Literature DB >> 29875420

Written pretest information and germline BRCA1/2 pathogenic variant testing in unselected breast cancer patients: predictors of testing uptake.

Martin P Nilsson1,2, Erik D Nilsson3, Barbro Silfverberg4, Åke Borg5, Niklas Loman5,6.   

Abstract

PURPOSE: This study aimed to evaluate predictors of testing uptake among unselected breast cancer patients who were offered germline BRCA1/2 testing in a prospective study.
METHODS: Pretest information was provided by a standardized invitation letter instead of in-person counseling. Data was abstracted from medical records. Using multivariate logistic regressions, predictors of testing uptake were analyzed.
RESULTS: The overall uptake of testing was 67% (539 of 805 patients). Low uptake rates were found for patients aged ≥80 years (33%), and patients born outside of Europe (37%). In adjusted analysis, age ≥80 years (odds ratio [OR] 0.10; P = 0.002), psychiatric disorders (OR 0.46; P = 0.006), occupation requiring at least 3 years of university or college education (OR 2.03; P = 0.003), and breast cancer or ovarian cancer in first-degree or second-degree relatives (OR 1.66; P = 0.02) were independently associated with uptake of BRCA1/2 testing. Somatic comorbidity in patients aged <70 years was associated with lower testing uptake.
CONCLUSION: Testing uptake varies across different subgroups according to patient-related factors that are readily available in the medical records. Knowledge about these factors enables health care professionals to identify patients who are less likely to pursue genetic testing.

Entities:  

Keywords:  Breast cancer; Genetic testing; Predictors; Uptake; Written information

Mesh:

Substances:

Year:  2018        PMID: 29875420     DOI: 10.1038/s41436-018-0021-9

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  25 in total

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Journal:  Gynecol Oncol       Date:  2015-04-28       Impact factor: 5.482

2.  Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer.

Authors:  Lynn C Hartmann; Noralane M Lindor
Journal:  N Engl J Med       Date:  2016-06-16       Impact factor: 91.245

3.  Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers.

Authors:  Allison W Kurian; Bronislava M Sigal; Sylvia K Plevritis
Journal:  J Clin Oncol       Date:  2009-12-07       Impact factor: 44.544

4.  Barriers to genetic testing in newly diagnosed breast cancer patients: Do surgeons limit testing?

Authors:  Laura Hafertepen; Alyssa Pastorino; Nichole Morman; Jennifer Snow; Deepa Halaharvi; Lindsey Byrne; Mark Cripe
Journal:  Am J Surg       Date:  2016-09-09       Impact factor: 2.565

5.  Factors associated with genetic counseling and BRCA testing in a population-based sample of young Black women with breast cancer.

Authors:  D Cragun; D Bonner; J Kim; M R Akbari; S A Narod; A Gomez-Fuego; J D Garcia; S T Vadaparampil; Tuya Pal
Journal:  Breast Cancer Res Treat       Date:  2015-04-14       Impact factor: 4.872

6.  Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer.

Authors:  Kathryn J Schlich-Bakker; Herman F J ten Kroode; Carla C Wárlám-Rodenhuis; Jan van den Bout; Margreet G E M Ausems
Journal:  Genet Med       Date:  2007-11       Impact factor: 8.822

7.  Determinants of genetic counseling uptake and its impact on breast cancer outcome: a population-based study.

Authors:  Aurélie Ayme; Valeria Viassolo; Elisabetta Rapiti; Gérald Fioretta; Hyma Schubert; Christine Bouchardy; Pierre O Chappuis; Simone Benhamou
Journal:  Breast Cancer Res Treat       Date:  2014-02-12       Impact factor: 4.872

8.  Age at diagnosis may trump family history in driving BRCA testing in a population of breast cancer patients.

Authors:  Hetal S Vig; Anne Marie McCarthy; Kaijun Liao; Mirar Bristol Demeter; Tracey Fredericks; Katrina Armstrong
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2013-08-05       Impact factor: 4.254

9.  BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study.

Authors:  Hildegunn Høberg-Vetti; Cathrine Bjorvatn; Bent E Fiane; Turid Aas; Kathrine Woie; Helge Espelid; Tone Rusken; Hans Petter Eikesdal; Wenche Listøl; Marianne T Haavind; Per M Knappskog; Bjørn Ivar Haukanes; Vidar M Steen; Nicoline Hoogerbrugge
Journal:  Eur J Hum Genet       Date:  2015-09-09       Impact factor: 4.246

10.  Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.

Authors:  Karoline B Kuchenbaecker; John L Hopper; Daniel R Barnes; Kelly-Anne Phillips; Thea M Mooij; Marie-José Roos-Blom; Sarah Jervis; Flora E van Leeuwen; Roger L Milne; Nadine Andrieu; David E Goldgar; Mary Beth Terry; Matti A Rookus; Douglas F Easton; Antonis C Antoniou; Lesley McGuffog; D Gareth Evans; Daniel Barrowdale; Debra Frost; Julian Adlard; Kai-Ren Ong; Louise Izatt; Marc Tischkowitz; Ros Eeles; Rosemarie Davidson; Shirley Hodgson; Steve Ellis; Catherine Nogues; Christine Lasset; Dominique Stoppa-Lyonnet; Jean-Pierre Fricker; Laurence Faivre; Pascaline Berthet; Maartje J Hooning; Lizet E van der Kolk; Carolien M Kets; Muriel A Adank; Esther M John; Wendy K Chung; Irene L Andrulis; Melissa Southey; Mary B Daly; Saundra S Buys; Ana Osorio; Christoph Engel; Karin Kast; Rita K Schmutzler; Trinidad Caldes; Anna Jakubowska; Jacques Simard; Michael L Friedlander; Sue-Anne McLachlan; Eva Machackova; Lenka Foretova; Yen Y Tan; Christian F Singer; Edith Olah; Anne-Marie Gerdes; Brita Arver; Håkan Olsson
Journal:  JAMA       Date:  2017-06-20       Impact factor: 56.272

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  1 in total

1.  Genetic testing in women with early-onset breast cancer: a Traceback pilot study.

Authors:  Annelie Augustinsson; Martin P Nilsson; Carolina Ellberg; Ulf Kristoffersson; Håkan Olsson; Hans Ehrencrona
Journal:  Breast Cancer Res Treat       Date:  2021-09-16       Impact factor: 4.872

  1 in total

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