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lynparza possiblity

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Posted 1/24/2020 2:22 PM (GMT 0)
Its been awhile since i have posted about my situation.i am still on xtandi for the 5th year, but my psa has increased to 32,from a low of .020.my scans show no growth of the mets.doc wants to continue on xtandi for awhile yet.he says lynparza would lower my psa some.has anyone here tried it?
Posted 1/24/2020 3:36 PM (GMT 0)
Its beyond my paygrade...but keep your faith and hang in there Captain


Mickey Childress(short e)...the name creates a character from a tale of which slides by me as a graze...from where and how...I know not...but the aura speaks well...no bull...good on ya mate...
Posted 1/24/2020 11:29 PM (GMT 0)
bump...alls I can do my friend
Posted 1/25/2020 12:46 AM (GMT 0)
Hi Mickey,

Have you been tested for the BRCA mutation?

You might want to change your subject to Lymparza to get more specific responses.

Jerry L.
Posted 1/25/2020 4:12 AM (GMT 0)
plus get your signature back up...its been awhile...and folks don't usually remember or bother to seek you out...tho some do...bless their hearts..er ah...no not me...ahem...Oh yes...umm...good luck...
Posted 1/25/2020 12:44 PM (GMT 0)
I know nothing....
Here's a Bump.
Posted 5/30/2020 9:16 PM (GMT 0)

Hello, Mickey Childress -----

You were looking at some possibilities a few months back ...

Wondering how you are doing, and how things are going for you?

We'll watch for your posts, and check for your updates.

Hope this finds you faring well & feeling your best, as we all set our sights on the summer ahead.

With my best,
Cyclone --- Iowa State University
Posted 6/1/2020 3:05 PM (GMT 0)
i havent had any scans yet after starting the lymparza.my psa continues to rise now to a level of 50+.side effects are a little rougher than the xtandi.i cant taste food nearly as good on the lymparza,but i am tolerating the other side effects pretty well.still no energy.i get scans this month,hopefully they will show some improvement in diminishing the spots on my bones.
Posted 6/1/2020 4:10 PM (GMT 0)
We're in the same HW in-coming class, late 2013.
You're more advanced than I, thoughts and prayers are with you brother!
Posted 6/1/2020 4:12 PM (GMT 0)
i do have the brca gene.
Posted 6/1/2020 9:01 PM (GMT 0)
Mickey good luck with the scans, please keep us posted.
Posted 6/2/2020 11:47 AM (GMT 0)

Keep us posted, Mickey. We all want the best for you.

Hope your scans show improvement.

Keep us posted and let us know how you're faring.

With my best,
Cyclone - # Iowa State University
Posted 6/19/2020 1:22 PM (GMT 0)
looks like the lynparza was a bust.psa went up again,scans showed spots were slightly larger.i start taxotere next week.heres hoping i can take the side effects and it works.
Posted 6/19/2020 6:23 PM (GMT 0)
Lynparza is a PARP inhibitor, one of the new genetically targeted treatments..I've been on it now for 2 weeks.. To early to tell if it's working..I'm running out of options....I did get a good response from the chemo ( taxotere) but side-effects were rough. Total hair loss and nuroplasty in my feet which you need to be careful with..It can be crippling.. Cabazitazel (Jevtana) worked better with fewer side-effects..Good luck to you..
Posted 6/20/2020 3:39 AM (GMT 0)

Hello, Mickey •••

Many of us here have pursued TAXOTERE chemotherapy infusions.

Be sure to use the search icon on the top of your screen and search for this thread title:

"Taxotere Side Effects"

It was started by Madeline Smith, and many of us here banded together and put together all our first-hand experiences.

Read through it, and you will find helpful navigational tips, and ways to mitigate side effects.

We're here for you, Mickey.

Stay strong, stay determined, one day at a time,
Cyclone ~ # Iowa State University
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