HBOC Genetic Counseling: A Genetic Counselor-Physician Partnership Model Joan Oliver, Amy Cronister Integrated Genetics, Laboratory Corporation of America® Holdings, Genetic Counseling Services, Monrovia, CA INTRODUCTION The American Society of Clinical Oncology (ASCO) has consistently addressed the oncologist’s role in integrating cancer genetic risk assessment and management into clinical practice and has supported pre-and posttesting counseling by a qualified health professional for patients at increased risk of hereditary cancer susceptibility.1 In 2014, Integrated Genetics began offering genetic counseling in collaboration with physicians whose patients have a personal or family history of breast or ovarian cancer. The goal of this study was to determine if a Telegenetic Counseling program for Hereditary Breast and Ovarian Cancer (HBOC) was operationally feasible and to test its utility for providers for whom cancer genetic counseling may not have been readily accessible. METHODS All referrals made in 2014 to Integrated Genetics for genetic counseling for a personal or family history of breast and/or ovarian cancer were analyzed. Genetic counseling was provided by active candidate/board certified Genetic Counselors who are licensed in the state of residence of the patient, where required by law. Data was gathered from 247 counseling sessions provided to patients from 23 states. Patients were referred for telegenetic counseling (TGC) by OB/GYN, Family Practice, Internal Medicine, or Oncologist providers and called one of two centralized appointment centers, depending on the patients’ time zone, as appropriate under applicable laws. Patients were scheduled and subsequently sent an invite to their TGC session to be conducted via WebEx. WebEx was selected for its easy-touse software which allows for the use of PowerPoint type visual displays, two-way webcam use, and HIPAA compliance. lThe scheduling staff requested medical records, such as previous molecular testing, and emailed the patient a cancer family history questionnaire, to be completed prior to the appointment. All patients were provided a comprehensive genetic counseling session including a three generation pedigree, review of records and test results, and discussion of principles of cancer genetics, benefits and limitations of genetic testing, and implications of potential test results. lGenetic risk assessment for HBOC was provided to all patients based on family and personal history and where applicable, cancer risk models such as BRCAPRO. Genetic testing options were discussed based on National Comprehensive Cancer Network® (NCCN®) testing criteria.2 lWhere available, NCCN screening and surveillance recommendations were discussed, but patients were referred back to their provider to discuss patient-specific management and treatment recommendations. All patients and referring providers received a written Genetic Counseling Report summarizing the genetic counseling session. Data on family and personal history of cancer, quantifiable genetic risk assessment, whether NCCN criteria were met, and testing decisions were entered in to the IG Genetic Counseling Information System. A subset of patients was seen via in-person genetic counseling, and received the same services as for TGC. RESULTS Figure 1. During 2014, 247 counseling sessions were provided to patients from 23 states. All patients had a personal or family history of breast or ovarian cancer and the average age of patients was 44 years (range: 16-85). Gene�cCounselingDemographics 247 Totalpa�entscounseled 198 Pre-test 49 Gene�cCounselingDemographics Post-test 247 23 Totalpa�entscounseled Statesserved 198 Pre-test 44(16-85) Averageage(range) 49 Post-test 23 Statesserved Averageage(range) 44(16-85) Figure 2. Sixty four percent (64%) of sessions Gene�cCounselingSessions were done via WebExWeb-Ex and 36% In-person in person. GCModality 159 88 Gene�cCounselingSessions % 64% 36% Web-Ex In-person GCModality 159 88 % 64% 36% Figure 3. Of the 247 sessions, 198 (80.2%) were for pre-test genetic counseling; of those, 173 (87.4%) met NCCN HBOC genetic testing criteria and genetic testing for BRCA1/2 was offered. Patients Seen for Pre-Test Counseling n=198 Figure 4. Of those offered testing, 70.52% desired testing, 27.75% declined, and 1.73% were undecided. Patients Offered BRCA1/2 Testing n=173 48 28% 25 12.6% 173 87.4% NCCN HBOC criteria not met Met NCCN HBOC criteria 3 2% 122 71% Accepted Declined Undecided The remaining sessions (n=49) included post-test counseling for pathogenic mutations or variants of uncertain significance (n=39), and patients who had accepted testing but whose results were pending (n=10). CONCLUSION REFERENCES The Integrated Genetics HBOC genetic counseling program extended comprehensive genetic counseling to patients at increased risk for BRCA1/2 mutations who might not otherwise have access to this service. According to the applicable guidelines, physicians appropriately selected patients for referral (87% met NCCN testing criteria). The genetic counselors provided cancer genetic risk assessment, time-intensive patient education to facilitate informed decision making, and counseling about the implications of results, including the complexities of variants of uncertain significance. This collaborative model ensured physicians retained full patient care oversight, including management of screening and surveillance, while leveraging genetic counselor expertise. 1.Robson, ME, Bradbury, AR, Arun, B, et al., American Society of Clinical Oncology policy statement update: Genetic and genomic testing for cancer susceptibility. J.Clin Oncol 2015 Nov 1; 33(31):3660-7; doi:10.1200/JCO.2015.63.0996. Epub 2015 Aug 31. 2.Hereditary Breast and/or Ovarian Cancer Syndrome. NCCN Guidelines Version 2.2015. Available at: http://www.nccn. org/professionals/physician_gls/pdf/genetics_screening.pdf. Accessed November 18, 2015. ©2015 Laboratory Corporation of America ® Holdings. All rights reserved.
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