BCG for male CPPS

Male pelvic pain, prostatitis, IC
jd

BCG for male CPPS

Post by jd »

Any thoughts of BCG for male patients with CPPS....in relation to the NIH funded BCG studies going on at 10 centers across the US now?

I know they are studying this for IC.....but aren't doctors starting to believe that CP/CPPS in is a variant(not sure if this is the right word) of IC?

In relation to that, I'm always wondering how many guys on this board have actually had a cystoscopy and bladder hydrodistention. In my case, my uro. told me I have "classic Prostatitis symtoms," and I had the cyst. and hydro. and it turned out I have IC.

I have read that BCG is one of the most promising future therapies for IC, I guess people who benefitted from it had a long term reduction of pain and IC symptoms from a well executed (but small) study.

Thoughts on all of this?
User avatar
Richard.N
Sage
Sage
Posts: 578
Joined: Wed Oct 30, 2002 6:05 pm
Location: Bristol, England

Post by Richard.N »

I had a BCG jab at school 20 years ago when I was 11, and I sometimes wonder (since I have calcification in my prostate - sometimes associated with TB scarring) whether it wasn't this that set the ball rolling...
Richard

Age: 39. | Onset Age: 30. Onset Date: January 2002. Symptoms (back then): Supra-pubic pain, back pain, urinary frequency, urgency and difficulty, weak stream, nocturia, (and variously) chronic fatigue, IBS. Current symptoms: more frequent than normal, but pretty much under control. Current amelioration: Xatral 10mg, Mirtazapine 30mg. | Worsened By: Stress, binge drinking, strained bowel movements, bloating, sitting on hard surfaces, jogging, and regularly - THE WINTER!

I'm not a medical expert. My comment is opinion. See your medical professional.
User avatar
webslave
Maintenance
Maintenance
Posts: 11432
Joined: Wed Oct 30, 2002 3:18 pm
Location: Please give your location so we can help better

Re: BCG for male CPPS

Post by webslave »

jd wrote:In relation to that, I'm always wondering how many guys on this board have actually had a cystoscopy and bladder hydrodistention.
I've had cystoscopy, but not hydrodistension. I don't think many men get hydrodistension.
In my case, my uro. told me I have "classic Prostatitis symtoms," and I had the cyst. and hydro. and it turned out I have IC.
IC may be the same/virtually the same as CPPS. The treatments don't differ all that much currently, and I expect the treatments to be identical eventually.
I have read that BCG is one of the most promising future therapies for IC, I guess people who benefitted from it had a long term reduction of pain and IC symptoms from a well executed (but small) study.
Unfortunately, BCG therapy is associated with a high incidence of granulomatous prostatitis (there are a bunch of papaers describing this). Granulomatous prostatitis is a kind of allergic reaction. One of the earliest papers describes it well:

Clin Exp Immunol 1976 Oct;26(1):137-47

Experimental cellular allergic reactions in normal canine and malignant human prostate.

Robinson MR, Rigby CC, Pugh RC, Vaughan LC, Dumonde DC.

This paper describes the histopathology of chronic tuberculin-type hypersensitivity reactions in the normal canine and malignant human prostate. Seven dogs were sensitized by injection of Freund's complete adjuvant and the histological response to the subsequent intra-prostatic injection of 6 mg tuberculin PPD was documented. A chronic mononuclear cell prostatitis persisted for 4 weeks and was accompanied by paracortical distension and follicular hyperplasia in regional lymph nodes. Six patients with carcinoma of the prostate were given multiple intraprostatic injections of BCG, which induced a chronic mononuclear cell prostatitis with some evidence of tumour-cell necrosis. The study indicated that the prostate can support chronic cell-mediated allergic reactions to extrinsic antigens and that intra-prostatic injections of BCG can be administered without harmful effects to patients with malignant prostatic disease
Good News! The great ProstaQ is BACK at last! You must try it.

HAS THIS SITE HELPED YOU?
Say Thanks by donating. Keep the
Forum alive on the Internet!
PayPal link at end of page ↓

Contact me at support at ucpps.men
User avatar
dshoskes
Urologist
Urologist
Posts: 204
Joined: Wed Oct 30, 2002 7:51 pm
Location: Cleveland Clinic, Ohio

Post by dshoskes »

Richard.N wrote:I had a BCG jab at school 20 years ago when I was 11, and I sometimes wonder (since I have calcification in my prostate - sometimes associated with TB scarring) whether it wasn't this that set the ball rolling...
He was referring to BCG instilled into the bladder. The problem with using it for chronic prostatitis / chronic pelvic pain syndrome IF the disease is in the prostate is that penetration into the prostate for the BCG is lousy. When we use BCG for bladder cancer that involves the prostate, we often have to resect the prostatic tissue first to get any penetration.
Daniel Shoskes MD
www.dshoskes.com
User avatar
Richard.N
Sage
Sage
Posts: 578
Joined: Wed Oct 30, 2002 6:05 pm
Location: Bristol, England

Post by Richard.N »

JD - I remember you saying that you were thinking of trying Elmiron. Any luck? Richard.
Richard

Age: 39. | Onset Age: 30. Onset Date: January 2002. Symptoms (back then): Supra-pubic pain, back pain, urinary frequency, urgency and difficulty, weak stream, nocturia, (and variously) chronic fatigue, IBS. Current symptoms: more frequent than normal, but pretty much under control. Current amelioration: Xatral 10mg, Mirtazapine 30mg. | Worsened By: Stress, binge drinking, strained bowel movements, bloating, sitting on hard surfaces, jogging, and regularly - THE WINTER!

I'm not a medical expert. My comment is opinion. See your medical professional.
jd

Post by jd »

Richard--

I talked with my Uro. and he thought it would be best to just stick with Algonot Plus, since I seem to be getting better with it and have been on it close to 4 1/2 months.