Hi-Risk/Recurrent/Advanced PCa Video Chat, March 31, 2025
- You can find out more about our 11 monthly prostate cancer meetings at https://ancan.org/prostate-cancer/
- Sign up to receive a weekly Reminder/Newsletter for this Group or others at https://ancan.org/contact-us/
- Under 60 Stage 3&4 Prostate Cancer – 2nd Thursdays @ 7pm Eastern in AnCan Barniskis Room
- Men (Only) Speaking Freely…1st & 3rd Thursdays @ 8.00 pm Eastern https://ancan.org/men-speaking-freely/
- Veterans Healthcare Navigation… 4th Thursday @ 8.00 pm Eastern https://ancan.org/veterans
Complete Richard Wassersug’s E2/estradiol survey – open to all https://qualtricsxmxjhxcwlhx.qualtrics.com/jfe/form/SV_2h2GxUXB1lWMT9I
Editor’s Pick: Mutations that favor and hinder Pluvicto success (rd)
Topics Discussed
CDMRP Prostate Cancer Research Program; new Pluvicto FDA approval; after 12 years, 78 yr old reaches 4+4 and must consider treatment; more around staying on bone strengtheners; could E2 be a twofer for bones and ADT?; which mutations enhance and which hinder Pluvicto; AUS complicates other surgical procedures; E2/estradiol survey to be presented at AUA25; RT proctitis; switching to Yale Smilow;
Chat Log
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John A
sent: 5:16 PM
If you are currently a reviewer, please send me a chat message. thanks, John dr.john@ancan.org
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Doug D Portland, OR
sent: 5:17 PM
Doug DuFresne participated
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Gary V Portland, Oregon
sent: 5:18 PM
Cut for 2025 was 57% of 2024 budget ..from $1.509 billion to $650 million
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Gary V Portland, Oregon
sent: 5:23 PM
That info came from “Perplexity” I did not do the math…
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AnCan – rick
sent: 5:27 PM
rd@ancan.org
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AnCan – rick
sent: 6:00 PM
Axumin
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AnCan – rick
sent: 6:07 PM
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AnCan – rick
sent: 6:07 PM
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Len Sierra
sent: 6:30 PM
APR-246, also known as eprenetapopt, is a small molecule that reactivates mutant p53, a tumor suppressor protein, and has shown promise in treating TP53-mutated cancers, particularly in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML).
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Len Sierra
sent: 6:31 PM
From ASCO GU 2024: TITLE: Association of prior PARP inhibitor therapy with response to 177Lu-PSMA-617 (LuPSMA) in men with DNA damage repair (DDR) mutations.
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Len Sierra
sent: 6:32 PM
Conclusions: Prior receipt of PARPi therapy appears to negatively associate with the clinical activity of LuPSMA. These data support the hypothesis that PARPi therapy may lead to clinically significant cross-resistance with LuPSMA