Factors associated with testicular self-examination among unaffected men from multiple-case testicular cancer families
© Vadaparampil et al; licensee BioMed Central Ltd. 2009
Received: 05 February 2009
Accepted: 29 May 2009
Published: 29 May 2009
The lifetime testicular cancer (TC) risk in the general population is relatively low (~1 in 250), but men with a family history of TC are at 4 to 9 times greater risk than those without. Some health and professional organizations recommend consideration of testicular self-examination (TSE) for certain high-risk groups (e.g. men with a family history of TC). Yet little is known about factors associated with TSE behaviors in this at-risk group.
We collected information on this subject during an on-going NCI multidisciplinary, etiologically-focused, cross-sectional Familial Testicular Cancer (FTC) study. We present the first report specifically targeting TSE behaviors among first- and second-degree relatives (n = 99) of affected men from families with ≥ 2 TC cases. Demographic, medical, knowledge, health belief, and psychological factors consistent with the Health Belief Model (HBM) were evaluated as variables related to TSE behavior, using chi-square tests of association for categorical variables, and t-tests for continuous variables.
For men in our sample, 46% (n = 46) reported performing TSE regularly and 51% (n = 50) reported not regularly performing TSE. Factors associated (p < .05) with regularly performing TSE in multivariate analysis were physician recommendation and testicular cancer worry. This is the first study to examine TSE in unaffected men from FTC families.
The findings suggest that, even in this high-risk setting, TSE practices are sub-optimal. Our data provide a basis for further exploring psychosocial issues that are specific to men with a family history of TC, and formulating intervention strategies aimed at improving adherence to TSE guidelines.
Although testicular cancer (TC) accounts for only 1% of all male cancers, it is the most common cancer in younger men aged 20–35 years old, with about 8,090 new cases estimated to occur during 2008 in the U.S. . TC incidence rates have been rising since the mid-twentieth century, especially among white males , while the rates of many other cancers have been decreasing. Although 5-year survival for TC has increased over the past several decades, long term survival remains related to stage at diagnosis , with localized TC 5-year survival rates of 99.5%, versus 70.1% for metastatic TC . In addition, earlier stage disease often requires less extensive treatment. Thus, early detection may minimize both TC-associated morbidity and mortality [5–7].
Leading health organizations debate the efficacy of testicular self-examination (TSE) in reducing TC related mortality , particularly with the advent of chemotherapeutic regimens that are highly-effective even for men with advanced disease during the last several decades. However, this decrease in mortality is accompanied by an increase in treatment-related morbidity, particularly for those cancers that are diagnosed at later stages [6, 9]. A recent review found little shift of the approximate 5-month delay from onset of TC symptoms to surgical diagnosis over the past seventy-five years . While TSE may not markedly improve the already high survival rates related to TC, early diagnosis does bring significant potential to reduce treatment-related morbidity, since surgery plus close surveillance is a viable management option for many early-stage patients . Education and instruction for men on the normal shape and texture of the testicles, plus information regarding signs and symptoms associated with TC could be a critical component in reducing treatment delay [11, 12].
Additionally, as epidemiological research identifies specific TC risk factors, some organizations have refined their screening recommendations to focus on high-risk groups. Established TC risk factors include cryptorchidism (undescended testes), prior contralateral TC and testicular intra-epithelial neoplasia. Testicular cancer risk is also increased in certain genetic conditions, such as Klinefelter and androgen insensitivity syndromes. Other conditions that may increase TC risk include urogenital malformations, testicular dysgenesis, testicular atrophy, history of infertility, and, possibly, exposures to a variety of etiologic agents during key developmental periods . Perhaps most importantly, family history is known to be an important independent risk factor. Approximately 1–3% of men with testicular cancer report the presence of another affected male in their family. Sons of men with TC have a four- to six-fold increase in risk of TC, and brothers carry an eight- to ten-fold increase in the risk when compared with the general population [14–16].
The American Cancer Society recommends that men with known risk factors such as family history seriously consider performing TSE regularly. This approach to modifying general population early cancer detection practices for high-risk populations is not unique to men with a familial risk for TC. For example, the National Comprehensive Cancer Network recommends routine breast self-examination (BSE) for women at increased risk of hereditary breast and ovarian cancer (HBOC) , despite randomized controlled trial data refuting the efficacy of BSE in reducing breast cancer mortality . In addition to the possibility that TSE recommendations for self-examination may reduce chemotherapy-related morbidity by increasing the proportion of early-stage TC diagnosed in high-risk men, there may also be further benefit in providing at-risk individuals with a management strategy that involves them directly in their own care, and gives them an enhanced sense of control over their lives .
We present an analysis of data collected from participants in a National Cancer Institute (NCI) multidisciplinary, etiologically-focused study of familial testicular cancer (FTC). Its primary aims include  identifying FTC susceptibility genes;  characterizing the FTC syndrome clinical phenotype; and  evaluating psychosocial and behavioral issues resulting from being a member of a family at increased risk of testicular germ cell tumor (TGCT). Segregation analysis has suggested that an autosomal recessive genetic model best explains the distribution of disease in FTC families although, to date, no specific TC susceptibility genes have been identified . The current exploratory sub-study describes the TSE practices of unaffected at-risk men from multiple-case families, and characterizes key demographic, medical, knowledge, health belief, and psychological factors associated with TSE using Health Belief Model (HBM) constructs and terminology . Specifically, we included the HBM variables of perceived benefits, barriers, susceptibility and severity. As previously discussed, TSE may improve high-risk men's sense of control over their own health [10, 29]. Thus, to examine this association we assessed health locus of control. Finally, previous behavioral research has emphasized the role of affect in health behaviors , thus we included the psychological variables of cancer worry and distress.
Materials and methods
The 99 TSE sub-study participants were members of 47 families enrolled on an NCI Clinical Genetics Branch (CGB) IRB-approved protocol (#02-C-0178) . Families were eligible for the main study if they had ≥ 2 confirmed cases of TC, or a single family member with bilateral TC. Eligible individuals included all TC cases age > 12 years, their first- and second-degree relatives), and blood relatives who either linked the two TC cases or who had themselves been diagnosed with cancer other than TC. In addition, spouses were included if they had children ≥ 12 years old who were study participants. Participants were ascertained through multiple referral mechanisms: 62/99 (63%) from healthcare providers (primarily physicians and genetic counselors), in response to mailed recruitment letters; 15/99 (15%) from the Testicular Cancer Resource Center (TCRC) http://tcrc.acor.org/, a patient advocacy group,; 13/99 (13%) self-referred through our study website http://familial-testicular-cancer.cancer.gov; and 9/99 (10%) from other sources. Unaffected males > age18 who were first- or second-degree relatives of a TC case were included in the current TSE analysis.
Data were collected via a mailed, written questionnaire (the Lifestyle and Attitudes Questionnaire [LAQ]), developed specifically for the FTC study. The present analysis was limited to those LAQ items pertaining to TSE and the relevant independent variables. These independent variables included items and scale scores from standardized, validated psychometric instruments, as well as items developed specifically for this study.
For this analysis, we chose variables of theoretical and practical interest related to predicting health behavior, as well as other factors which have been previously-implicated as related to cancer self-examination behavior.
Demographic and Medical Characteristics
Various sociodemographic and medical characteristics were assessed via self-report questionnaire: The age dichotomy (< 35; > 35) was selected based on ages of men at greatest TC risk; race (white; other); marital status (divorced/single/unknown; married); education (< high school; at least some college; post- graduate); relation to a TC case (first-degree relative; second-degree relative); and prior history of testicular abnormality (cryptorchidism, orchitis, epididymitis, or injury to testicle; no abnormalities).
Knowledge of TC
We measured knowledge regarding TC with the Testicular Cancer Knowledge Scale (TCKS), a 10-item scale (range of scores = 0–10 determined by the sum of questions answered correctly) based on an instrument developed to assess TC-related knowledge among young adults (Cronbach's alpha = .70) , including items regarding TC etiology, the timing and method of TSE, and the sequelae of TC. Each item had 3 possible answers: Agree, Disagree, or Don't Know.
Health Belief Model Variables
We evaluated critical HBM concepts: perceived TC susceptibility and severity, as well as perceived benefits and barriers to TSE. In keeping with more recent HBM applications [32, 33], we included the Cue to Action construct. We also included the health locus of control concept to assess individual belief that health is controlled by internal or external factors, such as performing self-examinations for cancer.
Perceived Susceptibility to Testicular Cancer Scale
Perceived susceptibility was assessed using previously-validated items associated with developing testicular  and breast cancer . Perception of TC susceptibility was measured by summing responses to 3 five-point Likert scale items (1 = strongly agree to 5 = strongly disagree) (Cronbach's alpha = 0.76). An example of an item from this scale: "It is likely that I will get testicular cancer."
Perceived Severity of Testicular Cancer Scale
Perceived severity was assessed using previously-validated items associated with developing testicular cancer . However, due to the low Cronbach's alpha for this scale in our sample , we included each item as a separate variable in the bivariate analyses. Thus, perception of severity was measured using individual values of three items with a five-point Likert scale (1 = strongly agree to 5 = strongly disagree). An example of an item from this scale: "If I got testicular cancer, its impact on my life would be severe."
Perceived Benefits of Testicular Self-examination
Perceived benefits were assessed using responses to 6 five-point Likert scale items (1 = strongly agree to 5 = strongly disagree) derived from previous health beliefs research regarding testicular  and breast cancer  risk (Cronbach's alpha = 0.77). An example of an item from this scale: "If I examined my own testicles regularly, I might find a lump sooner that if I just went to the doctor for a check up."
Perceived barriers were assessed using responses to 7 five-point Likert scale items (1 = strongly agree to 5 = strongly disagree) derived from previous health beliefs research regarding testicular  and breast cancer risk  (Cronbach alpha = 0.61).). An example of an item from this scale: "I am too busy to do TSE."
Cue to Action for TSE
Previous cancer prevention behavior studies identified physician recommendation as a key factor predicting uptake of cancer self-examination behaviors. We adapted a single 2000 National Health Interview Survey item to assess whether a physician had ever recommended performing TSE (yes, no).
Locus of Control
The Multidimensional Health Locus of Control (MHLC) Scale consists of 3 six-point Likert scales (total: 18 items) (1 = strongly agree to 6 = strongly disagree). Internal Health Locus of Control (IHLC) quantifies the belief that internal factors are responsible for health/illness (Cronbach's alpha = .78); Powerful Others Health Locus of Control (PHLC) quantifies the belief that one's health is determined by powerful others (Cronbach's alpha = .57); and Chance Health Locus of Control (CHLC) quantifies the belief that health illness is a matter of fate, luck or chance (Cronbach's alpha = .62). 
We measured cancer worry and cancer distress (intrusive and avoidant thoughts).
We modified the Lerman Breast Cancer Worry Scale to assess cancer worry among men at risk of TC . The scale assesses frequency of concerns about developing testicular cancer and the impact of cancer worry on mood and daily functioning on a 4-point scale (1 = not at all or rarely, to 4 = a lot) (Cronbach's alpha = 0.82) .
Cancer Distress via the Impact of Events Scale (IES)
The IES  measures the subjective impact of a specific event on an individual by assessing two major responses to stressful events: intrusion and avoidance. Intrusion is characterized by repetitive thoughts, mental images, disturbing dreams, and repetitive behavior, and is scored from 0 – 35 (Cronbach's alpha = .90). Avoidance is associated with denial of consequences from an event, blunted feelings, and emotional numbness related to an event , and is scored from 0 – 40 (Cronbach's alpha = .90). Respondents used a 4-point response scale (0 = 'not at all', 1 = 'rarely', 3 = 'sometimes', 5 = 'often') from a set of 15 TC-related statements to report the frequency with respect with which each occurred during the prior 7 days. It is a reliable and valid instrument for cancer-related distress among men and women either affected by or at risk of various cancers .
Practice of TSE
This was the primary analysis outcome. In the questionnaire, TSE was described as follows: "Testicular Self-examination (TSE) is when a man checks himself for any abnormalities in his testicles." Participants were then asked to provide a numerical response to the question "Have many times during the past year have you performed TSE?". We then classified men into two groups: those who regularly performed TSE (≥ 6 times in the past year) and those who did not regularly perform TSE (0–5 times in the past year). Previously- published research on TSE practices has used various standards to classify an individual as a regular performer of TSE, ranging from simply asking an individual whether they regularly perform TSE (yes, no) without defining the term "regular" , to categories based on a numeric response to a question about the frequency of TSE in a specified time frame [19, 26]. However, the cut points for categorizing an individual as a regular TSE performer differ among studies. For example, one study considered an individual who reported performing TSE 1 to 10 times a year as a regular performer , while another considered only individuals who reported practicing TSE 12 times in the previous year as a regular performer . There is current a lack of consensus among leading health and professional organizations on the recommended interval for TSE screening, and a lack of consistency in research studies regarding who is considered to be a "regular performer." Thus, we opted for a moderate approach whereby individuals who reported TSE > 6 times in the previous year were classified as regular performers, and those who reported TSE < 6 times as non-regular performers of TSE.
The main outcome of interest was Practice of TSE, a dichotomous variable consisting of those who reported they had regularly performed TSE (> 6 times in the previous year) compared to those who did not (< 6 times in the previous year). Descriptive statistics and reliability analyses were performed using the SPSS v. 15.0 statistical software package, and multivariate logistic regression employed SAS version 9.1.3. All analyses used two-tailed tests of significance. First, univariate analysis was used to compare TSE regular performers versus non-regular performers based on sociodemographic, medical, knowledge, HBM, and psychological factors. Independent variables that were significant at p < 0.05 (T-test, Chi square test) were then simultaneously entered into a multiple logistic regression model. Although the individual was the unit of analysis in this study, the familial nature of the cohort raised concerns regarding the assumption of observation independence. Therefore, all analyses that involved statistical testing (e.g. chi-square or t tests, logistic models) were conducted with a program that accounted for possible clustering within families (SAS Proc Surveyfreq, Proc Surveymeans, Proc Surveylogistic; SAS Institute, 2003). These procedures use the Taylor linearization method to estimate sampling errors of estimators based on potential clustering of responses between family members. Respondents with missing values for relevant variables were excluded from analyses.
Demographic and Medical Characteristics of Unaffected Men from Multiple-Case Testicular Cancer Familiesa
(n = 96)b, c
Regularly Performed TSE (n = 46)c, d
Did Not Regularly Performed TSE (n = 50)c, e
Age (%; n)
Marital Status (%; n)
Race (%; n)
Education (%; n)
Some college/college graduate
Relation to Case (%; n)
Prior history of TC abnormality (cryptorchidism, orchitis, epididymitis, or injury to testicle) (%; n)
Physician Rec. (Cue to Action) (%; n)
Performance of TSE
Of the 99 participants who met inclusion criteria for this sub-study, forty-six percent reported performing TSE six or more times in the previous year, while 51% reported performing TSE less than 6 times; the remaining 3% did not respond to this question.
Individual Factors Associated with Regular Performance of TSE
Knowledge, Health Belief and Psychosocial Characteristics of Unaffected Men from Multiple-Case Testicular Cancer Familiesa
(n = 96)b, c (X+SE)
Regularly Performed TSEb, c (n = 46) (X+SE)
Did Not Regularly Perform TSEb, d (n = 50) (X+SE)
Testicular Cancer Knowledge
Perceived Severity (impact of TC on life)
Perceived Severity (pain and suffering from TC)
Perceived Severity (chance of survival from TC)
Internal Health Locus of Control
Powerful Others Health Locus of Control
Chance Health Locus of Control
Factors not significantly associated with regular performance of TSE included marital status, education, having a prior testicular abnormality, perceived TC susceptibility, Health Locus of Control (internal, powerful others, or chance), and having avoidant thoughts.
Logistic Regression Model of Predictors of Testicular Self-examination among Unaffected Men from Multiple-Case Testicular Cancer Families (n = 91)
Odds Ratio (95% Confidence Interval)
Age > 35
0.4 (0.1, 1.3)
FDR of Case
2.2 (0.7, 8.0)
Physician Recommendation for TC
6.6 (2.0, 21.1)*
Testicular Cancer Knowledge
1.2 (0.84, 1.6)
1.1 (0.9, 1.4)
0.8 (0.6, 1.0)
1.6 (1.1, 2.3)*
1.0 (0.9, 1.1)
Forty six percent of unaffected, at-risk men from multiple-case TC families in our sample reported regular performance of TSE. The two factors significantly associated with regular performance of TSE were physician recommendation and higher levels of TC cancer worry.
In a 2005 review of TSE practices that included 6 studies of U.S. men ≥ age 18 , the percent of men practicing TSE on a monthly basis ranged from 6 to 36% Our TSE rates are not directly comparable to those data, which defined regular performance of TSE as once a month, since we used a broader inclusion for our regular performer category of 6 times a year or more. This may explain the higher proportion of men in our sample that were defined as regular performers of TSE (46%).
With respect to the HBM variables assessed in the current study, only Cues to Action (i.e. physician recommendation for TSE), remained a statistically significant predictor of TSE behavior in multivariate analysis. The importance of physician recommendation on TSE practice was striking, with men who reported a physician recommendation for TSE having at least six times higher odds of performing regular TSE compared with those who reported no such recommendation. This provides yet another example [33, 40, 41] of how potent an influence the physician can be with regard to cancer prevention behavior in patients, and underscores the importance of physicians including such recommendations in the course of ongoing health care discussions. Due to the lack of a strong evidence base to support the belief that TSE is associated with improved TC-related survival among those who practice it, and the remarkable therapeutic successes in managing TC patients even with far-advanced disease, it is unlikely that there ever will be a clinical trial testing this question. In this era of evidence-based medical practice, it is difficult for health care providers to insist that at-risk men adopt TSE practice, although common sense and logic suggest that a TC detected by TSE rather than symptoms should be more amenable to treatment regimens that do not include chemotherapy, or permit less intense or shorter chemotherapy regimens. This rationale is not unlike recommendations for both BSE, CA-125 testing, and transvaginal ultrasound recommendations for women at increased risk for hereditary breast and ovarian cancer . Given that TC is a disease which affects young men during the most productive period of their lives, there is potential for real economic and psychosocial benefit in attempting to minimize treatment-associated costs and morbidity.
Two previous studies of the HBM and TSE showed that perceived benefits and barriers were associated with TSE, as did our data [19, 29]. In our study, perceived cancer susceptibility was not associated with TSE. Although one previous study examining the relationship between TSE and perceived susceptibility found a significant association, there were only 12 men in the entire study who were considered to be "practicers" of TSE (i.e. reported practicing TSE > 4 times a year) [19, 29]. A larger study of TSE behaviors using multivariate analyses failed to replicate this finding . Perceived severity of TGCT was not a significant predictor of PSA testing. This finding is similar to two previous studies of TSE that used the HBM as a theoretical framework [19, 29]. Previous cancer screening research for a variety of sites has also found perceived susceptibility of little predictive value with regard to screening behaviors, possibly due to the almost universally held belief that cancer is a severe disease, regardless of type [43–48]. In our study, none of the HBM factors significant in bivariate analyses remained so when they were considered in a multivariate model which included physician recommendation. This result is consistent with many previous studies of cancer screening behaviors.
To our knowledge only one other study has examined HBM with respect to TSE using multivariate analysis. Overall, it appears that the HBM does not adequately explain TSE behavior. Similar to our study, HBM variables accounted for only a small proportion of the variance in TSE behavior (21%) . As discussed below, cancer-related worry was the main psychosocial predictor of TSE behavior in our study and may lend some support to the commonly-raised concern regarding the HBM and other cognitive models of health behavior, namely that they do not include affective variables as behavior predictors .
Cancer-related worry was the other major factor associated with TSE practice patterns in our study. From a theoretical perspective, several relationships between cancer worry and cancer prevention behaviors have been proposed. Some models posit that worry may serve as a facilitator to cancer screening behavior, others postulate worry acts a barrier, and some propose a curvilinear relationship between cancer worry and preventive behaviors, whereby worry is a facilitator to a certain level after which it becomes a barrier . The HBM, which was the theoretical basis of the present study, has been used to support the role of worry as both a barrier and facilitator for cancer screening behavior . In our sample, it appears that cancer worry motivates individuals to practice TSE, since those with higher levels of cancer worry were also more likely to perform TSE. However, the directionality of this relationship can only be established in the context of a prospective study; our data are cross-sectional. Studies in other high-risk populations provide some evidence that cancer worry may in fact precede screening behavior. In a review of the relationship between cancer worry and mammography screening among high-risk women, four of five prospective studies indicated that higher levels of cancer worry were associated with greater rates mammography screening and breast self-examination . However, no similar prospective studies of high-risk men are available. One cross-sectional study of prostate cancer screening among a sample of men at increased risk of hereditary prostate cancer found a negative relationship between cancer worry and screening behavior .
It is noteworthy that we observed no statistically significant differences in TSE practices between men with and without a prior history of a testicular abnormality. A personal history of cryptorchidism can increase the risk of TC up to 11-fold . Of the 13 men reporting a testicular abnormality in our series, 29% (n = 4) reported a history of cryptorchidism (data not shown). In a study by Blesch and colleagues, none of the 5 men with a history of cryptorchidism, reported regularly practicing TSE . While this finding may reflect the small number of men with this particular risk factor and the associated lack of statistical power to detect a difference in that study, it is possible that men may be unaware that testicular maldescent is among the most strongly-established TC risk factors. However, no study to date has focused specifically on the levels of awareness/knowledge of cryptorchidism as a risk factor for TC or as a multivariate predictor of TSE behavior.
In multivariate analyses, men age = 35 and those who were first-degree relatives of a TC case were no more likely to perform TSE than were older men or those whose affected family member was a more distant relative. In the 2005 review mentioned above , only 12–25% of participants in U.S. studies were aware of the age group most affected by TC. In the study by Blesch and colleagues , men with a family history of TC were significantly more likely to perceive greater benefits to TSE. However, the study did not assess the impact on actual TSE behavior. Taken together, the non-differential rates of TSE between men in younger and older age groups, men who are first versus second-degree relatives of a TC case, and men with a prior testicular abnormality compared with those without, suggest a lack of awareness on the part of unaffected family members regarding the additional risk conferred by having these characteristics. It is also possible that men recognize the implications of these characteristics, but they are not sufficiently concerned by this information to motivate screening behavior.
To our knowledge, this is the first study to examine TSE behaviors among unaffected men from multiple-case testicular cancer families. While the results provide important information about current rates and correlates of TSE in this high-risk group, they should be interpreted with caution due to certain limitations of our study. A goal of our study was to evaluate the utility of HBM in understanding TSE behavior. Ideally, use of an analytic technique such as structural equation modeling would allow us to definitively test the utility of HBM in predicting TSE behavior. However, our study was designed as a pilot study of the utility of HBM and it did not have a sample size sufficient to reach definitive conclusions. It is possible that the HBM did not adequately capture those factors that were important in TSE behavior. For example, one of the major criticism of HBM and other cognitive models of health behavior is the lack of inclusion of affective variables (e.g. distress) . To address this issue, we included scales for both cancer worry and cancer distress. Additionally, we included demographic and SES variables that may also impact screening behavior. Finally, in a study that compared the HBM to the Theory of Planned Behavior, the quality of the models was very similar. The TPB explained 22%of the variance in behavior versus 21% by the HBM, suggesting that applying another theoretical framework may have yielded similar results . Thus, based on our review of the literature related to theories of health behavior and predictors of screening, we feel that we adequately expanded the HBM to include other factors associated with TSE behavior. In addition, this was a cross-sectional study, making it difficult to establish that the beliefs and psychological factors we identified preceded the behavior, as hypothesized in the HBM. Additionally, men volunteering to participate in a study of familial TC may be more aware of and concerned about TC. Thus, the rates of TSE may be higher in this study population than men with a similar history not participating in such a study. Similarly, these men may be more knowledgeable about TC and have differing beliefs and psychological responses to TC.
As molecular genetic diagnosis improves, family history of TC will become an increasingly important risk factor on which to base decisions for primary, secondary, and tertiary prevention of TC. The present study showed that among men with a family history of TC, those who had higher levels of cancer worry were more likely to practice TSE regularly. However, findings also revealed that men at increased risk of TC due to a positive family history may be either less knowledgeable about and/or less motivated to perform TSE even if they are younger, have a prior testicular abnormality, or are a FDR of a man with TC. Thus, these are areas in which men may benefit from additional education and information upon which to base decisions about TSE practices. Physician recommendation emerged as the most important predictor of regular performance of TSE. Despite the absence of proof regarding the efficacy of TSE, it nonetheless remains prudent to encourage health care providers to recommend monthly TSE for high-risk patients, and to instruct their patients in performing this examination. Given the superficial/accessible location of the testes, and the existence of non-invasive imaging (testicular ultrasound) and tumor marker assays, the price one pays for a false-positive screening examination is likely to be substantially less than would be the case for ovarian cancer screening, for example. Finally, providing at-risk men information regarding accepted TC risk factors, as a means of deepening their understanding of their own risk, might help to correct some of the information deficiencies we identified. Despite the limitations in both our and other's studies, we have adopted the policy of recommending monthly TSE as a screening modality for unaffected bloodline males from multiple-case TC families, while clearly informing our patients that this represents our best clinical judgment rather than an evidence-based recommendation.
This research was supported in part by funding from the Intramural Research Program of the National Cancer Institute to NCI's Clinical Genetics Branch, and by support services contracts NO2-CP-11019 and N02-CP-65504 with Westat, Inc. The authors gratefully acknowledge the invaluable technical and programmatic support of Ann Carr, Janet Bracci and Jennifer Restrepo in the conduct of the study, Doug Banks and the Testicular Cancer Resource Center for their efforts in raising awareness of the research protocol in the familial testicular cancer community and facilitating referral of families, and the invaluable contributions made by study participants, without whom this work could not have been done.
- Edwards BK, Brown ML, Wingo PA, Howe HL, Ward E, Ries LA, Schrag D, Jamison PM, Jemal A, Wu XC, Friedman C, Harlan L, Warren J, Anderson RN, Pickle LW: Annual report to the nation on the status of cancer, 1975–2002, featuring population-based trends in cancer treatment. J Natl Cancer Inst 2005, 97: 1407–27.View ArticlePubMedGoogle Scholar
- Purdue MP, Devesa SS, Sigurdson AJ, McGlynn KA: International patterns and trends in testis cancer incidence. Int J Cancer 2005, 115: 822–7. 10.1002/ijc.20931View ArticlePubMedGoogle Scholar
- ACS: Cancer facts and figures – 2007. (ACS Publication No. 5008.07). Atlanta, GA: American Cancer Society; 2007.Google Scholar
- Ries LAG, Harkins D, Krapcho M, Mariotto A, Miller BA, Feuer EJ, Clegg L, Eisner MP, Horner MJ, Howlader N, Hayat M, ed: SEER Cancer Statistics Review, 1975–2003. Bethesda, MD: National Cancer Institute; 2006.
- Molina Saera J, Aparicio Urtasun J, Diaz Beveridge R, Palomar Abad L, Gimenez Ortiz A, Ponce Lorenzo J, Montalar Salcedo J: Epidemiological pattern and time trends in testicular germ-cell tumors: a single institution 20-year experience. Clin Transl Oncol 2006, 8: 588–93. 10.1007/s12094-006-0064-2View ArticlePubMedGoogle Scholar
- Moul JW, Paulson DF, Dodge RK, Walther PJ: Delay in diagnosis and survival in testicular cancer: impact of effective therapy and changes during 18 years. J Urol 1990, 143: 520–3.PubMedGoogle Scholar
- Ondrusova M, Ondrus D: Epidemiology and treatment delay in testicular cancer patients: a retrospective study. Int Urol Nephrol 2008, 40: 143–148. 10.1007/s11255-007-9245-3View ArticlePubMedGoogle Scholar
- Adelman WP, Joffe A: Controversies in male adolescent health: varicocele, circumcision, and testicular self-examination. Curr Opin Pediatr 2004, 16: 363–7. 10.1097/01.mop.0000131451.41322.43View ArticlePubMedGoogle Scholar
- Wishnow KI, Johnson DE, Preston WL, Tenney DM, Brown BW: Prompt orchiectomy reduces morbidity and mortality from testicular carcinoma. Br J Urol 1990, 65: 629–33. 10.1111/j.1464-410X.1990.tb14834.xView ArticlePubMedGoogle Scholar
- Moul JW: Timely diagnosis of testicular cancer. Urol Clin North Am 2007, 34: 109–17. 10.1016/j.ucl.2007.02.003View ArticlePubMedGoogle Scholar
- Chapple A, Ziebland S, McPherson A: Qualitative study of men's perceptions of why treatment delays occur in the UK for those with testicular cancer. Br J Gen Pract 2004, 54: 25–32.PubMedPubMed CentralGoogle Scholar
- Vasudev NS, Joffe JK, Cooke C, Richards F, Jones WG: Delay in the diagnosis of testicular tumours – changes over the past 18 years. Br J Gen Pract 2004, 54: 595–7.PubMedPubMed CentralGoogle Scholar
- Kramer JL, Greene MH, ed: Hereditary Testicular Cancer. Comprehensive Textbook of Genitourinary Oncology. Philadephia, PA: Lippincott; 2006.
- Dieckmann KP, Pichlmeier U: The prevalence of familial testicular cancer: an analysis of two patient populations and a review of the literature. Cancer 1997, 80: 1954–60. 10.1002/(SICI)1097-0142(19971115)80:10<1954::AID-CNCR12>3.0.CO;2-XView ArticlePubMedGoogle Scholar
- Hemminki K, Chen B: Familial risks in testicular cancer as aetiological clues. Int J Androl 2006, 29: 205–10. 10.1111/j.1365-2605.2005.00599.xView ArticlePubMedGoogle Scholar
- Hemminki K, Li X, Czene K: Familial risk of cancer: data for clinical counseling and cancer genetics. Int J Cancer 2004, 108: 109–14. 10.1002/ijc.11478View ArticlePubMedGoogle Scholar
- Daly M, Axilbund JE, Bryant E, Buys S, Eng C, Friedman S, Esserman LJ, Farrell CD, Garber J, Jeter J, Kohlman W, Lynch PM, Marcom PK, Nabell LM, Osarogiagbon RU, Pasche B, Reiser G, Sutphen R, Weitzel JN: The NCCN Genetic/Familial High-Risk Assessment: Breast and Ovarian Clinical Practice Guideline, version 1.2006.2006. [http://www.nccn.org]Google Scholar
- Thomas DB, Gao DL, Ray RM, Wang WW, Allison CJ, Chen FL, Porter P, Hu YW, Zhao GL, Pan LD, Li W, Wu C, Coriaty Z, Evans I, Lin MG, Stalsberg H, Self SG: Randomized trial of breast self-examination in Shanghai: final results. J Natl Cancer Inst 2002, 94: 1445–57.View ArticlePubMedGoogle Scholar
- Blesch KS: Health beliefs about testicular cancer and self-examination among professional men. Oncol Nurs Forum 1986, 13: 29–33.PubMedGoogle Scholar
- Katz RC, Meyers K, Walls J: Cancer awareness and self-examination practices in young men and women. J Behav Med 1995, 18: 377–84. 10.1007/BF01857661View ArticlePubMedGoogle Scholar
- Moore RA, Topping A: Young men's knowledge of testicular cancer and testicular self-examination: a lost opportunity? Eur J Cancer Care (Engl) 1999, 8: 137–42. 10.1046/j.1365-2354.1999.00151.xView ArticleGoogle Scholar
- Neef N, Scutchfield FD, Elder J, Bender SJ: Testicular self-examination by young men: an analysis of characteristics associated with practice. J Am Coll Health 1991, 39: 187–90.View ArticlePubMedGoogle Scholar
- Rodriguez JG, Velez M, Serrano E, Casado MP: Adolescent student's compliance with testicular self examination. Bol Asoc Med P R 1995, 87: 49–53.PubMedGoogle Scholar
- Singer AJ, Tichler T, Orvieto R, Finestone A, Moskovitz M: Testicular carcinoma: a study of knowledge, awareness, and practice of testicular self-examination in male soldiers and military physicians. Mil Med 1993, 158: 640–3.PubMedGoogle Scholar
- Trumbo CW: Mass-mediated information effects on testicular self-examination among college students. J Am Coll Health 2004, 52: 257–61. 10.3200/JACH.52.6.257-262View ArticlePubMedGoogle Scholar
- Ward KD, Weg MW, Read MC, Sell MA, Beech BM: Testicular cancer awareness and self-examination among adolescent males in a community-based youth organization. Prev Med 2005, 41: 386–98. 10.1016/j.ypmed.2005.02.003View ArticlePubMedGoogle Scholar
- Crockford GP, Linger R, Hockley S, Dudakia D, Johnson L, Huddart R, Tucker K, Friedlander M, Phillips KA, Hogg D, Jewett MA, Lohynska R, Daugaard G, Richard S, Chompret A, Bonaiti-Pellie C, Heidenreich A, Albers P, Olah E, Geczi L, Bodrogi I, Ormiston WJ, Daly PA, Guilford P, Fossa SD, Heimdal K, Tjulandin SA, Liubchenko L, Stoll H, Weber W, Forman D, Oliver T, Einhorn L, McMaster M, Kramer J, Greene MH, Weber BL, Nathanson KL, Cortessis V, Easton DF, Bishop DT, Stratton MR, Rapley EA: Genome-wide linkage screen for testicular germ cell tumour susceptibility loci. Hum Mol Genet 2006, 15: 443–51. 10.1093/hmg/ddi459View ArticlePubMedGoogle Scholar
- Janz NK, Champion VL, Strecher VJ, ed: The Health Belief Model. Health Behavior and Health Education. San Francisco, CA: Jossey-Bass; 2002.Google Scholar
- McClenahan C, Shevlin M, Adamson G, Bennett C, O'Neill B: Testicular self-examination: a test of the health belief model and the theory of planned behaviour. Health Educ Res 2007, 22: 272–84. 10.1093/her/cyl076View ArticlePubMedGoogle Scholar
- Slovic P, Peters E, Finucane ML, Macgregor DG: Affect, risk, and decision making. Health Psychol 2005, 24: S35–40. 10.1037/0278-6133.24.4.S35View ArticlePubMedGoogle Scholar
- Korde LA, Premkumar A, Mueller C, Rosenberg P, Soho C, Bratslavsky G, Greene MH: Increased prevalence of testicular microlithiasis in men with familial testicular cancer and their relatives. Br J Cancer 2008, 99: 1748–53. 10.1038/sj.bjc.6604704View ArticlePubMedPubMed CentralGoogle Scholar
- Bazargan M, Bazargan SH, Calderon JL, Husaini BA, Baker RS: Mammography screening and breast self-examination among minority women in public housing projects: the impact of physician recommendation. Cell Mol Biol (Noisy-le-grand) 2003, 49: 1213–8.Google Scholar
- Manne S, Lessin S: Prevalence and correlates of sun protection and skin self-examination practices among cutaneous malignant melanoma survivors. J Behav Med 2006, 29: 419–34. 10.1007/s10865-006-9064-5View ArticlePubMedGoogle Scholar
- Champion VL: Revised susceptibility, benefits, barriers scale for mammography screening. Res Nurs Health 1999, 22: 341–8. 10.1002/(SICI)1098-240X(199908)22:4<341::AID-NUR8>3.0.CO;2-PView ArticlePubMedGoogle Scholar
- Wallston KA, Wallston BS, DeVellis R: Development of the Multidimensional Health Locus of Control (MHLC) Scales. Health Educ Monogr 1978, 6: 160–70.View ArticlePubMedGoogle Scholar
- Lerman C, Daly M, Masny A, Balshem A: Attitudes about genetic testing for breast-ovarian cancer susceptibility. J Clin Oncol 1994, 12: 843–50.PubMedGoogle Scholar
- Horowitz M, Wilner N, Alvarez W: Impact of Event Scale: a measure of subjective stress. Psychosom Med 1979, 41: 209–18.View ArticlePubMedGoogle Scholar
- Vadaparampil ST, Ropka M, Stefanek ME: Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers. Fam Cancer 2005, 4: 195–206. 10.1007/s10689-004-1446-7View ArticlePubMedGoogle Scholar
- McCullagh J, Lewis G, Warlow C: Promoting awareness and practice of testicular self-examination. Nurs Stand 2005, 19: 41–9.View ArticlePubMedGoogle Scholar
- Aitken JF, Janda M, Lowe JB, Elwood M, Ring IT, Youl PH, Firman DW: Prevalence of whole-body skin self-examination in a population at high risk for skin cancer (Australia). Cancer Causes Control 2004, 15: 453–63. 10.1023/B:CACO.0000036451.39128.f6View ArticlePubMedGoogle Scholar
- Manne S, Fasanella N, Connors J, Floyd B, Wang H, Lessin S: Sun protection and skin surveillance practices among relatives of patients with malignant melanoma: prevalence and predictors. Prev Med 2004, 39: 36–47. 10.1016/j.ypmed.2004.02.028View ArticlePubMedGoogle Scholar
- Daly M, Axilbund JE, Bryant E, Buys S, Farrell CD, Ford JM, Friedman S, Garber J, Gruber S, Hampel H, Kaklamani V, Kohlmann W, Litton J, Marcom PK, Offitt K, Osarogiagbon RU, Pasche B, Reiser G, Shannon KM, Smith JR, Sutphen R, Weitzel JN: The NCCN Genetic/Familial High-Risk Assessment: Breast and Ovarian Clinical Practice Guideline, version 1.2009.2009. [http://www.nccn.org/professionals/physician_gls/PDF/genetics_screening.pdf]Google Scholar
- Champion VL, Scott CR: Reliability and validity of breast cancer screening belief scales in African American women. Nursing Research 1997, 46: 331–337. 10.1097/00006199-199711000-00006View ArticlePubMedGoogle Scholar
- Aiken LS, West SG, Woodward CK, Reno RR: Health beliefs and compliance with mammography-screening recommendations in asymptomatic women. Health Psychol 1994, 13: 122–9. 10.1037/0278-6184.108.40.206View ArticlePubMedGoogle Scholar
- Holm CJ, Frank DI, Curtin J: Health beliefs, health locus of control, and women's mammography behavior. Cancer Nurs 1999, 22: 149–56. 10.1097/00002820-199904000-00007View ArticlePubMedGoogle Scholar
- Stein JA, Fox SA, Murata PJ, Morisky DE: Mammography usage and the health belief model. Health Educ Q 1992, 19: 447–62.View ArticlePubMedGoogle Scholar
- Rudberg L, Nilsson S, Wikblad K, Carlsson M: Testicular cancer and testicular self-examination: knowledge and attitudes of adolescent Swedish men. Cancer Nurs 2005, 28: 256–62. 10.1097/00002820-200507000-00003View ArticlePubMedGoogle Scholar
- Vadaparampil ST, Jacobsen PB, Kash K, Watson IS, Saloup R, Pow-Sang J: Factors predicting prostate specific antigen testing among first-degree relatives of prostate cancer patients. Cancer Epidemiol Biomarkers Prev 2004, 13: 753–8.PubMedGoogle Scholar
- Hay JL, Buckley TR, Ostroff JS: The role of cancer worry in cancer screening: a theoretical and empirical review of the literature. Psychooncology 2005, 14: 517–34. 10.1002/pon.864View ArticlePubMedGoogle Scholar
- Bratt O, Damber JE, Emanuelsson M, Kristoffersson U, Lundgren R, Olsson H, Gronberg H: Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer. Eur J Cancer 2000, 36: 235–41. 10.1016/S0959-8049(99)00272-5View ArticlePubMedGoogle Scholar
- Kinkade S: Testicular cancer. Am Fam Physician 1999, 59: 2539–44. 2549–50PubMedGoogle Scholar
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