Prostatectomy + RT + ADT

Georges Calvez
Georges Calvez Member Posts: 547 Member
edited October 2018 in Prostate Cancer #1

I have created this new topic to document my case which I believe may be interesting to members .

I was diagnosed shortly after my 55th birthday with a PSA of around 130 and no other symptoms, nothing, nada, everything worked absolutely normally; I had a small prostate with about 40% of it filled with a Gleason 7 tumour. and seemingly not a lot else; nothing in the bones or internal organs that any scan could see
I have subsequently gone through an laparascopic prostatectomy; there are bad bits to these that only those that have shared them can tell you about. The gas pains, in France they give you ketamine for the postoperative pain and it results in hallucinations for a few days, bad constipation for a week and the odd nightmare for months after, the weeks after the catheter removal when you think you will never hold your pee again, etc.
Five weeks after the operation I had a PSA of 2 that fell to zero after a few weeks on Firmagon.
I have had 66 Gy of radiation plus 6 months of Firmagon now and I probably have another two and a half years, maybe less as I am doing so well or maybe the dreaded Luperon.
I am hoping that the residual cancer was concentrated in the urethra, bladder neck, etc which has been given an extra zapping or in the immediate pelvic area that was given a gentle roast, that and the Firmagon will hopefully destroy any little satellites.
I could be dead in more than five to fifteen or more, I  was a scientist and then I worked in IT so I am a bit of a dab hand at data but there is really no way to know.

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Comments

  • VascodaGama
    VascodaGama Member Posts: 3,707 Member
    #2
    Open RP

    GC,

    Thanks for sharing your story. Nowadays rarely we read in the forum from guys that did open RP. I am one of the open group too. My experience was easy with no troubles. I had the surgery in Japan done by an experienced Japanese surgeon, who was the director of the urology and in charge of the operations. His policy was not to discharge patients with the catheter on, so that made me stay at the hospital (big one) for additional 12 days.
    Along that period I benefited from the services of the many professionals (doctors, nurses and staff) that visited my room everyday checking everything. It sounds luxury when comparing with the guys on robot surgeries that go home 2 to 4 days later, but that was the standards. There were no robots around in those times and everyone were treated equally.
    In spite of the privileges I received from the several specialists, I still recurred and had to go through radiation and ADT along my 18 years as a survivor. I did it in sequential not as a combination therapy that is nowadays very much on demand. 

    I do not understand where you base your comment regarding survival. Were you classed on stage 4?

    I hope that you have fully recoperated from the interventions and want to listen about your zeros soon.

    Best wishes,

    VG

     

     

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #3
    Corrections

    Hi Vasco,

    I wrote the above rather quickly and late at night as it was originally posted in another thread so it has a few tiny errors.
    My surgery was actually laparoscopic so manual but done through small holes, a half way house!.
    The big debate is if the residual cancer evidenced by the post operative PSA of 2 is associated with the bladder or other structures or has gone off and formed micrometastases elsewhere.
    As far as anyone can tell I have not got any metastases in my bones or soft tissues on the basis of technetium scintillography, gadolinium MRI and iodine x ray.
    Pre operatively I was a Gleason ( 4 +3 ) 12 cores positive, post operatively I was staged pT3b pNO with peri prostatic, capsular and seminal vesicle invasion but the nerves were clear and as far as the surgeon could find the lymph system as well, so there is good and bad news there.
    I am on ADT for two to three years so I think I can bank zeros for those years and then maybe for at least a year or two after, after that who knows?
    If it does progress then I think it may progress quite slowly.
    One thing I know is that I am already pretty lucky most men with a PSA of 130 have got metastases all over the place, I am completely clean or only have tiny and at the moment undetectable ones.

    Best wishes,

    Georges

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #4
    Next twelve months

    Visited the urologist this morning, as I expected there is nothing to do in terms of scans, so it is now a waiting game.
    I have another twelve months of degarelix aka Firmagon and then we will see.
    Next blood test at the end of December, hopefully another zero as a Christmas present for me and my wife.

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #5
    Birthday

    It is my 56 th birthday tomorrow.
    I have lived a fairly stormy year with PCa, from the initial diagnosis when things looked bleak, through the RP, the radiation, etc, to now when things look better and I am in a  waiting game.
    Last night I told my penis, onwards and upwards but he was not listening!

    Best wishes all,

    Georges

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #6
    Circular letter

    Hi everybody,


    I have just had my copy of the circular letter sent from the urologist to the radiotherapist, general practitioner, me, etc, after our last meeting and it says not less than eighteen months of ADT.
    This is sounding a lot better than the two to three years that may have been on the table only three months ago.
    Two years or less may offer me more of a chance of fishing something out of the fire in terms of having the protective effect of testosterone recirculating in my body and even my sexuality.
    On verra, but I think stop after two years of Firmagon, if the cancer was undifferenciated and localised, maybe it really is all dead, and I can walk away, another year will have a lot of effects on me for not a lot of gain in terms of killing the beast.
    There is nothing to show cells with a Gleason number greater than four, OMS three.
    If I have metastases then another year may not matter a lot.

    Best wishes to everybody in your own private battles,

    Georges

  • VascodaGama
    VascodaGama Member Posts: 3,707 Member
    #7
    Longer ADT period in combos for aggressive cases

    Georges,

    I think that the ADT 18 months is attributed to your initial diagnosis (Gleason rate 4 in 12 cores) and stage pT3b. It is aggressive and the results of longer periods in ADT in the combo HT+RT have been better.

    ADT in RT wars works with two principles. It sensitizes cell's AR for better absorption of the radiation and it prolongs the radiation effects along cell's life cycle. This period goes from two to six months in one single cell but the longer period on ADT will also cover the cycle of newer cell's replicas that could have survived the RT's DNA destruction. I hope you manage the side effects and tell us about the good results when the ADT effects vanish.

    Congratulations on the low PSA. This is your first zero.

    Best wishes,

    VGama

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    edited January 2019 #8
    Update

    Hi Everybody,

    I have just updated my PSA timeline with my last result in December.
    I now have very high blood pressure and my blood glucose is close to type 2 diabetic with my cholesterol creeping up but my weight and BMI remain broadly constant.
    How far I will return to normal when the hormone therapy ends is a moot point, some men recover and others quite frankly do not.
    We do not have any data like a SHBG and testosterone assay prior to the debut of hormone therapy so all we can say is I am relatively young which is good but hypertension and a high blood glucose are not good omens.
    The good news is that metformin at 500mg twice a day does not seem to have any adverse effects but the effect on my glucose level is so far unknown, irbesartan has bought my blood pressure down but not by enough.
    I will be so glad when the hormone injections stop.

    Best wishes,

    Georges

  • VascodaGama
    VascodaGama Member Posts: 3,707 Member
    #9
    Interaction of drugs

    Just a note of precaution regarding the interaction of nsaid with high blood pressure drugs. Ibuprofen may be involved in your hypertension due to the hormonal manipulation and supplements. Do your research (webmd) on the matter and discuss with your doctor.

    Hope for the best.

    VG

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    edited February 2019 #10
    Ibuprofen

    Hi Vasco,

    I have already discussed the ibuprofen with the medecin traitant and there is no problem.
    If my psoriatic athritis bothers me I take it for a few days, same with the injections of Firmagon which hurt on the second day.
    I like www.drugs.com for researching drugs, the professional bit is really useful.

    Best wishes,

    Georges

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #11
    March PSA, etc

    Hi Everybody,

    Went down to the lab this morning for the pris de sang, resultats ce soir!
    Champagne and bennies or whisky and nembutal ce soir! :-)

    Best wishes,

    Georges

  • hewhositsoncushions
    hewhositsoncushions Member Posts: 411 Member
    #12
    Eh Bien, mon ami. Bon chance!

    Eh Bien, mon ami. Bon chance! I suggest Champagne washed down with Courvoisier!

    H

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #13
    One in the eye for Eeyore

    Hi there,

    This is one in the eye for Eeyore with his 'You're going to die young Christopher Robin!'
    Hopefully Tigger will be ecstatic and I will get off the degarelix in September.
    It is doing my head in.
    Parrrty tonight :-)
    25 March 2019 < 0,05 Architect Abbott chemiluminescence CMIA ( sérum )

    Best wishes,

    Georges

  • hewhositsoncushions
    hewhositsoncushions Member Posts: 411 Member
    #14
    Bravo sir!

    Bravo sir!

    I assume T levels were checked and are still low?

    H

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #15
    No point

    Hi Cushions,

    There is no point in testing the testosterone all the time on degarelix, it heads for the deck and stays there.
    One of the arguments for the superiority of degarelix over luprolide is that there are no microsurges after each injection which happens with some men on luprolide, this drips a little life to the cancer.
    There are also GnRH receptors on some types of prostate cancer cells and degarelix may block these as well, quite what the effect of this is no one seems to know.
    I am just hoping that I recover some testosterone when this stops.
    I lie there at night swearing at my leg pains, it drives the wife nuts.
    Off to drink Leffe and eat Toulouse sausage and chips.
    I am going to beard Tigger in his den 9:45 Jeudi matin!

    Best wishes,

    Georges

  • hewhositsoncushions
    hewhositsoncushions Member Posts: 411 Member
    edited March 2019 #16
    By eck I miss sausage and

    By eck I miss sausage and chips :)

  • Josephg
    Josephg Member Posts: 460 Member
    #17
    Super News

    I am so happy for you, Georges.

    I will toast you tonight!

  • VascodaGama
    VascodaGama Member Posts: 3,707 Member
    #18
    Zeros are always wellcome

    While having zeros is to celebrate I would prefer to have the champagne (Magic Door La Cle de la Femme Brut is my choice in celebrations) when the T levels are back to normal in close future.

    In any case I will toast this moment with a glass of my best red.

     Congratulatioins.

    VG

  • hewhositsoncushions
    hewhositsoncushions Member Posts: 411 Member
    edited March 2019 #19
    I think George's celebration

    I think George's celebration is around the fact that Eeyore predicted a lapse even whilst he was still inder the influence of hormones.

    H

  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #20
    No lapse for me!
    Hi there,

    My reasoning that I would not lapse was based on the following article;
    Hein Van Poppel, Lawrence Klotz, Gonatrophin- releasing hormone: An update review of the antagonists versus agonists International Journal of Urology 2012 19 594-601
    https://onlinelibrary.wiley.com/doi/epdf/10.1111/j.1442-2042.2012.02997.x

    Best wishes,

    Georges
  • Georges Calvez
    Georges Calvez Member Posts: 547 Member
    #21
    They seek him here, they seek him there, etc

    Hi Everybody,

    So here I am the day after the great rendevous with Tigger, we had  a case review and agreed on the following;

    Neither the MRI, CT scan or Tc scintillography showed any sign of metastases
    The biopsy showed no sign of cribriform
    The post prostatectomy examination showed no sign of nervous invasion but there was extra capsular extensions and invasion of the seminal vesicles
    My PSA fell remarkably post operatively from > 144 to 2.07
    It fell by up to 83% in around twelve days after the first Firmagon injection giving me a PSA half life of less than 0.1 months

    We agreed that the remaining postoperative cancer may well have been in the prostatic fossa but there is no way of knowing.

    Tigger then said that maybe it would be a good idea to go for two years, I told him that I was not happy with this and that I wanted to stick with the eighteen month plan.
    We agreed on eighteen months if my PSA is zero at the end of Sptember.
    I told him that if my PSA was not zero at the end of September considering that I would still be on degarelix then I would be in deep trouble and he agreed with this.
    So I will have to have a think about this eighteen months, maybe twenty one months, that would be eighteen months with non detectable PSA, or maybe two years?
    The longer I stay on degarelix, the less likely I will recover testosterone, etc and some normality, but maybe an extra few months will make a difference to the cancer or maybe not?
    These questions are essentially unanswerable but I have six months to think about them.
    Anyway I am feeling fit and well so I have a programme of walking, gardening, French improvement, etc to get on with.
    Circular letter to me and the doctors to look forward to next week.


    Best wishes,

    Georges

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