Collins M, Ransohoff D, Barry
M. Early detection of prostate cancer: serendipity strikes again. JAMA.
1997;278:1516-1519.
The authors address the issue of cancer detected
by chance. This phenomenon, termed serendipity, occurs when a screening
test (ie, digital rectal examination or prostate-specific antigen) is abnormal
due to benign conditions and cancer is coincidentally detected. The authors
caution us regarding the uncertainties regarding prognosis and impact of
aggressive treatment on the natural history of prostate cancer. They conclude
that the best approach for the early detection of prostate cancer has yet
to be defined.
Benoit RM, Naslund MJ. The
economics of prostate cancer screening. Oncology (Huntingt). 1997;11:1533-1543.
Concerns over the increased health care costs associated
with widespread screening are addressed. The authors discuss models to
calculate costs from screening and the impact of stage migration on these
costs. They estimate that screening for prostate cancer is more cost effective
than screening for cervical and breast cancer. The analysis presented in
this paper suggests that screening and the consequent early treatment of
prostate cancer may be cost effective.
Carlson GD, Calvanese CB, Partin
AW. An algorithm combining age, total prostate-specific antigen (PSA),
and percent free PSA to predict prostate cancer: results on 4298 cases.
Urology. 1998;52:455-461.
Various means to improve the performance of PSA have
been proposed. These include PSA density, PSA velocity, age-adjusted PSA,
and percent-free PSA. The authors propose a model that combines age, total
PSA, and percent-free PSA. In their study, this model had increased sensitivity
and specificity.
Fair WR, Fleshner NE, Heston
W. Cancer of the prostate: a nutritional disease? Urology. 1997;
50: 840-848.
The impact of nutrition in the promotion or prevention
of prostate cancer has been evaluated for decades. Fat and soy intake,
different vitamins, and the trace metal selenium have been previously studied.
In this comprehensive review, the authors discuss the current knowledge
regarding these nutritional agents.
Dalu A, Haskell JF, Coward
L, et al. Genistein, a component of soy, inhibits the expression of the
EGF and ErbB2/Neu receptors in the rat dorsolateral prostate. Prostate.
1998;37:36-43.
Asian men have a low incidence of prostate cancer.
Asian diet is rich in soy. The phytoestrogen genistein, a component of
soy, has been implicated as the reason for this decreased incidence. The
authors demonstrate that genistein inhibits tyrosine-phosphorylated proteins
in a rat model. They conclude that genistein downregulates the EGF and
ErbB2/Neu receptors in the rat prostate and that it may be useful in both
protecting against and treating prostate cancer.
Bova GS, Partin AW, Isaacs
SD, et al. Biological aggressiveness of hereditary prostate cancer: long-term
evaluation following radical prostatectomy. J Urol. 1998;160: 660-663.
Familial prostate cancer has been stratified recently
in two types: men with a family history of prostate cancer and the hereditary
prostate cancer syndrome (HPC). The former defines men with prostate cancer
who have a father or at least one brother with prostate cancer. HPC is
defined as a family with three generations affected, three first-degree
relatives affected, or two relatives affected before age 55. The investigators
compare the rate of PSA progression between men with and without a family
history of prostate cancer and men with or without HPC who underwent radical
prostatectomy. There was no statistically significant difference in the
probability of maintaining an undetectable PSA among the groups. They conclude
that there is no biologically important difference between hereditary and
sporadic prostate cancers.
Kallakury BV, Sheehan CE, Ambros
RA, et al. Correlation of p34cdc2 cyclin-dependent kinase overexpression,
CD44s downregulation, and HER-2/neu oncogene amplification with recurrence
in prostatic adenocarcinomas. J Clin Oncol. 1998;16:1302-1309.
As a product of the cell division control gene, p34cdc2
cyclin-dependent kinase (CDK) plays a role in the control of mammalian
somatic cell-cycle progression. CD44s, a transmembrane glycoprotein, plays
an important role in various cell-cell and cell-matrix interactions. The
HER-2/neu oncogene encodes a transmembrane glycoprotein member of the epidermal
growth-factor-receptor subgroup of the tyrosine kinase superfamily. The
investigators demonstrate that these proteins and oncogene are variably
expressed or amplified in prostate cancer and that such alterations may
affect tumor behavior. They suggest that CDK overexpression and HER-2/neu
amplification may be biologically related.
Hedlund TE, Duke RC, Schleicher
MS, et al. Fas-mediated apoptosis in seven human prostate cancer cell lines:
correlation with tumor stage. Prostate. 1998;36:92-101.
Fas, a member of the tumor necrosis factor receptor
superfamily, is a cell surface receptor capable of initiating an apoptotic
signaling pathway when bound to its ligand. This recent study supports
previous studies suggesting that the normal, differentiated prostatic epithelium,
as well as locally invasive prostate cancer, has the potential to undergo
fas-mediated apoptosis. Metastatic prostate cancer have a reduced potential
for apoptosis.
DAmico A, Whittington R, Malkowicz
B, et al. Biochemical outcomes after radical prostatectomy, external beam
radiation therapy, or interstitial radiation therapy for clinically localized
prostate cancer. JAMA. 1998;280:969-974.
Prostate-specific antigen (PSA) control after three
treatment modalities for clinically localized prostate cancer was estimated.
Patients were stratified in low-risk, intermediate-risk, and high-risk
groups. Low-risk patients had similar five-year PSA outcomes regardless
of treatment. Intermediate- and high-risk patients had a worst outcome
when treated with brachytherapy. The reader is cautioned that this observation
is currently well known and that contemporarily, patients with poor-risk
cancers are not treated with brachytherapy alone but with a combination
of preemptive hormonal therapy, external beam radiation therapy, and brachytherapy.
The Medical Research Council
Prostate Cancer Working Party Investigators Group. Immediate versus deferred
treatment for advanced prostatic cancer: initial results of the Medical
Research Council Trial. Br J Urol. 1997;79: 235-246.
Hormonal therapy has been the mainstay for the treatment
of advanced prostate cancer for over five decades. The optimal timing for
instituting treatment in advanced disease is still controversial. In this
randomized study of early vs deferred treatment, the investigators observed
better local control and delayed progression in patients treated immediately.