YANA - YOU ARE NOT ALONE NOW

PROSTATE CANCER SUPPORT SITE

BRONZE

JW Burford and Janet live in Missouri - USA. He was 61 when he was diagnosed on March 19, 2007. His initial PSA was 4.62 ng/ml, his Gleason Score was 8 and although he does not know what his staging was it seems from his narrative that he was staged T1c. His choice of treatment was Da Vinci robotic surgery. Here is his story.

After a regular visit to my Urologist which I have been seeing since 1998 for a Bladder cancer, he noticed I had a much higher PSA reading since my last PSA check a year before. He suggested that I have a biopsy due to the almost doubling PSA rate.

On March 19, 2007 I had my biopsy which revealed adenocarcinoma on the left side of the prostate. The biopsy Gleason Score was 4+4=8. I was then given some treatment options either surgery to remove or radioactive seed implants. I immediately had a bone scan scheduled which was negative for metastasis. I then consulted with a Da Vinci surgeon who indicated that I would probably be a good prospect for that type of surgery.

On April 24, 2007 I had the surgery, spent the night in the hospital then went home the next day and had a normal recuperative period. I suffered moderate incontinence and was impotent. I had my first post-op PSA test on June 12, 2007 which was a reading of 0.62....I then had another on June 24, 2007 with a reading of 0.59. I was then started on Lupron injections one every three months for a projected period of two years.

I also consulted a radiation oncologist who thought I needed adjuvant treatment right away. He made me an appointment with a medical oncologist who after interviewing me and looking at my records agreed that I needed IMRT (Intensity Modulated Radiation Therapy) radiation as soon as possible. My radiation doctor didn't want to start radiation until I was continent or close to being continent, so I didn't start IMRT treatments until September 13, 2007.

I had 35 daily treatments and finished on October 30, 2007. My first PSA reading just before finishing radiology treatments was 0.08. All subsequent readings to date have been <.05 or as low as the equipment would check. It has been 18 months since my surgery and I still am slightly incontinent, mostly stress, however I will have an occasional day where it seems I regress, but then again some days with none at all.

Naturally because I am taking Lupron I have maximum ED (no activity). I did take Viagra for a month or so but saw that I was wasting my money so have put that off until I finish Lupron injections, my last coming in April, 2009. Some additional items that I forgot to mention, the post operative path report...Gleason 4+5=9, positive surgical margin left side of prostate, and seminal vesicle invasion left side of prostate. Tumor involved 30% of prostate, mostly on the left side. Staging pT3b.

I feel fairly well, I do suffer some side effects of the Lupron injection, mostly hot flashes, however slight fatigue and maybe slight depression, however not enough to seek medical treatment. I feel some apprehension as what my first PSA after Lupron will be.....hoping for a lifetime of zeros!!!!

 

UPDATED

August 2009

 

 

I haven't had an update since my original posting on the forum. At that time I was taking Lupron every three months and had been on that regimen since June 27, 2007.

I just recently completed two years of that treatment and all my PSAs were registered at less than <.05%. I had my last shot in April of 2009 and as of today, August 10, 2009, I am still suffering from hot flashes, some fatigue and ED. I was hoping that soon some of the side effects of Lupron would be wearing thin, but not yet.

I have the important PSA test taken in October, which will be the one with no Lupron in my system for 3 months. The Doctor is going to check my testosterone also in October....he says he hopes it is low. I am still waiting for that firmness or stirring that so many of the posters on this forum speak of. I take a 100mg tab of Viagra about three times a week but so far no good.

I wish all members of the forum well, and to keep their chins up, you never know when some scientist might hit on a cure for this dreaded disease.

Best wishes,

J.W. Burford

JW's e-mail address is: jwburford@windstream.net