Literature DB >> 25933682

Adherence patterns to National Comprehensive Cancer Network (NCCN) guidelines for referral to cancer genetic professionals.

Terri Febbraro1, Katina Robison2, Jennifer Scalia Wilbur2, Jessica Laprise2, Amy Bregar3, Vrishali Lopes4, Robert Legare2, Ashley Stuckey2.   

Abstract

OBJECTIVE: Genetic predisposition is responsible for 5-10% of breast cancer, 10% of ovarian cancer and 2-5% of uterine cancer. The study objective was to compare genetic counseling and testing referral rates among women with breast cancer that met NCCN referral guidelines to the referral rates among women with gynecologic cancers and determine predictors of referral.
METHODS: Utilizing an institutional tumor registry database, patients from an academic women's oncology program were identified who met a subset of NCCN guidelines for genetic referral between 2004 and 2010. Patients diagnosed with ovarian cancer, breast cancer ≤50years of age, or uterine cancer <50years of age were included. A retrospective electronic chart review was conducted to evaluate for a genetic referral and uptake of genetic testing.
RESULTS: 820 women were included (216 uterine, 314 breast, and 290 ovarian cancer). The overall genetic referral rate was 21.7%. 34% of eligible breast cancer patients were referred compared to 13.4% of uterine cancer and 14.5% of ovarian cancer patients (p<0.0001). Younger age, breast cancer diagnosis, family history and earlier stage were all significant referral predictors. The odds of being referred increased with the number of affected family members. 70.8% of referred patients, consulted with genetics. Among those who consulted with genetics, 95.2% underwent testing.
CONCLUSIONS: Although increasing, genetic counseling remains underutilized across cancer diagnosis. Women with breast cancer are more likely to be referred than women with gynecologic cancers. Younger age, earlier stage and positive family history appear to be predictive of referral for genetic evaluation.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Genetic counseling; Hereditary cancer; Practice patterns

Mesh:

Year:  2015        PMID: 25933682      PMCID: PMC4868086          DOI: 10.1016/j.ygyno.2015.04.029

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


  34 in total

1.  Risk-reducing salpingo-oophorectomy (RRSO) in BRCA mutation carriers: experience with a consecutive series of 111 patients using a standardized surgical-pathological protocol.

Authors:  C Bethan Powell; Lee-may Chen; Jane McLennan; Beth Crawford; Charles Zaloudek; Joseph T Rabban; Dan H Moore; John Ziegler
Journal:  Int J Gynecol Cancer       Date:  2011-07       Impact factor: 3.437

2.  Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996.

Authors: 
Journal:  J Clin Oncol       Date:  1996-05       Impact factor: 44.544

3.  Prevalence of hereditary breast/ovarian carcinoma risk in patients with a personal history of breast or ovarian carcinoma in a mammography population.

Authors:  Francisco J Dominguez; Julie L Jones; Katherina Zabicki; Barbara L Smith; Michele A Gadd; Michele Specht; Daniel B Kopans; Richard H Moore; James S Michaelson; Kevin S Hughes
Journal:  Cancer       Date:  2005-11-01       Impact factor: 6.860

4.  Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.

Authors:  A M Burton-Chase; S R Hovick; S K Peterson; S K Marani; S W Vernon; C I Amos; M L Frazier; P M Lynch; E R Gritz
Journal:  Clin Genet       Date:  2013-03       Impact factor: 4.438

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

6.  Effect of BRCA1/2 mutations on long-term survival of patients with invasive ovarian cancer: the national Israeli study of ovarian cancer.

Authors:  Angela Chetrit; Galit Hirsh-Yechezkel; Yehuda Ben-David; Flora Lubin; Eitan Friedman; Siegal Sadetzki
Journal:  J Clin Oncol       Date:  2008-01-01       Impact factor: 44.544

7.  Keeping it simple: genetics referrals for all invasive serous ovarian cancers.

Authors:  R Demsky; J McCuaig; M Maganti; K J Murphy; B Rosen; S R Armel
Journal:  Gynecol Oncol       Date:  2013-05-22       Impact factor: 5.482

Review 8.  Management of extracolonic tumours in patients with Lynch syndrome.

Authors:  Jan J Koornstra; Marian Je Mourits; Rolf H Sijmons; Annemarie M Leliveld; Harry Hollema; Jan H Kleibeuker
Journal:  Lancet Oncol       Date:  2009-04       Impact factor: 41.316

9.  Attitude towards genetic testing for breast cancer susceptibility: a comparison of affected and unaffected women.

Authors:  M Bruno; M Digennaro; S Tommasi; B Stea; T Danese; F Schittulli; A Paradiso
Journal:  Eur J Cancer Care (Engl)       Date:  2009-11-13       Impact factor: 2.520

10.  Health care providers and direct-to-consumer access and advertising of genetic testing in the United States.

Authors:  Melanie F Myers
Journal:  Genome Med       Date:  2011-12-28       Impact factor: 15.266

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  35 in total

1.  Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer.

Authors:  Erin Tutty; Lara Petelin; Joanne McKinley; Mary-Anne Young; Bettina Meiser; Victoria M Rasmussen; Rowan Forbes Shepherd; Paul A James; Laura E Forrest
Journal:  Eur J Hum Genet       Date:  2019-04-08       Impact factor: 4.246

2.  A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment.

Authors:  Erica M Bednar; Holly D Oakley; Charlotte C Sun; Catherine C Burke; Mark F Munsell; Shannon N Westin; Karen H Lu
Journal:  Gynecol Oncol       Date:  2017-06-10       Impact factor: 5.482

Review 3.  Disparities in gynecologic cancer genetics evaluation.

Authors:  Emily M Hinchcliff; Erica M Bednar; Karen H Lu; J Alejandro Rauh-Hain
Journal:  Gynecol Oncol       Date:  2019-01-31       Impact factor: 5.482

4.  Evaluating the performance of National Comprehensive Cancer Network (NCCN) breast and ovarian genetic/familial high risk assessment referral criteria for breast cancer women in an Asian surgical breast clinic.

Authors:  Geok-Hoon Lim; Eillen Borje; John C Allen
Journal:  Gland Surg       Date:  2017-02

5.  National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.

Authors:  Christopher P Childers; Kimberly K Childers; Melinda Maggard-Gibbons; James Macinko
Journal:  J Clin Oncol       Date:  2017-08-18       Impact factor: 44.544

6.  Cancer Genetic Counseling and Testing: Perspectives of Epithelial Ovarian Cancer Patients and Gynecologic Oncology Healthcare Providers.

Authors:  Margaret I Liang; Deanna H Wong; Christine S Walsh; Robin Farias-Eisner; Joshua G Cohen
Journal:  J Genet Couns       Date:  2017-08-07       Impact factor: 2.537

7.  Disseminating universal genetic testing to a diverse, indigent patient population at a county hospital gynecologic oncology clinic.

Authors:  Erica M Bednar; Charlotte C Sun; Bethsaida Camacho; John Terrell; Alyssa G Rieber; Lois M Ramondetta; Ralph S Freedman; Karen H Lu
Journal:  Gynecol Oncol       Date:  2018-12-08       Impact factor: 5.482

8.  Breadth of Genetic Testing Selected by Patients at Risk of Hereditary Breast and Ovarian Cancer.

Authors:  J Brian Szender; Jasmine Kaur; Katherine Clayback; Mollie L Hutton; June Mikkelson; Kunle Odunsi; Cara Dresbold
Journal:  Int J Gynecol Cancer       Date:  2018-01       Impact factor: 3.437

9.  Genetic counseling referral for ovarian cancer patients: a call to action.

Authors:  Christine Garcia; Kara Harrison; Kari L Ring; Mackenzie W Sullivan; Lisa A Rauh; Susan C Modesitt
Journal:  Fam Cancer       Date:  2019-07       Impact factor: 2.375

10.  Creation and Implementation of an Environmental Scan to Assess Cancer Genetics Services at Three Oncology Care Settings.

Authors:  Erica M Bednar; Michael T Walsh; Ellen Baker; Kimberly I Muse; Holly D Oakley; Rebekah C Krukenberg; Cara S Dresbold; Sandra B Jenkinson; Amanda L Eppolito; Kelly B Teed; Molly H Klein; Nichole A Morman; Elizabeth C Bowdish; Pauline Russ; Emaline E Wise; Julia N Cooper; Michael W Method; John W Henson; Andrew V Grainger; Banu K Arun; Karen H Lu
Journal:  J Genet Couns       Date:  2018-05-16       Impact factor: 2.537

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