Medical Forum / Diseases and Disorders / Prostate Cancer / December 2004
Cryo, what you need to know.
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Canada Bob - 30 Nov 2004 11:52 GMT Thought that this link might help folks decide if Cryo is for them.
http://www.prostatepointers.org/prostate/lay/apilgrim/chapter12.html
Bob.
ron - 30 Nov 2004 15:38 GMT > Thought that this link might help folks decide if Cryo is for them. > > http://www.prostatepointers.org/prostate/lay/apilgrim/chapter12.html > > Bob. Hi Bob...That's an interesting article. It reports that Dr. Lee is preparing to publish his 6-year results; it will be interesting to see how his numbers come out. Drs. Lee and Onik are clearly two artists in the area of cryo. Their results will be among the best. Along these lines the article you referenced states, "Dr. Gary Onik reported negative biopsies in 82.6% of his patients at 3 months following cryosurgery. Dr. Fred Lee found no cancer in 92% of his patients at 3 months." This means that the PCa was not effectively removed from 17% of Dr. Onik's patients and 8% of Dr. Lee's. That's not a good starting point. Compare those 3 month numbers to Dr. Walsh's numbers at 10 years, where only about 5-8% of his low risk patients have biochemically failed!
Tha abstract that I posted previously on the 3rd Generation Cryo technique comparison, a multi-institutional study, showed that 22% of the low risk men had already failed at 12 months. On top of that 8% of the men remained on pads and 87% of the previously potent men were now impotent. By the way, one of the authors of this paper was Dr. Jeff Cohen who was listed along with Dr. Onik as the originators of the modern cryo procedure. Again, I just don't see the good news in these numbers in terms of cancer survival and morbidity...Best wishes and good health, Ron
Stephen Jordan - 30 Nov 2004 17:45 GMT > Thought that this link might help folks decide if Cryo is for them. > > http://www.prostatepointers.org/prostate/lay/apilgrim/chapter12.html My experience with cryosurgery is almost uniformly negative.
First, a few comments on the above article:
(1) it is somewhat outdated; Medicare will cover the cost, (2) incidence of impotence is well in excess of 80%, and (3) IMO, success, defined as "Destroy all the cancer in the prostate and achieve a non-detected PSA," (Dr. Lee), is an elusive goal at best.
My experience, which is of course anecdotal, is this:
9/30: biopsy, ten probes plus one through a palpable nodule discloses, on the right, "adenocarcinoma Gleason score 4+5 involving 6 of 7 cores...perineural invasion..." On the left *benign prostate tissue with acute and chronic inflammation*." This last turned out to be important.
11/03: cryosurgery. According to the summary, it was a "full prostate freeze."
7/04: due to rising PSA scores, another biopsy was performed, utilizing twelve probes. Result: on the *left* base, "Adenocarcinoma...Gleason score 4+4=8." The uro said he was surprised.
10/04: on the uro's referral (he apparently had no confidence in redoing the cryo, notwithstanding that the possibiity of a repeat is one of the sales points), completed IMRT treatment of 76Gy, plus some to seminal vesicles and lymph nodes, including adjuvant ADT (Lupron).
As of yesterday, November 29, the rad onc says he thinks I'm cured, although an indefinite course of ADT is to continue due to the aggressive Gleason 8 nature of the tumor, which MAY have shed some cells.
Now, here's the kicker: I had the cores from the July '04 biopsy restudied by Bostwick. Report confirms Gleason 8 adenocarcinoma at left base. Regarding the right base, which is where the Gleason 9 tumor supposedly frozen in 11/03 was situated, "atypical small acinar (granulous mass) proliferation highly suspicious for but not diagnostic of malignancy."
Swell. I'm presently unsure just what the 11/03 cryo really achieved. Did it transform the Gleason 9 tumor to the above suspicious mass? Dunno.
Bottom line, if I hadn't been stampeded into the cryo, I would not have done it. So far as I'm concerned, the result is poor, and the SE's, which I accepted in expectation that the cryo would succeed, are certainly not worth it. "Outrage" hardly touches the surface.
OK, maybe I had a fumbler for a uro. I don't know.
Regards,
Steve J __ "It is mistaken to attribute to malice things that can be satisfactorily explained by incompetence." -- Napoleon Bonaparte
Stephen Jordan - 01 Dec 2004 00:29 GMT Correction: I wrote that my first biopsy was "9/30." Should have been "9/03." Bad fingers, bad bad! (slap)
Steve J
ron - 04 Dec 2004 19:11 GMT In my earlier post in this thread, I mentioned an article (The Journal of Urology 2003; 170(4):1126-1130, Treatment of Organ Confined Prostate Cancer with Third Generation Cryosurgery: Preliminary Multicenter Experience) that, in my reading, didn't make a very favorable case in support of using cryo to treat PCa. While this study sampled a lot of doctors and hospitals, it did not include any of the cryo artists I am aware of like Duke bahn, Fred Lee or Gary Onik.
So to be "fair and balanced" I did a PubMed search on Duke Bahn. I found a number of publications, but thought the one I've included below to be most relevant, and recent. Since the study started in '93, not all the men were traeted with the 3rd Generation cryo technique. Presumably the results, on average, would be even better for men treated with the improvements contained in the 3rd Generation equipment. Also, I believe this targeted approach relates to partial, rather than total, prostate freezing, e.g. the male lumpectomy. I thought the following points worth noting: * The seven year projected results for low-risk men (61% using PSA>0.5 as the definition of failure) are far behind RCOG's or Walsh's 10-year projected results for SI + EBRT and surgery respectively (both >90% using a more stringent PSA>0.2 as a defintion of failure). * The results for high-risk men are encouraging. RT is generally thought to be more effective than surgery as risk group increases. RCOG reports a bNED of 61% (using the PSA>0.2 DOF) for high-risk men at 10 years. * Cryo's strength has always been that it is well tolerated (usually an out-patient procedure) and easily repeatable. Bahn finds that, of those re-treated with cryo for recurrence or incomplete initial removal, 68% are disease free after a mean follow-up of 63 months. Not bad! * It sounds like Bahn's morbidity data is much improved over that reported in the multi-institutional study. * Once again a large difference in success (30 points!) is noted depending whether ASTRO or PSA cutpoints are used to determine failure. This takes me back to our earlier threads on the Cleveland Clinic's paper earlier this year (International Journal of Radiation Oncology*Biology*Physics, Volume 58, Issue 1 , 1 January 2004, Pages 25-33, Radical prostatectomy, external beam radiotherapy <72 Gy, external beam radiotherapy 72 Gy, permanent seed implantation, or combined seeds/external beam radiotherapy for stage T1T2 prostate cancer, Patrick A. Kupelian M.D., Louis Potters M.D., Deepak Khuntia M.D., Jay P. Ciezki M.D., Chandana A. Reddy M.S., Alwyn M. Reuther M.P.H., Thomas P. Carlson M.D., and Eric A. Klein M.D.) where they compared various forms of RT (using ASTRO as the DOF) and RP (using PSA>0.2 as the DOF) and concluded that the 7-year bNEDs were similar for RT and RP, just because the numeric results happened to be the same even though different definitions of failure had been applied. In light of the now numerous studies that show large bNED differences when ASTRO or PSA cutpoints are used, it's not clear to me how the Cleveland Clinic conclusions made it into print. (I think I've digressed) Finally, let me note that there was another article I came across that made a strong case for use of cryo to treat recurrence after RT (sorry, I didn't note the reference)...Best wishes and good health, Ron
Urology. 2002 Aug;60(2 Suppl 1):3-11. Related Articles, Links Targeted cryoablation of the prostate: 7-year outcomes in the primary treatment of prostate cancer.
Bahn DK, Lee F, Badalament R, Kumar A, Greski J, Chernick M.
Prostate Institute of America, Community Memorial Hospital, Ventura, California 93003, USA. dkbahn@cmhhospital.org
The efficacy and safety of the long-term experience with targeted cryoablation of prostate cancer (TCAP) at a community hospital is retrospectively reviewed. A series of 590 consecutive patients who underwent TCAP as primary therapy with curative intent for localized or locally advanced prostate cancer from March 1993 to September 2001 were identified. Patients were stratified into 3 risk groups according to clinical characteristics. Biochemical disease-free survival (bDFS), post-TCAP biopsy results, and post-TCAP morbidity were calculated and presented. The mean follow-up time for all patients was 5.43 years. The percentages of patients in the low-, medium-, and high-risk groups were 15.9%, 30.3%, and 53.7%, respectively. Using a prostate-specific antigen (PSA)-based definition of biochemical failure of 0.5 ng/mL, results were as follows: (1) the 7-year actuarial bDFS for low-, medium-, and high-risk patients were 61%, 68%, and 61%, respectively; (2) the bDFS probabilities for a PSA cutoff of 1.0 ng/mL for low-, medium-, and high-risk patients were 87%, 79%, and 71%, respectively; and (3) the bDFS probabilities for low-, medium-, and high-risk patients using the American Society for Therapeutic Radiology and Oncology (ASTRO) definition of biochemical failure (3 successive increases of PSA level) were 92%, 89%, and 89%, respectively. The rate of positive biopsy was 13%. After a positive biopsy, 32 patients underwent repeat cryoablation. For those patients who underwent repeat cryoablation, 68%, 72%, and 91% remain bDFS using definitions of 0.5 ng/mL, 1.0 ng/mL, and the ASTRO criteria, respectively, after a mean follow-up time since repeat cryoablation of 63 months. The rates of morbidity were modest, and no serious complications were observed. TCAP was shown to equal or surpass the outcome data of external-beam radiation, 3-dimensional conformal radiation, and brachytherapy. These 7-year outcome data provide compelling validation of TCAP as an efficacious treatment modality for locally confined and locally advanced prostatic carcinoma.
PMID: 12206842 [PubMed - indexed for MEDLINE]
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