Surgery was better:
Evaluation of Cancer-Specific Mortali... - Advanced Prostate...
Evaluation of Cancer-Specific Mortality with Surgery Versus RT as Primary Therapy for Localized High-Grade PCa in younger Men
What is considered a young age? We have been recommended rediation at this point. 58 yr old Husband 7 months into treatment now. Gleason 7 no bone Mets, in a few lymph nodes and into the capsule on one side. Highest PSA before treatment 74. Jan 24 PSA at .34. Has steadily declined each month so far. MO says radiation within the year and then off ADT after total of 18 months. He does pretty consistent exercise with weights and elliptical, many supplements, a few preworkout aminos, and lots of organic veggie diet with fish. He personally would rather do radiation than surgery so there is that as well. Incontinence fears after surgery I think is his biggest fear, TBH.
One of the problems with those who give advice for primary treatment, is that it is often the same treatment as the person giving advice received.
I was puzzled when my urologist gave me (& my wife) a lot of information on the various therapies, to be read before our next visit. I expected to get an up-front recommendation from him. Given by biopsy results, wasn't there a logical choice? When I later questioned him on this, he said that it was to make the patient feel empowered.
But it also stops patients coming back to the doctor later & accusing him of choosing the wrong treatment.
I soon learned that the guy next door, who was treated before your diagnosis, will invariably recommend his own treatment - even if it was unsuccessful.
When we make the decision, we are wedded to it. And didn't I always say that surgery was better? LOL.
-Patrick
Your urologist did the ethical thing. Not just self interest. I understand thst there is a law requiring breat cancer patients be given information on all megically recognized treatments at diagnosis in some states
All urologists should do this at initial diagnosis of PC
The article said men under the age of 60 are considered young age. You can click on the link below and read about it. I may be better to do both --- in his case -- since the cancer is known to be in the lymph nodes already. Ask doctor if surgery to get the hornets nest out first and then radiate the prostate bed and surrounding lymph nodes. No one is a PC doctor on here, so don't rely on anything other than your doctors. You may want another doctors opinion before starting with radiation.
Very poor study. Most people who post studies on this site haven't a clue as to how to evaluate them. Here's how their peers responded (peer response is important in such journals). Patients should be wary of posts of research without commentary evaluating it and its context. Database analyses are often just a cheap and easy way for an academic to get published. They are notoriously plagued by selection bias. Here's a response to a similar database analysis:
"We read with interest the National Cancer Data Base (NCDB)
study by Berg et al. [1] comparing overall survival (OS)
between men aged 65 yr with high-risk prostate cancer
(PC) receiving radical prostatectomy (RP) and those receiving
external beam radiotherapy with a brachytherapy boost
(EBRT + BT). The authors conclude that EBRT + BT was
associated with significantly worse OS, with a hazard ratio
of 1.22 for all-cause mortality. When considering the validity
of this conclusion, three salient points must be considered.
First, cancer registries inherently cannot capture the
selection bias that affects treatment allocation to RP or
EBRT + BT, even among “healthy” patients. For example,
several different registry studies have shown implausible
OS differences among patients with low- and intermediate-
risk disease, with divergence of survival curves for RP and
EBRT—favoring RP—within 3 yr post-treatment, in stark
contrast to the level 1 evidence provided by the ProtecT
trial, which found no differences in all-cause mortality at
median follow-up of 10 yr [2,3].
Second, the dominant cause of death even in high-risk PC
is other-cause mortality [4]. The NCDB provides no
information on tumor control specifically, and one cannot
correct for unmeasured confounding variables that would
favor improved other-cause mortality in RP patients.
Therefore, any difference identified in OS is most likely
attributed simply to differences in other-cause mortality.
Third, the authors state that they did not account for the
use of androgen deprivation therapy (ADT) in the treatment
groups. Both the European Association of Urology/European
Society for Radiotherapy and Oncology/International Society
of Geriatric Oncology and National Comprehensive Cancer
Network guidelines recommend long-term ADT with EBRT
+ BT, reflecting the multiple randomized trials that have
demonstrated a robust OS benefit for use of long-term ADT
with EBRT. No high-level evidence exists to suggests that ADT
can be foregone with EBRT + BT, and hence all professional
societies consider it to be the standard of care to use ADT of
sufficient duration with EBRT + BT. Thus, the inclusion of
patients not receiving ADT (31% of EBRT + BT patients) and
the inability to account for ADT duration in this analysis are
troubling. This is evident if the results are contextualized
with two other studies with biopsy Gleason score 9–10
disease. The first found a PC-specific mortality benefit for
EBRT + BT (with median ADT duration of 12 mo) over RP
[5]. The second found an OS benefit for EBRT + BT (with
median ADT duration of 6 mo) overRP without postoperative
therapy, and equivalent OS between EBRT + BT and RP with
adjuvant EBRT [6]. Given the inherent differences between
patients who receive RP and those who receive EBRT + BT, we
acknowledge that all retrospective analyses are intrinsically
an “apples to oranges” comparison. However, in any such
comparison, it is even more imperative to enrich for explicitly
codified standard-of-care treatments.
Ultimately, the superiority or noninferiority of RP versus
EBRT + BT needs to be determined in a prospective,
randomized fashion. We would be highly supportive of a
clinical trial to help answer this question for the thousands
of patients diagnosed with high-risk disease annually.
References
[1] Berg S, Cole AP, Krimphove MJ, et al. Comparative effectiveness of
radical prostatectomy versus external beam radiation therapy plus
brachytherapy in patients with high-risk localized prostate cancer.
Eur Urol. In press. doi.org/10.1016/j.eururo.20....
[2] Pearlstein KA, Basak R, Chen RC. Comparative effectiveness of
prostate cancer treatment options: limitations of retrospective
analysis of cancer registry data. Int J Radiat Oncol Biol Phys. In
press. doi.org/10.1016/j.ijrobp.20....
[3] Hamdy FC, Donovan JL, Lane JA, et al. 10-Year outcomes after
monitoring, surgery, or radiotherapy for localized prostate cancer.
N Engl J Med 2016;375:1415–24.
[4] Johnston TJ, Shaw GL, Lamb AD, et al. Mortality among men with
advanced prostate cancer excluded from the ProtecT trial. Eur Urol
2017;71:381–8.
[5] Kishan AU, Cook RR, Ciezki JP, et al. Radical prostatectomy, external
beam radiotherapy, or external beam radiotherapy with brachy-
therapy boost and disease progression and mortality in patients
with Gleason score 9–10 prostate cancer. JAMA 2018;319:896–905.
[6] Tilki D, Chen M, Wu J, et al. Surgery vs radiotherapy in the manage-
ment of biopsy Gleason score 9–10 prostate cancer and the risk of
mortality. JAMA Oncol. In press. doi.org/10.1001/jamaoncol.
2018.4836.
Amar U. Kishan
William A. Hall
Daniel E. Spratt
I'm pretty sure the people who conducted the study would disagree. The facts are the facts.
I agree with Allen that some of the statistical models dealing with cohort studies are misspecified. It's unfortunate that the researchers cannot do a better job to get rid of biases in their analysis - maybe limitations of the databases, and/or the publish or perish culture?
The real question is how to adjust for the biases, now that we now it's there. Can we create upper and lower limit "bands" around the impact of these biases on the results? I'm inclined to think that's plausible. There has been some studies that have attempted to take the state of "health" of the individual into accounts, using it as a proxy for the selection bias.
What was the time period that was studied? Did they use RT data from the 1990’s? I recall that the SEER database goes back decades.
Also, high risk PCa today is treated with the triple play of EBTR, BT, and ADT. As Allen stated, where does this study assess the RT combo?
While the authors do mention other studies with conflicting results, I’m not convinced that they made their case that “surgery is superior “.
then there's the Whack-a-Mole theory, it sometimes comes back no matter what treatment is chosen. No one knows why, so we just have to keep beating it back down.
Bob, G9, proton, adt (18 months)
Diagnosed at 58 with Gleason 9. Urologist wanted RP. Went to Johns Hopkins for second opinion. They said they would not operate over a 6 as chances were too great it was out of the capsule. Took their advice did 43 IMRT radiation and then ADT with Dr. Myers. That was in 2004. PSA currently undetectable after doubling in 2015 for a few months. Still on a Dr. Myers "cocktail". Think I have done pretty well and think the side effects of radiation and ADT are less than with RP. Never had incontinence although did have nausea.
One of the problems here is the rapid evolution of both radiotherapy, sytemic tehapies and surgical procedures. With all of us living so much longer a study that loikd at ten year survival, which was considered a cure 20 years ago is not comparing apples to apples
Very conplex dosease which varies dramaticslly from individusl to individual
Ten years from now there will be other treatments and what is done now will be considered primitive
RCOG2000, Good point. It takes years to see if a treatment really works better than another -- over the long haul.
Hey wait a minute.....Young? Old? I say you're as old as the woman you feel.
Good Luck, Good Health and Good Humor.
j-o-h-n Thursday 02/14/2019 6:17 PM EST