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Re: exwannabe post# 749811

Sunday, 02/16/2025 2:02:05 PM

Sunday, February 16, 2025 2:02:05 PM

Post# of 822798
How many tumor specific antigens can Provenge present to immune system?

You and your buddies are trying to make things look so complicated in the hope of tricking and deceiving people. In the case of DCVax-L, things are rather simple.

Is there another company which has the technology enabling dendritic cells to present hundreds of tumor-associated antigens to immune system? The answer is no. NWBO is the only company on this planet that has the technology. Unlike other immunotherapy treatment, DCVax-L can trigger massive and sustainable t-cell infiltration into tumor site.

That's why I can say with 100% certainty that the technology adopted in the following trial is the same pulsing technology for the combo trial.

Therapy to Treat Ewing's Sarcoma, Rhabdomyosarcoma or Neuroblastoma
https://clinicaltrials.gov/study/NCT00923351

Adjuvant Immunotherapy to Improve Outcome in High-Risk Pediatric Sarcomas
https://aacrjournals.org/clincancerres/article/22/13/3182/79179/Adjuvant-Immunotherapy-to-Improve-Outcome-in-High

Autologous tumor lysate, cell therapy, and CYT107
Tissue was obtained via percutaneous core needle biopsy and/or fine needle aspiration (n = 26) or surgical resection (n = 3).




Results: Forty-three patients enrolled and 29 received immunotherapy. The regimen was well tolerated. Intent-to-treat analysis demonstrated 5-year OS of 51% with significant differences based upon histologic group (63% vs. 0% for Ewing/rhabdomyosarcoma vs. other sarcomas) and response to standard therapy (74% no residual disease vs. 0% residual disease). Five-year intent-to-treat OS of patients with newly diagnosed metastatic Ewing/rhabdomyosarcoma was 77%, higher than previously reported in this population and higher than observed in a similar group treated with an earlier adjuvant immunotherapy regimen (25% 5-year OS). T-cell responses to autologous tumor lysate were identified in 62% of immunotherapy recipients, and survival was higher in those patients (73% 5-year OS with vs. 37% without immune response, P = 0.017). Immune reconstitution, measured by CD4 count recovery, was significantly enhanced in subjects treated with recombinant human IL7.





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