RE:RE:RE:RE:RE:RE:RE:Can we soon start treating terminal children ( brain cancer Thanks Eog - didn`t hear back from Lazer00 with his alleged toxicity issues but if TLD-1433 is safe Rutherrin is safer and a lot of preclinical work in GBM has confirmed this as per my previous post.
There are at least two other legs - vaccine and CLT - to TLT`s GBM Treatment.These were the further subject of separate papers at that International Congress (see below).
Paper 11070-110: A New Platform Technology RuVaCare™, an Extracorporeal Anti-Cancer Vaccine is Efficient in Breaking Immune Barrier to Target Cancer Cells
This paper discusses the successful application of Theralase®'s PDT technology as a cancer vaccine, known as RuVaCare™, and highlights the study's outcome and the significant increase of survival obtained in the RuVaCareTM vaccinated RG2-GBM model. RuVaCare™ was designed to break the suppressive tumours barriers and to selectively boost the activation of an effective immune response, specifically toward malignant cancer cells.
Paper 11070-353: Photobiomodulation Inhibits Warburg Metabolism and Potentiates a Dose Dependent Response By GBM Cells to Ruthenium-Based PDT
This paper discusses the impact of Photo Bio Modulation ("PBM") on the Warburg Effect and how it increases the efficacy of TLD-1433 in the destruction of GBM brain tumours.
If the PDT alone can push survival out beyond 5 years` then in combination with vaccine and CLT (leaving aside for now cannabis) results should be spectacular. PDT is repeatable not only within the 16 hour window of the therapeutic dwell-time but as a separate procedure at a later date. The serious prospect of a non-invasive treatment to defeat this terrible disease.