Blog Archive

Sunday, December 25, 2016

Sunday, December 18, 2016

Plasma-Derived vs Recombinant

A year ago we renewed a match between two heavy-weight contenders in hemophilia: plasma-derived products versus recombinant. The question: which product is more likely to cause inhibitor formation? In the fight to avoid inhibitor formation, some groups and opinion leaders read the initial results of the SIPPET project and declared plasma-derived the winner. But it's a bit more complicated than that. Read Paul Clement's excellent article on SIPPET; it will take many more rounds before we declare an outcome. The good news is that so much clinical scrutiny is underway.

The SIPPET Bombshell
Paul Clement


A bombshell was dropped at the Plenary Scientific Session of the 57th annual meeting of the American Society of Hematology (ASH) on December 6, 2015, in Orlando. Study coordinators of the SIPPET project (Study on Inhibitors in Plasma-Product Exposed Toddlers)1 presented surprising preliminary findings: recombinant factor VIII products are associated with an 87% increased risk of inhibitor development compared to plasma-derived factor VIII products. 2
            In other words, for every 10 people treated with recombinant factor VIII as opposed to plasma-derived factor VIII, 1 patient can be expected to develop high-titer inhibitors.
            As a parent of a toddler who does not have inhibitors, you may feel stunned, angry, or scared when you read these findings. Should you be? Before you rush to make a product change, learn how the study was conducted, what its potential shortfalls are, and why you should take a deep breath!

Shock and Awe
Understandably, many consumers are concerned. Some news releases describing the study results only heightened the alarm. Hemophilia Federation of America (HFA) issued a press release requesting that National Hemophilia Foundation’s (NHF) Medical and Scientific Advisory Council (MASAC) “consider the temporary suspension of recommendations… that state any preference for recombinant factor products until the results of the full SIPPET study can be reviewed.” 3
            Is this a reasonable reaction, or is this jumping the gun? It helps to examine how the study was conducted—and why.

Fighting Invaders
Why was the study looking to see if plasma-derived products are less immunogenic than recombinant products—that is, less likely to lead to developing inhibitors?
            In the blood, factor VIII is normally tightly bound to another protein called von Willebrand factor (VWF). VWF has several functions, including protecting factor VIII from being digested and cleared from the bloodstream. Some researchers suggest that in doing this, VWF masks some of the sites on the factor VIII protein where antibodies attach, potentially making factor VIII with VWF less immunogenic. Note:
            • Intermediate/high-purity plasma-derived factor VIII products are the only ones that contain VWF.
            • Recombinant and ultra-high-purity (monoclonal purified) plasma-derived factor VIII products contain no VWF.
Without the protection of its VWF “bodyguard,” the immune system may recognize these factor VIII products as intruders and develop inhibitors to neutralize them.
The problem is, no one really knows for sure what causes inhibitors, and no one knows whether factor VIII with VWF is less immunogenic.

SIPPET Strategy
SIPPET set out to answer this question: Is plasma-derived factor VIII with VWF less immunogenic compared to recombinant factor VIII without VWF?
            SIPPET researchers designed a study called a prospective randomized controlled trial (RCT). Prospective means looking forward, before the patient has developed an inhibitor (in contrast to retrospective studies, in which researchers look backward, after someone has developed an inhibitor). Controlled means that there are two groups: (1) an experimental group that will use factor VIII containing VWF, and (2) a control group that will use factor VIII without VWF. This second group is used as a standard of comparison against the experimental group. Randomized means that no one involved in the study influenced which group a patient was assigned to. Randomization is often done by a computer.
            RCT studies are often considered the gold standard, thought to produce more reliable data than other types of studies. Although an RCT can show relationships between variables being studied, it cannot prove causality. So the RCT used for SIPPET can’t prove that the presence or absence of VWF in factor VIII caused the observed results.
            SIPPET was conducted between 2010 and 2015, and data was collected on 251 patients from 42 participating sites in 14 countries from Africa, the Americas, Asia, and Europe. The patients were younger than six years old, had severe hemophilia A, were previously untreated with factor, and had minimal exposure (less than five times) to blood components. Of the 251 patients, 125 were treated with one of the plasma-derived factor VIII products containing VWF. The remaining 126 patients were treated with a VWF-free recombinant factor VIII product.4 The patients were followed to see if they developed an inhibitor, for 50 exposure days (days they received factor infusions) or three years, whichever came first.
            It’s important to note that only one of the plasma-derived products used in this study is available in the US, and that the study was funded by manufacturers of plasma-derived products. Is this a conflict of interest? Does it influence the findings?

SIPPET Shortcomings?
The preliminary findings were startling: of the 251 patients, 76 developed an inhibitor, and 50 of those were high-titer inhibitors. And 90% of these inhibitors developed in the first 20 days of treatment. Most important: recombinant factor VIII products were associated with an 87% increased risk of developing an inhibitor compared to plasma-derived factor VIII products containing VWF.
            Remember, these are not final results and have not yet been reviewed by researchers outside of the study. Before you decide whether to switch your toddler to a plasma-derived factor VIII containing VWF, know that many other variables affect inhibitor formation. In any experiment, variables not directly being tested, but which could have an effect on the outcome, are called confounding variables.
            For example, the single greatest risk factor for developing inhibitors is the type of genetic mutation that caused your child’s hemophilia. If the mutation in the factor VIII gene resulted in no factor VIII being produced in his body, then he is already at significantly higher risk of developing an inhibitor. This is one of many confounding variables in the SIPPET study.
            One way to reduce the effects of confounding variables on the data is to use a large study sample. If the sample size is large enough and patients are randomly assigned to two groups, then each group should have about the same number of patients with the same confounding variable, so its effect will be canceled. The problem is that the more confounding variables you have, the larger your study sample size must be—perhaps several thousand patients. And many variables affect inhibitor development.
            Another way to account for the effects of confounding variables is to identify and measure them, and then to separately compare and analyze the data from patients who share the same confounding variable. This process is called stratification (meaning to separate into layers) and was used by SIPPET along with other statistical analysis methods. But the study identified and measured only six confounding variables: (1) age at first treatment, (2) intensity of treatment, (3) type of factor VIII gene mutation, (4) family history, (5) ethnicity, and (6) country site. What about the effects of the other confounding variables that were not measured? If the study sample size was too small to reduce the effects of other, unmeasured, confounding variables, then the study’s conclusions are questionable and might be explained in other ways.

Don’t Jump Ship Yet
At the time of this writing, SIPPET has not been published in a medical journal. That means researchers—outside of those conducting the study—don’t know much more about the study than you do after reading this article. Only a short synopsis of the SIPPET study was presented at the ASH annual meeting—just enough to cause a stir and raise many questions. You can be sure that as soon as the journal article is released, it will be examined by bleeding disorder experts worldwide. Questions will undoubtedly be asked about the handling of confounding variables and whether the study sample size was large enough.
            And experts will have another question, too: Why didn’t the study include any of the new prolonged half-life products, several of which appear to have a lower immunogenicity than other recombinant factor VIII products?
            Should you switch your toddler from a recombinant to a plasma-derived factor VIII product containing VWF based on the preliminary SIPPET results, in the hope that it will reduce the risk of developing an inhibitor? This is a question for you and your hematologist, but if you were a betting person, the answer would be no. To bleeding disorder experts, the results of SIPPET are not a bombshell, but merely a piece of the puzzle that is inhibitors.5 The conclusions of this study contradict those of several other studies. It may take years, and several additional studies, to sort everything out. MASAC is on top of this, and as the data becomes available, you can be assured that NHF will share its expert opinion. So keep calm and carry on!



1. https://ash.confex.com/ash/2015/webprogram/Paper82866.html (accessed Feb. 7, 2016).
2. Inhibitors are a major complication of hemophilia in which a person’s immune system mistakenly recognizes infused factor as a foreign (and potentially dangerous) protein, and develops antibodies (inhibitors) to inactivate the factor, making factor infusions ineffective.
3. http://www.hemophiliafed.org/news-stories/2015/12/update-2-sippet-study-2/ (accessed Feb. 7, 2016).
4. The VWF-rich plasma-derived factor VIII concentrates used by SIPPET: Alphanate (Grifols), Fandhi (Grifols), Emoclot (Kedrion), or Factane (LFB). The VWF-free recombinant factor VIII products used: Recombinate (Baxalta), Advate (Baxalta), Kogenate SF (Bayer), or Refacto AF (Pfizer).
5. Visit the Believe Limited website for an excellent interview by Patrick James Lynch of bleeding disorder expert Dr. Steven Pipe about the SIPPET findings: http://believeltd.com/inhibitors-sippet-and-the-double-edged-internet/ (accessed Feb. 7, 2016).



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Sunday, December 11, 2016

See how James found the factor IX option he’d been searching for

As we’re full swing into the holiday spirit and a new year is just around the corner, it seems like the perfect time to share this inspiring story of a young man with hemophilia B named James. Please read below to learn about his story and his choice of treatment.
Laurie

After missing out on much of his life because of bleeds, James found a fresh start with the help of the right treatment for him…IXINITY® [coagulation factor IX (recombinant)].

Watch James share his story at IXINITY.com.

Interested in learning more about IXINITY? Connect with a Hemophilia Territory Manager near you at MyIXINITYRep.com.

And remember, this is James’ experience; different people may have different results. You should always talk to your doctor to decide which treatment is right for you.

Meet James

"Since birth I’ve used different hemophilia B products, and regardless of treatment, I continued to have breakthrough bleeds most every other week. I felt I had no control over my health, and that led me down a bad path as I started making some unhealthy choices in my teen years.

When I was 21, I saw an ad for a clinical trial of a new recombinant hemophilia B treatment. I thought, 'I have nothing to lose.'

After a few weeks in the clinical trial, I stopped having bleeds almost entirely. I realized I didn’t know what feeling good felt like. I felt more in control, and it was a liberating experience.

One day I decided to go running—I don’t know what made me decide to because I'd never really done it before. But I thought, 'I'm just going to go for a run,' and about a mile later, I thought, 'Huh! This is awesome'

After talking with my doctor, I’ve now developed a habit of running 3 times each week with my dog, and exercising regularly. To be honest, switching to IXINITY was the best decision I ever made. I don’t feel like someone with hemophilia; I forget I even have it."

See more of James’ journey at IXINITY.com.

James’ experience with IXINITY may not be typical. Speak with your doctor to see if IXINITY is the right treatment for you.

The content of this post is provided and sponsored by Aptevo Therapeutics.

IXINITY INDICATIONS AND IMPORTANT SAFETY INFORMATION

What is IXINITY®? 

IXINITY [coagulation factor IX (recombinant)] is a medicine used to replace clotting factor (factor IX) that is missing in adults and children at least 12 years of age with hemophilia B. Hemophilia B is also called congenital factor IX deficiency or Christmas disease. Hemophilia B is an inherited bleeding disorder that prevents clotting. Your healthcare provider may give you IXINITY to control and prevent bleeding episodes or when you have surgery.

IXINITY is not indicated for induction of immune tolerance in patients with hemophilia B.

IMPORTANT SAFETY INFORMATION for IXINITY®

• You should not use IXINITY if you are allergic to hamsters or any ingredients in IXINITY.
• You should tell your healthcare provider if you have or have had medical problems, take any medicines, including prescription and non-prescription medicines, such as over-the-counter medicines, supplements, or herbal remedies, have any allergies, including allergies to hamsters, are nursing, are pregnant or planning to become pregnant, or have been told that you have inhibitors to factor IX.
• You can experience an allergic reaction to IXINITY. Contact your healthcare provider or get emergency treatment right away if you develop a rash or hives, itching, tightness of the throat, chest pain, or tightness, difficulty breathing, lightheadedness, dizziness, nausea, or fainting.
• Your body may form inhibitors to IXINITY. An inhibitor is part of the body’s defense system. If you develop inhibitors, it may prevent IXINITY from working properly. Consult with your healthcare provider to make sure you are carefully monitored with blood tests for development of inhibitors to IXINITY.
• If you have risk factors for developing blood clots, the use of IXINITY may increase the risk of abnormal blood clots.
• Call your healthcare provider right away about any side effects that bother you or do not go away, or if your bleeding does not stop after taking IXINITY.
• The most common side effect that was reported with IXINITY during clinical trials was headache.
• These are not all the side effects possible with IXINITY. You can ask your healthcare provider for information that is written for healthcare professionals.

For more information about IXINITY, please see full Prescribing Information, including Important Patient Information.

You are encouraged to report side effects of prescription drugs to the Food and Drug Administration. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.


Aptevo BioTherapeutics LLC, Berwyn, PA 19312

IXINITY [coagulation factor IX (recombinant)] and any and all Aptevo BioTherapeutics LLC brand, product, service and feature names, logos, and slogans are trademarks or registered trademarks of Aptevo BioTherapeutics LLC in the United States and/or other countries.

© 2016 Aptevo Biotherapeutics. All rights reserved. CM-FIX-0093

Sunday, December 04, 2016

AIDS: Lest We Forget

"Get out!"
The threat of HIV to those with hemophilia was made vividly clear in September 1987. On August 21, 1987, two weeks before my son with hemophilia was born, the Ray brothers had been fire-bombed from their trailer park home in Arcadia, Florida--a warning to the family to leave. It made headlines nationwide and was considered a landmark act in the history of HIV in the US. The story was of shocking interest to everyone, even those of us who didn't know hemophilia was about to enter our lives.


I still have my copy of People magazine, which had a story on it. Two weeks later, my son was diagnosed and a chill went through me. He was lucky to have just missed the window for contracting HIV through contaminated blood products. But there was national hysteria, misunderstanding about HIV transmission, and paranoia.


There are now fantastic drugs available now that can treat HIV and prolong the lives of those who have it. So much public education has been done to alleviate ignorance and the spread of the virus. From 2005 to 2014, the annual number of new HIV diagnoses declined 19%. And December 1 is World AIDS Day, to remember those who died as a result of this insidious virus. The US hemophilia community alone lost an estimated 10,000 with hemophilia, and this doesn't include the spouses who were infected. Ten thousand people made up half of our community at the time. 

World AIDS Day remembers those who died, and a ceremony was held at the National AIDS Memorial Grove in San Francisco. Both HFA and NHF were honored to have been invited to participate.
 http://www.aidsmemorial.org/

World AIDS Day also serves to remind us that the work is not yet done. I was reading Time magazine on a plane ride yesterday, and was shocked at the statistics I read. 


  • In 2015, 39,513 people were diagnosed with HIV infection in the United States. 
  • More than 1.2 million people in the US are living with HIV, and 1 in 8 of them don't know it.
  • Gay and bisexual men accounted for 82% (26,375) of HIV diagnoses among males and 67% of all diagnoses.
  • Black/African American gay and bisexual men accounted for the largest number of HIV diagnoses (10,315), followed by white gay and bisexual men (7,570).
  • Heterosexual contact accounted for 24% (9,339) of HIV diagnoses
  • Six percent (2,392) of HIV diagnoses in the United States were attributed to injection drug use (IDU).
  • Louisiana has the second highest new-infection rate: due to poverty, large incarcerated population, stigma, abstinence-only sex ed (CDC data, Time magazine, Nov 28-Dec 5, 2016)
  • Miami: cuts in health spending contributed to a 23% rise in those with HIV since 2004, the fastest-growing rate of infection in US. (CDC data, Time magazine, Nov 28-Dec 5, 2016)

World AIDS Day is an important day for two reasons: to remember the loved ones we lost, and to remind a sometimes still ignorant or risk-taking public that HIV still lives among us, is transmitted through unprotected sex or shared needles with someone who has it (and you cannot tell by looking who has it), and that there is no cure. The hemophilia community warriors have from day 1 led the charge for a safer blood supply, safer blood products, and greater information about HIV/AIDS. 

Read: And the Band Played On by Randy Shilts, Dying in Vein by Kathy MacKay
Note: The spread of HIV in the US was originally blamed on a gay French Canadian flight attendant, Gaetan Dugas, but new analysis of stored blood samples have exonerated him of this. And the Band Played On opens with Dugas's story and alleged link as Patient Zero.

 
Bayer