Hello,
I would like to ask, what is usual to expect after Docetaxel + Hormonotherapy?
Thanks.
Hello,
I would like to ask, what is usual to expect after Docetaxel + Hormonotherapy?
Thanks.
Not sure about the question? Do you mean the disease or side effects or something else? What stage and Gleason is your cancer?
My father was diagnosis of prostate adenocarcinoma, Gleason (3 + 4), initially staged with a T2b N0 M0, last year, at the age of 60.
On May 1, 2019 he underwent radical radiotherapy without hormone therapy. Completed treatment on May 22, 2019. 5 intense sessions. PSA after treatment dropped from 9.3 to 7.6.
However, starting in March 2020, he had biochemical recurrence criteria, underwent examinations and presented bone and ganglionic metastasis with a PSA of 47.5.
It was suggested by his doctor to do hormone therapy with an LHRH analogue and evaluation in Medical Oncology to perform concomitant chemotherapy (docetaxel).
He also started with the treatment (just one session).
Yikes that is pretty aggressive for a Gleason 7. Yes the current standard of care would be Lupron or similar and chemotherapy for 6 cycles and see how he responds. He should respond pretty well for several years I would think. The side effects are not pleasant but I worked the entire time of chemo except days 7-10 after the infusions.
I think something is wrong with the diagnosis. I wasn't supposed to be in this situation right now: /
I’m a little surprised that radiation was used instead of surgery. Was surgery an option?
I cannot say because I was not at the multidisciplinary consultation.
I think that at least it was not placed as the best chance for his problem. The radiologist say after treatment that everything went well, and said to my father that he doesn't worry about the prostate anymore.
Why would "surgery" be an option, given the diagnosis, "T2b N0 M0", so wondering your assertion?
This was in a diagnosed curable situation, furthermore, even knowing now that it became spine (ganglion) mestatisis.
Sounds like he's on a good treatment plan. I've been through chemo and it was well tolerated for me as it is with most. I sat around a lot for the first 5 days of each cycle, but still able to do light chores around the house and even cooked. I never lost my appetite (I actually gained weight) and never threw up. Had runny eyes and some diarrhea, leg and ankle swelling, but that's about it. It all went away.
He's probably going to see his PSA decline from the combination of the androgen deprivation therapy and chemotherapy. Sometime down the road, hopefully in long time, he will eventually become castrate resistant and need to add another drug like Xtandi or Zytiga. That could be a long time from now so you just have to put one foot in front of the other with this disease. That's what I had to do, especially at the beginning when everything was so overwhelming,
Wishing the best for him and you.
It has been difficult to accept that the disease could have been better controlled at diagnosis. I don't know...
Our family has been very discouraged.
We are afraid, because it looks like a sentence.
I know where you are at from the patients side of it. It's tough to take for sure and scary because you don't what to expect. I went straight to stage 4 with a PSA of 463 at diagnosis. I was in total shock, figured I'd have a year to live at most. Here I am 3 1/2 years later and my life is fantastic, even with cancer.
Do everything I can to fight the cancer, but I'm also determined to have the best life I can have as long as I can.
I do remember how it was in the beginning. I found that just taking one step at time kept me from being overwhelmed. Like: the next step is I have to have a CT done or the next step is I have an appointment with the doctor, etc. and just get through things one step at a time.
Don't be afraid to reach out for help. I got some counseling that really helped me a lot.
A sense of discouragement is expected but not permanent and not necessary. My father was diagnosed about age 74 with stage 4 and lived until age 83. During this time I was diagnosed at age 44 and my father inlaw now is in stage 4. I suppose in my own way I have accepted that I have disease. I will pursue the best treatment avaialble. I recognize that I am mortal and that I will die. I do the best that I can to not let worry and anxiety of what lay ahead ruin the days that God has given me to live no matter how numbered. Disease and poor health can rob the patient and their loved ones of happiness and time if we dwell too much on it.
I am surprised he didn't receive an ADT drug before and during radiation.
To answer your question an ADT drug would be the next step. I would start with Lupron then add casodex if needed.
Here's the optimal sequence:
prostatecancer.news/2019/12...
But maybe Xofigo if there are bone metastases, pain and no visceral organs are involved.
If it was a truss biopsy it might not have correctly located the full extent of the tumour(s) or lesions. In that case the treatment might have not been adequate for the stage of the disease. That is the only reason I can think that this turned to BCR so quickly.
Sorry, but what BCR means?
Thank you for your time.
I am open to recommendations that can help my father to better results.
Sorry, but what BCR means? YOUR QUESTION, answered by Tall_Allen 11 months ago.
Tall_Allen•
11 months ago
While there is a standard definition of biochemical recurrence (BCR) after prostatectomy (i.e., confirmed PSA ≥ 0.2 ng/ml), there is a confusing array of definitions of biochemical recurrence (BCR) after salvage radiation (SRT). I'm not sure that we're ready for a standardized definition yet. And perhaps the definition of the FIRST BCR bears scrutiny.
pcnrv.blogspot.com/2019/08/...
Good Luck, Good Health and Good Humor.
j-o-h-n Thursday 07/09/2020 4:59 PM DST
Thank god for chemo I say
I was in loads of pain had to quit my job as a result
I had mets all over the place
Sturnum ,shoulders ,pelvis ,spine and ribs
After treatment
Very small residual amount left 7th and 8th rib
Clear everywhere else
Moving on to targeted radiotherapy to the prostrate on the 21st
K would be back to work if not for Covid
I feel 100% better now
It was worth the days of fatigue and hair loss
My PSA is now 1.54
It was 13.5 when diagnosed
My hormone drug is Decapeptyl
My side effects were mild
I trained most days after chemo
I am a bodybuilder
I find resistance training works wonders for restoring energy keeping my appetite and strengthens my body
I am very appreciative of what medicine has done
JNunes, sounds normal. For example, in 2003 at age 56, I had Brachytherapy followed by 25 sessions of IMRT with a PSA of 6.7. I was given a 92% success rate. At 10 months I had two mets. My research medical oncologist told me to not second guess my primary treatment as minute cancer cells had already escaped. This is called micro-metastasis where the unseen cells travel through the lymphatic and vascular systems. Kind like the lick of the draw.
In 2004, I immediately enrolled in a six month chemotherapy plus hormone therapy trial. I was most fortunate to be able to stop Lupron in 2010. Today, at 73, I remain undetectable, <0.1 PSA.
Keep killing the little bastards. Worrying is your enemy. You are on the right track. Should your cancer progress, Tall Allen has shown you a typical progression of magic bullets in case you need them.......
Gourd Dancer
your story really is v inspiring 💫