| by:
Gil Lederman, M. D.
Epidemiologic studies are often important because of trends
that may be observed. Associations between diseases in studies
of large groups of a population, may lead to the determination
of risk factors - factors that may lead to finding causation
of disease or more importantly, the prevention of disease.
A recent report in the Journal of Clinical Oncology by Ahsan
et al evaluated other cancers that occur in patients with
malignant brain tumors. As the authors noted, this separate
epidemiologic study can help determine whether there are "shared
risk factors, effective treatment for one primary tumor on
the risk of another cancer or genetic predisposition to multiple
cancers."
This is especially critical as there is very little known
about the etiology or cause of primary malignant brain tumors.
In that effort, the SEER Program was used to collect this
data. The SEER Program is run by the National Cancer Institute
and has been collecting cancer-related information for more
than two decades through major cancer registries. These registries
document disease in 10% of the American population. More than
1-1/2 million Americans with cancer were evaluated between
1973 and 1990.
The authors evaluated those patients who had other cancers
followed by the development of malignant brain tumors. Furthermore,
the brain tumor had to be diagnosed more than six months after
the initial cancer as the authors desired to eliminate coincidental
findings during staging or evaluation of the first cancer.
Additionally the researchers broke out the observations into
five year sequences.
So, which cancers were associated with a higher risk of developing
subsequent brain tumors? There was an increased risk of brain
tumors after the diagnosis of bladder cancer in both men and
women - although in women this did not reach statistical significance.
Thus, only in men was statistical significance reached to
verify whether the observed phenomenon was a trend or an actual
reality. In men, there were elevated risks of developing brain
tumors in those who had sarcomas or leukemias.
In women, the only increased risk of developing brain tumors
was in those who had prior colon or rectum cancer. There was
a slight risk of developing brain tumors after breast cancer
and endometrial cancer, but those associations were not statistically
significant. The role of hormonal factors was felt to be "further
implicated by our finding of elevated relative risks of brain
tumor after both breast cancer and endometrial cancer."
Of interest was that the authors found no increased risk of
malignant brain tumors after the development of tobacco-related
cancers such as those afflicting the lung or head and neck
area. In fact, the opposite was true in that there was significantly
lower risk of brain tumors after lung cancers in men. This
would suggest that smoking is not related to the development
of brain tumors. Finally, a negative disclaimer the tobacco
industry can place on cigarette packages!!
This study is important for a variety of reasons. It is the
first that evaluated the development of brain cancers after
other cancers. An earlier evaluation suggested the risk of
brain tumors was greater after only the diagnosis of melanoma
but it was not confirmed.
The authors speculated that the association of brain tumors
and bladder cancers might suggest that causes of bladder malignancies
such as chemicals and dyes have similar effect on the brain.
Another possibility is that bladder cancers and brain tumors
might have a genetic link, predisposing certain individuals
to both.
This data should help other investigators search for the cause
of brain and other cancers. Important medical observations
are made on the shoulders of giants.
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