Advertisement
Research Article| Volume 149, ISSUE 3, P565-569, June 2018

Download started.

Ok

Implementation of a quality improvement project for universal genetic testing in women with ovarian cancer

      Highlights

      • Improvement needed in efforts for universal testing in gynecology oncology.
      • Implementation of simple measures can have large impact on achieving this goal.
      • Education of providers is an effective way of impacting universal testing rates.
      • Patients who see genetic counselors have a high rate of testing completion.

      Abstract

      Objective

      The National Comprehensive Cancer Network recommends all women with ovarian cancer be offered genetic testing. Despite a decade of endorsement, many oncology practitioners have yet to make this a part of routine practice. Referral to genetic counseling and completion of genetic testing among patients at substantial risk of germline mutations are significantly lacking, adversely affecting patient care and squandering an opportunity to maximize cancer prevention efforts. This project determined the impact and feasibility of implementing a basic model for universal referral to genetic counseling and completion of genetic testing in women with a diagnosis of ovarian cancer in an academic gynecology oncology practice with access to electronic health records (EHRs).

      Methods

      Patients diagnosed with ovarian cancer from January 2008 to November 2013 were retrospectively reviewed to determine the baseline referral rate for genetic counseling and testing completion in our practice. Implementation of a process change model combining provider training, patient education, enhanced electronic health record documentation and improved patient appointment scheduling strategies were implemented. We then prospectively collected data on all newly diagnosed ovarian cancer patients that had not already undergone genetic testing presenting from December 1, 2013 to November 30, 2016.

      Results

      Genetic referral rates, genetic counseling and testing completion rates were markedly improved. Pre-implementation our genetic testing rate was 27% and post implementation our testing rate was 82% (p-value ≤ 0.001).

      Conclusions

      Low cost interventions that target education of both providers and patients regarding the importance of genetic testing along with utilization of the EHR and streamlined patient appointment services can significantly increase rates of genetic testing completion.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Gynecologic Oncology
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Pal T.
        • Lee J.H.
        • Besharat A.
        • Thompson Z.
        • Monteiro A.N.
        • Phelan C.
        • Lancaster J.M.
        • Metcalfe K.
        • Sellers T.A.
        • Vadaparampil S.
        • Narod S.A.
        Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers.
        Clin. Genet. 2014; 85: 49-53https://doi.org/10.1111/cge.12130
        • Manchanda R.
        • Loggenberg K.
        • Sanderson S.
        • Burnell M.
        • Wardle J.
        • Gessler S.
        • Side L.
        • Balogun N.
        • Desai R.
        • Kumar A.
        • Dorkins H.
        • Wallis Y.
        • Chapman C.
        • Taylor R.
        • Jacobs C.
        • Tomlinson I.
        • Mcguire A.
        • Beller U.
        • Menon U.
        • Jacobs I.
        Population testing for cancer predisposing BRCA1/BRCA2 mutations in the Ashkenazi-Jewish community: a randomized controlled trial.
        J. Natl. Cancer Inst. 2015; 107: 379https://doi.org/10.1093/jnci/dju379
        • Nelson H.D.
        • Huffman L.H.
        • Fu R.
        • Harris E.L.
        • U.S. Preventive Services Task Force
        Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force.
        Ann. Intern. Med. 2005; 143: 362-379
        16144895
        • National Comprehensive Cancer Network
        Clinical Practice Guidelines in Oncology Genetic/Familial High-risk Assessment: Breast and Ovarian Version 1.
        2007 (03/22/07)
        • American College of Obstetricians and Gynecologists
        Hereditary breast and ovarian cancer syndrome. ACOG practice bulletin no. 103.
        Obstet. Gynecol. 2009; 113: 957-966
        • Hampel H.
        • Bennet R.L.
        • Buchanan A.
        • Pearlman R.
        • Wiesner G.L.
        • Guideline development group ACoMG
        • et al.
        A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
        Genet. Med. 2015; 17: 70-87
      1. American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
        J. Clin. Oncol. Nov 1 2015; 33 (Epub 2015 Aug 31): 3660-3667https://doi.org/10.1200/JCO.2015.63.0996
        26324357
        • Randall L.M.
        • Pothuri B.
        • Swisher E.M.
        • Diaz J.
        • Buchanan A.
        • Witkop C.T.
        • Powel C.B.
        • Smith E.B.
        • Robson M.E.
        • Boyd J.
        • Coleman R.L.
        • Lu K.
        Multidisciplinary summit on genetics services for women with gynecologic cancers: a Society of Gynecologic Oncology white paper.
        Gynecol. Oncol. 2017; 146: 217-224https://doi.org/10.1016/j.ygyno.2017.06.002
        • Chen S.
        • Parmigiani G.
        Meta-analysis of BRCA1 and BRCA2 penetrance.
        J. Clin. Oncol. 2007; 25: 1329-1333https://doi.org/10.1200/jco.2006.09.1066
        • Norquist B.M.
        • Harrell M.I.
        • Brady M.F.
        • Walsh T.
        • Lee M.K.
        • Gulsuner S.
        • et al.
        Inherited mutations in women with ovarian carcinoma.
        JAMA Oncol. 2016; 2: 482-490https://doi.org/10.1001/jamaoncol.2015.5495
        • Malander S.
        • Rambech E.
        • Kristoffersson U.
        • Halvarsson B.
        • Ridderheim M.
        • Borg A.
        • Nilbert M.
        The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
        Gynecol. Oncol. 2006; 101: 238-243https://doi.org/10.1016/j.ygyno.2005.10.029
        • Pennington K.P.
        • Swisher E.M.
        Hereditary ovarian cancer: beyond the usual suspects.
        Gynecol. Oncol. 2012; 124: 347-353https://doi.org/10.1016/j.ygyno.2011.12.415
        • Demsky R.
        • McCuaig J.
        • Maganti M.
        • Murphy K.J.
        • Rosen B.
        • Armel S.R.
        Keeping it simple: genetics referrals for all invasive serous ovarian cancers.
        Gynecol. Oncol. 2013; 130: 329-333https://doi.org/10.1016/j.ygyno.2013.05.003
        • Metcalfe K.A.
        • Fan I.
        • McLaughlin J.
        • Risch H.A.
        • Rosen B.
        • Murphy J.
        • Bradley L.
        • Armel S.
        • Sun P.
        • Narod S.A.
        Uptake of clinical genetic testing for ovarian cancer in Ontario: a population-based study.
        Gynecol. Oncol. 2009; 112: 68-72https://doi.org/10.1016/j.ygyno.2008.10.007
        • Petzel S.V.
        • Vogel R.I.
        • Bensend T.
        • Leininger A.
        • Argenta P.A.
        • Geller M.A.
        Genetic risk assessment for women with epithelial ovarian cancer: referral patterns and outcomes in a university gynecologic oncology clinic.
        J. Genet. Couns. 2013; 22: 662-673https://doi.org/10.1007/s10897-013-9598-y
        • Powell C.B.
        • Littell R.
        • Hoodfar E.
        • Sinclair F.
        • Pressman A.
        Does the diagnosis of breast or ovarian cancer trigger referral to genetic counseling?.
        Int. J. Gynecol. Cancer. 2013; 23: 431-436https://doi.org/10.1097/IGC.0b013e318280f2b4
        • Childers C.P.
        • Childers K.
        • Maggard-Gibbons M.
        • Macinko J.
        National estimates of genetic testing in women with a history of breast or ovarian cancer.
        J. Clin. Oncol. 2017; 35: 1-7https://doi.org/10.1200/JCO.2017.74.7899
        • Petzel S.V.
        • Vogel R.I.
        • McNiel J.
        • Leininger A.
        • Argenta P.A.
        • Geller M.A.
        Improving referral for genetic risk assessment in ovarian cancer using an electronic medical record system.
        Int. J. Gynecol. Cancer. July 2014; 24: 1003-1009
        • Bednar E.M.
        • Oakley H.D.
        • Sun C.C.
        • Burke C.C.
        • Munsell M.F.
        • Westin S.N.
        • Lu K.H.
        A universal genetic testing initiative for patients with high grade epithelial ovarian cancer and implications for treatment.
        Gynecol. Oncol. 2017; 146: 399-404
        • Meyer L.A.
        • Anderson M.E.
        • Lacour R.A.
        • Suri A.
        • Daniels M.S.
        • Urbauer D.L.
        • Nogueras- Gonzalez G.M.
        • Schmeler K.M.
        • Gershenson D.M.
        • Lu K.H.
        Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.
        Obstet. Gynecol. 2010; 15: 945-952
        • Febbraro T.
        • Robison K.
        • Wilbur J.S.
        • Laprise J.
        • Bregar A.
        • Lopes V.
        • Legare R.
        • Stuckey A.
        Adherence patterns to National Comprehensive Cancer Network (NCCN) guidelines for referral to cancer genetic professionals.
        Gynecol. Oncol. 2015; 138: 109-114https://doi.org/10.1016/j.ygyno.2015.04.029
        • Geer K.P.
        • Ropka M.E.
        • Cohn W.F.
        • Jones S.M.
        • Miesfeldt S.
        Factors influencing patients' decisions to decline cancer genetic counseling services.
        J. Genet. Couns. 2001; 10: 25-40
        • Novetsky A.P.
        • Smith K.
        • Babb S.A.
        • Jeffe D.B.
        • Hagemann A.R.
        • Thaker P.H.
        • Powell M.A.
        • Mutch D.G.
        • Massad S.
        • Zighelboim I.
        Timing of referral for genetic counseling and genetic testing in patients with ovarian, fallopian tube, or primary peritoneal carcinoma.
        Int. J. Gynecol. Cancer. 2013; 23: 1016-1021https://doi.org/10.1097/IGC.0b013e3182994365
        • Kentwell M.
        • Dow E.
        • Antill Y.
        • Wrede C.D.
        • McNally O.
        • Higgs E.
        • Hamilton A.
        • Ananda S.
        • Lindeman G.
        • Scott C.L.
        Mainstreaming cancer genetics: a model integrating germline BRCA testing into routine ovarian cancer clinics.
        Gynecol. Oncol. 2017; 145: 130-136https://doi.org/10.1016/j.ygyno.2017.01.030
        • Senter L.
        • O'Malley D.M.
        • Backes F.J.
        • Copeland L.J.
        • Fowler J.
        • Salani R.
        • Cohn D.E.
        Genetic consultation embedded in a gynecologic oncology clinic improves compliance with guideline care.
        Gynecol. Oncol. 2017; 14: 110-114
        • Fox E.
        • McCuaig J.
        • Demsky R.
        • Shuman C.
        • Chitayat D.
        • Maganti M.
        • Murphy J.
        • Rosen B.
        • Ferguson S.
        • Randall Armel S.
        The sooner the better: genetic testing following ovarian cancer diagnosis.
        Gynecol. Oncol. Jun 2015; 137 (Epub 2015 Apr 11): 423-429https://doi.org/10.1016/j.ygyno.2015.03.057
        • Cohen P.A.
        • Nichols C.B.
        • Schofield L.
        • Van Der Werf S.
        • Pachter N.
        Impact of clinical genetics attendance at a gynecologic oncology tumor board on referrals for genetic counseling and BRCA mutation testing.
        Int. J. Gynecol. Cancer. 2016; 26: 892-897
        • Pokharel H.P.
        • Hacker N.F.
        • Andrews L.
        Improving attendance to genetic counselling services for gynaecological oncology patients.
        Gynecol. Oncol. Res. Pract. Jan 10 2018; 5 (eCollection 2018): 2https://doi.org/10.1186/s40661-018-0059-z
        • Chen Z.
        • Kolor K.
        • Grosse S.D.
        • Rodriguez J.L.
        • Lynch J.A.
        • Green R.F.
        • Dotson W.D.
        • Bowen M.S.
        • Khoury M.J.
        Trends in utilization and costs of BRCA testing among women aged 18–64 years in the United States, 2003–2014.
        Genet. Med. Sep 21 2017; (Epub ahead of print)https://doi.org/10.1038/gim.2017.118
        • Scott C.L.
        • Swisher E.M.
        • Kaufmann S.H.
        Poly (ADP-ribose) polymerase inhibitors: recent advances and future development.
        J. Clin. Oncol. Apr 20 2015; 33: 1397-1406https://doi.org/10.1200/JCO.2014.58.8848
        • Ledermann J.
        • Harter P.
        • Gourley C.
        • Friedlander M.
        • Vergote I.
        • Rustin G.
        • Scott C.
        • Meier W.
        • Shapira-Frommer R.
        • Safra T.
        • Matei D.
        • Macpherson E.
        • Watkins C.
        • Carmichael J.
        • Matulonis U.
        Olaparib maintenance therapy in platinum-sensitive relapsed ovarian cancer.
        N. Engl. J. Med. Apr 12 2012; 366: 1382-1392https://doi.org/10.1056/NEJMoa1105535
      2. New York Times Most Visited Content of 2013.
        • Juthe R.H.
        • Zaharchuk A.
        • Wang C.
        Celebrity disclosures and information seeking: the case of Angelina Jolie.
        Genet. Med. 2015; 17: 545-553
        • Offit K.
        • Bradbury A.
        • Storm C.
        • et al.
        Gene patents and personalized cancer care: impact of the myriad case on clinical oncology.
        J. Clin. Oncol. 2013; 31: 2743-2748
        • Acheson L.S.
        • Stange K.C.
        • Zyzanski S.
        Clinical genetics issues encountered by family physicians.
        Genet. Med. 2005; 7: 501-508
        • Anderson B.
        • McLosky J.
        • Wasilevich E.
        • Lyon-Callo S.
        • Duquette D.
        • Copeland G.
        Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
        J. Cancer Epidemiol. 2012; 2012298745
        • Brandt R.
        • Ali Z.
        • Sabel A.
        • McHugh T.
        • Gilman P.
        Cancer genetics evaluation: barriers to and improvements for referral.
        Genet. Test. 2008; 12: 9-12
        • D'Agincourt-Canning L.
        Genetic testing for hereditary cancer: challenges to ethical care in rural and remote communities.
        HEC Forum. 2004; 16: 222-233
        • Cohen S.A.
        • Marvin M.L.
        • Riley B.D.
        • Vig H.S.
        • Rousseau J.A.
        • Gustafson S.L.
        Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
        J. Genet. Couns. Aug 2013; 22: 411-421
        23615968
        • Bonadies D.C.
        • Brierley K.L.
        • Barnett R.E.
        • Baxter M.D.
        • Donenberg T.
        • Ducaine W.L.
        • Ernst M.E.
        • Homer J.
        • Judkins M.
        • Lovick N.M.
        • Powers J.M.
        • Stanislaw C.
        • Stark E.
        • Stenner R.C.
        • Matloff E.T.
        Adverse events in cancer genetic testing: the third case series.
        Cancer J. Jul–Aug 2014; 20: 246-253
        25098283
        • Brierley K.L.
        • Campfield D.
        • Ducaine W.
        • Dohany L.
        • Donenberg T.
        • Shannon K.
        • Schwartz R.C.
        • Matloff E.T.
        Errors in delivery of cancer genetics services: implications for practice.
        Conn. Med. 2010 Aug; 74: 413-423
        20806621
        • Brierley K.L.
        • Blouch E.
        • Cogswell W.
        • Homer J.P.
        • Pencarinha D.
        • Stanislaw C.L.
        • Matloff E.T.
        Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications.
        Cancer J. Jul–Aug 2012; 18: 303-309https://doi.org/10.1097/PPO.0b013e3182609490
        22846730
      3. Committee opinion no. 693: counseling about genetic testing and communication of genetic test results.
        Obstet. Gynecol. Apr 2017; 129: e96-e101
        28333821
        • Robson M.E.
        • Bradbury A.R.
        • Arun B.
        • Domchek S.M.
        • Ford J.M.
        • Hampel H.L.
        • Lipkin S.M.
        • Syngal S.
        • Wollins D.S.
        • Lindor N.M.
        American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
        J. Clin. Oncol. Nov 1 2015; 33 (Epub 2015 Aug 31): 3660-3667https://doi.org/10.1200/JCO.2015.63.0996