Literature DB >> 20160272

Coherence and completeness of population-based family cancer reports.

Louise Wideroff1, Anne O Garceau, Mark H Greene, Marsha Dunn, Timothy McNeel, Phuong Mai, Gordon Willis, Lou Gonsalves, Michael Martin, Barry I Graubard.   

Abstract

BACKGROUND: Although family history of cancer is widely ascertained in research and clinical care, little is known about assessment methods, accuracy, or other quality measures. Given its widespread use in cancer screening and surveillance, better information is needed about the clarity and accuracy of family history information reported in the general population.
METHODS: This telephone survey in Connecticut examined coherence and completeness of reports from 1,019 respondents about 20,504 biological relatives.
RESULTS: Of 2,657 cancer reports, 97.7% were judged consistent with malignancy (versus benign or indeterminate conditions); 79% were site specific, 10.1% had unspecified cancer sites, and 8.6% had "ill-defined" sites. Only 6.1% of relatives had unknown histories. Unknown histories and ambiguous sites were significantly higher for second-degree relatives. The adjusted percentage of first-degree relative reports with ambiguous sites increased with decreasing education and African-American race of survey respondents, and with deceased vital status of relatives. Ambiguous second-degree relative reports were also associated with deceased vital status and with male gender of respondents.
CONCLUSIONS: These findings suggest that family history of cancer reports from the general population are generally complete and coherent. IMPACT: Strategies are needed to improve site specificity and thus maximize the utility of such information in primary care settings.

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Year:  2010        PMID: 20160272      PMCID: PMC3102427          DOI: 10.1158/1055-9965.EPI-09-1138

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


  36 in total

1.  Research priorities for evaluating family history in the prevention of common chronic diseases.

Authors:  Paula W Yoon; Maren T Scheuner; Muin J Khoury
Journal:  Am J Prev Med       Date:  2003-02       Impact factor: 5.043

Review 2.  Achieving utility with family history: colorectal cancer risk.

Authors:  Deborah J Bowen; Evette Ludman; Nancy Press; Thuy Vu; Wylie Burke
Journal:  Am J Prev Med       Date:  2003-02       Impact factor: 5.043

Review 3.  Reconsidering the family history in primary care.

Authors:  Eugene C Rich; Wylie Burke; Caryl J Heaton; Susanne Haga; Linda Pinsky; M Priscilla Short; Louise Acheson
Journal:  J Gen Intern Med       Date:  2004-03       Impact factor: 5.128

4.  Cancer risk assessment from family history: gaps in primary care practice.

Authors:  Randa D Sifri; Richard Wender; Nina Paynter
Journal:  J Fam Pract       Date:  2002-10       Impact factor: 0.493

Review 5.  Collection and use of cancer family history in primary care.

Authors:  Nadeem Qureshi; Brenda Wilson; Pasqualina Santaguida; June Carroll; Judith Allanson; Carolina Ruiz Culebro; Melissa Brouwers; Parminder Raina
Journal:  Evid Rep Technol Assess (Full Rep)       Date:  2007-10

Review 6.  Cancer genetics in primary care.

Authors:  Duane Culler; Sarah J Grimes; Louise S Acheson; Georgia L Wiesner
Journal:  Prim Care       Date:  2004-09       Impact factor: 2.907

7.  Reported family history of cancer in the prostate, lung, colorectal, and ovarian cancer screening trial.

Authors:  Paul F Pinsky; Barnett S Kramer; Douglas Reding; Saundra Buys
Journal:  Am J Epidemiol       Date:  2003-05-01       Impact factor: 4.897

8.  American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.

Authors: 
Journal:  J Clin Oncol       Date:  2003-04-11       Impact factor: 44.544

9.  Familial risk for common diseases in primary care: the Family Healthware Impact Trial.

Authors:  Suzanne M O'Neill; Wendy S Rubinstein; Catharine Wang; Paula W Yoon; Louise S Acheson; Nan Rothrock; Erin J Starzyk; Jennifer L Beaumont; James M Galliher; Mack T Ruffin
Journal:  Am J Prev Med       Date:  2009-06       Impact factor: 5.043

10.  Can family history be used as a tool for public health and preventive medicine?

Authors:  Paula W Yoon; Maren T Scheuner; Kris L Peterson-Oehlke; Marta Gwinn; Andrew Faucett; Muin J Khoury
Journal:  Genet Med       Date:  2002 Jul-Aug       Impact factor: 8.822

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  11 in total

1.  A model for patient-direct screening and referral for familial cancer risk.

Authors:  Kristin B Niendorf; Melissa A Geller; Rachel Isaksson Vogel; Timothy R Church; Anna Leininger; Angela Bakke; Robert D Madoff
Journal:  Fam Cancer       Date:  2016-10       Impact factor: 2.375

Review 2.  ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.

Authors:  Sapna Syngal; Randall E Brand; James M Church; Francis M Giardiello; Heather L Hampel; Randall W Burt
Journal:  Am J Gastroenterol       Date:  2015-02-03       Impact factor: 10.864

3.  Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.

Authors:  Anne Marie McCarthy; Mirar Bristol; Susan M Domchek; Peter W Groeneveld; Younji Kim; U Nkiru Motanya; Judy A Shea; Katrina Armstrong
Journal:  J Clin Oncol       Date:  2016-05-09       Impact factor: 44.544

Review 4.  What characterizes cancer family history collection tools? A critical literature review.

Authors:  J E Cleophat; H Nabi; S Pelletier; K Bouchard; M Dorval
Journal:  Curr Oncol       Date:  2018-08-14       Impact factor: 3.677

5.  Family health information sharing among older adults: reaching more family members.

Authors:  Sato Ashida; Ellen J Schafer
Journal:  J Community Genet       Date:  2014-07-30

6.  Automatic Genetic Risk Assessment Calculation Using Breast Cancer Family History Data from the EHR compared to Self-Report.

Authors:  Margaret Sin; Julia E McGuinness; Meghna S Trivedi; Alejandro Vanegas; Thomas B Silverman; Katherine D Crew; Rita Kukafka
Journal:  AMIA Annu Symp Proc       Date:  2018-12-05

7.  Uptake of genetic testing for germline BRCA1/2 pathogenic variants in a predominantly Hispanic population.

Authors:  Julia E McGuinness; Meghna S Trivedi; Thomas Silverman; Awilda Marte; Jennie Mata; Rita Kukafka; Katherine D Crew
Journal:  Cancer Genet       Date:  2019-04-24

8.  The context of collecting family health history: examining definitions of family and family communication about health among African American women.

Authors:  Tess Thompson; Joann Seo; Julia Griffith; Melanie Baxter; Aimee James; Kimberly A Kaphingst
Journal:  J Health Commun       Date:  2015-03-02

9.  "You don't have to keep everything on paper": African American women's use of family health history tools.

Authors:  Tess Thompson; Joann Seo; Julia Griffith; Melanie Baxter; Aimee James; Kimberly A Kaphingst
Journal:  J Community Genet       Date:  2013-02-09

10.  An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.

Authors:  Mary Pritzlaff; Arielle Yorczyk; Linda S Robinson; Sara Pirzadeh-Miller; Tirun Lin; David Euhus; Theodora S Ross
Journal:  J Genet Couns       Date:  2014-06-12       Impact factor: 2.537

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