Thursday, 13 May 2010

Initial meeting with radiologist

Attended St. Mary's,Newport today with Sue to meet with the oncology specialist who will be overseeing the treatment at the Queen Alexandra near Cosham. The main purpose was to sign the disclaimer (10% - 15% chance of long term impotence and incontinence). The treatment will be for seven and a half weeks (37 days in total) given Monday to Fridays. The aim will be to treat the pelvic area generally to target the known cancer in the lymph nodes there with a concentrated burst after that on the prostate itself.
Apparently it will be easy peasy for the first month but then gets increasingly difficult as the cumulative effects start to kick in. This will be reddening of the skin ,bleeding, fatigue and diarrhoea for starters. Not got a start date yet but given that they like to have 3 months of hormone treatment first (to shrink the prostate) I am expecting it to be the latter part of June or early July. Great news in that our booked trip to Lords for England v Bangladesh Test with overnight stay in Central London is still on!
I had a blood test a couple of days ago and the PSA level is down to 0.7 which is the expected result of the hormone treatment. Other effects have been weight gain (comfort eating) -diet now underway (hide the crisps and biscuits).Hot flushes have started which only last a few minutes but occur throughout the day. We have booked a consultation with the erectile dysfunction nurse - Viagra was mentioned and that will be the subject of my next blog.

Thursday, 22 April 2010

First 3 monthly hormone injection

I have had the first of what will be one every three months hormone implants. The drug is Goserelin (Zoladex)which is injected into the abdomen after local anaesthetic. It is in the form of a pellet about 1cm long and 2mm thick and can be felt under the skin. Here is the boring science bit - it is a gonadotrophin releasing hormone super-agonist (GnRH agonist)also known as a lutenizing hormone releasing hormone (LHRH). The effect is to inhibit production of testosterone and estrogen (it is also used in the treatment of advanced breast cancer).
Prostate cancer cells and some breast cancer cells are hormone dependent so when the hormones are eliminated the cancer cells are inhibited.
So how is this making me feel -well pretty good actually. Apart from the dreaded loss of libido (all too evident!)I am feeling OK in myself and have taken a different view on life and the meaning of everything. My wife, family and friends have been very loving and supportive and I have become even more in touch with my feminine side!
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Tuesday, 6 April 2010

MRI Scan results

Just got back having had the scan results revealed. Quite good news all things considered. The cancer has been staged as T3a N1.
Basically this means the cancer has spread into surrounding lymph nodes (potentially not good) and is breaking through the capsule of the prostate - known as locally advanced disease. Considering the specialist reckons I have had this for up to 15 years this diagnosis is better than worse case scenario. If the cancer had spread to nearby organs such as the bladder neck,back passage or pelvic wall then it would have been categorised as advanced disease. The scan shows that the cancer has not spread to other parts of the body (metastasised)as far as can be established - (micrometastises cannot be detected but may be there?)

So the next step is an appointment with the radiologist specialist on 13th May. I will undergo a course of daily treatment over several weeks at a Portsmouth Hospital while continuing with the hormone therapy. It is hoped that the hormone therapy will shrink the cancer cells prior to the X-ray treatment.
The blood test for PSA levels came back at 11.1 - down from 47 at initial diagnosis so this shows the hormone treatment is working.

Monday, 5 April 2010

Hormone treatment - mind and matter!

The treatment I am having so far is called an androgen blockade. This is designed to cut off the production of male sex hormones with the hope of shrinking and slowing the growth and spread of the cancer cells. In the past this was acheived by castration and this still remains a posibility further down the line. The tablets and injections are categorized as chemical castration and the thought of having this treatment is not a happy one for the average male. This is a similar treatment that is offered to some American sex offenders and you cannot avoid being affected both emotionally and physically.

My wife is very understanding over my concerns which typically are far more important to a man than a woman. Her response has been that I have "had a good run". I am grateful that this is true but it is difficult to realise that something you hold dear may have come to an end.

The all too obvious effects of impotency have increased as the days have gone by and the refusal of my "equipment" to perform is not yet in tune with what my mind wants.This may sound like the least I should be worried about given a life threatening condition but the fact is at the moment it is the main thing to occupy my thoughts given the fact I am not in pain and do not yet have a prognosis.

Typical man,thinking about sex six times every hour (Prince Charles quote).

First hormone implant

Its the day after the second MRI scan and a trip to my home doctor for the first hormone injection. This is given in the stomach and was painless. I laid horizontally on the couch,loosened my belt and was given a local pain killing injection. Then the actual implant was injected and I didn't feel a thing. Nor could I feel anything under the skin afterwards.

This dose is for 4 weeks and then I am to switch to three montly injections. The initial course of tablets stop in two weeks and are to prevent this injection causing tumor flare. As I understand it the injection causes a temporary spike in testosterone (opposite to what is required) and this can cause the tumor to flare or cause pain in any areas it may have spread into,commonly the bones.

I book one more blood test as it is back to the urologist on 6th April. He will announce the scan results and hopes the blood test will indicate that the hormone treatment so far will have resulted in a PSA score down to single figures.

The MRI scans

Having started on the hormone therapy the scan appointments come through. Two are ordered. A pelvic scan and a full body scan a week apart. The first is the pelvic scan carried out at St. Mary's Magnetic Resonance Imaging dept. I'm first in at 08.30 so no waiting. Strip off to underpants and don the robe and go through to the MRI suite. Questionaire to make sure I have no metal implants etc and its onto the machine. Having read up on this and been sent a leaflet - nothing to worry about, harmless, no side effects, maybe a bit noisy other than that easy peasy. Well it wasn't that bad as I was not sucked fully into the machine. It was noisy but I was given headphones through which I could occassionally hear classical music when it was not being drowned out by the pneumatic drill like noise of the magnets.

A week on and its the full body scan. This will take longer (up to an hour)and involves imaging the whole body. Over the week I have become increasingly anxious despite my earlier practice. This session was more difficult. As I was moved further into the machine my mouth went dry and a feeling of panic began. With my ankles strapped together and arms pinned down my sides and the curved roof of the machine inches from my face (keep eyes shut throughout)I fought hard to stay still and supress my fear. After all I have been potholing and would be ashamed if I had to press the emergency button that was being gripped increasingly tightly in my left hand.

After 35 minutes I was extracted from the machine and the proceedure was over. Two teas later in the hospital cafe and I was still rattling the cup in the saucer. Strange really as I really thought it would have been easier than that.

Biopsy Result and Gleason score

Today its off to St. Marys to get the biopsy results.Sue is coming with me to hear the news as we have decided it is important to share this journey together and I am very grateful for her moral support. I have been hanging on to the idea that the high PSA and lumpy enlarged gland may have been caused by stones or something else.

Hopes dashed. The "Gleason Score" is a high risk 8 out of 10 . This is an analysis of the abnormality of the cells taken from the biopsy and is used to determine the GRADE of the cancer (how aggressive it is). Both sides of the prostate are affected. Information comes thick and fast. Most shocking is that the specialist reckons this means I have had the disease for between 10-15 years. He confirms that it will be no good doing a prostatectomy (surgical removal of the prostate) as this would be shutting the door after the horse has bolted. As I am still young by prostate cancer standards he reckons this must be an inherited disease.

Hormone therapy is to be initiated immediately. I am prescribed tablets to start taking tonight. These are to reduce the male sex hormones -androgen's, including testosterone which the cancer cell "feed" on. I am also given a letter for my doctor to give me a further injection of hormone treatment in two weeks time. It is important that I take the oral tablets for one month and have the injection half way through this period. Something about reducing tumor flare?

I make a follow up appointment in a months time before which I have to have two MRI scans to see how far the cancer may have spread - called the STAGE.

Another booklet is provided "Living With Hormone Therapy" and I realise this whole thing is real.