Literature DB >> 19019415

Uptake of clinical genetic testing for ovarian cancer in Ontario: a population-based study.

Kelly A Metcalfe1, Isabel Fan, John McLaughlin, Harvey A Risch, Barry Rosen, Joan Murphy, Linda Bradley, Susan Armel, Ping Sun, Steven A Narod.   

Abstract

BACKGROUND: Approximately 13% of ovarian cancers in Canada are attributable to a mutation in BRCA1 or BRCA2. In 2001, genetic testing for BRCA1 and BRCA2 became freely available to all women in Ontario with a diagnosis of invasive ovarian cancer. It is unknown what proportion of women with ovarian cancer receive genetic testing as a result of this recommendation.
METHODS: Patients in Ontario who had been diagnosed with epithelial ovarian cancer from 2002 to 2004 were identified using the Ontario Cancer Registry. Information was collected on demographic and risk factors, including information on previous testing for BRCA1 and BRCA2. Women were asked to provide a blood sample for genetic testing or to provide a genetic test result if clinical testing had been done. Genetic testing for BRCA1 and BRCA2 mutations was conducted on all blood samples.
RESULTS: Of the 416 women, 80 women (19%) had undergone previous clinical genetic testing for BRCA1 and BRCA2. Of these 80 women, 30% had a positive genetic test result, compared to 5% of 336 women who had not had clinical genetic testing (p<0.0001). Sixty percent of all mutations were identified within this group of 80 women.
CONCLUSIONS: Genetic testing is available in Ontario to all women with invasive ovarian cancer. However, only a small proportion of women are being referred for testing. This study suggests that increased public awareness directed at physicians and at women with cancer may expand the use of genetic testing.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19019415      PMCID: PMC3074978          DOI: 10.1016/j.ygyno.2008.10.007

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  20 in total

1.  Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer families.

Authors:  B B Biesecker; N Ishibe; D W Hadley; T R Giambarresi; R G Kase; C Lerman; J P Struewing
Journal:  Am J Med Genet       Date:  2000-08-14

2.  A fluorescent multiplex-DGGE screening test for mutations in the BRCA1 gene.

Authors:  Graciela Kuperstein; Elaine Jack; Steven A Narod
Journal:  Genet Test       Date:  2006

3.  Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.

Authors:  Lisa R Susswein; Cécile Skrzynia; Leslie A Lange; Jessica K Booker; Mark L Graham; James P Evans
Journal:  J Clin Oncol       Date:  2008-01-01       Impact factor: 44.544

4.  Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years.

Authors:  Kathleen E Malone; Janet R Daling; David R Doody; Li Hsu; Leslie Bernstein; Ralph J Coates; Polly A Marchbanks; Michael S Simon; Jill A McDonald; Sandra A Norman; Brian L Strom; Ronald T Burkman; Giske Ursin; Dennis Deapen; Linda K Weiss; Suzanne Folger; Jennifer J Madeoy; Danielle M Friedrichsen; Nicola M Suter; Mariela C Humphrey; Robert Spirtas; Elaine A Ostrander
Journal:  Cancer Res       Date:  2006-08-15       Impact factor: 12.701

5.  BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer.

Authors:  R Moslehi; W Chu; B Karlan; D Fishman; H Risch; A Fields; D Smotkin; Y Ben-David; J Rosenblatt; D Russo; P Schwartz; N Tung; E Warner; B Rosen; J Friedman; J S Brunet; S A Narod
Journal:  Am J Hum Genet       Date:  2000-03-16       Impact factor: 11.025

6.  Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada.

Authors:  Harvey A Risch; John R McLaughlin; David E C Cole; Barry Rosen; Linda Bradley; Isabel Fan; James Tang; Song Li; Shiyu Zhang; Patricia A Shaw; Steven A Narod
Journal:  J Natl Cancer Inst       Date:  2006-12-06       Impact factor: 13.506

7.  A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes.

Authors:  G Kuperstein; W D Foulkes; P Ghadirian; J Hakimi; S A Narod
Journal:  Clin Genet       Date:  2000-03       Impact factor: 4.438

8.  Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.

Authors:  Katrina Armstrong; Ellyn Micco; Amy Carney; Jill Stopfer; Mary Putt
Journal:  JAMA       Date:  2005-04-13       Impact factor: 56.272

9.  Low rates of acceptance of BRCA1 and BRCA2 test results among African American women at increased risk for hereditary breast-ovarian cancer.

Authors:  Chanita Hughes Halbert; Lisa Kessler; Jill E Stopfer; Susan Domchek; E Paul Wileyto
Journal:  Genet Med       Date:  2006-09       Impact factor: 8.822

10.  Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families.

Authors:  T Peelen; M van Vliet; A Bosch; G Bignell; H F Vasen; J G Klijn; H Meijers-Heijboer; M Stratton; G J van Ommen; C J Cornelisse; P Devilee
Journal:  Br J Cancer       Date:  2000-01       Impact factor: 7.640

View more
  24 in total

1.  Personalized medicine: a personal view.

Authors:  S A Narod
Journal:  Curr Oncol       Date:  2010-10       Impact factor: 3.677

2.  Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing.

Authors:  Barbara M Norquist; Kathryn P Pennington; Kathy J Agnew; Maria I Harrell; Christopher C Pennil; Ming K Lee; Silvia Casadei; Anne M Thornton; Rochelle L Garcia; Tom Walsh; Elizabeth M Swisher
Journal:  Gynecol Oncol       Date:  2012-12-19       Impact factor: 5.482

Review 3.  Predictors of genetic testing decisions: a systematic review and critique of the literature.

Authors:  Kate Sweeny; Arezou Ghane; Angela M Legg; Ho Phi Huynh; Sara E Andrews
Journal:  J Genet Couns       Date:  2014-04-11       Impact factor: 2.537

4.  Providers' perceptions and practices regarding BRCA1/2 genetic counseling and testing in African American women.

Authors:  Kristi D Graves; Juleen Christopher; Toni Michelle Harrison; Beth N Peshkin; Claudine Isaacs; Vanessa B Sheppard
Journal:  J Genet Couns       Date:  2011-08-06       Impact factor: 2.537

5.  BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group.

Authors:  Kathryn Alsop; Sian Fereday; Cliff Meldrum; Anna deFazio; Catherine Emmanuel; Joshy George; Alexander Dobrovic; Michael J Birrer; Penelope M Webb; Colin Stewart; Michael Friedlander; Stephen Fox; David Bowtell; Gillian Mitchell
Journal:  J Clin Oncol       Date:  2012-06-18       Impact factor: 44.544

Review 6.  Personalised medicine and population health: breast and ovarian cancer.

Authors:  Steven A Narod
Journal:  Hum Genet       Date:  2018-10-17       Impact factor: 4.132

7.  Universal BRCA1/BRCA2 Testing for Ovarian Cancer Patients is Welcomed, but with Care: How Women and Staff Contextualize Experiences of Expanded Access.

Authors:  Hannah Shipman; Samantha Flynn; Carey F MacDonald-Smith; James Brenton; Robin Crawford; Marc Tischkowitz; Nicholas J Hulbert-Williams
Journal:  J Genet Couns       Date:  2017-05-24       Impact factor: 2.537

8.  Genetic risk assessment for women with epithelial ovarian cancer: referral patterns and outcomes in a university gynecologic oncology clinic.

Authors:  Sue V Petzel; Rachel Isaksson Vogel; Tracy Bensend; Anna Leininger; Peter A Argenta; Melissa A Geller
Journal:  J Genet Couns       Date:  2013-05-16       Impact factor: 2.537

Review 9.  Delivering widespread BRCA testing and PARP inhibition to patients with ovarian cancer.

Authors:  Angela George; Stan Kaye; Susana Banerjee
Journal:  Nat Rev Clin Oncol       Date:  2016-12-13       Impact factor: 66.675

10.  Improving referral for genetic risk assessment in ovarian cancer using an electronic medical record system.

Authors:  Sue V Petzel; Rachel Isaksson Vogel; Jena McNiel; Anna Leininger; Peter A Argenta; Melissa A Geller
Journal:  Int J Gynecol Cancer       Date:  2014-07       Impact factor: 3.437

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.