Factors Pointing to the Development of Metastatic Prostate Cancer

It is inevitable; most men with prostate cancer, who require treatment with androgen deprivation therapy (ADT), will eventually become resistance to treatment leading to the development of metastatic disease. Men who develop metastatic castrate-resistant disease have a very poor prognosis. Historically, their overall survival is estimated only to be 24 to 36 months.

A study at the Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, Ohio tried to identify predictors of clinical disease progression in patients with prostate cancer who were receiving ADT.

They evaluated 13,740 men with biopsy-confirmed prostate cancer who were enrolled in the Cancer of the Prostate Strategic Urological Research Endeavor (CaPSURE) database from 1995 to 2007. The primary endpoint of the study was the development of bone metastasis. They compared clinical and pathologic characteristics between men who developed metastasis and those who did not using chi-square tests in a Cox proportional hazards regression model.

The mean age of the 13,740 men was 70 years, with a range of 39-94 years. One hundred ninety-one men (4.8%) progressed to metastatic disease at a median of 18 months from the initiation of ADT (range, 1-139 months). On multivariate analyses, risk category (hazards ratio

[HR], 2.58; P < .0001), percent of biopsies positive >33% (HR, 3.36; P = .003), age < /=65 years at diagnosis (HR, 2.11; P = .001, and prostate-specific antigen velocity on ADT (HR, 1.04; P < .001) were found to be significantly associated with the development of metastatic disease after ADT.To review their findings they found the following items as significant risk factors for the development of metastatic disease:1- Men younger than 65 years with high-risk disease

2- Men with higher than 33% of positive biopsies at diagnosis

3- Higher PSA velocity while on ADT

These items are not the only potential factors that can herald the development of metastatic disease, but they are among the most important. If you have any of these factors, make sure that your doctor is aggressive with your treatment and that you seriously consider participating in a clinical trial.

Reference:
Cancer. 2009 Jul 27. Epub ahead of print.
doi:10.1002/cncr.24526; Abouassaly R, Paciorek A, Ryan CJ, Carroll PR, Klein EA.
PubMed Abstract
PMID:19637339

Joel T Nowak MA, MSW

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Tom Panks September 7, 2009 at 6:18 am
Thanks for the update Joel; but I am a bit concerned about this. You state…”make sure that your doctor is aggressive with your treatment” ….
If ADT becomes in-effective after a given amount of time…. why do we then hasten that end time by aggressively medicating ourselves w/ADT? Shouldn’t extending a program of on/off treatment using PSA as a marker be more beneficial?
Thank You..Looking forward to your reply as I expect others are too.
Joel September 9, 2009 at 2:58 pm
Tom,
Once hormone therapy stops working there are other treatments that do have the ability to slow down the growth of the cancer. Being aggressive with these treatments is important in extending your survival.