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  1. Artikel ; Online: Urologists' Perceptions of Active Surveillance and Their Recommendations for Low-risk Prostate Cancer Patients.

    Xu, Jinping / Bock, Cathryn / Janisse, James / Schwartz, Kendra L / Triest, Jeffrey / Cher, Michael L / Goodman, Michael

    Urology

    2021  Band 155, Seite(n) 83–90

    Abstract: Objective: To assess practicing urologists' attitudes and perceptions of active surveillance (AS) and other treatment options for low-risk prostate cancer.: Methods: This was a cross-sectional survey of urologists practicing in Michigan and Georgia. ... ...

    Abstract Objective: To assess practicing urologists' attitudes and perceptions of active surveillance (AS) and other treatment options for low-risk prostate cancer.
    Methods: This was a cross-sectional survey of urologists practicing in Michigan and Georgia. Urologists were asked about perceptions and practices pertaining to AS.
    Results: Overall, 225 urologists completed the survey; 147 (65%) were from Michigan and 78 (35%) were from Georgia. Most urologists reported they provided (99%), discussed (97%), and offered (61%) AS to all of their low-risk patients. Most believed AS is effective (97%) and underused (90%), while 80% agreed that curative therapy (surgery, radiation) is overused in the United States. Although most (79%) endorse that Black men are more likely to have aggressive low-risk disease, 89% reported feeling comfortable recommending AS to Black men. In multivariable analysis, significant provider-related predictors of AS recommendation were practice location, number of years in practice, beliefs pertaining to survival benefit of prostatectomy and effectiveness of AS, and expectation that patients are not interested in AS. The patient characteristics of race, age, life expectancy, fear of cancer progression, and fear of treatment side effects were also significant predictors of AS recommendations.
    Conclusion: Most urologists surveyed stated that AS is effective and underused for low-risk prostate cancer . Overall, urologists are much less likely to recommend AS to younger men and slightly less to Black men. AS recommendations varied by practice location and by years in practice. These findings indicate targeted educational efforts in the US are needed to influence urologists toward greater acceptance of AS.
    Mesh-Begriff(e) Adult ; Attitude of Health Personnel ; Cross-Sectional Studies ; Female ; Georgia ; Humans ; Male ; Michigan ; Middle Aged ; Practice Patterns, Physicians'/statistics & numerical data ; Prostatic Neoplasms/therapy ; Surveys and Questionnaires ; Urologists ; Watchful Waiting/statistics & numerical data
    Sprache Englisch
    Erscheinungsdatum 2021-01-19
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 192062-5
    ISSN 1527-9995 ; 0090-4295
    ISSN (online) 1527-9995
    ISSN 0090-4295
    DOI 10.1016/j.urology.2020.12.037
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Lifetime personal cigarette smoking and risk of young-onset breast cancer by subtype among non-Hispanic Black and White women in the Young Women's Health History Study.

    Ihenacho, Ugonna / Hamilton, Ann S / Mack, Wendy J / Wu, Anna H / Unger, Jennifer B / Pathak, Dorothy R / Hirko, Kelly A / Houang, Richard T / Press, Michael F / Schwartz, Kendra L / Marcus, Lydia R / Velie, Ellen M

    Breast cancer research and treatment

    2022  Band 195, Heft 3, Seite(n) 353–366

    Abstract: Purpose: To evaluate the association between lifetime personal cigarette smoking and young-onset breast cancer (YOBC; diagnosed <50 years of age) risk overall and by breast cancer (BC) subtype, and whether risk varies by race or socioeconomic position ( ... ...

    Abstract Purpose: To evaluate the association between lifetime personal cigarette smoking and young-onset breast cancer (YOBC; diagnosed <50 years of age) risk overall and by breast cancer (BC) subtype, and whether risk varies by race or socioeconomic position (SEP).
    Methods: Data are from the Young Women's Health History Study (YWHHS), a population-based case-control study of non-Hispanic Black (NHB) and White (NHW) women, ages 20-49 years (n = 1812 cases, n = 1381 controls) in the Los Angeles County and Metropolitan Detroit Surveillance, Epidemiology, and End Results (SEER) registry areas, 2010-2015. Lifetime personal cigarette smoking characteristics and YOBC risk by subtype were examined using sample-weighted, multivariable-adjusted polytomous logistic regression.
    Results: YOBC risk associated with ever versus never smoking differed by subtype (P
    Conclusion: Findings confirm prior reports of a positive association between cigarette smoking and Luminal A YOBC and identify a novel association between smoking and HER2-type YOBC.
    Mesh-Begriff(e) Adult ; Breast Neoplasms/epidemiology ; Breast Neoplasms/etiology ; Case-Control Studies ; Cigarette Smoking/adverse effects ; Cigarette Smoking/epidemiology ; Female ; Humans ; Middle Aged ; Pregnancy ; Receptor, ErbB-2 ; Receptors, Estrogen ; Receptors, Progesterone ; Risk Factors ; Young Adult
    Chemische Substanzen Receptors, Estrogen ; Receptors, Progesterone ; Receptor, ErbB-2 (EC 2.7.10.1)
    Sprache Englisch
    Erscheinungsdatum 2022-08-04
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 604563-7
    ISSN 1573-7217 ; 0167-6806
    ISSN (online) 1573-7217
    ISSN 0167-6806
    DOI 10.1007/s10549-022-06675-4
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Attitudes towards health research participation: a qualitative study of US Arabs and Chaldeans.

    Campbell-Voytal, Kimberly D / Schwartz, Kendra L / Hamade, Hiam / Dallo, Florence J / Neale, Anne Victoria

    Family practice

    2018  Band 36, Heft 3, Seite(n) 325–331

    Abstract: Background: The Arab Muslim and Chaldean Christian American community is unified by language but culturally diverse. Researchers are challenged to engage the Arab/Chaldean community to meet immigrant health needs. Arabs/Chaldeans are identified as white ...

    Abstract Background: The Arab Muslim and Chaldean Christian American community is unified by language but culturally diverse. Researchers are challenged to engage the Arab/Chaldean community to meet immigrant health needs. Arabs/Chaldeans are identified as white in clinical data sets making it difficult to identify health behaviours and patterns unique to the community.
    Objectives: To explore the views of members of the Arab/Chaldean community, including researchers and the lay public, regarding health research participation and the role of clinicians, researchers and community leaders in the research process.
    Methods: A qualitative study of Arab and Chaldean adults and researchers conducted in a US community with a large Arab/Chaldean population. Five semi-structured focus group discussions were triangulated with five in-depth semi-structured interviews with Arab or Chaldean primary care researchers. Responses were audio-recorded and transcribed verbatim. Transcripts were coded and thematically analysed, and findings confirmed with community representatives.
    Results: Three themes were identified: (i) research expectations: risks and benefits; (ii) health care environment: clinicians as recruiters and (iii) research participations: risks and benefits. Themes captured concerns with social relationships, reputation or trust and the cost and benefit of research participation. In the Arab/Chaldean community, institutional and political fears and distrust are amplified. Respect for physicians, teachers and faith leaders connected with or recruiting for studies enhances likelihood of research participation.
    Conclusion: Clinical researchers should address the cultural and immigration histories of Arab/Chaldean research participants. Studies that maximize trust will minimize participation bias and lay the groundwork for improved health. Institutional, sociocultural and personal factors require a pre-study phase to engage and educate participants.
    Mesh-Begriff(e) Adult ; Aged ; Arabs ; Attitude to Health/ethnology ; Cultural Characteristics ; Emigrants and Immigrants ; Female ; Focus Groups ; Humans ; Interviews as Topic ; Male ; Michigan ; Middle Aged ; Motivation ; Patient Selection ; Primary Health Care ; Qualitative Research ; Researcher-Subject Relations ; Trust ; Young Adult
    Sprache Englisch
    Erscheinungsdatum 2018-09-14
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 605939-9
    ISSN 1460-2229 ; 0263-2136
    ISSN (online) 1460-2229
    ISSN 0263-2136
    DOI 10.1093/fampra/cmy071
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: A Review of Research on Disparities in the Care of Black and White Patients With Cancer in Detroit.

    Simon, Michael S / Raychaudhuri, Sreejata / Hamel, Lauren M / Penner, Louis A / Schwartz, Kendra L / Harper, Felicity W K / Thompson, Hayley S / Booza, Jason C / Cote, Michele / Schwartz, Ann G / Eggly, Susan

    Frontiers in oncology

    2021  Band 11, Seite(n) 690390

    Abstract: Racial disparities in cancer incidence and outcomes are well-documented in the US, with Black people having higher incidence rates and worse outcomes than White people. In this review, we present a summary of almost 30 years of research conducted by ... ...

    Abstract Racial disparities in cancer incidence and outcomes are well-documented in the US, with Black people having higher incidence rates and worse outcomes than White people. In this review, we present a summary of almost 30 years of research conducted by investigators at the Karmanos Cancer Institute's (KCI's) Population Studies and Disparities Research (PSDR) Program focusing on Black-White disparities in cancer incidence, care, and outcomes. The studies in the review focus on individuals diagnosed with cancer from the Detroit Metropolitan area, but also includes individuals included in national databases. Using an organizational framework of three generations of studies on racial disparities, this review describes racial disparities by primary cancer site, disparities associated with the presence or absence of comorbid medical conditions, disparities in treatment, and disparities in physician-patient communication, all of which contribute to poorer outcomes for Black cancer patients. While socio-demographic and clinical differences account for some of the noted disparities, further work is needed to unravel the influence of systemic effects of racism against Black people, which is argued to be the major contributor to disparate outcomes between Black and White patients with cancer. This review highlights evidence-based strategies that have the potential to help mitigate disparities, improve care for vulnerable populations, and build an equitable healthcare system. Lessons learned can also inform a more equitable response to other health conditions and crises.
    Sprache Englisch
    Erscheinungsdatum 2021-07-07
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2021.690390
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Racial Differences in Treatment Decision-Making for Men with Clinically Localized Prostate Cancer: a Population-Based Study.

    Xu, Jinping / Janisse, James / Ruterbusch, Julie / Ager, Joel / Schwartz, Kendra L

    Journal of racial and ethnic health disparities

    2015  Band 3, Heft 1, Seite(n) 35–45

    Abstract: Purpose: Racial differences in prostate cancer treatment patterns have motivated concerns about over- and undertreatment. We surveyed black and white patients with localized prostate cancer (LPC) regarding their treatment decision-making processes to ... ...

    Abstract Purpose: Racial differences in prostate cancer treatment patterns have motivated concerns about over- and undertreatment. We surveyed black and white patients with localized prostate cancer (LPC) regarding their treatment decision-making processes to gain a better perspective on factors associated with LPC treatment choice.
    Methods: We conducted a population-based, cross-sectional survey of 260 men (132 black, 128 white) aged ≤75 years, with newly diagnosed LPC. Our primary outcome was treatment choice (either surgery, radiation, or watchful waiting/active surveillance (WW/AS)), and our primary predictors were race and tumor risk level.
    Results: Overall, treatment choice did not differ by race. As cancer risk increased, both black and white patients were more likely to undergo surgery and less likely to receive radiation. However, the pattern of WW/AS was different between white and black men. White men were less likely to select WW/AS as cancer risk increased, while risk level was unrelated to black men undergoing WW/AS. Urologist's recommendation had the greatest impact on men's treatment choice, followed by tumor risk level, age, and personal preferences.
    Conclusions: Although there were no overall racial differences in treatment choice, when stratified by tumor risk level, the pattern of WW/AS was different between white and black patients, suggesting that over- and undertreatment is a larger concern for black than white men. A risk-stratified approach to understand racial disparities in LPC treatment and better strategies to aid black men in their treatment decision-making are needed to reduce racial disparities in prostate cancer outcomes.
    Mesh-Begriff(e) African Americans/psychology ; African Americans/statistics & numerical data ; Aged ; Cross-Sectional Studies ; Decision Making ; European Continental Ancestry Group/psychology ; European Continental Ancestry Group/statistics & numerical data ; Humans ; Male ; Prostatic Neoplasms/ethnology ; Prostatic Neoplasms/therapy ; Risk ; Watchful Waiting
    Sprache Englisch
    Erscheinungsdatum 2015-05-05
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2760524-3
    ISSN 2196-8837 ; 2197-3792
    ISSN (online) 2196-8837
    ISSN 2197-3792
    DOI 10.1007/s40615-015-0109-8
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel: A primer of the HIPAA Privacy Rule for practice-based researchers.

    Neale, Anne Victoria / Schwartz, Kendra L

    The Journal of the American Board of Family Practice

    2004  Band 17, Heft 6, Seite(n) 461–465

    Mesh-Begriff(e) Health Insurance Portability and Accountability Act/legislation & jurisprudence ; Humans ; Physicians/legislation & jurisprudence ; Privacy/legislation & jurisprudence ; Research Personnel/legislation & jurisprudence ; United States
    Sprache Englisch
    Erscheinungsdatum 2004-11-01
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 1036289-7
    ISSN 0893-8652
    ISSN 0893-8652
    DOI 10.3122/jabfm.17.6.461
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: The Epidemiology of Cancer Among Homeless Adults in Metropolitan Detroit.

    Holowatyj, Andreana N / Heath, Elisabeth I / Pappas, Lisa M / Ruterbusch, Julie J / Gorski, David H / Triest, Jeffrey A / Park, Hyo K / Beebe-Dimmer, Jennifer L / Schwartz, Ann G / Cote, Michele L / Schwartz, Kendra L

    JNCI cancer spectrum

    2019  Band 3, Heft 1, Seite(n) pkz006

    Abstract: Background: Homeless individuals suffer and die disproportionately from chronic diseases and disorders. We describe the epidemiology of cancer among homeless persons in metropolitan Detroit.: Methods: A retrospective cohort study was performed using ... ...

    Abstract Background: Homeless individuals suffer and die disproportionately from chronic diseases and disorders. We describe the epidemiology of cancer among homeless persons in metropolitan Detroit.
    Methods: A retrospective cohort study was performed using 1973-2014 data from the Metropolitan Detroit Cancer Surveillance System, a population-based cancer registry and member of the National Institutes of Health-National Cancer Institute's Surveillance, Epidemiology, and End Results program. Homeless adults were identified through address at diagnosis listed as a homeless shelter, hospital, or supplemental field indicating homelessness. Age-adjusted, sex-specific proportional incidence ratios (PIR) compared cancer incidence proportions by primary tumor site of homeless patients to the nonhomeless referent population. Kaplan-Meier curves depicted unadjusted survival differences in a propensity score matched sample. Differences in 10-year survival were assessed using the score test with a sandwich estimator accounting for matched cluster effects. Statistical tests were two-sided.
    Results: A total of 388 individuals experienced homelessness at first primary invasive cancer diagnosis. Statistically significantly higher proportions of respiratory system (PIR = 1.51; 95% confidence interval = 1.28 to 1.79) and female genital system (PIR = 1.83; 95% confidence interval = 1.31 to 2.55) cancers were observed among homeless men and women, respectively. Homeless persons had poorer overall and cancer-reported survival compared with a propensity score matched referent population (median: overall survival, 20.0 vs 38.0 months, respectively,
    Conclusion: Disparities in disease burden exist between adults who are experiencing homelessness compared with the nonhomeless population at cancer diagnosis. These findings provide clinically relevant information to understand the cancer burden in this medically underserved population and suggest an urgent need to develop cancer prevention and intervention programs to reduce disparities and improve the health of homeless persons.
    Sprache Englisch
    Erscheinungsdatum 2019-03-25
    Erscheinungsland England
    Dokumenttyp Journal Article
    ISSN 2515-5091
    ISSN (online) 2515-5091
    DOI 10.1093/jncics/pkz006
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Physical activity and quality of life in African American cancer survivors: The Detroit Research on Cancer Survivors study.

    Beebe-Dimmer, Jennifer L / Ruterbusch, Julie J / Harper, Felicity W K / Baird, Tara M / Finlay, David G / Rundle, Andrew G / Pandolfi, Stephanie S / Hastert, Theresa A / Schwartz, Kendra L / Bepler, Gerold / Simon, Michael S / Mantey, Julia / Abrams, Judy / Albrecht, Teri L / Schwartz, Ann G

    Cancer

    2020  Band 126, Heft 9, Seite(n) 1987–1994

    Abstract: Background: The benefit of regular exercise in improving cancer outcomes is well established. The American Cancer Society (ACS) released a recommendation that cancer survivors should engage in at least 150 minutes of moderate to vigorous physical ... ...

    Abstract Background: The benefit of regular exercise in improving cancer outcomes is well established. The American Cancer Society (ACS) released a recommendation that cancer survivors should engage in at least 150 minutes of moderate to vigorous physical activity (PA) per week; however, few report meeting this recommendation. This study examined the patterns and correlates of meeting ACS PA recommendations in the Detroit Research on Cancer Survivors (ROCS) cohort of African American cancer survivors.
    Methods: Detroit ROCS participants completed baseline and yearly follow-up surveys to update their health and health behaviors, including PA. This study examined participation in PA by select characteristics and reported health-related quality of life (HRQOL) as measured with the Functional Assessment of Cancer Therapy and Patient-Reported Outcomes Measurement Information System instruments.
    Results: Among the first 1500 ROCS participants, 60% reported participating in regular PA, with 24% reporting ≥150 min/wk. Although there were no differences by sex, prostate cancer survivors were the most likely to report participating in regular PA, whereas lung cancer survivors were the least likely (P = .022). Survivors who reported participating in regular PA reported higher HRQOL (P < .001) and lower depression (P = .040).
    Conclusions: Just 24% of African American cancer survivors reported meeting the ACS guidelines for PA at the baseline, but it was encouraging to see increases in activity over time. Because of the established benefits of regular exercise observed in this study and others, identifying and reducing barriers to regular PA among African American cancer survivors are critical for improving outcomes and minimizing disparities.
    Mesh-Begriff(e) Adult ; African Americans ; Aged ; Cancer Survivors ; Cohort Studies ; Exercise ; Female ; Humans ; Life Style ; Male ; Michigan ; Middle Aged ; Quality of Life ; Young Adult
    Sprache Englisch
    Erscheinungsdatum 2020-02-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1429-1
    ISSN 1097-0142 ; 0008-543X ; 1934-662X
    ISSN (online) 1097-0142
    ISSN 0008-543X ; 1934-662X
    DOI 10.1002/cncr.32725
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Patients' Survival Expectations With and Without Their Chosen Treatment for Prostate Cancer.

    Xu, Jinping / Janisse, James / Ruterbusch, Julie J / Ager, Joel / Liu, Joe / Holmes-Rovner, Margaret / Schwartz, Kendra L

    Annals of family medicine

    2016  Band 14, Heft 3, Seite(n) 208–214

    Abstract: Purpose: Overtreatment of screen-detected localized prostate cancer (LPC) is an important public health concern, since the survival benefit of aggressive treatment (surgery or radiation) has not been well established. We investigated the survival ... ...

    Abstract Purpose: Overtreatment of screen-detected localized prostate cancer (LPC) is an important public health concern, since the survival benefit of aggressive treatment (surgery or radiation) has not been well established. We investigated the survival expectations of patients who had LPC with and without their chosen treatment.
    Methods: A population-based sample of 260 men (132 black, 128 white) 75 years old or younger with newly diagnosed LPC completed a self-administered survey. How long the patients expected to live with their chosen treatment, how long they would expect to live with no treatment, and factors associated with the difference in perceived life expectancy were assessed using multivariable analysis.
    Results: Without any treatment, 33% of patients expected that they would live less than 5 years, 41% 5 to 10 years, 21% 10 to 20 years, and 5% more than 20 years. With their chosen treatment, 3% of patients expected to live less than 5 years, 9% 5 to 10 years, 33% 10 to 20 years, and 55% more than 20 years. Treatment chosen, age, general health perception, and perceived cancer seriousness predicted the differences in perceived life expectancy, while race and actual tumor risk did not. After adjustment for other covariates, men who choose surgery or radiation expected greater gain in survival than men who chose watchful waiting or active surveillance.
    Conclusions: Most patients with LPC underestimated their life expectancy without treatment and overestimated the gain in life expectancy with surgery or radiation. These unrealistic expectations may compromise patients' ability to make informed treatment decisions and may contribute to overtreatment of LPC. Primary care physicians, when included in the decision process, should focus on helping patients develop realistic expectations and choices that support their treatment goals.
    Mesh-Begriff(e) Aged ; Choice Behavior ; Cross-Sectional Studies ; Decision Making ; Humans ; Life Expectancy ; Linear Models ; Male ; Michigan ; Middle Aged ; Prostatic Neoplasms/diagnosis ; Prostatic Neoplasms/mortality ; Prostatic Neoplasms/therapy ; Radiography ; Surgical Procedures, Operative
    Sprache Englisch
    Erscheinungsdatum 2016-05
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2171425-3
    ISSN 1544-1717 ; 1544-1709
    ISSN (online) 1544-1717
    ISSN 1544-1709
    DOI 10.1370/afm.1926
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: The Detroit Research on Cancer Survivors (ROCS) Pilot Study: A Focus on Outcomes after Cancer in a Racially Diverse Patient Population.

    Beebe-Dimmer, Jennifer L / Albrecht, Terrance L / Baird, Tara E / Ruterbusch, Julie J / Hastert, Theresa / Harper, Felicity W K / Simon, Michael S / Abrams, Judith / Schwartz, Kendra L / Schwartz, Ann G

    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

    2018  Band 28, Heft 4, Seite(n) 666–674

    Abstract: Background: African Americans are often diagnosed with advanced stage cancer and experience higher mortality compared with whites in the United States. Contributing factors, like differences in access to medical care and the prevalence of comorbidities, ...

    Abstract Background: African Americans are often diagnosed with advanced stage cancer and experience higher mortality compared with whites in the United States. Contributing factors, like differences in access to medical care and the prevalence of comorbidities, do not entirely explain racial differences in outcomes.
    Methods: The Detroit Research on Cancer Survivors (ROCS) pilot study was conducted to investigate factors related to short- and long-term outcomes among patients with cancer. Participants completed web-based surveys, and mailed saliva specimens were collected for future genetic studies.
    Results: We recruited 1,000 participants with an overall response rate of 68%. Thirty-one percent completed the survey without any interviewer support and the remaining participated in an interviewer-administered survey. Seventy-four percent provided a saliva specimen and 64% consented for tumor tissue retrieval. African American survivors required more interviewer support (
    Conclusions: In this pilot study, we demonstrated that a web-based survey supplemented with telephone interviews and mailed saliva kits are cost-effective methods to collect patient-reported data and DNA for large studies of cancer survivors with a high proportion of minority patients. The preliminary data collected reinforces differences by race in factors affecting cancer outcomes. Our efforts continue as we expand this unique cohort to include more than 5,000 African American cancer survivors.
    Impact: Formal investigation of factors influencing adverse outcomes among African American cancer survivors will be critical in closing the racial gap in morbidity and mortality.
    Mesh-Begriff(e) Adult ; Aged ; Cancer Survivors/statistics & numerical data ; Ethnic Groups ; Female ; Humans ; Male ; Middle Aged ; Neoplasms/ethnology ; Neoplasms/mortality ; Pilot Projects ; Treatment Outcome
    Sprache Englisch
    Erscheinungsdatum 2018-11-27
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1153420-5
    ISSN 1538-7755 ; 1055-9965
    ISSN (online) 1538-7755
    ISSN 1055-9965
    DOI 10.1158/1055-9965.EPI-18-0123
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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