DIPG/DIPT Discussion

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Just One More Day for Love, Hope & a Cure


A searchable blog on DIPG research, DIPG news, recent publications, DIPG Foundations, DIPG researchers, clinical trials as well as other issues relating to Diffuse Intrinsic Pontine Tumors- both Diffuse Intrinsic Pontine Gliomas (DIPGs) and Atypical Pontine Lesions (APLs).

For parents, family and friends of children with DIPG looking for information and connection to others dealing with DIPG please check the buttons on the right hand side for resources.

Monday, April 6, 2009

Wall of Courage




~A message from Heide Randall


May is Brain Tumor Awareness Month

As you all know, May is Brain Tumor Awareness Month, and I wanted to make some gear to mark it as such. So, I've created designs for shirts, buttons, magnets, caps, mugs, mousepads, etc. etc. etc.

It was originally only intended for our youngest BT warriors and angels, but due to popular demand I've added designs for adult BT warriors and angels, as well.

The products are available here: http://cafepress.com/btwallofcourage ...

There is a special section featuring products with pictures of over 120 of our youngest BT warriors and angels.

There is gear available to support your: Son, Daughter, Survivors (Had/Have a Brain Tumor), Brother, Sister, Grandson, Granddaughter, Niece, Nephew, Cousin, Father, Mother, Husband, Wife, Grandmother, Grandfather, Uncle, Aunt, and Friend (boy/girl).

For those interested, proceeds from the sale of these products will be distributed among the following:
Jessica C. Randall Memorial Scholarship FundChildren's Brain Tumor Foundation (http://cbtf.org/)

The Brain Candy Project (http://braincandyproject.org/)

Jacob's Smiles (http://jacobssmiles.com/ -- site not functional yet, but I think many of you know Christine and her son, ^Jacob^.)and,

pending: Aimee's Army (http://aimeesarmy.org/)

I hope you all enjoy the gear. I figure I'll be wearing gray all year long!!!! :)


~Heide Randallm/o ^Jessica^ (Forever 17) & Jake (17)




Monday, March 30, 2009

FDA to Discuss DIPG Biopsies

On April 27, 2009, the Committee will meet to discuss the scientific and ethical issues involved in obtaining and using brain biopsy specimens to evaluate gene expression patterns in children with diffuse pontine gliomas.


DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Joint Meeting of the Pediatric Advisory Committee and the Oncologic Drugs Advisory Committee
This meeting is open to the public.


Date and Time of Meeting:
April 27, 2009, from 8 a.m. to 6 p.m.

Date and Time of the Open Public Hearing:
April 27, 2009, between approximately 1 p.m. and 2 p.m.

Deadline to Request Speaking during Open Public Hearing:
On or before April 3, 2009 (see "How to Participate in the Open Public Hearing" below)

Address of Meeting:
Washington DC North/Gaithersburg Hilton,
620 Perry Pkwy.,
Gaithersburg, MD 20877.

Contact Person:
Carlos Pena
Office of the Commissioner (HF-33)
Food and Drug Administration,
5600 Fishers Lane (for express delivery, rm. 14B-08)
Rockville, MD 20857,
301-827-3340
or
e-mail: carlos.pena@fda.hhs.gov

Agenda:
On April 27, 2009, the Committee will meet to discuss the scientific and ethical issues involved in obtaining and using brain biopsy specimens to evaluate gene expression patterns in children with diffuse pontine gliomas.

FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA's Web site after the meeting. Background material is available at
http://www.fda.gov/ohrms/dockets/ac/acmenu.htm, click on the year 2009 and scroll down to the appropriate advisory committee link.

How to Participate in the Open Public Hearing:
Oral presentations from the public will be scheduled between approximately 1 p.m. and 2 p.m. on April 27, 2009.

Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Notify the contact person (listed above) on or before April 3, 2009, if you would like to make a formal oral presentations the day of the meeting. Submit a brief statement of the general nature of the evidence or arguments they wish to present, the names and addresses of proposed participants, and an indication of the approximate time requested to make their presentation. The contact person (listed above) will notify interested persons regarding their request to speak by April 6, 2009.

Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session.

Written submissions may be made to the contact person (listed above) on or before April 13, 2009.

Persons attending FDA's advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets. FDA welcomes the attendance of the public at its advisory committee meetings and will make every effort to accommodate persons with physical disabilities or special needs. If you require special accommodations due to a disability, please notify the contact person (listed above) at least 7 days in advance of the meeting.

FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at http://www.fda.gov/oc/advisory/default.htm for procedures on public conduct during advisory committee meetings.

Saturday, March 28, 2009

Avastin

On March 31, 2009 -- this Tuesday -- the FDA will hold an open public hearing to discuss approval of Avastin as a single agent in previously treated glioblastoma multiforme. The hearing will take place from 8:30 a.m. to 4:30 p.m. at the Hilton Washington DC/Silver Spring. Although this hearing is for an adult indication, we believe this matter deserves the attention of the brain tumor community at large. Moreover, we are seeing Aavastin being used with our DIPG kids more and more frequently.

There is some concern in the adult community that a negative review from the FDA will result in insurance companies refusing to pay for Avastin for any brain tumor patient.

Because this is an issue that may very well directly impact the DIPG community specifically, and most certainly will impact the entire brain tumor community, we delivered the following letter in support of Avastin for the Committee's consideration:


ODAC Committee Members:

We, the Board members of Just One More Day, are writing to urge the Committee to recommend approval of Avastin as a single agent in recurrent glioblastoma multiforme.
Just One More Day is a non-profit foundation formed by parents to help other parents whose children have been diagnosed with pediatric diffuse intrinsic pontine gliomas (“DIPG”), a cancerous tumor which invades the brainstem. DIPGs are almost always terminal, with most children dying within one year of diagnosis. In thirty years, and despite multiple different trials, no chemotherapy has been found to be effective against DIPG. With Avastin, however, there is hope.

Although DIPGs are generally considered inoperable, DIPG lesions were biopsied as part of a recent French study. The study revealed that the vast majority of DIPGs are high-grade gliomas, with many being glioblastoma multiforme.

In our network of parents we have seen many of our children with DIPGs stabilize with Avastin. In fact, we have recently been overjoyed by dramatic regression of the DIPG in Andrew, son of one of our Board members, after he received a single cycle of Avastin. Avastin has provided a flicker of hope in the dismal world of diffuse intrinsic pontine gliomas.

We realize that the question before the committee is whether to recommend approval of Avastin as a single agent in recurrent glioblastoma. Unfortunately, the call for written testimony did not indicate whether the question addresses both adults and children or only adults. Regardless, we believe it is important that our voice be heard on the matter. We are directly impacted by what is being done for adults with brain tumors, as treatments are usually not approved for children until they pass through the approval process for adults. Articles such as Antiangiogenic Therapy Using Bevacizumab in Recurrent High-Grade Glioma: Impact on Local Control and Patient Survival (J. Neurosurg. 2009 Jan; l 10(1): 173-80)) are encouraging and reflect what we are seeing with our children.

We ask the committee pause and reflect on the impact of this recommendation to the entire brain tumor community -- including our children. Previously there has been so little hope for children with DIPGs. Even a little more time with our children – even, as our name reflects, just one more day -- is incredibly precious to us. Please help the flame of this hope continue to burn and, we hope, to grow even brighter.

None of our board members have financial conflicts regarding the approval of Avastin.

Thank you for your time and consideration.



Background information is available at-
Meeting background http://www.fda.gov/ohrms/dockets/ac/cder09.html#OncologicDrugs
27 page document from Genetech http://www.fda.gov/ohrms/dockets/ac/09/briefing/2009-4427b1-01-FDA.pdf

Tuesday, March 17, 2009

May is Brain Tumor Awareness Month


Please join us for UmbrELLA of HOPE a family fun event in remembrance of Ella Hope Hauschildt and families fighting Diffused Intrinsic Pontine Glioma (DIPG).

On December 7, 2007 our lives changed forever, our daughter Ella Hope was diagnosed with a DIPG a rare and inoperable brain tumor. During Ella’s fight we tried conventional and alternative treatments, but to this day there is still no known treatment that is able to destroy this tumor.

Ella was born into heaven on November 21, 2008 after an 11 ½ month battle. On that day our focus changed from fighting for our little girl’s life, to fighting for brighter days for all children and families dealing with this dreadful tumor.

I ask that you join us in this fight on Saturday May 16, 2009 at the UmbrELLA of HOPE family fun event http://www.umbrellaofhope.com/ to remember Ella and all children fighting this disease and to support Just One More Day.org.

Just One More Day.org is committed to providing information and support for families affected by Diffused Intrinsic Pontine Glioma, promoting awareness and funding research for a cure. The event will include a family walk on the trails of Lake Front Park in Prior Lake, Minnesota. Other events include:

* Kids bounce houses
* Face painting
* Clowns
* Music entertainment
* Story telling
* Much more.

To register for the Family Fun Event please go to http://www.umbrellaofhope.com/ . We look forward to seeing you and we appreciate and applaud your willingness to walk with us in this battle!!!

Donations of coloring books, crayons, markers, colored pencils and craft items will also be collected for Riah’s Rainbow http://www.riahsrainbow.org/. Riah’s Rainbow was created by the Klien family in memory of little Mariah Klien who passed away from DIPG on August 31, 2008. Their goal is to bring smiles to the faces of children who have to endure a day, a week or even months in the hospital. All donations will be delivered to Fairview University Hospital. Please consider bringing a donation to bring smiles to kids who are battling cancer or chronic illnesses.