BAT & Nivolumab: New from Demeade... - Fight Prostate Ca...

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BAT & Nivolumab

pca2004 profile image
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New from Demeade/Antonarakis & Co. [1]

"Nivolumab is a human IgG4 monoclonal antibody that blocks PD-1. It is a type of immunotherapy and works as a checkpoint inhibitor, blocking a signal that prevents activation of T cells from attacking the cancer." [2]

"The primary endpoint of a confirmed PSA50 response rate was met and estimated at 40% (N = 18/45 ... against the 25% null hypothesis). Sixteen of the PSA50 responses were achieved before the addition of nivolumab." !!!

Interestingly: "In paired metastatic tumor biopsies, BAT induced pro-inflammatory gene expression changes that were restricted to patients achieving a clinical response."

{I see that Mary-Ellen Taplin (Dana-Farber) was the only non-Hopkins team member. She has been around a while - 198 PCa hits on PubMed since 1995, including some important studies imo.}

-Patrick

[1] pubmed.ncbi.nlm.nih.gov/381...

[2] en.wikipedia.org/wiki/Nivol...

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pca2004
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Ramp7 profile image
Ramp7

I wonder if Propionate would effect the results even further in a positive direction. I took Cypionate once, and it took over 6 weeks to achieve a low Testosterone reading.

KocoPr profile image
KocoPr in reply toRamp7

Oh i bet propionate would make difference for the good

KocoPr profile image
KocoPr

Mary Ellen Taplin is awesome. Some amazing articles including this neuroendocrine liquid biopsy test of CTC on men that are still androgen responsive.

A clinical-grade liquid biomarker detects neuroendocrine differentiation in prostate cancer. J Clin Invest. 2022 11 01; 132(21). View in: Pubmed

pubmed.ncbi.nlm.nih.gov/363...

Maxone73 profile image
Maxone73

Very good! I am trying to see if I can find a stratification of data based on gene mutations prior to therapy

MateoBeach profile image
MateoBeach

16 of the 18 PSA50 responders achieved it before starting Nivolumab. So the responders were largely due to BAT alone. That is within the expected range of responders in previous trials of traditional BAT given the low sample size. The increased "pro-inflammatory" response in paired biopsies in the responders is very interesting. Perhaps yet another mechanism for benefit from BAT, at least for some. Nivolumab does not appear to me to be worth the added toxicity.

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