Thursday, October 29, 2015

Auvi-Q and Allerject Recall

The Auvi-Q has returned in ownership to its original inventors and their company, kalĂ©o. An updated post will be published. 

Voluntary, Precautionary Recall of ALL 
Auvi-Q and Allerject Epinephrine Auto-Injectors
Due to Potential Inaccurate Dosage Delivery

Click here to watch a video from the Dr. Paul Chew, Global Chief Medical Officer, Sanofi

Click here for details on the reimbursement process.

Recall details can be found here (U.S.) and here (Canada.) I reached out to Sanofi US to get some clarification on a few issues and received the following information: (emphasis and [comments] added...)

  • The Sanofi US voluntary recall includes ALL Auvi-Q® (epinephrine injection, USP) devices currently in the market.  The Lot number information shared in our announcement includes every consecutive lot number beginning with #2299596 through 3037230
    • (I'm still awaiting on specific clarification on the set I have, which expires 10-2015 and has a lot number that does not fall in the noted range. Though it may only be "good" for another few days, it will have to be my backup until I can get replacement EAIs.)
  • This recall is specific to Auvi-Q in the U.S. and Allerject in Canada
  • People with Auvi-Q devices should immediately contact their healthcare professional for a prescription for an alternate epinephrine auto-injector [e.g. Adrenaclick, EpiPen, Generic Epinephrine]
  • They can then call 1-866-726-6340 for information about how to return their Auvi-Q devices (Due to high volume of calls being received on the Auvi‑Q customer service phone line, callers may periodically receive a message that the line is down. We appreciate your patience and please call back.) 
    • [A second line has been added, due to the high call volume: 1-877-319-8963)
  • Sanofi US will reimburse patients for the full out-of-pocket cost [of the newly purchased EAIs] when they receive a new epinephrine auto-injector [with proof of purchase - so save your receipts!]
  • Information and updates about the recall will be posted as they are available on

Tuesday, October 20, 2015

Kyle Dine Eczema Song Contest

I SING SO ECZEMA WON’T WIN!  New Video Contest Featuring YOUR CHILD!
Dedicated to all the courageous kids who battle eczema every day, The Eczema Song hopes to make the struggle of applying creams and wearing wet wraps a bit more fun. The song was created by Kyle Dine, food allergy singer/song writer and all around AMAZING guy, in collaboration with Jennifer Roberge, owner of The Eczema Company, in honor of National Eczema Awareness Month.

Enter to win the I SING SO ECZEMA WON’T WIN! video contest by sharing a video of your little one(s) singing the new empowering song, The Eczema Song. Have your child show us that eczema doesn’t define them and that they WON’T LET IT WIN!
The video with the most votes wins! So, make sure to share your entry with friends and family and ask them to vote every day.
+ First place prize $100 from The Eczema Company (natural eczema treatments) 
& $100 from Blue Bear Aware (one-stop food allergy shop)!
+ (Second place prize is an awesome gift pack from The Eczema Company worth $50+!
Hurry! Contest ends November 23, 2015 at 12:00AM.

How to enter
+ Post or upload your video to your YouTube, Instagram or Vine account and then provide the link in the entry form found here.
+ Give your video a title of 100 characters or fewer, and include a brief description about your battle with eczema and how you won’t let it win!
+ Be creative!
+ Make sure to share the contest and ask for votes! The video with the most votes wins first place. The video with the second most votes wins second place.
+ Contest closes midnight, Monday, November 23, 2015.
+ The winner will be notified on or before Monday, November 30.
+ Open to all eczema super heroes on planet Earth.
+ Submitted videos become property of The Eczema Company but will not be used for any other purpose without expressed consent.

Watch the The Eczema Song together with your child. And then read the lyrics to get ready to enter….
The Eczema Song
Eczema, makes me itch everywhere
Eczema, it can be so hard to bear
Eczema, I know when it begins
I’m strong and I won’t let it win!

Uh oh! I’m starting to feel an itch…
Get the eczema fighting cream and quick!

And rub it on my hands and my feet, and my elbow crease, on my chest, and behind my knees.
Ear and nose the itch it goes, even right between my toes.

Ahhhh so much better. My cream works like a dream
And if I put it on quick, it will do the trick, rub it all around, you can’t slow me down!


Uh oh! I’m starting to feel an itch…
Get the eczema fighting cream and quick!

And rub it on my front and back, I need some mitts don’t want to scratch my armpit.
Behind my ear, fingers and thumb, even some cream for my (funny horn sound).

Ahhhh so much better. My cream works like a dream
And if I put it on quick, it will do the trick, rub it all around, you can’t slow me down!


Uh oh! I’m starting to feel an itch…
Get the eczema fighting cream and quick!

And I rub it on my cheeks and chin, I work it in, especially on any hidden skin (shot of inside elbow or knee)
I rub it in up high, rub it in down low, that’s how I make the itching go!

Ahhhh so much better. My cream works like a dream
And if I put it on quick, it will do the trick, rub it all around, you can’t slow me down!

Eczema, makes me itch everywhere
Eczema, it can be so hard to bear
Eczema, I know when it begins
I’m strong and I won’t let it win!

Yes, I’m awesome and I won’t let Eczema win!

Sunday, August 23, 2015

Seeing Dr. Xiu-Min Li in New York - 18-Month Progress Report

Time has been flying by, as it's known to do, and I realized that I have not posted about our journey, seeing Dr. Xiu-Min Li, in private practice. We recently had our in-person, follow-up appointment in New York, which reminded me that I wanted to provide an update. Bear with me as I try to summarize these past 18 months!

In January 2014, my daughter began treatment with Dr. Xiu-Min Li. To bring anyone up to speed, who doesn't know of Dr. Li's work, here is an excerpt to provide an overview: (from my post, "Food Allergy Treatments 2015 - Research Starter Kit"...)

Description: “Dr. Xiu-Min Li studied both traditional Chinese medicine (TCM) and Western medicine in China before coming to the United States to do research at three of the world's premier medical schools—Stanford and Johns Hopkins followed by Mount Sinai as part of the Jaffe Food Allergy Institute, where she is a tenured professor of pediatrics. She has worked to adapt and refine classical TCM formulas to treat allergic diseases such as eczema, asthma, and food allergies that have resisted standard medications and avoidance strategies, and proven their effectiveness in rigorous laboratory studies that meet the highest standards and protocols. She has simultaneously maintained a small private practice.” --Excerpt from a Q&A with Henry Ehrlich, author of the book Food Allergies: Traditional Chinese Medicine, Western Science, and the Search for a Cure. (This book* is an excellent reference, explaining the origins and science behind Dr. Li’s work.) *affiliate link

 FAHF-2 (FAHF = Food Allergy Herbal Formula) and its latest refinement, B-FAHF-2 (Butanol-refined) are Investigational New Drugs (INDs) that are undergoing trials en route to FDA approval. FAHF-2 has been shown to completely block peanut anaphylaxis in murine (mouse) models and has a proven safety profile in humans. 

 Dr. Li also has an herbal asthma medication called ASHMI (Antiasthma Simplified Herbal Medicine Intervention.) “In contrast with prednisone, ASHMI had no adverse effect on adrenal function and had a beneficial effect on T(H)1 and T(H)2 balance.” 

 FAHF, ASHMI, and other medicines are making their way through the FDA approval process. In the meantime, Dr. Li’s limited private practice uses a collection of herbal supplements for the treatment of patients with a wide variety of atopic conditions. These come in the form of tablets, capsules, teas, bath additives and creams. Getting the active compounds into the system via multiple routes (digestive system, skin) offers a greater chance at optimal absorption and uptake into the cells. 

Dr. Li is a supporter of combined therapeutic approaches. Though the majority of her patients are seeing her, exclusively, she has many patients concurrently undergoing OIT, SLIT, etc. She is working with other researchers, such as Dr. Kari Nadeau, to study the synergistic effects of therapies.

In the beginning, we started out with just a single "Digestion Tea" capsule, that I emptied into a small dish with some applesauce, an herbal bath additive and after-bath cream. My daughter didn't have any obvious stomach issues, but given all that I had read about the importance of the "gut", I asked if we could include it in our protocol. Dr. Li agreed that it would be beneficial. My daughter started treatment when she was 5, and she wasn't able to swallow the pills, so for items that were in pill form, I used a pill crusher and added them to applesauce, as well. In the picture below, you can see a sampling of pill/capsule sizes (this is not an all-inclusive set.)

Digestion Tea in applesauce
We definitely went through an adjustment period. I'd say it took a good 6 months for us to get to a speedy routine for pill taking. I believe this was mainly due to the fact that she could not swallow the pills. In the early months, we sat with her pleading, and sometimes even bribing her to take her herbs. There were some days when it took her an hour and a half to get them all down, due to stalling tactics! I made up so many random "games" to get her through the herb-taking process. She was only 5 at the time, and I am amazed at her ability to get it all done, despite the stalling. We're about 18 months into treatment and she has only missed a handful of doses.

Along the way, my daughter learned to swallow pills and that greatly improved the whole process, though she still takes capsuled items as teas, with apple juice. The bath and creams process takes about 30 minutes, since bath soaking time is 15-20 minutes, nightly. Luckily, my daughter has always worn long sleeves and long pant pajamas, so the creams haven't caused a problem with furniture or anything. There is certainly a lot to the protocol, but after a while, it becomes part of the daily routine.

We have monthly or bi-monthly phone consultations, where we go over progress and Dr. Li makes any needed changes to the protocol. In private practice, there is a lot of tweaking and customization. This is definitely personalized medicine! Calls are usually very brief (about 15 minutes) but with some planning, it all gets covered. I typically write up a list of what items we're currently taking, how much I have of each item, and a bullet-point list of things I want to remember to ask/tell her about.

The first 6 months of treatment involved slowly ramping up to the full set of items, at full-dose quantities based on her weight and age at the time. So, for our particular case (everything is case-by-case and we can't really make any generalizations) we did our first set of labs at the 1-year-mark by the calendar, but it was closer to 6 months on "full dosing". When we got those first labs back, I was so happy to see that all of her IgE values had dropped! There was only one that made a tiny increase, which I will explain under the "Ara h" peanut component chart. Total IgE (not charted) has basically remained the same, but I am not really concerned, given that Dr. Li is not concerned. IgE tends to trend upward as a child ages, so only a little movement is good.

17 calendar months, ~12 months on full protocol for age/weight
(click to enlarge)
I am definitely happy to see the continued drops in IgE. The foods, above, are not all that were tested, but they are the ones for which I have a baseline/pre-treatment value and a recent value for comparison. My daughter's IgE values were falling pre-treatment, but I feel that the drops during treatment are more "meaningful" in the sense that there are other changes going on at the cellular level that can help these positive changes turn into more complete healing, rather than just the drop in IgE that can come from strict avoidance, alone.

Below I have a chart of the peanut "Ara h" components. The thing about these results is that I only had them done once, before, in 2012, and then again, this past June of 2015. Therefore, I can't say this is completely within the "Dr. Li Treatment" time frame, but I was still amazed by the drops. Ara hs 1, 3, and 8 went from low values to "<0.10" and Ara h2 dropped 73%, down to 9.81.
2012-2015 Ara h Values - Can't completely attribute to treatment, but I'm guessing it was a decent part of it!
(click to enlarge)
(Charts made with the help of
The only anomaly in this whole thing was her Ara h 9 value. It was previously "<0.10" and is now 0.21. I was perplexed by this one, since it was the only value that went up and is the Lipid Transfer Protein (LTP) which can be linked to several foods. I really think this might have something to do with the fact that my daughter recently starting eating apples on a daily basis. The LTP section of the Phadia site reads, "Ara h 9 shares 60-70% amino sequence identity with LTPs from a number of commonly consumed foods, including peach, apple, pear, plum, cherry, hazelnut, lentils, sunflower, beans, chestnut and strawberry." My daughter can eat the fruits in bold without any OAS issues or any problems, so it doesn't seem to be an issue, so far. She just hasn't eaten the others for me to know how she'd do with them. I must say, though, that I was really amazed when she ate plum, for the first time, a couple of weeks ago, and it didn't bother her one bit. No itchy mouth, no rash, etc. It's not that she reacted to them in the past, or anything, but I get an itchy mouth, myself, and a weird change in my tongue texture when I eat certain fruits, so I see them as "irritating," and plums are "stone fruits" but thankfully, she didn't have an issue with them.

(Side note: Apparently, the grocery store has this growing wave of hybrid fruits that I never noticed, before - plumcots, apriums, etc. - which are apricot/plum hybrids, along with other combinations. I had bought those a couple of times by mistake, so in a way, she has had some exposure to apricots.)

I'd like to point out that before treatment, I would have been entirely too scared to try such fruits. I grew fearful of food, in general, feeling that they are all "guilty until proven innocent," but being in treatment with Dr. Li has boosted my confidence levels and is easing my food anxieties, little by little. As time on treatment goes on, I feel my daughter's immune system is stronger and not so reactive.

My daughter had never undergone skin testing, so a few months back, we decided to do some SPTs for some low-IgE foods, in anticipation of introducing them. I was really surprised when they all came up positive. The thing is, I have no point of reference for the tests. We also had them done in two separate visits, with two separate methods and I think a number of variables affected the results (like the amount of pressure placed on the poking device, using fresh items vs. extracts, etc.)

Dr. Li wasn't as surprised, though, as she says that the skin cells have a longer memory and are slower to catch up. The whole process reinforced my disdain for SPTs. I just don't find them reliable in the least. I tested foods that I know she has eaten in the past, without experiencing a major reaction, and they came up positive. I also feel a shift in my considerations of IgE testing, as treatment progresses. I feel that once this kind of immune-modulating treatment commences, the tests have to be viewed differently. I certainly enjoy seeing the IgE values come down, but I don't think it means as much that they remain at certain levels, or that they could go higher. The things we need to look at are not readily available, just yet. (Biomarkers, biomarkers, biomarkers!)

Here is a sampling of improvements I've noticed:

  • We've tapered off daily antihistamine use and drastically reduce the number of "as needed" doses. My daughter was taking daily a/h for about 3 years prior to tapering off. It was a very slow, gradual process.
  • We've discontinued the regular use of topical corticosteroids. In these 18 months, we only had to use one a single time, when she developed a rash from a waterpark "kiddie pool," in the earlier months of treatment. 
  • We've also tapered off topical hydrocortisone ointment. I hadn't realized how often I was relying on it!
  • My daughter is "eligible" to taper off her daily Qvar asthma medication. This is due in large part to the effectiveness of Qvar, whose effects we saw before starting with Dr. Li, but I wouldn't feel as confident in tapering off Qvar, without knowing that Dr. Li's treatment is working on strengthening her system for the transition. One of the things Dr. Li has said, repeatedly, is that it's not just about tapering off of medications, but being off of them and remaining asymptomatic
  • I've noticed a change in the nature of my daughter's illnesses. When she was younger, if she got sick, we'd hunker down for round-the-clock nebulizer use, and I felt like I was in battle-mode. A while back she got her first cold while on treatment and I was preparing for the onslaught and it was over in a day or so without needing any albuterol! She spent one night really looking sick and had a mild fever, and I put cold compresses on her forehead to ease the heat, and the next day she was already doing better. It was a bit magical. That's the only illness she has had these 18 months, though she sprouted a bit of a cough, last week, from some post-nasal drip that also went away after using Dr. Li's Cough and Cold Teas. 

So, I feel that things are moving right along and I look forward to the future! I feel so remiss in my reporting, so if anyone has any questions, please let me know!

Edited to add: I totally forgot to add that we also saw our first "negative" (<0.35) value and it was for walnut! I hadn't added it to the chart, because I only tested walnut, once, at 18 months, and again, during this most recent round, so I can't tie it directly to the treatment time frame, but it's still an exciting development. It is on the list for future challenges/additions, but further down ahead of some other foods.

Thursday, May 28, 2015

Food Allergy Treatments 2015 - Research Starter Kit
I created this document as a reference for my local support group, to share information on a selection of the food allergy treatment options that are currently in the works. I would also like to share it with anyone else who is interested.

Please note that this is not an all-encompassing document and there are many more treatments in the early stages of  research and development. There are so many seeds of hope!


Monday, April 6, 2015

AAAAI 2015 Pro-Con Session: Is OIT Ready for Prime Time?

The following is a summary of the Pro/Con Session on whether food OIT (Oral Immunotherapy) is ready for “prime time”. (Being ready for “prime time,” in this sense, means ready for widespread use.) This session was on the final day of the AAAAI 2015 Annual Meeting in Houston, TX, on February 24, 2015. (In case anyone might be interested, the “Virtual Annual Meeting” (VAM) can be purchased from AAAAI for $259, for non-members. This session was among those recorded for the VAM.)

Session Details:

Jonathan M. Spergel , MD PhD FAAAAI 

Pro Speaker:                                                       
James W. Baker , MD FAAAAI                        

Con Speaker:
Robert A. Wood , MD FAAAAI

Starting off, Dr. James W. Baker, speaking on the "Pro" side:

  • Protection from the dangers of an accidental bite of their allergen “represents a desirable state for parents of children with food allergies.” 
  • Dr. Baker described the "slow" and "rapid" challenges that he performs. If he does not expect a problem, he performs the rapid challenge and if "the danger seems more imminent" he does the slow challenge.
  • He described his 4 categories for patients - "Recent Positive", "Past Positive", "Unsure History", and "Negative History"
  • Dr. Baker stated, "[For] the patient that has a positive history/recent positive [recent reaction] [...] the majority of these patients who are well-adjusted to the avoidance management strategy, I stay there. We don't automatically go into the slow challenge/desensitization protocol, unless there is a maladaptive psychology approach to it. Many, many children now have their lives dramatically changed because of food allergy and this is really the driving force behind things."
  • Dr. Baker stated, "it turns out that the slow-graded challenge and the desensitization protocol are essentially the same"
  • He has learned over time that certain factors affect the threshold response - exercise, infection, menstruation, total allergic load, gastroenteritis, vaccination, and uncontrolled asthma.
  • In his practice, he chooses daily dosing, “because compliance data with inhalers, pills or topicals always showed that once daily is the most reliable compliant pattern.”
  • To his way of thinking, he is doing a “graded peanut challenge, interspersed by sub-threshold doses to achieve a 'bite-proof' state dependent on persistent exposure.” He stated that it’s fine if some want to call that desensitization, and the words sometime “mean different things to different people.”
  • Baker spoke about his “first 128 patients” on whom he collected and analyzed long-term data.
    • 18 of the them essentially had a negative challenge (meaning they passed their initial challenge, completely)
    • For some of the patients they experienced a positive (failed) challenge if he used his rapid challenge protocol and when he did a slow challenge, they had a negative result (they passed.)
  • “11% of patients who've actually outgrown [a peanut allergy] will get it back if they don’t add it to their diet."
    • Whether the allergy was outgrown or he has desensitized them, Dr. Baker wants them eating peanuts regularly and “biting the dog that bit them.”
  • Reviewing the studies, “they clearly documented that tolerance was not achieved.” [...] Dr. Baker quoted from a paper of Dr. Wood’s: “If only desensitization is achieved, patients who are being treated with peanut oral immunotherapy who have an accidental ingestion will most likely be protected from an allergic reaction.”
  • In most practices, patients span a spectrum from “false positive diagnosis to a patient who had actually outgrown their food allergy, all the way down to the true anaphylaxis.”
    • However, all patients are treated the same and he feels more options are needed. “We have too many patients with these disorders and their lives are being changed, often unnecessarily, because of it.”
  • (Showing a slide) Referring back to the “first 128 patients, “we’re successful about 75% of the time. For “about 80% of these patients, their first symptoms included hives or facial swelling, with about 30% having GI symptoms and about 25% had airway symptoms. It takes me roughly 6 visits and about 5.6 hours, with an hour at the end of each visit of waiting.”
  • His first chosen endpoint is about 165 mg of peanut, “that’s about 1/4th of a peanut.”
  • For those who discontinued, the GI symptom group is the large group, so “now when we get the GI symptom as the first symptom, we go much slower in that group and now we’re batting about 95% of patients making it to the maintenance dose.”
  • Dr. Baker instructed some to discontinue treatment...
    • Some parents decided on their own that the “benefit-bother ratio was not in their favor”.
    • Poor compliance
    • Vigorous athletes (concerns of “exercise-induced food-dependent anaphylaxis”)
  • Data from the “first 128 patients”
    • 89,000 doses, 183 patient years
    • “using various reaction rates, the one I chose was 12.5% per year [...] Dr. Wood, in his editorial, chose a lower rate, but we had no unmonitored reactions in our entire patient group, in other words no reactions that occurred out in the street...”
  • Dr. Baker summarized his arguments:
    • “I think there is a lower rate of un-monitored reactions [...] The reactions that did occur, occurred under supervision…”
    • “There was significant quality of life improvement for the child and for the parents. I could go on and on about that.”
    • Dr. Baker’s discussion of the reasons not to do it:
      • “Dan Atkins came up with [...] the ‘perfect storm’ - this is the patient who makes more than one mistake at a time [...] This is the patient that really scares me." (Dr. Baker mentions that he took a patient off the protocol for this…)
      • “The second thing is that management is part art, part science and I don’t think a group practice can do this.” He stated the requirements for one 24/7/365 nurse and one 24/7/365 doctor “to intimately deal with these patients with multiple phone calls every time there’s a question. This is a high-energy area that you have to take care of…”
      • It was discovered during the administration of a questionnaire that 5 of the 60 respondents were under the impression that they “had been cured and were eating peanuts sporadically. They all got a phone call from me telling them, ‘Look, you gotta keep taking your peanut - we don’t know whether you’re cured or not.’”
      • “Another lesson I learned the hard way is that the health care decisions for an adolescent change somewhere between 16 and 20.” He explained that parents make the decision to treat and then that gets passed to the child and they want to ensure that the child will be willing to keep up with things after they turn 18 and leave home.
      • As for the risk of EOE, he stated that it is rare. He has scoped 3 patients for it and none of them have had it.
    • Dr. Baker returned back to summarizing his arguments: We are “doing more than just desensitizing the patient - we’re reminding them every day that they have a peanut allergy, which is something that is not found in the avoidance-management strategy - every day, they are checking where the adrenaline kit is - this does not happen often in the avoidance-management strategy. We’re selecting our parents and our patients according to those we think would succeed. This doesn't happen with the other group.”
    • Dr. Baker further summarized: Desensitization equals empowerment for patients and is a daily reminder to avoid their allergen and it represents an unmet need. He believes the indications for Oral Food Challenges (OFCs) needs to be expanded and that the protocols for safe food OIT need to be standardized, along with the designing of new guidelines. He described OIT as a “disruptive” form of therapy, but feels that “unmet needs are fertile ground for disruptive innovation.”

Next up was Dr. Wood, speaking on the "Con" side...

  • We all agree - “Food allergy can have significant effects on nutrition and quality of life and that a safe and effective treatment for food allergies is highly desirable.”
  • First, “has the risk:benefit ratio of food OIT been appropriately established? Are the numbers [presented] really sufficient to move forward with this as a ‘prime time’ therapy?”
  • “Second, and maybe even most important, should the usual steps required for the development of a new treatment, for any disease, be followed for food OIT?”
  • Dr. Wood’s position is that the answer to the first point is “No” and a “Yes”/”Of course” to the second question.
  • “How can we even argue that we should be moving forward with a potentially dangerous treatment before we've done the usual studies that would be required to bring a new treatment to the prime time. [In fact], the only reason we can do it, is because the treatment is available in the grocery store. If this was a drug, it would be far from approval, far from use, and no one in this room would touch is in their practice, as it has not been adequately studied.”
  • Back to the risk:benefit ratio - what are the risks of the disease?
    • Reactions to accidental exposures
      • They certainly occur, but it is hard to determine exact frequency, and there is variability based on the allergen. There are differences by age and other variables, such as those Dr. Baker described that can affect the tolerance of the food being taken.
      • Fatalities - scary, but rare - "2 deaths per million persons in those with true food allergies"
      • Other risks of the disease related to nutrition and quality of life
  • “Now, what are the risks of treatment with OIT?”
    • Chronic, non-dose related symptoms
      • “We do see exacerbations of any co-existing/co-morbid allergic disease - atopic dermatitis being one of them, but the chronic gastrointestinal complaints, which are so common in treatment is a really big issue and it is a [barrier] to providing this treatment to at least 10-20% of patients.”
      • “EOE is diagnosed in 1-2%, but our bias would be that many of these kids who drop out of treatment because of these chronic GI symptoms would have EOE, if scoped. Our usual pattern, though, is to remove the treatment from their life and they feel better in 1-3 weeks and we don’t feel the need to scope, so we don’t [know] and won’t unless and until we have non-invasive measures, [...] the true incidence of EOE in this treatment.”
    • Frequency of acute reactions during OIT
      • Reaction rates vary based on how the patient is monitored and how reactions are defined, but there is some general consensus on the following:
        • “overall [as opposed to per-dose] reaction rates are extremely high - that they affect virtually all patients, but thankfully most reactions are mild.”
        • “moderate reactions, again the definition may vary, they occur in less than 5% of doses, but cumulatively, because you’re giving doses every day over a period of months and years, it turns out that they are very common on a per-patient basis.”
        • “Severe reactions, again, thankfully, for those reactions requiring epinephrine are also rare - less than 1% of all doses.
      • Citing examples from 3 different studies:
        • First study - Co-authored by Dr. Baker and first-authored by Richard Wasserman - analyzing Peanut OIT in various private practices:
          • High number of doses 240,000 doses for 352 patients - 27% of said patients had a reaction requiring epinephrine.
          • “Other adverse reactions were not reported and that’s because even though Dr. Baker claimed this was “monitored” reactions, these patients are not necessarily being monitored in a rigorous manner, like you would use in an FDA-approved, IRB-approved [Institutional Review Board] clinical trial.”
        • 2nd study -  Dr. Wood on Milk OIT
          • 10,000 doses and 20 subjects
          • Lower respiratory symptoms 1.5%
          • Multi-system reactions 0.5%
          • Epinephrine needed in about 20% of all patients
        • 3rd study - Comparison of Peanut SLIT and Peanut OIT
          • “SLIT had far fewer significant reactions.”
          • 4,000 doses
          • Doses with symptoms: 48%
          • Doses with moderate reactions 3.4%
      • Dr. Wood feels that looking at the reaction rates on a per-dose basis is not as important as looking at it from a per-patient perspective: “What is that individual patient at risk for undergoing this type of therapy? 100% had dosing symptoms, 64% had moderate reactions, and 37% had reactions that required epinephrine.” [...] “On a per-patient basis, significant reactions are very common…”
      • “reactions when you’re being treated are dramatically higher than they are when you practice strict avoidance. Ten times, probably twenty times more common than you would expect to see in your average patient, who is complying with their avoidance diet.”
    • The risk of chronic disease, including EOE, are “markedly increased with treatment compared to the practice of strict avoidance.”
  • “Long-term outcomes are really the crux of the matter, here.” Dr. Wood stated that he would gladly accept a fairly risky therapy, if there was a great long-term result, but without any proof of the long-term outcomes, it limits that discussion.
    • A couple of published papers on the subject show that there may or may not be a true quality of life (QOL) improvement post-treatment.
    • Dr. Wood did a long-term follow-up on QOL study and the results were not positive, in terms of QOL - “in fact, we've had many patients electively go back to strict avoidance, because having to keep peanut in their diet was so much more difficult than strict avoidance and carrying epinephrine.”
    • The risks do not disappear post-treatment Dr. Wood contends that these risks may actually increase.
  • A long-term Milk OIT study was done - 32 patients from their original two Milk OIT studies were followed for 3-5 years. Even though most of the subjects completed with study and were able to incorporate milk into their diets, the long-term results “were very disappointing.” 
    • At the end of the 3-5 year period:
      • 19% were on an unrestricted diet
      • 16% had returned to strict avoidance
      • 25% had no symptoms
      • large group with “occasional or even frequent symptoms"
      • 31% had systemic reactions
      • 9% required epinephrine
    • “One of the scary things that came out [of the milk study] is that one subject that had used up to 30 shots of epinephrine in the follow-up period - had milk reactions while she was off at boarding school.”
    • Conclusions from long-term milk study:
      • Only 25% consuming milk, regularly and without symptoms
      • Many patients were far more reactive in the follow-up period than in the study period
      • Long-term success appears contingent on on-going exposure, which "turns out to be far more difficult to do for a large number of patients.”
      • “We appreciated that it would be hard for peanut, both because of aversion and maybe not feeling well or fear, but with milk we thought it would be quite easy, but it was not easy, at all. And the key question there - is it really more aversion, is it really more fear, or is it that they’re just not feeling well? And when you have a stomach ache every day, you’re inclined in a lot of instances to ratchet down your rate of exposure to that food and as you ratchet down exposure, you will run the risk of becoming more reactive..."
      • "my greatest concern [...] is that some patients may be at highest risk after being treated and even though Jim is going to argue that getting their daily dose makes them cognizant of their allergy and more likely to keep their epi with them, I’d say that the complete opposite is true. I’d say they’d walk around with a false sense of security [...] I am far more worried about deaths occurring in the post-treatment phase than I am in the during-treatment phase, when things are being monitored more carefully.”
  • "If we're going to move this treatment forward, what are the outcomes that would really justify the use of OIT in clinical practice?"
    • Increase in challenge threshold? - Dr. Wood stated that this can be done, except for the 10-20% of patients who cannot tolerate treatment, but "we recognize that in most people that will only be sustained with on-going exposure."
    • A sustained increase in challenge threshold, which would persist without exposure? "That would be a slam dunk. We would accept, I think, the risks of treatment if we really had something that was more approaching a cure and one of the things that Jim & I agree upon is that we're nowhere near that."
    • Improved quality of life? Dr. Wood stated that this was really important and could not be discounted, "but without adequate safety it is not going to be a final indication for approval of OIT, certainly, by the FDA."
    • Reduced risk of reactions during treatment compared to strict avoidance? Dr. Wood stated that this will not happen, and "you're going to have more reactions when you're being treated, but if you could have a long-term outcome that really lead to sustained tolerance, that would be, again, potentially a very acceptable risk:benefit ratio."
    • Reduced risk of reactions after treatment - Dr. Wood stated that this is our goal, but we are not quite there, yet.
  • "[What] are the studies that are actually needed, exactly, to bring OIT to clinical practice?" Dr. Wood referred to the traditional drug approval process, "by usual FDA mechanisms." Dr. Wood reiterated that this treatment has only been able to move forward, due to the ease of acquiring the food products for dosing, "but does that really mean we should be completely bypassing the drug approval process, especially with a very dangerous drug?"
    • Dr. Wood stated that at this point, we would be going through clinical phases I, II, and III and we are currently at the equivalent of perhaps late Phase II, "but there are no Phase III trials for food allergy and one of the problems in moving this forward, is that every trial that will be done is going to take 2, or 3, or 5 years..."
  • "My summary is that OIT holds great promise for the treatment of food allergy. There are other treatment modalities that are not part of this debate, today, that we think also hold promise, that OIT does carry significant risks, that the risks of food allergies - the disease - is very real, but potentially far less than the risk of treatment. As far as risk goes, I believe without a doubt this will be the most dangerous treatment you ever prescribe to a patient. There is nothing you prescribe that's in this, even remotely in this realm of risk. And how then can you argue that the usual trials of drug development should be bypassed for any treatment, much less this one, that carries such significant and potentially lethal risks. So, I really am completely in favor of on-going OIT studies, I am completely in favor of the development of other treatment modalities, but to run this treatment, at this phase of research, out to the public is completely wrong."

Moderator: The moderator stated that there would be two 5-minute rebuttals, first by Dr. Baker and then by Dr. Wood, followed by a brief panel session, with questions from the audience.

Dr. Baker Rebuttal
  • "I think that what I'm worried about is waiting for an expensive solution. I think that would take it out of the realm for a lot of people. I'm worried about that. I worry that quality of life issues are dramatic and I still think that warrants taking some risks in this regard."
  • "There are only 3 conditions that I can think of where immunotherapy has been used in a life-threatening disease - bee sting allergy, aspirin allergy, and food allergy. Now, I don't think we've cured anybody, or cured 100% of people in any one of those categories. [...] We've reduced the risk in those categories, but I don't think we are absolutely successful. And the null hypothesis for a preventative study is much more difficult than for a remedial study." 
    • Dr. Baker explained that the "null hypothesis has to include the words such as 'had you not been on this you would have had more trouble?' and I think that would be an extremely difficult thing, to ever produce a drug that's going to achieve that type of efficacy."
  • Dr. Baker contends that post-treatment, patients "pass their challenge every day" and he admits that there are tremendous compliance problems, and "exercise-induced food-dependent anaphylaxis is a huge problem and with my high school athletes we separate this treatment by at least 5 hours from any vigorous exercise."
  • Dr. Baker said that he most wanted to argue for a change in the indication for food challenges, more of which he thinks need to be done. He observed that none of his patients with a history of atopic dermatitis had flares as a result of treatment.
  • Dr. Baker stated, "I agree that milk is the one to stay away from - it's the most difficult one to desensitize." He believes egg is the easiest, peanut is in between, but "milk patients surprise you and so I discourage it in that group."
Dr. Wood Rebuttal
  • Dr. Wood agreed with Dr. Baker and said if the topic of the debate was "Should We Do More Food Challenges" then the answer would be a definite yes, and there would be nothing to debate.
  • However, Dr. Wood continued, "[T]he diagnostic food challenge is an incredibly important tool, but I really think you're being misleading by equating a graded OIT escalation to a food challenge. I don't think they're the same and we need to be very careful about how that message goes out." [See bullet points #5 and #8 in Dr. Baker's opening remarks]
  • Dr. Wood stated that, "expense is not a reason not to do the appropriate studies." He mentioned that most of them know of drugs that they would love to have in their clinics, but "we need to wait for the studies to be done to show what its proper indications are, it's risk:benefit ratio is..."
  • Dr. Wood closed his rebuttal stating that he is concerned that the information has not been obtained on the long-term risk:benefit ratio and that "just showing that you get some bump in challenge threshold is many steps away from that kind of study, not just showing a short-term risk:benefit ratio, but a long-term risk:benefit ratio."
Audience Q&A [Just FYI, none of these questions were asked by me.]

Audience Member (A/M) #1: The A/M stated that Dr. Wood might have done too good a job at convincing them that OIT is not only not ready for prime time, and that perhaps it might even be a bad approach, all together.

Dr. Wood: Dr. Wood stated that it would depend on the long-term outcome. He stated that he would love if in 5-10 years, we could have a variety of options and "OIT should be on the table, but there may be other options that won't provide the dramatic increase in threshold, but may provide the same level of safety that our patients really want." He mentioned that information on the peanut patch would be presented later in the afternoon, and he thinks that people will have options in a few years. However, "saying that because you might like to give your patient the patch, because it's a little safer, but because [OIT is accessible now] you're going to do OIT, instead, that is not the right way to move this field forward."

Audience Member #2: The A/M stated that they started out and remain ambivalent about OIT and that they have visited Dr. Baker's center and read many papers and their hope is that both Drs. Baker and Wood could get together and either "define protocols that would allow appropriately trained individuals" to do OIT, or decide that OIT has been tried and it's time to move on to some other treatment. The A/M stated, "I'm a little bit bothered by the fact that 10+ years down the road we seem to still be at the same point of debating not only whether or not it's ready for prime time, but is it ready for patient intervention." The A/M asked for their thoughts.

Dr. Baker: "I've always felt that we should do the most dangerous thing that the patient's ever going to do, in the office and we get over that hurdle and then everything they do at home is less dangerous than what they do in the office, and so I've always taken that approach." Dr. Baker reiterated that he still uses the avoidance-management strategy "in patients that are well-adjusted to it. The ones I really go after are those whose parents are paralyzed by this" and he feels the benefit:risk ratio is favorable in those cases. He continued on to say, "These kids lose their identity - their name is no longer 'Johnny' it's 'the kid with the peanut allergy' and these kids' lives are tremendously changed and I'm extremely sensitive to that and that's why I'm willing to go out on a limb and it is disruptive to academia to do this and I fully recognize that."

Dr. Wood: Dr. Wood agreed that we should feel ambivalent, given that we don't have all the data. He agrees that the large studies need to occur and in many data centers, etc. As for 10 years' time, he said that is, in the development of a new treatment, a very short time and we should not get discouraged. He clarified, though, that it has actually been slightly less than 10 years, as "the first double-blind study of food immunotherapy" was started in 2006. He stated that this field will move more slowly, out of necessity, as safety needs to be the driving force and due to the length of each phase of study. "We use the word 'equipoise' when we're talking about this and this is my most perfect example of equipoise - we just don't know enough to say if we're on one side of the fence or the other."

Moderator: The moderator chimed in to mention that two companies were at AAAAI who just finished Phase II clinical trials - Allergen Research Corp. (ARC) [Now Aimmune Therapeutics] and DBV Technologies - and he felt that a Phase III will probably be somewhere in the near future.

Dr. Baker then asked Dr. Wood how he would have managed his hypothetical patient (17-year-old soccer player, originally seen at age 2 with hives and shortness of breath after eating peanuts, positive SPT and had successfully avoided peanuts until the present. The patient developed EIA [exercise-induced asthma] at age 12. He had an accidental bite of a candy bar, which he discovered contained peanuts, but he did not react, despite coming in and finding he still had a "very positive" skin test...) Dr. Wood responded that he was "a perfect example of a kid who went 15 years with no reaction and he might have been highly allergic - and that's my average patient. You know, my average patient, their worst complaint is that 'I've now thrown away 65 EpiPens, because I never had to use one' and I say, 'that's the best insurance plan you ever had' [...] most of my patients are going 5...8...10...15 years with no reactions, whereas my patients in these studies...And you were completely correct, this is a 24/7/365-day monitoring, because there's not a day that my phone will not ring - I give them direct access to my phone, when they're undergoing this treatment because reactions are so common and it's so different from the patient who is on strict avoidance, where reactions are so uncommon."

Dr. Baker: "What do you think about my plea for [more] food challenges?"
Dr. Wood: "I completely agree."

Audience Member #3: An audience member asked a question bringing up the Lack study (The LEAP Study) but Dr. Wood stated that it was not pertinent, as it was a different approach, so the A/M clarified their question to ask if any study had been done to compare the severity of reactions in OIT versus the severity of reactions in the placebo arm.

Dr. Wood stated that they had not really looked at the data in that way, but there was data on the frequency of severe reactions.

Audience Member #4: The A/M expressed their concern, feeling that this was a vulnerable population that would "do anything for a cure." They expressed their concern for their ability to get informed consent as they "don't know enough about the long-term to tell them what they'll wind up with and I do worry about the long-term follow-up...I think we really need to see that, because I don't think families think about that - they think about the immediate, 'I want to get beyond this, my child could potentially die.' and I'd also like to have markers or some way to tell who's not going to tolerate this from the start, so that we don't put patients on it..." They stated that they can ask question to see if things like EOE are developing, but they are not sure if just removing peanut will make it go away or "will we have started a process that other foods will become sensitizing and now we've given them a long-term problem in addition to the one they had before."

Dr. Wood: Dr. Wood mentioned that he had 5 other slides that he didn't get to that were just on those very points. He added, "I think the risk of this approach is only going to be magnified as it goes out to greater numbers..." [...] "This is a very hands-on, one-on-one kind of thing - it's going to be very hard to duplicate in the real world."

Dr. Baker: Dr. Baker agreed, noting that he now has about 300 patients and it's difficult to maintain an intimate relationship with that many patients. He stated that the "manpower issue" is very problematic. Due to this issue, he is not currently accepting new patients.

Audience Member #5: "A couple of comments and a question - Should we be calling this 'oral desensitization' instead of 'oral immunotherapy'? And what happens if there is a fatality and we're providing this oral immunotherapy or desensitization in an office where there might not be the oversight that we have in the clinical studies? What will that do for the progress of the research? And then, finally, how ethical is it to provide such a treatment, if it seems likely it may be worse than the disease?"

Dr. Wood: Dr. Wood noted that as long as the word "tolerance" isn't used, it doesn't really matter whether you call it immunotherapy or desensitization, though he mentioned that he felt the term "specific oral tolerance induction" was "just wrong." As to the question of a fatality, he stated, "When somebody dies this whole process will shut down pretty quickly, and especially it will be a problem if it is not done in an FDA-approved protocol. And I think anyone doing this outside the confines of an IRB protocol is, right now, at substantial risk and this is what the next studies are needed for." He noted that some will say FDA approval is not needed, since foods can be purchased in the grocery store for treatment, but he stated that bypassing the FDA would be an extremely worrisome direction.

Dr. Baker: "My brother's a malpractice defense attorney and he does say that an error of commission is much harder to defend than an error of omission by a patient and so I'm acutely aware of that." He noted that they, instead, use a "memorandum of understanding" with the patient and practice agreeing to do their respective parts. He stated that "Informed consent never gets into evidence. Informed consent is part of the battery law and not part of the negligence laws and the negligence law's where we could be in trouble. It's a significant problem and I can't erase it."

Audience Member #6: This A/M recounted a story about a patient they had on OIT that experienced side effects and dropped out. That patient was also on asthma medication and after a while was feeling better and decided, on their own, to stop taking their medication. The patient later developed a viral respiratory illness and ended up in the ICU. The hospital staff questioned the patient/patient's family, wondering what kind of bad doctor they had, but the patients confessed that they were the ones that unilaterally decided to discontinue taking their asthma medication. The A/M's point, they stated, was that if the patient had still been doing OIT, "I would have been completely at risk for what happened to him, as everyone would have assumed that anything that happened to him, that illness was worse because of [the OIT], rather than the viral illness. So I think there is a risk to people doing this, because if anything unusual happens it's going to be brought back to the fact that this patient's on oral immunotherapy. I think it's also going to muddy the waters about how effective it is."

[No commentary from either doctor and another A/M stepped up to the microphone.]

Audience Member #7: This A/M expressed their frustration that there didn't seem to be any consistency among the experts. "We have posters and presentations [on OIT] for quite a few years and they'll play up the safety and the efficacy of it and they won't find a big problem with it and then we come to a Pro/Con debate where there are some really big problems, sometimes, so I think that has to be ironed out, there has to be some kind of consistency of approach." The A/M commented that there are so many protocols that even if they agreed to offer OIT, there isn't yet a standard to follow.