Experience with Triplet therapy followed by IMRT and SBRT
Hello and thank you for reading this. I’m 62, G9 with 3 bone metastases and a couple involved small pelvic lymph nodes (de novo oligometastatic prostate cancer). Currently, I’m on dual hormone therapy and will begin docetaxel in mid August (6 cycles, one every three weeks). The plan after chemo, assuming all goes well, is to have radiation to my prostate and to the spots where mets were. I will remain on hormone therapy for a year after I complete radiation. I know I need to hit this as hard as I can from the start but it seems like such a large undertaking and I don’t know what to expect along the way. Not sure how I will feel during chemo and radiation.
I was hoping to hear from some of you, who have been through the same treatment, what your experience was or currently is, how you handled it, and how you’re doing post treatment.
Thank you in advance for sharing your experiences. I really appreciate your support.
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We got by with one pair. We kept them ‘assembled’ in our freezer and fill a small cooler with bags of ice, load the frozen mittens/socks, top it off with more bags of ice, and take the cooler. We put the mittens/socks on 15 min before the start of the docetaxel which comes first and left them in til about 15 after the Carboplatin, a total of 1:45-2hrs. Some say it’s only the docetaxel that can impact neuropathy, but we just kept them on. If the items don’t stay cold, we have the ice… but haven’t had to go that route. If you can afford a 2nd pair , that would be awesome if you can keep them cold. Good luck and from what I hear of neuropathy from chemo, it’s work the effort.
@wooldridgec
Thank you for posting this.
Hubby is doing triplet therapy now for stage 4 G8.
First round of six chemo done.
His also manifested in extreme back pain. Relugolux helped tremendously within a couple of weeks. Darolutemide and docetaxel added.
We have an appt to talk to the radiologist right before round 2 of chemo. Not sure what to expect.
His GP delivered the diagnosis in a way that made us think there was really no hope. After appointments with the oncologist and other specialists, we now know while there isn’t a ‘cure’, there’s hope.
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