Have bone mets but been on Nubequa since 01/22 and have more mets now at Sacrum and tail bone. Orch last year with good PSA since. Either 3D or IMRT to start soon x 10 days for 3D, (not sure time for IMRT). RO says mets there on scans of 2/22 but small, now larger. We didn't know. MO wants to start Olaparib (Lymparza) 30 days after finishing radiation, but to stay on Nubequa with it. Foundation report on liquid biopsy says good results with Olaparib, Zytiga, and Prednisone in a Phase 3 trial. This is the wife and he is 80 now. Appreciate any comments.
Anyone on Lymparza with positive resu... - Advanced Prostate...
Anyone on Lymparza with positive results?
Good luck with the trial!
He's not in a trial? Am I missing something your saying TA?
Would you mind sending me a message to explain? I'm the wife, 78 years old, and trying my best to understand this disease by myself. He can't help. So if I ask dumb questions, it's because I'm trying to help him. But, I've had questions about his treatment. And I appreciate you people more than you know. Thanks
Did they study if the cancer has mutations making it susceptible to treatment with Olaparib?
Yes, a mutation CDK12
Have biallelic BRCA2 - using Olaparib for 18 months bringing PSA down to 0.1. Almost no side effects, swallowing the pills with yoghurt.
Radiation induces SSB, single strand breaks in the DNA threads. Olaparib which is a PARP inhibitor prevents the cancer cells repairing SSB. This leads to double strand breaks. If you have the BRCA2 loss of functionality the cancer cells can not repair DSB and the cells die.
Thus it makes sense to start Olaparib just before radiation.
Thank you. His MO wants radiation first, then start Olaparib 30 days later? His psa the first of Sept. was still down, <0.1. He has had an Orch. Did you take it with Zytiga and Prednsione or any other drug? Thanks
Is there literature supporting this? Sounds interesting... Would love to be able to read and share with my MO as well.
Thanks
The most relevant documentation: aacrjournals.org/mct/articl...
Appreciate the link, thank you. But I will say that exhibits results vs Pancreatic Cell structure, not PCa. And my MO and O have gone down this road before, and I do agree somewhat, that it's apples/oranges when comparing different cancers (cells). What works for one does not often translate to others, Interesting otherwise we would all be using the same drugs regardless of the the cancer, which we know doesn't work so well.... I may forward to him regardless.
Thanks again
I have BRAC2 and Lynparza reduced PSA from 20 to 2 in 3 months.
I just want to say monitor your husband closely on Lynparza. After 5 months my guy ended up in the hospital. Stopped eating and drinking. Dementia like behavior. Organs began failing. Took months to get him back up and about again.
Thank you! I do have concerns about this med and is it even right for his mutation? Is he ok now? Did all those symptoms leave? Thank you for responding and wishing you both all the best.
he has the BRCA2 mutation. He recovered but it took at least six months to get him back on his feet. I wish I’d pulled him off sooner. We went to Jevtana after that. He’s finished that and did OK on it. But his PSA is rising again. We’re still hoping it’ll stabilize. But we’re preparing for LU 177 if it doesn’t. Of course, the problem is that it’s not that available in the US yet. Even though the FDA approved it in a limited number of cases. He’s in that number but it doesn’t help if you can’t get it.
My husbands mutation is CDK12 and Lynparza does not work on it as well as on BRAC2. Do you mind me asking how old your guy is? Mine is 80 so all treatments are scary. Not sure where you live but Duke U is using Pluvicto, which I think is LU177? Also MD Anderson in Houston is but says it's hard to get the meds. used for it. Glad you found a med he's tolerating. I guess with all meds, there will be some who have more trouble than others tolerating it but cannot imagine how scared you both were. So glad he's back on his feet. Our MO says he will need to have monthly labs while on Lynparza.
My guy is 68. Diagnosed 6 years ago. Stage 4 with extensive bone nets. PSA over 1,500. We’re in Atlanta. From what I’ve been told only one hospital about an hour from us has LU 177 right now in N. GA. I’ll do more research soon if PSA doesn’t level out from Jevtana
Best of luck in finding what you need.
My husband had a good 8 month run with Lynparza. Little or no side effects, thankfully.