Literature DB >> 31062229

Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review.

Siang Ing Lee1, Mitesh Patel1, Brittany Dutton1, Stephen Weng1, Jocelyn Luveta, Nadeem Qureshi2.   

Abstract

This systematic review evaluated the effectiveness of strategies to identify and manage patients with familial risk of breast, ovarian, colorectal and prostate cancer in primary care to improve clinical outcomes. MEDLINE, EMBASE, CINAHL and Cochrane library were searched from January 1980 to October 2017. We included randomised controlled trials (RCT) and non-randomised studies of interventions (NRSI). Primary outcomes were cancer incidence, cancer-related clinical outcomes or the identification of cancer predisposition; secondary outcomes were the appropriateness of referral, uptake of preventive strategies and cognitive and psychological effect. From 11,842 abstracts, 111 full texts were reviewed and three eligible studies (nine articles) identified. Two were cluster RCTs and one NRSI; all used risk assessment software. No studies identified our primary outcomes, with no consistent outcome across the three studies. In one RCT, intervention improved the proportion of genetic referrals meeting referral guidelines for breast cancer (OR 4.5, 95% CI 1.6 to 13.1). In the other RCT, there was no difference in screening adherence between the intervention and control group. However, there was borderline increased risk perception (OR 1.89, 95% CI 0.99 to 3.59) in the subgroup that under-estimated their colon cancer risk. In the NRSI, there was no change in psychological distress in patients at increased familial breast cancer risk, but population risk patients had reduced anxiety after intervention (state anxiety mean change - 3, 95% CI - 5 to - 2). Future studies should have better-defined comparator groups and longer follow-up and assess outcomes using validated tools.

Entities:  

Keywords:  Breast neoplasm; Colorectal neoplasms; Genetic predisposition to disease; Ovarian neoplasms; Primary health care; Prostatic neoplasms

Year:  2019        PMID: 31062229      PMCID: PMC6962422          DOI: 10.1007/s12687-019-00419-6

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  33 in total

1.  Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening.

Authors:  S Paluch-Shimon; F Cardoso; C Sessa; J Balmana; M J Cardoso; F Gilbert; E Senkus
Journal:  Ann Oncol       Date:  2016-09       Impact factor: 32.976

2.  Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.

Authors:  Susan M Domchek; Tara M Friebel; Christian F Singer; D Gareth Evans; Henry T Lynch; Claudine Isaacs; Judy E Garber; Susan L Neuhausen; Ellen Matloff; Rosalind Eeles; Gabriella Pichert; Laura Van t'veer; Nadine Tung; Jeffrey N Weitzel; Fergus J Couch; Wendy S Rubinstein; Patricia A Ganz; Mary B Daly; Olufunmilayo I Olopade; Gail Tomlinson; Joellen Schildkraut; Joanne L Blum; Timothy R Rebbeck
Journal:  JAMA       Date:  2010-09-01       Impact factor: 56.272

3.  A cohort study of cancer risk in relation to family histories of cancer in the Utah population database.

Authors:  Richard A Kerber; Elizabeth O'Brien
Journal:  Cancer       Date:  2005-05-01       Impact factor: 6.860

4.  Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.

Authors:  H J Järvinen; M Aarnio; H Mustonen; K Aktan-Collan; L A Aaltonen; P Peltomäki; A De La Chapelle; J P Mecklin
Journal:  Gastroenterology       Date:  2000-05       Impact factor: 22.682

5.  Online self-test identifies women at high familial breast cancer risk in population-based breast cancer screening without inducing anxiety or distress.

Authors:  A van Erkelens; A S Sie; P Manders; A Visser; L E Duijm; R M Mann; M Ten Voorde; H Kroeze; J B Prins; N Hoogerbrugge
Journal:  Eur J Cancer       Date:  2017-04-14       Impact factor: 9.162

6.  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

7.  Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation.

Authors:  Larissa Shamseer; David Moher; Mike Clarke; Davina Ghersi; Alessandro Liberati; Mark Petticrew; Paul Shekelle; Lesley A Stewart
Journal:  BMJ       Date:  2015-01-02

Review 8.  Cancer genetic risk assessment for individuals at risk of familial breast cancer.

Authors:  Jennifer S Hilgart; Bernadette Coles; Rachel Iredale
Journal:  Cochrane Database Syst Rev       Date:  2012-02-15

9.  Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey.

Authors:  Maren T Scheuner; Timothy S McNeel; Andrew N Freedman
Journal:  Genet Med       Date:  2010-11       Impact factor: 8.822

10.  Clinical utility of a Web-enabled risk-assessment and clinical decision support program.

Authors:  Lori A Orlando; R Ryanne Wu; Rachel A Myers; Adam H Buchanan; Vincent C Henrich; Elizabeth R Hauser; Geoffrey S Ginsburg
Journal:  Genet Med       Date:  2016-03-03       Impact factor: 8.822

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  2 in total

1.  Association of Disparities in Family History and Family Cancer History in the Electronic Health Record With Sex, Race, Hispanic or Latino Ethnicity, and Language Preference in 2 Large US Health Care Systems.

Authors:  Daniel Chavez-Yenter; Melody S Goodman; Yuyu Chen; Xiangying Chu; Richard L Bradshaw; Rachelle Lorenz Chambers; Priscilla A Chan; Brianne M Daly; Michael Flynn; Amanda Gammon; Rachel Hess; Cecelia Kessler; Wendy K Kohlmann; Devin M Mann; Rachel Monahan; Sara Peel; Kensaku Kawamoto; Guilherme Del Fiol; Meenakshi Sigireddi; Saundra S Buys; Ophira Ginsburg; Kimberly A Kaphingst
Journal:  JAMA Netw Open       Date:  2022-10-03

2.  Improving primary care identification of familial breast cancer risk using proactive invitation and decision support.

Authors:  Nadeem Qureshi; Brittany Dutton; Stephen Weng; Christina Sheehan; Wendy Chorley; John F R Robertson; Denise Kendrick; Joe Kai
Journal:  Fam Cancer       Date:  2020-06-11       Impact factor: 2.375

  2 in total

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