Here's the latest stats regarding my dad's treatment:
Diagnosis July 2018
PSA - 680 (mets to 5 retroperitoneal lymph nodes and 2 bones)
PSA doubled to 1200 in one month!
Began treatment 8/18 starting with Casodex. In one week, his PSA dropped to 470! (just Casodex)
Last week received his first Docetaxel infusion, Lupron and Xgeva. WBC=12
WBC dropped to below 1 today. Received Neuopgen. He will probably do more Neupogen the next few days.
Side effects so far: abdominal pain, intermittent constipation, diarrhea and FOUL gas (lol) Feeling fatigued and worn down. Magase is helping his appetite and nausea.
After my first Docetaxel infusion, my wbc dropped to 0.5. They pumped me full of Neulasta and a week later my wbc was up to 6 something, (within normal range). Don't despair,(If you are) they gave me Neulasta after my next five infusions and everything was good. Sounds like your father is going to get through his chemo treatments just fine.
in reply to
Bill48162-
That's great encouragement! We are nervous about the WBC and I was hoping to hear that this was par for the course. I'm glad to learn that your numbers went up. With a little boost from the Neupogen this week, perhaps his will, too. Thank you for easing my mind.
I would suggest taking a claratin and an aleve the day before , day of and day after nuelasta/Nuepogen to relieve bone pain in legs and hips caused by nuepogen drawing white blood cells out of bones. If his temperature goes to 101, that is an emergency, call the Dr in middle of night. That said I think the Nuepogen will work just fine and raise those WBC.
This forum has truly been one of the most beneficial resources since his diagnosis. I've put a lot of time into researching PCa recently....trying to understand it myself so as to better help him but honestly, all the research in the world can not compare to the real life expressions and suggestions of people actually going through it. So, just today after checking the forum, I went out and got Claritin and a new thermometer! Your helpful advice is helping others! Thanks so much
in reply to
I would recommend getting a professional thermometer, the same ones they use at the hospital. I will not do chemo again without one. I ended up going to the ER with a borderline fever, but had a 3 degree spread between the 3 thermometers we have. It was frustrating and stressful.
in reply to
Oh my Greg57-
That's a good point! I purchased a regular digital from the local pharmacy. Probably not as accurate. I will check into a professional grade
in reply to
I may have made an unnecessary trip to the ER because I couldn't be sure which one of three was correct. When I got there, my temperature was slightly elevated, but below 100.4 so not sure whether it went down on the way or was never really above 100.4. They found nothing wrong and by the time I left, my temperature was pretty much back to normal. I had a lot of stress and some good sized co-pays. I could always argue that it's better to err on the side of safety, but even better to have an accurate thermometer.
in reply to
His wbc will go up, don't worry. It it were me I would keep your father away from crowds, etc until his count raises, which it will. Dan59 gave great advice regarding body temperature. Neutropenic fever is a slight concern. Have his temp checked if he complains of fever like symptoms. He will be just fine. My doctor freaked out when I told her I was out running (miles) with a wbc of .90. Hey, i felt fine! Relax, this happens.
in reply to
Running miles!!!!! That's incredible! Thank you for the positive reinforcement. All of the grandchildren went back to the Petri dish.....I mean......school yesterday. 😃 He will have to monitor visits with them I suppose. When he is feeling better, I suggested a mask.
It sounds like your dad is getting the best medical care possible, is on a good treatment plan, and has a great advocate in you. Dealing with this is a constant learning process, isn’t it?
The neupogen should take care of the neutropenia, and I’m sure they will continue to monitor it regularly. When I had my docetaxel my Neutrophils dropped, but not enough to require Neulasta. Also watch his RBC counts. If his hemoglobin and hematocrit drop too far below the WNL level he may need a transfusion. Mine went below WNL during chemo, but not enough for a transfusion. Having a medical grade thermometer, as Gregg57 suggested, is a good idea...much more accurate. If his temp goes over 100.4 go to the ER.
Most of the other side effects (diarrhea, constipation, etc. can be treated with OTC meds. Gas-X or othe simethicone products may help with the foul gas issue. My wife tells me that my gas smelled like lilacs. 😎
My oncologist prescribed dexamethasone for me, to be taken on the 2nd day after each chemo cycle. It gave me a little boost before I slipped to the nadir.
That's my fear. I'm happy to say the Neupogen is working but we will have to watch him each cycle. Hope that you are doing well. Thank you for the reminder. 😃
Megace for appetite, which he is currently taking, also helps his cancer. I was on it for a while and I gained too much weight but it helped slow down my cancer. It is a female hormone which will add another angle to his existing hormone therapy. If his appetite needs another boost, consider medical marijuana and it may also help with the nausea. Zofran under the tongue is excellent for nausea.
I completed 6 cycles of Docetaxel/Carboplatin chemo in January 2018.
Here are my hints:
1. Med Onc prescribed Aloxi drip before chemo to eliminate nausea and it worked.
2. Prescribed Dexamethasone day before, day of, and day after chemo to moderate side effects.
3. Med Onc suggested 100mg B6 orally daily to mitigate peripheral neuropathy. I also iced my hands and feet.
4. Left each session with On Body Injector of Neulasta to boost white blood cells. Advised by Med Onc to take Claritin beginning one day before chemo and continuing for 6 days to reduce bone pain.
5. Use Biotene products for mouth care.
6. Took Wisconsin American ginseng for chemo fatigue--google Mayo Clinic and ginseng for their trial.
Chemo worked for me, dropping PSA from 10.8 to .4 and reducing liver lesions!
No, I have minor tingling/numbness in right foot and more pronounced tingling/numbness in left foot. Hands OK. Taking Lyrica to moderate. Still taking B6.
I hope it gets better for you Mark. My dad's sister received Chemo for breast cancer and didn't know to take B6 or ice hands and feet. She suffers with horrible numbness that's rendered her disabled. I'm so glad to have learned how to at least minimize the symptoms. Thank you so much
You are most welcome! I have been in this battle for six years (please see bio for complete treatment history), and my calling now is to share my learnings from drugs, radiation, and chemo. My initial prognosis was three years, so I have been blessed for a reason.
Mark
Dear DWDaughter, moral support and love, laughter and empathy are strong healing forces. He has by his side. APC is a bumpy trail..I wont worry about him ,because he has you . Take special care of self so you can be strong for him to lean on. Good Daughter!
in reply to
Thank you Lulu700
in reply to
Your father must be proud of a daughter with such integrity and love for Papa.. That wonderful smile can heal..🦋
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.
First PSA result after treatment 
PSA Rising After Initial Treatment Success - Thoughts On What To Do Next (and When)
Initial Test Results after First 3 Months 
Freaking out over latest blood test results
Advanced Prostate Cancer Treatment
