered with us to care for our little girl.
Unfortunately, the outcome was inevitable:
On Monday, May 7th, Addy and my wife were once again in Monterrey for treatment. We were anxious about this trip because Addy had been presenting some symptoms and we were unsure of what was causing them. After her MRI, the doctors came out and informed us that she had developed hydrocephalus, a fluid build up in her brain, and that she would need a shunt placed immediately to drain the fluid. Treatment was postponed and my wife booked a flight straight to Little Rock. Addy’s shunt was placed and an MRI performed on her spine based on some things the doctors saw on another MRI of her brain. On Wednesday the 9th, we found out that Addy’s cancer had spread to the lower part of her brain and on down her spine as well. Her Mexico treatment that has kept her cancer stabilized is no longer working either because the protocol has changed, or because the tumor has mutated.
And so Addy’s story ended tragically, leaving a devastated family having spent a quarter of a million dollars for a treatment whose components we don’t even know. As is usually the case with unproven treatments like this, it’s not the doctors’ fault the treatment didn’t work. The tumor must have mutated.
Addy Joy’s not alone, either. There is a veritable pipeline from Australia to Monterrey for patients with DIPG to be treated in the same clinic where Addy Joy Sooter was treated, as you will see.
I observed at the beginning of this post how the lack of mention of the name of the clinic in Mexico where Addy Joy Sooter was treated in so many news stories was one of the things that first got my skeptical antennae twitching (well, that and the $200,000—and counting—bill for the treatments). It was difficult to learn, but, as it turns out, not impossible. Some persistent Googling and perusing of the Sooters’ Facebook page revealed the name of the clinic in a story in—where else—The Daily Mail:
A week before the bad news, Addy was accepted to receive experimental treatment at the 0-19 Clinic in Monterrey, Mexico, which is where they headed on Tuesday morning.
There, she will receive intra-arterial delivery method of chemotherapy, which will hopefully be able to get as close to the tumor as possible in order to kill it.
Her family found out about the clinic through DIPG groups they are a part of on Facebook, according to her father, Matt.
‘Some others in the group were already there receiving treatment, others were asking about it,’ Matt told Daily Mail Online. ‘I was given a couple of names to contact. Through them we started talking about getting her down here and sending MRI results and her medical info.’
When I read this, I shuddered. Intra-arterial chemotherapy? Into the brainstem? Well, it is an experimental therapy. I found some references to a trial at Johns Hopkins, for instance. It is, however, a phase I trial. It involves the use of intra-arterial Melphalan, two doses. Because it is a phase I trial, it is definitely not an efficacy trial; indeed, the ClinicalTrials.gov entry specifically states that it is a feasibility study to “perform a qualitative evaluation of whether or not we can safely deliver IA chemotherapy to patients with progressive DIPG.” Also, the status of the trial is listed on ClinicalTrials.gov as “Suspended (Study has been placed on hold for an interim review.)” In this context, “suspended” means that the trial was halted early but might start up again. Interestingly, the Johns Hopkins website says the trial is “currently closed for analysis.” To me, a suspension makes me wonder if there were toxicity problems, but there is no way of knowing why the trial was suspended without contacting the PI or when (if ever) the trial will be restarted. It’s also hard not to note that the study start date was in 2013. Five years is a long time to take to accrue to a phase I study, given how small phase I studies usually are, even if the investigators are allowing two years for assessment of progression-free survival. A search of PubMed reveals that the results of the trial haven’t been published yet; hopefully the study will be completed and published soon.
Let’s just put it this way. Whatever the status of the Johns Hopkins phase I trial, the thought of intra-arterial chemotherapy being done outside of an academic medical center, much less by dubious doctors in Mexico, makes my skin crawl. Remember, this is a technique that’s being done at Hopkins, but that the group there hasn’t published on yet. That makes it not only experimental, but nowhere near proven or even shown to be promising yet. That’s assuming that the doctors at the Mexican clinic are even doing the same or a similar protocol. Then they’re adding some sort of immunotherapy. It’s all unspecified, though. Nowhere is there published a protocol, results, or anything other than testimonials and anecdotes, as you will see.
So what do we know about this clinic? When I did a Google search for “DIPG Monterrey,” the first website that came up was Making DIPG History in Monterrey, along with the site’s Facebook and Instagram pages. These sites are all run by a naturopath named Kim Beauchamp, who has a relative with DIPG:
The cost of one year of treatment in Monterrey amounts to over $300,000—without accounting for unexpected complications and extended hospital stays. But when parents find something that can help save their child’s life, they’ll stop at nothing to provide it for them.
Kim Beauchamp is a naturopathic doctor and writer. In the fall of 2016, her cousin Jeni’s daughter Kira was diagnosed with DIPG. Since then, Kim’s become intimately involved in the DIPG community—researching, advocating for families, and spreading awareness of DIPG with the hope of stopping this devastating disease.
After spending a week with Jeni and Kira in Mexico and witnessing first hand the effects of DIPG on children, the incredible demands on their caretakers, and the profound changes that the treatment in Monterrey is making for the children receiving it, Kim reached out to photographer and pediatric cancer awareness Project 3.8 founder Robyn Ivy about going to Monterrey to chronicle these children’s journeys with DIPG together.
Although this website is not directly affiliated with Clínica 0-19, there’s no doubt that it provides excellent PR given that it is very likely the first site most parents with DIPG encounter when searching for alternatives to conventional treatment in Mexico and how positively it presents stories of children treated by Drs. Siller and Garcia. Amusingly, Ms. Beauchamp also includes what skeptics like to call a “quack Miranda warning” on every page of her website:
The information contained in this site is for educational and/or informational purposes only, and is not intended to diagnose, treat, or prevent any condition. If you have any concerns about your own health or that of a family member, you should always consult with a healthcare professional.
I definitely consider a quack Miranda warning fitting for a site run by a naturopath. It turns out that Clínica 0-19 does have a website. My Spanish isn’t so great, but, bolstered with Google Translate, it’s good enough to figure out what’s being offered. For instance, the website declares that “we are experts in the integrative and alternative management of cancer” and boasts about using the “most advanced techniques of traditional and alternative medicine.” I also must say that I wasn’t too impressed by this passage:
Requesting a Second Medical Opinion is a fundamental right that every patient and their family have in order to know more about their condition or type of cancer.
In the United States, medical errors are already the eighth cause of death and the great majority occurs due to the lack of a Second Medical Opinion. In other countries, it has been shown that in 15% of the cases a change or precision in the diagnosis is necessary and in up to 70% of the patients a modification in their treatment is required.
I suppose I should be relieved Clínica 0-19 didn’t repeat the trope that medical errors are the third most common cause of death in the US. Looking at the clinic’s list of doctors didn’t exactly give me confidence, either, given that there is an “orthomolecular therapist.” Orthomolecular medicine, as you might recall, is a quackery that basically uses megadoses of vitamins and nutrients to treat all manner of diseases. Linus Pauling’s high dose vitamin C treatments for cancer.
Basically, there wasn’t much in the way of information on either Beauchamp’s website or the Clínica 0-19 website. So my Googling went on. Searching for the name of the medical director, Dr. Alberto J. Siller, however, did lead me somewhere, but not anywhere good.
Drs. Alberto Siller and Alberto García and the Instituto de Oncología Intervencionista
So what is this “experimental treatment” at Clínica 0-19 that attracted Addy Joy Sooter’s family as the last resort to try to save their daughter? It all boils down to Drs. Alberto Siller and Alberto Garcia of Instituto de Oncología Intervencionista (IDOI), which also has a slick website declaring it to be ” leader of the intra-arterial brain tumors procedure and recognized for its Diffuse Intrinsic Pontine Glioma (DIPG) treatment.” There’s also an application to be treated asking for basic information (name, age, etc.), clinical history, plus videos of the child eating, walking, and speaking, along with MRI files. Demonstrating that crowdfunding is basically a part of this “institute’s” business model, there is also a question, “If the patient has a funding campaign, please share it with us so we can promote it with local nonprofit organizations who focus on raising funds for these causes.” Basically, what I gathered from various websites is that IDOI sees its patients in consult and followup at Clínica 0-19 but does the actual invasive radiology procedures at local hospitals in and around Monterrey, primarily at Hospital Angeles, admitting them there for treatment.
That’s all well and nice, but what is the treatment? Here, I was frustrated again to find just this:
The intra-arterial treatment exists since long and is performed continuously in diverse countries. What IDOI does differently is the preparation, mixing, dosage and sequential administration of the different medications that integrates the treatment’s model. It also uses the intrathecal route to administer certain medication.
The interventional oncology that IDOI performs consists in a puncture made in the femoral artery through which a micro catheter is inserted and directed by fluoroscopy to the blood supply site of the tumor.
The risks related with the procedure are minimal and imply the formation of a hematoma in the puncture site (less than 5%) and a possible vascular event such as a stroke (less than 0.7%). The other part of the procedure consists in making a lumbar puncture after the intra-arterial treatment with the application of medications.
The inherent risks of this procedure are pain in the puncture site, the formation of a hematoma and some irritation of the cauda equine(radiculitis) that occurs in less than 1% of the cases.
All medication used by IDOI are approved by Cofepris and FDA.
Imagine my relief that all the drugs are FDA-approved.
A particularly glaring omission here is…oh…you know…the risk of injecting chemotherapy right into the major arteries leading to the brainstem! The institute does, however, include a video from the University of Rochester about using intraarterial treatment for stroke, which is totally the same thing. The FAQ isn’t any more illuminating:
How successful are you in your treatments?
The treatment program of the Institute of Interventional Oncology for patients with DIPG began many years ago. We have treated adult and child patients with different types of brain tumors in addition to DIPG. The response rate to our management scheme is very high and treatment-related toxicity is very low. Many of these patients are free of disease years after their treatment has been discontinued and some have died from accidents or situations unrelated to the tumor and / or treatment.
Are there any publications in the peer-reviewed medical literature or statistics provided? Of course not! (More on that later.) Even worse, they will not even give examples of which drugs are used:
What agents are being administered?
Since the beginning of our program the treatment scheme has maintained a basic structure of medicines used to treat cancer. We are constantly evaluating new drugs and replacing each one with the purpose of improving our results. All the medications we use are FDA approved. What makes this program different is not only the route of administration but the dosage and sequence of administration of the products. With the arrival of a new category of products called molecular targeted therapy, our results have significantly improved.
This is utter nonsense. Dr. Siller could provide examples of the drugs (or a subset of the drugs) used if he wished to. He does not, and that is utterly irresponsible. Indeed, Dr. Siller is providing even less information about his treatment than cancer quack Frank Arguello provides about his “atavistic chemotherapy,” and he provided very little. At least Stanislaw Burzynski tells his patients what he is giving them. He might not inform them adequately how toxic it is, but he does tell them what they’re getting. In terms of transparency, these guys are worse than Burzynski!
But what about the “immunotherapy”? This is about all the clinic website says:
Can you explain the immunotherapy done in your program?
Our Immunotherapy program consists in the application of patient’s own immunological cells extracted previously and “activated” to recognize and destroy the tumor cells of the patient.
Who knows what this means? This could mean anything from just removing the patient’s white blood cells and treating them with various cytokines to “activate” them all the way to doing a poor man’s CAR-T therapy. Color me cynical, but somehow I doubt that level of expertise and equipment are available at a clinic like this or even the hospitals they work with, to do something as sophisticated as CAR-T, particularly since the FAQ also includes questions about high dose vitamin C treatment, hyperbaric oxygen chamber therapy, and hydrogen peroxide therapy, all quackery. The bottom line, I have to conclude, is that I have no idea what these guys are doing and calling “immunotherapy.” I also have little idea what they are doing except injecting chemotherapy into arteries leading to the brainstem given that they don’t state which drugs they are using or on what basis a chemotherapy regimen is chosen for each patient. Their treatment is, in essence, a black box, and they’re basically asking parents to trust that they know what they’re doing without anything resembling good evidence to support it.
Meanwhile, Drs. Siller makes excuses:
While Dr Siller admitted they are to an extent making things up as they go along, he said this was driving their success. He said the main problem with established medical protocol was that “you cannot move a millimetre outside what is written because you are out of the protocol. We are not using that. We are tailoring our treatment to every patient based on the circumstances.
“That’s a big, big issue. And nobody seems to understand that we are not in the protocol world. We understand that, but we rather prefer to take every single child according to their…circumstance.”
In other words, we make it up as we go along and can’t tell you how we do it in a sufficiently clear manner to make it possible to write a protocol to do it in a clinical trial. This, of course, also means that they can’t teach their technique for picking chemotherapy drugs to anyone else. How convenient. It’s the same damned excuse that homeopaths use to dismiss clinical trials of homeopathy that don’t include “personalization” of the treatment. I also can’t help but retort that there are now ways to test “personalized” treatments. Doctors are doing it all over the place.
The Australian connection
It didn’t take me long to discover that there is a direct pipeline between Clínica 0-19 and Australia, because multiple stories came up of children from Australia being treated at this clinic. Australian newspapers have published several Daily Mail-like credulous articles about Australian children with DIPG being taken to Monterrey by their parents for “last resort” experimental therapy. For example, in February, there was a headline in the Daily Telegraph “Little Annabelle Potts and her family have found hope with brain tumour treatment in Mexico.” Annabelle Potts is a now six year old Australian girl with, sadly, DIPG. Like so many other families of children with DIPG, Annabelle’s family is desperate to do anything to save her. It’s $30,000 a treatment, and the objections of Australian doctors are waved away:
But Annabelle’s battle is far from over. Her family know she isn’t cured, and even though Australian doctors don’t support the findings from Dr Siller and Dr Garcia in Monterrey, Annabelle’s parents believe they are their best shot at buying time until there is a cure.
So that means every six weeks, they cough up $30,000 from anywhere they can find it, sometimes through Facebook fundraising, and Adam takes time off work as a carpenter to fly Annabelle from their Canberra home to visit Clinica 0-19.
There’s another girl with DIPG being treated named Annabelle, Annabelle Nguyen. I learned some useful things from her GoFundMe page. First, it tells me one thing I needed to know about Annabelle Ngyen’s cancer, namely that it is less aggressive than the usual DIPG. After all, she survived well over a year and a half after her diagnosis without progression having received only conventional treatment. I also learned this:
They combined around 11 cocktail of drugs go in through the groin and then through the back with catheters, and inject a certain sequence of drugs to the brain stem and then they combine with Immunotherapy. We are looking at lifelong treatment till we get NED.
NED means “no evidence of disease.” It’s what we look for in tumor response, basically the equivalent of, “We can’t find any cancer anywhere with our imaging studies.” Eleven drugs, though? Eleven? That is an incredible, shocking number. What are these drugs? How is the sequence in which they are given determined? Again, we don’t know. Dr. Siller doesn’t say. Lifetime treatment? How do you know? You don’t. But lifetime treatment at $30,000 a pop is an excellent revenue stream.
We’ll return to Annabelle Potts and Annabelle Nguyen later. In the meantime, I point to similar stories about other children from Australia, such as Doris Sun, Riaa Kulkarni, and several others.
“We’re too busy saving patients to publish our results!!!”
Drs. Siller and Garcia have not gone without criticism, of course, although it’s hard to find much specific criticism among the glowing testimonials because so little is known about just what these doctors are doing. There was, however, a story in the Daily Telegraph in January describing some of the issues the international oncology community has with Clínica 0-19. The article starts with a discussion of Doris Sun and her cancer treatment, noting:
There is only one small but relevant condition keeping Doris from receiving the treatment back home: there are no peer-reviewed studies proving it works, only anecdotes of its effectiveness.
The controversial intra-arterial chemotherapy and immunotherapy treatment is the brainchild of Monterrey-based doctors Alberto Siller and Alberto García, who developed their technique two decades ago and offer it through their clinic, Instituto de Oncología Intervencionista. They have refused to cooperate with the international medical community and have never published their results.
Refuse to cooperate with the international medical community? That strongly suggests to me that these guys are quacks right there. In any case, next comes a quote from an Australian oncologist:
But leading Sydney paediatric oncologist Professor David Ziegler is highly critical of the Mexican doctors.
“They have been doing this for 20 years, so if it works, why don’t they publish their findings? I don’t know why they don’t, but you’d be concerned that it is not working and that’s why they don’t want to release the information,” Prof Ziegler said.
Neurologist Dr Brian Owler, from Cure Brain Cancer, said the regulatory system in Australia required “proof of principle” that a trial may work based on peer-reviewed studies, which the Mexican doctors have not published. Until that exists, no Australian trial can take place.
Exactly. Siller and Garcia have been at this two decades. They should be able to publish at least a case series, but they don’t. They should be able to publish their statistics for overall survival and recurrence-free survival, so that they can be at least compared with historical controls. It’s not ideal, but significantly higher survival statistics might indicate that they are on to something, although I can’t help but note that even in that case the figures would still have to be interpreted with caution. This is, after all, a highly selected population of children with families able to raise $300,000 in a short period of time and who are also able to endure multiple long trips to Mexico to receive therapy. They’re likely in better physical shape than the average DIPG patient. It doesn’t matter though. Siller and Garcia haven’t published their survival and recurrence statistics. Why?
The doctors have received criticism from Australian experts because they have not published any data on their techniques or their success rate, but the doctors say they are too busy treating 70 plus patients from around the world.
It was at this point that I wanted to throw something at my computer screen. Fortunately, I restrained myself. “I’m too busy saving lives to publish my results or do clinical trials to test my treatment” is the oldest and lamest quack excuse there is. It’s also hard not to wonder whether the reason they don’t cooperate with Australian oncologists is that, if their treatment actually did work and were available outside of Mexico, their lucrative revenue stream would dry up in short order.
The only thing Drs. Siller and Garcia seem to cooperate for is publicity, which unfortunately they got, thanks to a highly credulous Daily Telegraph article with a nauseating teaser, “Miracle Cancer Clinic Saving Aussie Kids.” I don’t have access to it because it’s behind a paywall. Fortunately, I got a hold of it through PressReader. The title, “Where Hope Lives,” is entirely credulous. There was also another story for the Sunday Times entitled “Inside the Miracle Factory in Suburban Mexico Keeping Our Kids Alive.” Both are largely the same article with some minor differences.
Inadvertently, though, the article reveals a very Burzynski-like practice:
Professor David Ziegler, paediatric oncologist at the Kids Cancer Centre, Sydney Children’s Hospital, Randwick, has been highly critical of the doctors because they have never released their research and findings to be peer reviewed. “I have not seen any results that show this treatment is effective,” Prof. Ziegler said.
“On occasion the team in Mexico has released limited scans which do not accurately depict the tumour” and are not able to be used to tell if the treatment is doing anything at all.
This is exactly the sort of thing Burzynski does. Dr. Siller also appears to share another trait in common with Burzynski, arrogance:
“I told an Italian doctor… ‘if you have something to give to your patient better than what we are using, feel free’,” Dr. Siller said.
Elsewhere in the story, Dr. Siller is quoted as saying that he and Dr. Garcia aren’t making much money from their treatment. Never mind that the story also reports that their DIPG treatment makes up the bulk of their business now, that they now employ ten physicians, and have struck deals with local hospitals, such as Hospital Angeles, to treat their patients there. They also claim that they’d love to publish their results, but, sorry, they’re too darned busy working 18 hour days to save lives.
They do, however, add:
“We are starting to do some basic numbers,” Dr. Siller said. “Our thoughts are to start publishing the results in the coming months.”
Wait a minute. You’ve been doing this for twenty years, and you’re only now “starting to do some basic numbers”? That’s the excuse of quacks.
As a result of the Telegraph story, though, in early March the Cure Brain Cancer Foundation responded to the call for Australian authorities to investigate Dr. Siller and Garcia’s claims of anecdotal success treating DIPG:
“We’re willing to sponsor a DIPG expert to visit the lab and verify Clinica 0-19’s claim,” Michelle Stewart, CEO of CBCF said.
“Last week’s report (in The Sunday Telegraph) said the doctors were too busy to report their findings, and if we can provide assistance for them to get this information out, we are more than happy to.
“We want to send a DIPG expert who can report back on the drugs used so if any learning can be found, we can use that to treat patients locally. “
The CBCF has sent a letter requesting permission for the expert to attend and research the procedure and drugs used.
“We want to make the information available so that if researchers wanted to do a trial here, we could provide funding,” Ms Stewart said.
And what was Clínica 0-19’s the answer? Let’s just say that it was…not unexpected:
Violeta Montes de Oca, a public relations consulted hired by the clinic, said they needed time to “be able to develop a program that allows receiving invited doctors”.
“Today, the clinic’s only priority is to devote all its attention and energy to trying to restore health and improve the quality of life of patients under treatment,” she said.
“As you will understand, it is very difficult at this time to offer a date to receive them.”
That sure sounds as though the clinic was continuing to make excuses and trying its best to delay. It’s been nearly four months, and, to the best of my ability to search, I have found no evidence that Clínica 0-19 has not allowed an outside expert to visit and help Drs. Siller and Garcia to do the required analyses for publication. In the meantime, there have been developments.
NED? Not so fast…
Drs. Siller and Garcia also claim they have four patients with NED, including Annabelle Potts and Annabelle Nguyen, who were discussed above. Let’s look at updates for Annabelle Potts first. On her GoFundMe page we find an update from last month:
Last week, Annabelle just had her 10th IA treatment. The results from the MRI is not the news is not what we have hoped for. The original tumour is still essentially ‘dead’, but it looks as if there is some small new growth into the cerebellum. While this is absolutely not what we hoped for, we are so grateful that the doctors in Mexico picked this up before treatment and treated the area immediately!
Sadly, this is not NED. It’s also not unexpected. I also can’t help but wonder if some of the progression observed in some of these patients was the same phenomenon that so often fooled Burzynski: Pseudoprogression. Pseudoprogression is a common phenomenon in brain tumors where, after conventional treatment with radiation and/or chemotherapy, the tumor will appear to be progressing because inflammation around the dying tumor appears indistinguishable from tumor on MRI. Any treatment, even ineffective treatment, will appear to “work” if administered while the cancer is in pseudoprogression because eventually the inflammation settles down and the area that lights up as a mass on MRI shrinks. The problem, of course, is that one can’t say whether apparent progression is pseudoprogression or real progression except in retrospect. Also, these are real pediatric oncologists treating many of these children who should be (and almost certainly are) aware of the phenomenon. Of course, confounding factors like this are yet another reason why anecdotes don’t cut it for showing efficacy. Clinical trials are needed, with rigorous monitoring of tumor sizes by neuroradiologists who know what they’re doing, careful survival and recurrence measurements, and monitoring for adverse reactions.
Speaking of adverse reactions, I feel compelled and at the same time deeply sad to finish on a horrific cautionary note, and unfortunately that note is an update on Annabelle Nguyen in the form of a story over the weekend in The West Australian. Basically, Annabelle Nguyen has fallen into a coma, and her family is stuck in Monterrey:
But after initial success, when the tumour disappeared and the family packed up to move home, it returned and Annabelle fell into a coma, which she remains in to this day.
“She said she had a monster in her head and she wants to fight it, I believe she is fighting it,” Sandy said.
But while Annabelle silently fights, her prognosis is not improving. Her family is spending $2500 a day to keep her in a hospital in Monterrey and desperately wants to bring her back to Australia.
That flight, however, cannot be taken commercially and will cost the best part of $250,000.
“A lot of people tell me that we’re holding her back, that we should let her go but they are not in our shoes,” Sandy told 7 News.
As I said before, it is not surprising that the tumor returned. It’s not even clear to me from anything that I can find out online that Siller and Garcia’s treatments actually did Annabelle any good, although it’s very clear that they cost her parents a whole lot of money. Now Annabelle is trapped in an ICU in a foreign country thousands of miles from home, her parents racking up $2,500 a day in medical bills, unable to leave because a medical flight back to Australia would cost a quarter of a million dollars, this after having already spent $300,000. And the greatest tragedy of all? Their daughter will die soon regardless, and from an ethical standpoint, as painful and horrible as it is to contemplate, taking her off life support and instituting comfort measures only almost certainly represent the best course of action for Annabelle. Unfortunately, the Nguyen family are victims of arrogant and unscrupulous doctors, aided and abetted by social media that lead new victims to their clinic.
If Drs. Siller and Garcia truly have made a major advancement in the treatment of DIPG, they have a moral obligation to publish their existing results and to accept help from the international medical oncology community to test their treatment in proper clinical trials. Continuing to charge $30,000 a pop for an unproven treatment for 10+ treatments is immoral given that there is no evidence that their treatment is superior to existing therapies. The longer they fail to do that, the more I suspect that the reason they don’t do it is because they don’t want to endanger their revenue stream.
34 replies on “Clínica 0-19 and IDOI: Not making DIPG history in Monterrey (part 1 of 4)”
One of the things I find fascinating and frightening at the same time is that alternative practitioners often charge outrageous sums. They certainly can’t claim that they have to recuperate 100s of millions of dollars in research cost as the pharmaceutical companies, though exaggerated, do. I surmise that part of the hype, the selling point, for desperate people is the obscene costs. Somehow, psychologically, it must convince them it will work. Simply, the more expensive, the more likely it works. Not logical; but certainly understandable from the point of view of desperate people. However, of course, the alternative practitioners are just making out like bandits.
At the same time, the county hospital in my home town which serves as a training location for the nursing program at the Community college is going broke and having to cut staff because of low reimbursement for services provided.
I have also noticed that alt-med is expensive, whether it’s these guys, people like Dr. Bob (who generally does not accept insurance), or that RMB278 (in China) Chinese snake oil that was discussed on this site a few weeks ago.
For cancer patients, the issue is desperation. Parents do not want to admit that their young child is dying of cancer, and often they will ignore things that people not in similar situations would easily identify as red flags. The parents want some kind of hope, and these alternative practitioners offer a form of hope, however false it may be.
There is a point at which these practitioners become predatory. I think Burzynski has long since crossed that line, and I think these guys have as well.
There’s also a societal pressure. When news of a diagnosis like this gets out, families to get support but also a lot of questions about what the family is looking at in terms of treatment.
“Don’t give up” is a refrain these parents hear a lot.
We’ve got to get away from this idea that accepting a terminal illness is “giving up.”
The societal pressure is definitely a biggie. While I’ve no experience of DIPG, my husband died of GBM last year and I seemed to have to spend an awful lot of time explaining to well-meaning relatives why the hospice didn’t have him on a drip after he fell into his final coma (and wasn’t taking in any fluids, obviously). Although I’m sure they meant well, there was a very strong undercurrent of ‘not doing enough’.
Incidentally, being a long-time reader here meant that I knew exactly how bleak the prognosis was when he was diagnosed. But it was still difficult to resist the idea that somebody somewhere has a treatment that will offer some hope. I can only imagine how much stronger that feeling would be if it were a child.
I surmise that part of the hype, the selling point, for desperate people is the obscene costs.
I dunno. Back in the days before crowd-funding, families could only manage to raise smaller amounts, and the scammers were quite happy with charging correspondingly less.
Sure, con men tend to adjust their fees to what their victims can scrape together.
I guess not saying what you’re doing is one way to avoid criticism.
Addy’s is such a heartbreaking story.
Besides milking desperate families for all they’re worth, several problems arise:
If there is a valid scientific treatment that may not cure someone; but prolong their life, opting for alternative medicines could actually shorten what time they have left;
Even if there is no current treatment, some alternative medicines may actually shorten whatever time they have left.
And the alternative medicines, though not working, deprives people of the time they could be spending with family, time to cherish, rather than reducing that time with false hopes and, of course, leaving near and dear in financial ruin.
One last thing is how total strangers will contribute to save one kid; but vote against improving medical care for lots of poor kids who could be saved. The power of images.
And then there is a 6 year old Dutch boy who has already died from DIPG, who in December 2016 raised money for the Red Cross, for children with pneunomia..
In his name there is also raised money for a CED (convection-enhanced delivery).
No money for quacks.
“We are looking at lifelong treatment”
“We’re going to keep squeezing the parents for $$$ right up until the child dies”.
CDC of chs/course publishes statistics about causes of death:
Ninth cause is various kidney problems.
My child has died from DIPG, the ideal of intrarterial delivery of medication to the tumor is ideal, the fact the treatment is 8ndividualized to the patient is ideal, the multimodal drug and immunotherapy approach is ideal. My son didn’t go through this treatment, but it is up to parents to choose what direction they decide to take. When you are given limited option and you want to save your child, you will seek what may work. In America, we are limited on the trials that can and cant be done on children. There are few drugs for childhood cancer and those that exist came from trials on adults. There is little government funding for pediatric research, and all the 27 child cancer research facilities are competing for the same grants from this pool. Drug companies do not want a cure, and politicians have a vested interest in prolonging agony. My sons cost for treatment far exceeded what it cost in Mexico, and he survived 8 months. Your article calls these doctors quacks, but what other options have you explored for these families? What other treatments exist for DIPG families? Hope sometimes is a greater thing then any science, and given what other options exist, hope is all these families have. Sloan Ketterling has started an intrarterial program and are using the same drugs as doctor Siller. The fact that this method bypasses the blood brain barrier is far beyond anything that exists in the states. To think outside the norm is what will change our medical approach to any and all cancers. Society does not agree with this. So when you want to condemn a treatment, also offer an alternative.
Sadly, that’s not how EBM/SBM works. Sometimes there is no alternative.
These quacks play on this and pretend that there is.
Mr. Kohler, a grieving father; just said: “Hope sometimes is a greater thing than any science …” yet you continue to insist that he kneel at the alter of your gods?
Mr. Kohler seems to be an educated & articulate man & I am willing to bet that he is well connected with & speaking on the behalf of; a community of families affected by DIPG.
This is what could accurately be referred to as a “Deal Breaker” regarding the credibility of E/SBM.
Christine, you are going to die. E/SBM says you cannot live forever, at least not with existing or foreseeable procedures and drugs. But do not give up hope! I will offer you a chance at eternal life. As proof, look at me. I have partaken of this new procedure and here I am, still alive! All you need to do is send me all your money. Once the check clears we can proceed. How about it?
“Sloan Ketterling has started an intrarterial program and are using the same drugs as doctor Siller.”
You have this information? Please name the drugs Siller is using.
William, I am sorry for your loss.
I hope that some day science will find better answers for children like yours.
It doesn’t bypass the blood brain barrier to inject into an artery. That is where the blood is. Intramural therapy would bypass the barrier.
Nope. There are many clinical trial options in the U.S., some supported by pharmaceutical companies:
Not really, they are using 124I-8H9.
What very little we know about 0-19, they are using conventional agents off-label.
It’s understandable that desperate people do desperate things, but participating in a legitimate trial appears to offer far more opportunity for promising technologies that might help a child and add to the body of knowledge for future children with DIPG at less cost (borne by the study sponsor, not the patient), compared with a quack using anecdotes, old approaches, and off-label approved drugs, require tens of thousands of dollars and fail to report of outcomes to make a difference for the future.
I’m sorry your son had to endure that experience. I’m sorry you had to.
But we have rules about experimental treatments for good reason: there have been too many instances of well meaning doctors using real people as experimental subjects with no controls for safety. These rules didn’t spring up over night: they were the development of decades of learning the hard way what doesn’t work.
I do, however, take issue with your claim that drug companies and doctors don’t want a cure. That is simply not true. Even in the most cynical light, drug companies want cures: they’d make millions on cures. Politicians have no reason to not want a cure; supporting the mechamism for cures would give them great political capital–again if you look at things in the most cynical of lights.
Note that I said cures, not a cure. Every cancer needs variation in approach because cancer treatment is so hard. The type of cancer, place of cancer, staging, genetics, all play a role in what treatments work, what treatments don’t, and why some cancers have no or next to no realistic chance of cure at all.
The people who run drug companies, and serve in elected office are just that. People. It’s not that they don’t care. It’s that they can’t always be all things to all people. If they run their business into the ground, then there are no cures for anyone. If they exhuast taxpayer resources, there are no cures for anyone.
I would agree that conservative politicians in this country have cut money for the NIH and other agencies who do most of the legwork on treatments, to the bone. State and local politicians have cut higher education as well. Sometimes their reasons are disingenuous, I’ll agree. Political advocacy towards funding these institutions would help.
Hope is a good thing, I’ll grant you. Hope . . . not false hope. That’s what quackery is. False hope. These people know they are not offering real hope. They know they are lying to patients. Even the well meaning ones know there is nothing behind what they do but belief. They can’t demonstrate how or why their “treatments” work, and when they invariably fail, they always find something other than their quackery to blame.
An oncologist would tell you, “We know the limitations of this drug. We know which side effects are common or rare. We know the odds of survival for 1, 3, and 5 years. We know based on the stage of the cancer which treatments are mostly likely to have a chance of helping you.” It’s not medicine’s fault they can’t always tell you what you want to hear. A quack will always come up with a reason to try something else, they will never tell you it’s time to look into hospice.
That is why they are so disliked here. They lie to you, the patient or the family, and those lies cause great harm.
You and your wife had my sincere condolences. Ever since I started learning a lot about DIPG in 2011, when I started paying close attention to another doctor who specialized I treating DIPG patients (Stanislaw Burzynski), I’ve come to hate this disease. However, I hate doctors who take advantage of these desperate, hurting families even more.
When I first encountered Clínica 0-19, I gave Drs. Siller and Garcia the benefit of the doubt, even as I raised an eyebrow at the $300,000 bills parents were facing. Then, the more I looked into Clínica 0-19, the more alarmed and horrified I became. The stories of children taken down there started to give me a huge sense of déjà vu. Basically, the stories were so similar to those of children I had written about who had been taken to be treated by Dr. Burzynski that it was eerie. It was even worse, though, because at least Burzynski made a pretense of doing clinical trials. Drs. Siller and Garcia answer criticism that they don’t have any evidence and have never published even the most basic data about their treatment (such as what it is and their survival statistics) by using a reprise that I’ve only ever seen used by quacks: We’re too busy saving lives to publish our results or do clinical trials. (How do they know they’re saving lives if they haven’t done clinical trials or even analyzed their survival statistics? That’s my retort.) Worse, in March the Australian charity Cure Brain Cancer Foundation offered to sponsor a DIPG effort to travel to Monterrey and help Drs. Siller and Garcia analyze their survival statistics and validate their treatment. Dr. Siller’s excuse? The same: We’re too busy to host someone. It’s four months later, and Dr. Siller hasn’t taken CBCF up on its offer.
I know parents like you want an answer and want it urgently. I can understand why you would think that I shouldn’t shoot down Dr. Siller and Garcia’s treatment without offering an alternative, but that’s a false dichotomy. I don’t have to offer an alternative to know that Dr. Siller and Garcia have no evidence to support their treatment. I don’t have to offer an alternative to know that what they’re doing doesn’t make biological sense, given the 10+ chemotherapy drugs they use and the very low doses of some of them. I don’t need to offer an alternative to know that only 200 ml of blood is not going to produce very many dendritic cells (as a reader on my other blog pointed out to me), which means that the “immunotherapy” being offered is, from a scientific an immunological standpoint, nonsense. It almost certainly can’t work. I explain all of this in detail in today’s post.
Sadly, I don’t have any alternatives, but I do know that this alternative almost certainly doesn’t work, is toxic, subjects children to repeated invasive procedures (angiography) and anesthesias, and costs hundreds of thousands of dollars. I know that this alternative is one to be avoided for the sake of children with DIPG. For that, I make no apologies. I’m very sorry that my analyses of this treatment, which I have come to view as quackery over the last couple of weeks, causes distress to parents of children with DIPG who read it, but I’m hoping that other parents who read it will at least consider this skeptical analysis before traveling to Monterrey. I plan on writing a third installment sometime this month that illustrates how this treatment doesn’t help children and harms some.
I am sorry for the oss of your son. But while what this clinic says they are doing might be ideal, it’s just words. There is no proof they are doing anything except taking people’s money. There’s not a person standing against this kind of quackery who doesn’t want to offer hope to these families, but we want to offer real hope, to all families, not false hope to families with money and despair to families without.
Sadly, the alternative is accepting that there is no viable treatment to save such a child. Nobody wants to do that, which is understandable; but paying off a scam artist and throwing away every dollar you have (or worse, going into debt) in pursuit of a false hope is not, repeat NOT, a better option. It just ensures that the quack will thrive and be able to exploit other suffering families in the future.
You want to talk about ‘prolonging suffering’? How about holding out false hope, which the quack knows will inevitably fail?
“Drug companies do not want a cure, and politicians have a vested interest in prolonging agony.”
This kind of argument assumes that no one working for or running a drug company, or any politician ever had a child with cancer, or that they are deliberately condemning their own kids and families in order to make money.
Is that what William and others who make such statements truly believe?
[…] Clínica 0-19: Not making DIPG history in Monterrey (part 1 of 3) July 3, 2018 […]
Shit, I’ve worked 18 hour days on cats lately, and even I could dash off a report.
And it looks like I found another victim, through a Go Fund Me page:
It’s in Dutch, but there is a translation in the replies, though it’s not complete, because the translation doesn’t mention a clinic in Monterey. In the Dutch piece there is a link to an article about another patient in the Daily Mail http://www.dailymail.co.uk/femail/article-4570944/Terminally-ill-British-miracle-recovery.html
[…] Clínica 0-19: Not making DIPG history in Monterrey (part 1 of 3) July 3, 2018 […]
I’m retracting my comment here after reading Part 3. I was wrong. I was wrong for what I thought were the right reasons: The child with nothing left to lose & the parents with everything to lose & doctors who I thought were helping with something innovative that gave them hope.
But now I don’t think that the doctors are trying to help anybody but themselves because a parent asked uncomfortable questions & the doctors responded with discomfort.
Now, THAT; I know. And I know that it means that something is not right.
[…] Mexico and quackery? When last I discussed a clinic and hospital in Monterrey, I was discussing Clínica 0-19, where Drs. Alberto Siller and Alberto Garcia have been subjecting children with the diffuse […]
[…] in the child’s home country and not paid for by the government or insurance companies. We saw it for Addy Joy Sooter. We saw it for Annabelle Nguyen, whose parents didn’t just pay hundreds of thousands of […]
[…] clinics, quack stem cell clinics, and, most recently, Clínica 0-19 in Monterrey, Mexico, which treats children with diffuse intrinsic pontine glioma (DIPG) with an unproven (and secret) combination of chemotherapy agents administered every few […]