Literature DB >> 23354368

Does the diagnosis of breast or ovarian cancer trigger referral to genetic counseling?

C Bethan Powell1, Ramey Littell, Elizabeth Hoodfar, Fiona Sinclair, Alice Pressman.   

Abstract

OBJECTIVE: Kaiser Permanente Northern California is a large integrated health care delivery system in the United States that has guidelines for referring women with newly diagnosed BRCA1-and BRCA2-associated cancers for genetic counseling. This study assesses adherence to genetic counseling referral guidelines within this health system.
METHODS: Chart review was performed to identify patients with cancer who met the following pathology-based Kaiser Permanente Northern California guidelines for referral for genetic counseling: invasive breast cancer, younger than age 40; nonmucinous epithelial ovarian, fallopian tube, or peritoneal cancer, younger than age 60; women with synchronous or metachronous primary cancers of the breast and ovaries; and male breast cancer. We assessed compliance with referral guidelines. An electronic notice was sent to the managing physician of patients with newly diagnosed cancer to assess the feasibility of this intervention.
RESULTS: A total of 340 patients were identified with breast cancer at younger than age 40 or with ovarian, peritoneal, or tubal cancer between January and June, 2008. Upon chart review, 105 of these patients met pathology-based criteria for referral to genetic counseling, of whom 47 (45%) were referred within the 2-year study period. Of the 67 subjects with breast cancer, 40 subjects (60%) were referred. In contrast, only 7 (21%) of 33 patients with ovarian cancer were referred (P < 0.001). A pilot study was performed to test the feasibility of notifying managing oncologists with an electronic letter alerting them of eligibility for genetic referral of patients with new diagnosis (n = 21). In the 3 to 6 months after this notification, 12 of these 21 patients were referred for counseling including 5 of 7 patients with a diagnosis of ovarian cancer.
CONCLUSION: There is a missed opportunity for referring patients to genetic counseling, especially among patients with ovarian cancer. A pilot study suggests that alerting treating physicians is a feasible strategy to increase appropriate referral.

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Year:  2013        PMID: 23354368     DOI: 10.1097/IGC.0b013e318280f2b4

Source DB:  PubMed          Journal:  Int J Gynecol Cancer        ISSN: 1048-891X            Impact factor:   3.437


  20 in total

1.  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 2.  Ovarian Cancer Prevention in High-risk Women.

Authors:  Sarah M Temkin; Jennifer Bergstrom; Goli Samimi; Lori Minasian
Journal:  Clin Obstet Gynecol       Date:  2017-12       Impact factor: 2.190

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

Authors:  Terri Febbraro; Katina Robison; Jennifer Scalia Wilbur; Jessica Laprise; Amy Bregar; Vrishali Lopes; Robert Legare; Ashley Stuckey
Journal:  Gynecol Oncol       Date:  2015-04-28       Impact factor: 5.482

Review 4.  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

5.  Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer: A Population-Based Study in Southern Sweden.

Authors:  Annelie Augustinsson; Carolina Ellberg; Ulf Kristoffersson; Håkan Olsson; Hans Ehrencrona
Journal:  Public Health Genomics       Date:  2020-07-08       Impact factor: 2.000

6.  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

7.  Predictors of genetic testing uptake in newly diagnosed breast cancer patients.

Authors:  Mary K Ladd; Beth N Peshkin; Claudine Isaacs; Gillian Hooker; Shawna Willey; Heiddis Valdimarsdottir; Tiffani DeMarco; Suzanne O'Neill; Savannah Binion; Marc D Schwartz
Journal:  J Surg Oncol       Date:  2020-04-28       Impact factor: 3.454

8.  The value of a genetic counselor: improving identification of cancer genetic counseling patients with chart review.

Authors:  Jennifer N Eichmeyer; Christa Burnham; Patty Sproat; Rick Tivis; Thomas M Beck
Journal:  J Genet Couns       Date:  2013-10-25       Impact factor: 2.537

9.  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

10.  Strategies to enhance identification of hereditary breast cancer gene carriers.

Authors:  Sonya Reid; Lucy B Spalluto; Tuya Pal
Journal:  Expert Rev Mol Diagn       Date:  2020-09-11       Impact factor: 5.225

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