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Wednesday, 16 October 2019

Good afternoon, Stephen and all!

Thank you so much for this blog, for the large amount of useful information that can be found here. This is very important for everyone who has faced such a terrible disease. We would like to tell you about our situation and we really look forward to your help, since we do not know at all what is best to do in our case. My sister (48 years old) was diagnosed with glioblastoma multiforme in April that affects affecting the insular lobe of the telencephalon and the right frontal lobe of the brain (IDH wild type; MGMT is unmethylated; ATRX obtained). At the moment, we do not have any other data on genetic mutations, a full genetic analysis will be available only after 3 weeks. 4 days after diagnosis, an operation was performed to remove the tumor, a resection of more than 95%. During the operation, a displacement of the neoplasm with affecting the pyramidal tract (about 8 mm) was found. On the third day after the operation, my sister was already perfectly normal, feeling quite satisfactory. At the end of May, a course of radiation therapy began, 6 weeks (TMZ 75 mg / m2 per day, concomitant radiotherapy 59-60 Gy). Immediately upon completion of the course, edema began to develop, tumor recurrence was recorded, and the condition began to deteriorate steadily. The size of the new tumor at that time was already slightly larger than the removed one. We attribute the deterioration of the condition to the consequences of therapy, since a month and a half from the operation to the start of therapy, everything was fine. As a result, the sister began to choke, it became difficult for her to walk and talk, constantly lacking oxygen. Dexamethasone 12-8 mg began to be used. In July, we had an MRI in one of the best clinics in Germany (where the first operation, radiation, chemotherapy was performed), as a result of which German doctors refused us and gave us a couple of weeks ... By the end of July, she practically stopped moving on her own, could only reach from the bed to the toilet and vice versa, her left arm was almost inactive. In August, we started using Optune, took a chemotherapy course (TMZ, 240 mg / m2 for 5 days). In early September, literally a day after the completion of chemotherapy, the condition became critical, she simply did not wake up in the morning. Doctors were able to perform a miracle, brought back to life. And they insisted on a second operation, which became, as it turned out, the last available opportunity to save her life (without an operation, it's a matter of days). The operation was carried out on September 13, the tumor was removed by 90%. Dexamethasone 3 days before surgery - 20 mg, now reduced to 5 mg. A biopsy revealed that the removed tissue is radiation necrosis. But doctors can not be sure about the remaining 10% - this is necrosis or nevertheless a tumor. After the operation, the sister successfully recovers, the doctors are satisfied with the process. Memory, speech, motor functions were not affected. Now she can take several dozen steps a day with support. Every day we work out with a fitness trainer, two days ago we started going to the pool and exercise on a stationary bike. A few days ago MRI was done, the tumor does not develop, the displacement decreased by half.
And now the main thing. We need to decide on the next steps. We wanted to participate in poliovirus trials in the USA, but they refused (complex tumor location, low Karnowski score).

Considered as options for participation in studies of the Canadian vaccine VAL-083 (interested, because its effect does not depend on MGMT methylation), the DCVax vaccine. But at the moment for us it is all inaccessible in connection with the functional state of the patient.

In addition, immediately after the second operation, we sent the tumor material for the manufacture of the dendritic vaccine. Our neurosurgeon (who performed the second operation) spoke out against its use. But we still plan to try it. Avastin was abandoned, and in general, we are actively studying alternative medicine options, we want to make our own cocktail. But while we still haven’t figured it out enough, we don’t understand how to correctly compile it, what additional information is needed for this. It’s very scary to harm her! We are afraid of the traditional treatment, because before our eyes a person literally died away with its use. And now, every day, even small, but progress and improvement is noticeable. And we are afraid to make a mistake in the independent choice of funds - what if she suddenly gets worse?

Do you believe in alternative methods in general or choose traditional treatment?

Has anyone tried soda solutions, what do you think of this method?

I understand that the question is very vague, that everything is very individual, and now I’m carefully studying all the information on the blog, but maybe you can recommend which drugs you should definitely pay attention to? What worked for many?

We will be very grateful for your reply!


5 comments:

  1. I think this patient should take contact with the IOZK for a combined strategy approach including multimodal immunotherapy.

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  2. Dear Yulia,
    Thank you for everything you are doing for your sister. It does seem like a miracle she was able to recover from such a low point.

    A few questions. You mentioned the tumor tissue being sent away for a dendritic cell vaccine. Where was it sent to? There are several clinics offering commercial vaccines, apart from DCVax.

    In general I advocate not an either/or approach (alternative versus conventional), but a broader approach that builds off the conventional approach.

    I have never offered anyone a specific cocktail, not least of all because I'm not a doctor, but also because this is highly experimental, and there isn't enough information to say what an optimal cocktail might look like in general, let alone for a specific individual. However, I made an information sheet in the Brain Tumor Library with a list of many commonly used or studied drugs and supplements that people are experimenting with. At one point I tried to give them an approximate rating to show which ones I would prioritize (based on the level of evidence or the ease of access).

    I will share the Library with you and direct you to that sheet.

    As far as genetic testing, the main genetic alteration common in IDH wild-type adult GBMs that is actually targetable with available drugs is EGFR. If you could get them to test for EGFR amplification/overepression/mutation this might provide additional therapeutic insights, although I'm not sure it would make a difference for you in terms of clinical trials.

    Was Avastin tried and then abandoned, or was it just never tried?

    I hope you are continuing in your study and learning alot, and I hope your sister continues to improve.

    In Germany you might be able to reach out to Marc-Eric Halatsch of the University of Ulm, to find out how the CUSP9 trial is going. This is a 9 drug cocktail of commonly available repurposed drugs, and is the only extensive cocktail of this type that has made it to trial for GBM.

    Best wishes

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  3. Steven, thank you so much for your reply!!

    We live in Russia (although the first operation took place in Germany), and the second operation was done here. Dendritic cell vaccine was also made in Russia. We planned to participate in vaccine trials in the USA, Canada or Europe, but as I said, they refuse us because of the current functional state and location of the tumor. Therefore, while we are recovering from the operation and are looking for options that will be available now.

    As for the mutation of the EGFR, we will try to do the necessary test, I understand that this is really important.

    We did not try Avastin, we were afraid of possible side effects. During chemotherapy, temozolomide was used.

    I will be very grateful if you add me to the Library (my mail y.dyatlova2347@gmailcom)

    Thanks for the tip about CUSP9, we’ll try to find out about it.

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  4. Hi Yulia,
    I've recently had the opportunity to meet Prof. Halatsch and he is very open minded tries to go out of his way to help every patient. He will probably send the CUSP9 protocol if you ask him, but if you have to buy the drugs on your own they are very expensive (in Germany about 2500 € / month as far as I know).

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  5. Hi Yulia, we are from Belarus but live in the UK. My husband was diagnosed with glioblastoma Grade IV in May 2016 (original diagnosis was astrocytoma in September 2015) and he is still with us - Thanks to God! In addition to radio and chemo treatment he also been taking Valgoncyclovir for 1 year together with Themozolomide, and started Avastin every 2 weeks and now we have increased the interval to 3 months. His condition is considered stable at the moment. As Stephen says, all the advice or information everyone provides here is very individual but with the help of this site we built up our confidence about Avastin and many supplements. We also went for PAT MRI to St Petersburg in August 2016 where the overall picture was very negative but there was a senior couple where the husband had glioblastoma for 2 years but after taking Avastin treatment in Burdenko clinic in Moscow, his PAT MRI has shown no cancer cells - they went straight from the clinic to pray to St Ksenija and St Matrona... Regarding soda, my husband was measuring his PH on a daily basis with PH strips (urine and saliva) for about 2 years ate least and with soda he was able to keep the PH balance over 7.5 mark, without it it wasn't possible. I've just posted a response to another case with supplements that my husband was taking. In addition to the supplements, he was also taking DCA+B1 and keeping to a very strict diet( no sugar, white flour, rice, etc), following breakfast recommendations from Budwig diet (4 years now) and exercising a lot (running from 500 meters early days and increasing to 10km now). Miracles do happen, please believe and ask Saints and our God to send your sister the healing with your help and support via Holy Communion.. All the very best and wishing your sister a very speedy full recovery!

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