I thought about posting this a few days ago, and the recent post on chemo by AlvinSD reminded me to do it. It's been a full week since I did my 5th Pluvicto infusion, and I am still suffering from some side effects. Some of those SEs are new to this infusion, some are ones I experienced after prior sessions but are worse this time.
While I can't be sure, I attribute this primarily to insufficient hydration this time around. For all four of the prior infusions, I made a point of drinking LOTS of fluids not just on the day of (and after) the treatment, but for a few days BEFOREHAND. This time I had been suffering some non-cancer-related back pain for the few weeks prior and had not been sleeping well at all. I was exhausted, groggy and depressed during the days leading up to my Pluvicto and I completely neglected any conscious effort to pre-hydrate, let alone stay well-hydrated on that day. Trying to catch up the day after isn't gonna cut it.
Fatigue has been much worse, and still persists. I am having minor headaches and generally feel like crap. My appetite exists but has not returned to normal, as I am only happy now with carbs like bread, beans, pasta and fruit and even the thought of many vegetables, healthy-fat and high-protein foods -- that I normally enjoy -- can repel me. [Actual nausea is the one side effect I am experiencing LESS OF than I did with a few prior infusions, thanks to taking Zofran (ondansetron) for a few days. I highly recommend this medication for preventing nausea... it worked not just for the Pluvicto, but for the contrast used with CT scans that had been causing me problems.]
A side effect new to me arose with this infusion: dry mouth. Even after a week, I am finding I need to sip something multiple times during the night, mouth completely dry. This is not due to dehydration I am experiencing NOW, but it seems to make sense that my salivary glands could have suffered due to the dehydration I was experiencing last week.
Maybe it's just the the glands took more of a hit this time because they got increasingly PSMA-avid relative to the cancer cells in my body. But that's not something I can control. Drinking water is. So please remember to stay WELL-hydrated with this therapy!