
Cancer Epidemiology Biomarkers & Prevention Vol. 9, 1323-1328, December 2000
© 2000 American Association for Cancer Research
Intention to Be Tested for Prostate Cancer Risk among African-American Men1
Ronald E. Myers2,
Terry Hyslop,
Kathleen Jennings-Dozier,
Thomas A. Wolf,
Desiree Y. Burgh,
Julie A. Diehl,
Caryn Lerman and
Gerald W. Chodak
Behavioral Epidemiology Section, Division of Medical Oncology and Medical Genetics [R. E. M., T. A. W., D. Y. B., J. A. D.], and Biostatistics Section, Division of Clinical Pharmacology [T. H.], Department of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania 19107; College of Nursing and Health Professions, MCP Hahnemann University, Philadelphia, Pennsylvania 19102 [K. J-D.]; Georgetown University Medical Center, Washington DC 20007-4104 [C. L.]; and Weiss Memorial Hospital, Chicago, Illinois 60640 [G. W. C.]
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Abstract
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This
study was conducted to identify factors associated with intention to be
tested for prostate cancer risk among African-American men.
Participants in this study included African-American men
(n = 548) who were patients at the University
Health Service at the University of Chicago, were 40 to 70 years of
age, and did not have a personal history of prostate cancer. Baseline
telephone survey data were collected for 413 (75%) men. Respondents
were asked if they intended to have a blood test to assess prostate
cancer risk. Univariate and multivariate analyses of intention to be
tested for risk were performed. Eighty-six percent of the men said that
they intended to be tested. Multivariate analysis results show that
belief in the efficacy of prostate cancer screening [odds ratio
(OR) = 3.6; 95% confidence interval (CI) = 1.4, 9.1] and
intention to undergo a prostate cancer-screening (i.e.,
digital rectal examination and prostate-specific antigen testing;
OR = 2.8; 95% CI = 1.3, 6.3) were positively associated with
intention to be tested for prostate cancer risk. Being older (OR =
0.4; 95% CI = 0.2, 0.9), having had a prostate cancer-screening
examination in the past year (OR = 0.5; 95% CI = 0.2, 1.0),
perceiving ones prostate cancer susceptibility to be high (OR =
0.4; 95% CI = 0.2, 0.8), and being fatalistic about
prostate cancer prevention (OR = 0.3; 95% CI = 0.2, 0.7)
were negatively associated with intention to be tested for risk.
Intention to be tested for prostate cancer risk was high among men in
the study. Past screening, perceived susceptibility, and beliefs
related to early detection might influence receptivity to genetic
testing for prostate cancer risk.
 |
Introduction
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The lifetime risk of developing prostate cancer and of dying from
the disease rises substantially among men after the age of 50
(1)
, and a 2-fold greater risk exists among
African-American men (2, 3, 4)
. Along with age and race,
having a family history of prostate cancer is also a well-established
risk factor for the disease (5, 6, 7, 8, 9, 10)
. Evidence that there
is a genetic link for prostate cancer susceptibility is mounting with
increased attention being directed toward understanding the basis for
elevated risk among African-American men (11, 12, 13)
.
Recent reports have identified a gene located on the long arm of
chromosome 1q2425 (i.e., HPC1) that may
be involved in the development of hereditary prostate cancer
(14)
. The MAX-interacting protein-1 (i.e.,
MXI1) on chromosome 10q and the KAI1 prostate
cancer antimetastasis gene on chromosome 11p are genes that may be
involved in the origin or progression of prostate cancer
(15)
. Predisposition for early onset prostate cancer has
been attributed to 1q42.2-q43 located on chromosome 1q, but distant
from the HPC1 locus (16)
. Genetic testing for
prostate cancer risk is performed currently only in the context of
research investigations, including a project that focuses on
African-American families (i.e., the African American
Hereditary Prostate Cancer
Study.3
) In
the future, however, genetic testing for prostate cancer susceptibility
may become a health care option for men at increased risk. Therefore,
it is important to identify determinants of receptivity to
susceptibility testing among African-American and other high-risk men.
Knowledge in this area will help to gauge the potential utilization of
this modality.
A number of researchers have assessed the extent to which family
members of patients with different types of cancer are interested in
being tested for risk (17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30)
. Several studies have also
addressed this matter among members of the general population
(31, 32, 33, 34, 35, 36, 37, 38, 39)
. Most of these studies have been conducted in
relation to breast and colorectal cancer. However, relatively little
research has been published on the receptivity of at-risk racial and
ethnic populations to genetic testing for cancer susceptibility
(20
, 22
, 24
, 32
, 34)
. In the study presented here, we
measured the extent to which African-American men reported that they
intended to be tested for prostate cancer risk when such testing
becomes available in the future. We also sought to identify variables
that were associated with this outcome.
The PHM4
was
used to guide the collection and analyses of cross-sectional data in
the study. The PHM is a theory-based explanatory framework that is
grounded in Antonovskys work on the coherence of health behavior in
everyday life (40)
, the Health Belief Model
(41)
, Theory of Reasoned Action (42)
, and
Social Cognitive Theory (43)
. Constructs included in the
model, which include personal background, cognitive and psychological
representations, social support and influence, and intention, have been
validated elsewhere (44)
. The PHM has been useful in
explaining cancer-screening intention and adherence to screening
(45, 46, 47, 48, 49)
.
 |
Materials and Methods
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Recruitment of Study Participants.
In 1995, we initiated a study of adherence to prostate cancer screening
with DRE and PSA testing among African-American men in Chicago. We used
computerized patient files of the University Health Services of the
University of Chicago to identify men who were 40 to 70 years of age,
lived in neighborhoods (defined by zip codes) near the University of
Chicago, and had visited the University Health Services in the previous
two years. Men who had a personal history of prostate cancer were
excluded. A total of 2473 patients satisfied these initial eligibility
criteria. We randomly selected 1000 patients from this sampling frame
for medical chart review. This review resulted in the identification of
750 men who were African American and had a mailing address and
telephone number. A telephone survey company (Mathematica Policy
Research, Inc., Princeton, NJ) attempted to contact the men to
administer a survey questionnaire. It was determined that 202 subjects
(27%) were not available for contact for the following reasons: 164
(81%) did not have a working telephone number; 30 (15%) were
deceased; and 8 (4%) had moved without leaving a forwarding address or
new phone number. Of the 548 remaining men, 413 (75%) completed the
survey and consented to participate in the study, 56 (10%) refused, 42
(8%) were not available for survey contact during the field period, 10
(2%) were unable to complete the survey because of physical
difficulties (i.e., communication problems attributable to
hearing or speech impairment), and 27 (5%) did not complete the survey
for a variety of other reasons.
Variables Measured on the Baseline Survey.
The Baseline Survey instrument, which has been published elsewhere
(46)
, included established PHM constructs. Personal
background was measured in terms of participant age, level of formal
education, marital status, and medical and prostate cancer screening
history. Cognitive and psychological representations related to
prostate cancer screening were measured for participants using a
four-level Likert-type response pattern (i.e., 1 =
strongly disagree, 2 = sort of disagree, 3 = sort of agree,
4 = strongly agree). Some individual survey items were combined to
form scale scores with a high degree of reliability, as indicated by
Cronbach
correlation coefficient. The following scales were formed:
perceived efficacy of prostate cancer screening (three items,
= 0.72); the salience and coherence of prostate cancer screening (four
items,
= 0.85); personal susceptibility to prostate cancer
(two items,
= 0.74); the belief that prostate cancer screening
can improve well-being (two items,
= 0.75); concern about
exam-related pain and anxiety (two items,
= 0.75); and
finally, each respondents confidence in University of Chicago Health
Services medical staff (four items,
= 0.78). Other
variables were measured as individual survey items. These items
included the following: the belief that fate is related to the
diagnosis of prostate cancer; the belief that the benefits of prostate
cancer screening are greater than the costs; the feeling that having a
prostate exam is embarrassing; the belief that a lack of symptoms
indicates no need for a prostate exam; the worry about the cost of
having a prostate exam; belief that African-American men are more
likely to get prostate cancer; and intention to have a prostate cancer
early detection exam.
Social support and influence also was measured using a Likert-type
response pattern. Items inquired about family member support for
prostate cancer screening, respondent receptivity to family member
support for prostate cancer screening, perceived primary care physician
support for prostate cancer screening, and receptivity to physician
support for prostate cancer screening.
Intention to be tested for prostate cancer risk was assessed by asking
each man to respond to the following scenario:
In the future, a new blood test may become available that will help to
find out if you are likely to get prostate cancer at some time later in
life. This test would also be a way to find out if prostate cancer runs
in your family. If the test were offered to you free of charge, how
likely is it that you would choose to have the test?
A four-level Likert-type response was obtained (i.e., 1 = not likely, 2 = somewhat likely, 3 = very likely, 4 =
I am certain I would go in for further testing). Responses were
dichotomized as high (= 4) and low (<4). Selection of this coding
scheme was based on the assumption that a score that indicates absolute
certainty of intention will be highly predictive of actual behavior.
We anticipated that some men might not want to be tested for prostate
cancer risk. For men who had low intention to be tested for prostate
cancer risk, we presented the following scenario:
Different things might stop you from having the new blood test. I will
read a list of reasons why you might not have the new test. Please tell
me whether it is very likely, somewhat likely, or not likely that each
reason would stop you from having the new test.
Response options included: cost of the test; time involved in going for
test; concern about physical discomfort of the test; worry that the
test would show you are likely to get prostate cancer; other people
might find out about the test results; and the test results might be
wrong. We also allowed for open-ended responses other than those given.
A three-level response pattern was provided for each option
(i.e., 1 = not likely, 2 = somewhat likely, 3 = very likely). Responses were dichotomized as not likely or
somewhat likely (
2) versus very likely (>2). This
categorization scheme was chosen to reflect responses about which
individuals held strong feelings.
Data Analysis.
Frequency distributions for survey variables were generated to create a
profile of study participants. Univariate analyses were also performed
using a 2 x n
2
statistic, or a generalized Fishers exact test, to assess
whether observed associations between explanatory variables and
intention to undergo genetic testing for prostate cancer risk were
statistically significant at P < 0.10. Intention to be
tested for prostate cancer risk was modeled using variables that were
significantly associated (P < 0.10) in univariate
analysis. Backward stepwise logistic regression analysis was performed
beginning with participant background characteristics. Significant
background characteristics were retained, and PHM cognitive and
psychological representation, social support and influence, and
intention variables were considered. For explanatory variables with
>5% missing data, regression analysis included two corresponding
dummy variables, one that indicated if a response was given and
one that indicated if the response was missing. This method allowed for
all responses to be considered in the analyses.
Interaction terms involving all independent variables were also
assessed at P < 0.05.
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Results
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Profile of Study Participants.
Seventy-one percent of study participants were 50 or more years of age,
54% had 12 years or less of formal education, and 60% were married.
In terms of medical and screening history, many of the men (59%) had
had a DRE or a PSA test in the previous 12 months, whereas fewer men
(15%) had a personal history of benign prostatic hyperplasia or a
family history of prostate cancer (i.e., having a
first-degree male relative diagnosed with prostate cancer; 7%).
Overall, 409 men responded to the survey item that asked about
intention to be tested for prostate cancer risk. Eighty-six percent of
these men stated that they intended to be tested for this risk.
Univariate Analyses.
Tables 1
and 2
show that a number of PHM variables
were positively and significantly associated with intention to be
tested for prostate cancer risk. Specific variables included: belief
that prostate cancer can be prevented; belief that prostate cancer can
be cured; interest in knowing whether one has prostate cancer; belief
that prostate cancer early detection should be done in the absence of
symptoms; belief that early diagnosis and treatment of prostate cancer
has a positive impact on personal well-being; perceived efficacy
related to prostate cancer screening; belief in the importance of
prostate cancer early detection; physician support for prostate cancer
screening; and intention to have a prostate cancer early detection
examination. The following PHM factor variables were negatively and
significantly associated with intention to be tested for prostate
cancer susceptibility: being more than 50 years of age; having had a
DRE or PSA test in the past 12 months; having high-perceived personal
susceptibility to prostate cancer; fatalism about developing prostate
cancer; and being worried that having an early detection exam would
result in a diagnosis of prostate cancer.
View this table:
[in this window]
[in a new window]
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Table 1 Univariate analysis of participant background and intention to have
genetic screening test for prostate cancer (n = 409)
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View this table:
[in this window]
[in a new window]
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Table 2 Univariate analysis of participant cognitive/psychological and social
support/influence and intention to have genetic screening test
for prostate cancer (n = 409)
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Multivariate Analyses.
Findings from logistic regression analysis (see Table 3
) show that belief in the efficacy of
prostate cancer screening and intention to have a prostate
cancer-screening examination were positively associated with intention
to be tested for prostate cancer risk. Being older and having had a DRE
or PSA test in the past year were negatively associated with intention
to be tested for prostate cancer risk. In addition, perceived prostate
cancer susceptibility and fatalism about prostate cancer prevention
were also negatively associated with intention to be tested.
Reported Barriers to Being Tested.
Men who reported a relatively weaker intention to be tested for
prostate cancer risk (n = 58) were asked to indicate
whether defined barriers would keep them from being tested. The
following distribution of responses was obtained: cost of the test
(58%); time involved in going for the test (52%); worry that other
people might find out about test results (47%); belief that the test
result might be wrong (45%); worry that test results might show that
they were at increased risk (43%); and concern about the physical
discomfort of testing (42%). Because respondents were able to choose
more than one response, recorded percentages sum to more than 100%.
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Discussion
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The overwhelming majority of men in the study population reported
a high level of intention to be tested for prostate cancer risk when
such testing becomes available. This finding is similar to results
reported in most studies of interest in genetic testing conducted among
patients with a family history of cancer and in the general
population. It is also consistent with the results of studies in
which men who were family members of prostate cancer patients have been
asked about their intention to be tested for prostate cancer risk
(17
, 19
, 27)
.
Men with high-perceived prostate cancer screening efficacy were more
likely to state that they intended to be tested for prostate cancer
risk than men with low-perceived screening efficacy. Intention to have
a prostate cancer-screening exam in the future was also positively and
significantly associated with intention to be tested for prostate
cancer risk. These findings suggest that men who were predisposed to
taking preventive action were also interested in knowing whether they
were at risk for developing prostate cancer in the future.
Men in the study who were 50 or more years of age were significantly
less likely than younger men to say that they intended to be tested.
Tambor, Rimer, and Strigo (35)
also reported that interest
in testing for genetic risk for breast cancer was negatively correlated
with age. Glanz et al. (22)
, however, found
that age was positively associated with intention to be tested for
colorectal cancer risk. Reasons for this lack of consistency across
studies in the relationship between age and intention to be tested is
not clear. Older participants in the current study may have been more
skeptical about genetic testing than younger participants
(50, 51, 52, 53)
. Older men, as compared with younger men, may
have viewed the prostate cancer-screening exam as providing sufficient
information for their use in protecting their health. This line of
reasoning is supported by the finding that men who had had a prior
prostate cancer-screening exam were less likely to say that they
intended to be tested for prostate cancer risk.
Interestingly, we also found that men who believed themselves to be
susceptible to prostate cancer were less likely to intend to be tested
for prostate cancer risk than those who thought they were not
susceptible to the disease. This finding was surprising, because it has
been reported elsewhere (17
, 22
, 24
, 30
, 31 , 37
, 38
, 54
, 55)
that perceived susceptibility is positively associated with
interest in being tested for cancer risk. It is possible that men in
the current study who thought they were at risk did not want to expose
themselves to the possibility of receiving information that might
support this belief. Another novel finding was that men in the study
group who were fatalistic about preventing prostate cancer were less
likely to say that they intended to be tested for prostate cancer risk.
It may be assumed that men who thought there was little hope of
preventing prostate cancer also would be likely to question the value
of predictive genetic testing.
Several studies (20
, 23
, 54, 55, 56, 57, 58, 59, 60)
have shown that interest
in being tested for breast and colorectal cancer risk does not
necessarily translate into an increase in susceptibility testing
among both men and women. It is likely that the same situation will
pertain to the relationship between the intention to be tested and
actually being tested for prostate cancer risk in the future.
Among African-American men, access problems (i.e., the
expense and time involved in testing), information confidentiality,
concern about test accuracy, worry about being found to be at increased
risk, and the perceived discomfort of the testing procedures may limit
the utilization of susceptibility testing. Other factors, such as lack
of knowledge about genetic testing procedures, skepticism about the
motivations of medical authority, and concern about confidentiality,
are likely to influence decision making about being tested for prostate
cancer risk. It should be possible to begin systematically identifying
factors that will influence decision making in this area through
studies that involve African-American men who are now being asked to
participate in prostate cancer genetic testing research projects, such
as the African American Hereditary Prostate Cancer
Study3
. This area of research is also relevant,
of course, to other high-risk groups. By applying theory-based
cognitive and psychosocial constructs in studies related to decision
making in this area, the process of identifying variables that are
useful in predicting actual behavior will be facilitated.
The study described here has important limitations. First, the
participating men were patients in an established health care system in
one metropolitan area and agreed to participate in a research project.
In terms of data collection, information on personal background
(e.g., family history of prostate cancer and past screening
history) was obtained only on the basis of self-report. As these
measures were based only on participant recall, they may have been to
some degree inaccurate. Prostate-screening status was assessed via the
inspection of clinic medical records. Study participants who were
screened elsewhere could have been classified as not having had a
screening exam. We have no evidence suggesting that this situation
actually occurred, however. It should be mentioned that intention to be
tested for prostate cancer risk was assessed at the same time as other
variables included in the study data set. We did not have a prospective
measure of intention to be tested for risk or of being tested for risk.
The aim of our analyses was to identify variables that were associated
with, not predictive of, this outcome. In addition, we sought to
determine barriers to being tested for prostate cancer risk only among
men with low intention scores. A more complete approach to ascertaining
this information would have been to ask all study participants to
identify potential barriers.
 |
Acknowledgments
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We want to express our appreciation to Drs. Leonard Gomella,
Elisabeth Kunkel, Walter Hauck, and Timothy Rebbeck for their critical
review of the manuscript. We also want to thank Martha Keintz and Trena
Diggs for their careful editorial work.
 |
Footnotes
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The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
1 Supported by the National Cancer Institute
(Grant R01 CA67464). 
2 To whom requests for reprints should be
addressed, at Behavioral Epidemiology Section, Division of Medical
Oncology, Department of Medicine, Thomas Jefferson University, 125
South Ninth Street, Philadelphia, PA 19107. Phone: (215) 503-4085; Fax
(215) 923-9506; E-mail: ron.myers{at}mail.tju.edu 
3 National Human Genome Research Institute.
National cooperative study of prostate cancer in African
Americans. URL:
www.nhgri.nih.gov/About_NHGRI/Dir/Prostate_Study/about.html. 
4 The abbreviations used are: PHM, Preventative
Health Model; DRE, digital rectal exam; PSA, prostate-specific
antigen. 
Received 5/10/00;
revised 9/22/00;
accepted 9/29/00.
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