Skip to main content

Advertisement

Log in

A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland

  • Original Article
  • Published:
Familial Cancer Aims and scope Submit manuscript

Abstract

In the Republic of Ireland (ROI), BRCA1/BRCA2 genetic testing has been traditionally undertaken in eligible individuals, after pre-test counselling by a Clinical Geneticist/Genetic Counsellor. Clinical Genetics services in ROI are poorly resourced, with routine waiting times for appointments at the time of this pilot often extending beyond a year. The consequent prolonged waiting times are unacceptable where therapeutic decision-making depends on the patient’s BRCA status. “Mainstreaming” BRCA1/BRCA2 testing through routine oncology/surgical clinics has been implemented successfully in other centres in the UK and internationally. We aimed to pilot this pathway in three Irish tertiary centres. A service evaluation project was undertaken over a 6-month period between January and July 2017. Eligible patients, fulfilling pathology and age-based inclusion criteria defined by TGL clinical, were identified, and offered constitutional BRCA1/BRCA2 testing after pre-test counselling by treating clinicians. Tests were undertaken by TGL Clinical. Results were returned to clinicians by secure email. Onward referrals of patients with uncertain/pathogenic results, or suspicious family histories, to Clinical Genetics were made by the treating team. Surveys assessing patient and clinician satisfaction were sent to participating clinicians and a sample of participating patients. Data was collected with respect to diagnostic yield, turnaround time, onward referral rates, and patient and clinician feedback. A total of 101  patients underwent diagnostic germline BRCA1/BRCA2 tests through this pathway. Pathogenic variants were identified in 12 patients (12%). All patients in whom variants were identified were appropriately referred to Clinical Genetics. At least 12 additional patients with uninformative BRCA1/BRCA2 tests were also referred for formal assessment by Clinical Geneticist or Genetic Counsellor. Issues were noted in terms of time pressures and communication of results to patients. Results from a representative sample of participants completing the satisfaction survey indicated that the pathway was acceptable to patients and clinicians. Mainstreaming of constitutional BRCA1/BRCA2 testing guided by age- and pathology-based criteria is potentially feasible for patients with breast cancer as well as patients with ovarian cancer in Ireland.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Abbreviations

BC:

Breast cancer

CNS:

Clinical nurse specialist

ER:

oEstrogen receptor

HGSOC:

High grade serous ovarian cancer

KPI:

Key performance indicator

LGSOC:

Low grade serous ovarian cancer

OC:

Ovarian cancer

PR:

Progesterone receptor

PV:

Pathogenic variant (mutation)

RMH:

The Royal Marsden NHS Foundation Trust

TNBC:

Triple Negative Breast Cancer

VUS:

Variant of Uncertain Significance

VRE:

Variant Requiring Evaluation

References

  1. Witjes VM, van Bommel MHD, Ligtenberg MJL, Vos JR, Mourits MJE, Ausems MGEM et al (2022) Probability of detecting germline BRCA1/2 pathogenic variants in histological subtypes of ovarian carcinoma a meta-analysis. Gynecologic Oncol 164(1):221–230

    Article  CAS  Google Scholar 

  2. Lin J, Sharaf RN, Saganty R, Ahsan D, Feit J, Khoury A et al (2021) Achieving universal genetic assessment for women with ovarian cancer: are we there yet? A systematic review and meta-analysis. Gynecol Oncol 162(2):506–516

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Buys SS, Sandbach JF, Gammon A, Patel G, Kidd J, Brown KL et al (2017) A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes. Cancer 123(10):1721–1730

    Article  CAS  PubMed  Google Scholar 

  4. Beitsch PD, Whitworth PW, Hughes K, Patel R, Rosen B, Compagnoni G et al (2019) Underdiagnosis of hereditary breast cancer: are genetic testing guidelines a tool or an obstacle? J Clin Oncol 37(6):453–460

    Article  PubMed  Google Scholar 

  5. Copson ER, Maishman TC, Tapper WJ, Cutress RI, Greville-Heygate S, Altman DG et al (2018) Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study. Lancet Oncol 19(2):169–180

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Greenup R, Buchanan A, Lorizio W, Rhoads K, Chan S, Leedom T et al (2013) Prevalence of BRCA mutations among women with triple-negative breast cancer (TNBC) in a genetic counseling cohort. Ann Surg Oncol 20(10):3254–3258

    Article  PubMed  Google Scholar 

  7. Evans DG, Howell A, Ward D, Lalloo F, Jones JL, Eccles DM (2011) Prevalence of BRCA1 and BRCA2 mutations in triple negative breast cancer. J Med Genet 48(8):520–522

    Article  CAS  PubMed  Google Scholar 

  8. Pal T, Agnese D, Daly M, La Spada A, Litton J, Wick M et al (2020) Points to consider: is there evidence to support BRCA1/2 and other inherited breast cancer genetic testing for all breast cancer patients? A statement of the American college of medical genetics and genomics (ACMG). Genet Med 22(4):681–685

    Article  PubMed  Google Scholar 

  9. Yadav S, Reeves A, Campian S, Sufka A, Zakalik D (2017) Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis. Hered Cancer Clin Pract 15:11–11

    Article  PubMed  PubMed Central  Google Scholar 

  10. Metcalfe KA, Narod S, Eisen A, Lerner-Ellis J (2016) Treatment decision making and psychosocial outcomes associated with rapid genetic testing for BRCA1 and BRCA2 in women newly diagnosed with breast cancer. J Clin Oncol 34 (15_suppl) 1586-1586

  11. Sæther NH, Skuja E, Irmejs A, Maksimenko J, Miklasevics E, Purkalne G et al (2018) Platinum-based neoadjuvant chemotherapy in BRCA1-positive breast cancer: a retrospective cohort analysis and literature review. Hered Cancer Clin Pract 16:9–9

    Article  PubMed  PubMed Central  Google Scholar 

  12. Tan DS, Kaye SB (2015) Chemotherapy for patients with BRCA1 and BRCA2-mutated ovarian cancer: same or different? Am Soc Clin Oncol Educ Book 35:114–21

    Article  Google Scholar 

  13. Miller RE, Leary A, Scott CL, Serra V, Lord CJ, Bowtell D et al (2020) ESMO recommendations on predictive biomarker testing for homologous recombination deficiency and PARP inhibitor benefit in ovarian cancer. Ann Oncol 31(12):1606–1622

    Article  CAS  PubMed  Google Scholar 

  14. Pujade-Lauraine E, Ledermann JA, Selle F, Gebski V, Penson RT, Oza AM et al (2017) Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol 18(9):1274–1284

    Article  CAS  PubMed  Google Scholar 

  15. Moore K, Colombo N, Scambia G, Kim BG, Oaknin A, Friedlander M et al (2018) Maintenance olaparib in patients with newly diagnosed advanced ovarian cancer. N Engl J Med 379(26):2495–2505

    Article  CAS  PubMed  Google Scholar 

  16. Poveda A, Floquet A, Ledermann JA, Asher R, Penson RT, Oza AM et al. (2020) Final overall survival (OS) results from SOLO2/ENGOT-ov21: a phase III trial assessing maintenance olaparib in patients (pts) with platinum-sensitive, relapsed ovarian cancer and a BRCA mutation. J Clin Oncol 38(15_suppl) 6002–6002

  17. Coleman RL, Oza AM, Lorusso D, Aghajanian C, Oaknin A, Dean A et al (2017) Rucaparib maintenance treatment for recurrent ovarian carcinoma after response to platinum therapy (ARIEL3): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet 390(10106):1949–1961

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Mirza MR, Monk BJ, Herrstedt J, Oza AM, Mahner S, Redondo A et al (2016) Niraparib maintenance therapy in platinum-sensitive, recurrent ovarian cancer. N Engl J Med 375(22):2154–2164

    Article  CAS  PubMed  Google Scholar 

  19. González-Martín A, Pothuri B, Vergote I, DePont Christensen R, Graybill W, Mirza MR et al (2019) Niraparib in patients with newly diagnosed advanced ovarian cancer. N Engl J Med 381(25):2391–2402

    Article  PubMed  Google Scholar 

  20. Ray-Coquard I, Pautier P, Pignata S, Pérol D, González-Martín A, Berger R et al (2019) Olaparib plus bevacizumab as first-line maintenance in ovarian cancer. N Engl J Med 381(25):2416–2428

    Article  CAS  PubMed  Google Scholar 

  21. Coleman RL, Fleming GF, Brady MF, Swisher EM, Steffensen KD, Friedlander M et al (2019) Veliparib with first-line chemotherapy and as maintenance therapy in ovarian cancer. N Engl J Med 381(25):2403–2415

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Robson M, Im SA, Senkus E, Xu B, Domchek SM, Masuda N et al (2017) Olaparib for metastatic breast cancer in patients with a germline BRCA Mutation. N Engl J Med 377(6):523–533

    Article  CAS  PubMed  Google Scholar 

  23. Litton JK, Rugo HS, Ettl J, Hurvitz SA, Gonçalves A, Lee K-H et al (2018) Talazoparib in patients with advanced breast cancer and a germline BRCA mutation. N Engl J Med 379(8):753–763

    Article  CAS  PubMed  Google Scholar 

  24. Tutt ANJ, Garber JE, Kaufman B, Viale G, Fumagalli D, Rastogi P et al (2021) Adjuvant olaparib for patients with BRCA1- or BRCA2-mutated breast cancer. N Engl J Med 384(25):2394–2405

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Mateo J, Porta N, Bianchini D, McGovern U, Elliott T, Jones R et al (2020) Olaparib in patients with metastatic castration-resistant prostate cancer with DNA repair gene aberrations (TOPARP-B): a multicentre, open-label, randomised, phase 2 trial. Lancet Oncol 21(1):162–174

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Sandhu SK, Hussain M, Mateo J, Fizazi K, Saad F, Shore N et al (2019) PROfound: phase III study of olaparib versus enzalutamide or abiraterone for metastatic castration-resistant prostate cancer (mCRPC) with homologous recombination repair (HRR) gene alterations. Ann Oncol 30:ix188–ix189

    Article  Google Scholar 

  27. Golan T, Hammel P, Reni M, Van Cutsem E, Macarulla T, Hall MJ et al (2019) Maintenance olaparib for germline BRCA-mutated metastatic pancreatic cancer. N Engl J Med 381(4):317–327

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. AstraZeneca KA (2022) Lynparza approved in the US as adjuvant treatment for patients with germline BRCA-mutated HER2-negative high-risk early breast cancer. AstraZeneca. Press release available from: https://www.astrazeneca.com/media-centre/press-releases/2022/lynparza-approved-in-the-us-as-adjuvant-treatment-for-patients-with-germline-brca-mutated-her2-negative-high-risk-early-breast-cancer.html. Accessed 1 Jun 2022

  29. Merck, LYNPARZA® (olaparib) Receives Positive Opinion From EU CHMP as Adjuvant Treatment for Germline BRCA-Mutated, HER2-Negative High-Risk Early Breast Cancer (2022) Press release available from: https://www.merck.com/news/lynparza-olaparib-receives-positive-opinion-from-eu-chmp-as-adjuvant-treatment-for-germline-brca-mutated-her2-negative-high-risk-early-breast-cancer/. Accessed 1 Jul 2022

  30. Gotlieb WH. (2017) The society of gynaecologic oncology of canada (GOC) position statement: no woman left behind: toward a pan-canadian strategy for universal BRCA testing in ovarian cancer

  31. National Comprehensive Cancer Network (NCCN) clinical practice guidelines in oncology: ovarian cancer including fallopian tube cancer and primary peritoneal cancer (2019)

  32. Ledermann JA, Sessa C, Colombo N. (2016) eUpdate—ovarian cancer treatment recommendations (ESMO guidelines committee)

  33. ACOG Practice Bulletine Clinical Management Guidelines for Obstetrician-Gynecologists. (2017). 130(3)

  34. Vergote I, Banerjee S, Gerdes AM, van Asperen C, Marth C, Vaz F et al (2016) Current perspectives on recommendations for BRCA genetic testing in ovarian cancer patients. Eur J Cancer 69:127–134

    Article  PubMed  Google Scholar 

  35. Desai S, Jena AB (2016) Do celebrity endorsements matter? Observational study of BRCA gene testing and mastectomy rates after Angelina Jolie’s New York times editorial. BMJ 355:i6357

    Article  PubMed  PubMed Central  Google Scholar 

  36. Henneman L, Vermeulen E, van El CG, Claassen L, Timmermans DR, Cornel MC (2013) Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010. Eur J Hum Genet 21(8):793–799

    Article  PubMed  Google Scholar 

  37. McVeigh TP, Sweeney KJ, Kerin MJ, Gallagher DJ (2016) A qualitative analysis of the attitudes of Irish patients towards participation in genetic-based research. Ir J Med Sci 185(4):825–831

    Article  CAS  PubMed  Google Scholar 

  38. Hoskovec JM, Bennett RL, Carey ME, DaVanzo JE, Dougherty M, Hahn SE et al (2018) Projecting the supply and demand for certified genetic counselors: a workforce study. J Genet Couns 27(1):16–20

    Article  PubMed  Google Scholar 

  39. Jenkins BD, Fischer CG, Polito CA, Maiese DR, Keehn AS, Lyon M et al (2021) The 2019 US medical genetics workforce: a focus on clinical genetics. Genet Med 23(8):1458–1464

    Article  PubMed  PubMed Central  Google Scholar 

  40. Maiese DR, Keehn A, Lyon M, Flannery D, Watson M, Working Groups of the National Coordinating Center for Seven Regional Genetics Service, C (2019) Current conditions in medical genetics practice. Genet Med 21(8):1874–1877

    Article  PubMed  PubMed Central  Google Scholar 

  41. Penon-Portmann M, Chang J, Cheng M, Shieh JT (2020) Genetics workforce: distribution of genetics services and challenges to health care in California. Genet Med 22(1):227–231

    Article  PubMed  Google Scholar 

  42. Dragojlovic N, Borle K, Kopac N, Ellis U, Birch P, Adam S et al (2020) The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review. Genet Med 22(9):1437–1449

    Article  PubMed  Google Scholar 

  43. Seoighe C, Bracken A, Buckley P, Doran P, Green R, Healy S et al (2020) The future of genomics in Ireland ? Focus on genomics for health [version 1; peer review: 2 approved]. HRB Open Res 3:89

    Article  PubMed  PubMed Central  Google Scholar 

  44. Lynch SA, Borg I (2016) Wide disparity of clinical genetics services and EU rare disease research funding across Europe. J Community Genet 7(2):119–126

    Article  PubMed  Google Scholar 

  45. Clark T, Giffney C, Lambert D, Peyton C, Turner J, White N et al. (2018) Irish association of genetic counsellors (IAGC): Setting up a professional body and working towards regulation, in 21st meeting of the irish society of human genetics. Dublin

  46. Review of the Clinical Genetics Medical Workforce in Ireland (2019) Health Service Executive National Doctors Training & Planning. Available from: https://www.hse.ie/eng/staff/leadership-education-development/met/plan/specialty-specific-reviews/clinical-genetics-2019.pdf. Accessed 1 Jun 2022

  47. Bradley L, Lynch SA (2021) Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences? J Community Genet 12(1):121–127

    Article  PubMed  Google Scholar 

  48. O'Shea MT, Collins C. A survey of GP experience with the work of the National Cancer Control Programme and their views in relation to service priorities 2016, National Cancer Control Programme and Irish College of General Practitioners. Available from: https://www.hse.ie/eng/services/list/5/cancer/pubs/reports/a-survey-of-gp-experience-with-the-work-of-the-national-cancer-control-programme-and-their-views-in-relation-to-service-priorities.pdf. Accessed 1 Jun 2022

  49. Pierle JM, Mahon SM (2019) Genetic service delivery models: exploring approaches to care for families with hereditary cancer risk. Clin J Oncol Nurs 23(1):60–67

    PubMed  Google Scholar 

  50. ClinicalTrials.gov. Digital Delivery of Information About Genetic Testing for Breast Cancer (BRCA-DIRECT). 2022 07 July 2022]; Available from: https://clinicaltrials.gov/ct2/show/NCT04842799

  51. Barwell J, Snape K, Wedderburn S (2019) The new genomic medicine service and implications for patients. Clin Med (Lond) 19(4):273–277

    PubMed  Google Scholar 

  52. Kemp Z, Turnbull A, Yost S, Seal S, Mahamdallie S, Poyastro-Pearson E et al (2019) Evaluation of cancer-based criteria for use in mainstream BRCA1 and BRCA2 genetic testing in patients with breast cancer. JAMA Netw Open 2(5):e194428

    Article  PubMed  PubMed Central  Google Scholar 

  53. George A, Riddell D, Seal S, Talukdar S, Mahamdallie S, Ruark E et al (2016) Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients. Sci Rep 6:29506

    Article  PubMed  PubMed Central  Google Scholar 

  54. Rumford M, Lythgoe M, McNeish I, Gabra H, Tookman L, Rahman N et al (2020) Oncologist-led BRCA ‘mainstreaming’ in the ovarian cancer clinic: a study of 255 patients and its impact on their management. Sci Rep 10(1):3390

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Kentwell M, Dow E, Antill Y, Wrede CD, McNally O, Higgs E et al (2017) Mainstreaming cancer genetics: a model integrating germline BRCA testing into routine ovarian cancer clinics. Gynecol Oncol 145(1):130–136

    Article  PubMed  Google Scholar 

  56. Flaum N, Morgan RD, Burghel GJ, Bulman M, Clamp AR, Hasan J et al (2020) Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of England. Eur J Hum Genet 28(11):1541–1547

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Rahman B, Lanceley A, Kristeleit RS, Ledermann JA, Lockley M, McCormack M et al (2019) Mainstreamed genetic testing for women with ovarian cancer: first-year experience. J Med Genet 56(3):195–198

    Article  PubMed  Google Scholar 

  58. Scott N, O’Sullivan J, Asgeirsson K, Macmillan D, Wilson E (2020) Changing practice: moving to a specialist nurse-led service for BRCA gene testing. Br J Nurs 29(10):S6-s13

    Article  PubMed  Google Scholar 

  59. Grindedal EM, Jørgensen K, Olsson P, Gravdehaug B, Lurås H, Schlichting E et al (2020) Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway. Fam Cancer 19(2):133–142

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Bokkers K, Zweemer RP, Koudijs MJ, Stehouwer S, Velthuizen ME, Bleiker EMA et al (2022) Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer. Fam Cancer 21(3):295–304

    Article  PubMed  Google Scholar 

  61. Hegarty J, Flaherty SJ, Egan S, Jones MM, Odisigo C, Chakraborty S, O'Reilly D, Saab MM. (2021) The unmet need in cancer genetic services: conducting an environmental scan of the cancer genetics services in an Irish context underpinned by a mixed methods approach. Irish Cancer Society www.cancer.ie

  62. Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J et al (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American college of medical genetics and genomics and the association for molecular pathology. Genet Med 17(5):405–423

    Article  PubMed  PubMed Central  Google Scholar 

  63. McVeigh TP, Cody N, Carroll C, Duff M, Farrell M, Bradley L et al (2017) Recurrent large genomic rearrangements in BRCA1 and BRCA2 in an Irish case series. Cancer Genet 214–215:1–8

    Article  PubMed  Google Scholar 

  64. NICE guideline 2013: Classification and care of people at risk of familial breast cancer and management of breast cancer and related risks in people with a family history of breast cancer. (2013)

  65. Lee AJ, Cunningham AP, Kuchenbaecker KB, Mavaddat N, Easton DF, Antoniou AC (2013) BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface. Br J Cancer 110:535

    Article  PubMed  PubMed Central  Google Scholar 

  66. Mazzola E, Blackford A, Parmigiani G, Biswas S (2015) Recent enhancements to the genetic risk prediction model BRCAPRO. Cancer Inform 14(Suppl 2):147–157

    PubMed  PubMed Central  Google Scholar 

  67. Carver T, Hartley S, Lee A, Cunningham AP, Archer S, de Babb VC et al (2021) CanRisk tool-a web interface for the prediction of breast and ovarian cancer risk and the likelihood of carrying genetic pathogenic variants. Cancer Epidemiol Biomark Prev 30(3):469–473

    Article  CAS  Google Scholar 

  68. Evans DG, Lalloo F, Cramer A, Jones EA, Knox F, Amir E et al (2009) Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing. J Med Genet 46(12):811–817

    Article  CAS  PubMed  Google Scholar 

  69. Manchanda R, Patel S, Antoniou AC, Levy-Lahad E, Turnbull C, Evans DG et al (2017) Cost-effectiveness of population based BRCA testing with varying ashkenazi jewish ancestry. Am J Obstet Gynecol 217(5):578.e1-578.e12

    Article  PubMed  Google Scholar 

  70. Evans DGR, Lalloo F, Wallace A, Rahman N (2005) Update on the manchester scoring system for BRCA1 and BRCA2 testing. J Med Genet 42(7):e39–e39

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Weitzel JN, Lagos VI, Cullinane CA, Gambol PJ, Culver JO, Blazer KR et al (2007) Limited family structure and brca gene mutation status in single cases of breast cancer. JAMA 297(23):2587–2595

    Article  CAS  PubMed  Google Scholar 

  72. NIH. The Cost of Sequencing a Human Genome. 2016; Available from: https://www.genome.gov/27565109/the-cost-of-sequencing-a-human-genome/. Accessed 1 Jun 2022

  73. Manchanda R, Patel S, Gordeev VS, Antoniou AC, Smith S, Lee A et al (2018) Cost-effectiveness of population-based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 mutation testing in unselected general population women. J Natl Cancer Inst 110(7):714–725

    Article  PubMed  Google Scholar 

  74. Kennedy JM (2017) National Cancer Strategy 2017–2026, An Roinn Sláinte. Available from: https://www.gov.ie/en/publication/a89819-national-cancer-strategy-2017-2026/. Accessed 1 Jun 2022

  75. Percival N, George A, Gyertson J, Hamill M, Fernandes A, Davies E et al (2016) The integration of BRCA testing into oncology clinics. Br J Nurs 25(12):690–694

    Article  PubMed  PubMed Central  Google Scholar 

  76. Davies S (2016) Chief medical officer’s summary, in annual report of the chief medical officer—generation genome C. Langenberg, Editor

  77. Maxwell KN, Domchek SM, Nathanson KL, Robson ME (2016) Population frequency of germline BRCA1/2 mutations. J Clin Oncol 34(34):4183–4185

    Article  PubMed  Google Scholar 

  78. McHugh JK, Offiah G, Daly S, El Beltagi N, Barry MK, O’Reilly S et al (2022) Postgraduate training in cancer genetics-a cross-specialty survey exploring experience of clinicians in Ireland. Ir J Med Sci 191(3):1427–1434

    Article  PubMed  Google Scholar 

  79. Coakley M, Cleary V, Power N, O’Reilly S (2017) BRCA1/2 germline testing in non-mucinous epithelial ovarian carcinoma: changing international practice and implications for service provision. Eur J Hum Genet 25(2):167–168

    Article  CAS  PubMed  Google Scholar 

  80. Lalloo F, Varley J, Ellis D, Moran A, O’Dair L, Pharoah P et al (2003) Prediction of pathogenic mutations in patients with early-onset breast cancer by family history. Lancet 361(9363):1101–1102

    Article  CAS  PubMed  Google Scholar 

  81. Gonzalez KD, Noltner KA, Buzin CH, Gu D, Wen-Fong CY, Nguyen VQ et al (2009) Beyond li fraumeni syndrome: clinical characteristics of families with p53 germline mutations. J Clin Oncol 27(8):1250–1256

    Article  CAS  PubMed  Google Scholar 

  82. Nelen MR, Kremer H, Konings IB, Schoute F, van Essen AJ, Koch R et al (1999) Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations. Eur J Hum Genet 7(3):267–273

    Article  CAS  PubMed  Google Scholar 

  83. McGarrity TJ, Amos CI, Baker MJ. (2016) Peutz-Jeghers syndrome, in genereviews. In: MP Adam et al. (Eds). 2001: Seattle (WA): University of Washington, Seattle

  84. Win AK, Jenkins MA, Dowty JG, Antoniou AC, Lee A, Giles GG et al (2017) Prevalence and penetrance of major genes and polygenes for colorectal cancer. Cancer Epidemiol Biomark Prev 26(3):404–412

    Article  CAS  Google Scholar 

  85. Idos G, Valle L. Lynch Syndrome. 2004 Feb 5 [Updated 2021 Feb 4]. In: Adam MP, Everman DB, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022

  86. Skerl P, Krajc M, Blatnik A, Novakovic S (2017) Genetic testing and counseling of a recipient after bone marrow transplant from a sibling harboring a germline BRCA1 pathogenic mutation. Oncol Rep 38(1):279–282

    Article  PubMed  Google Scholar 

  87. HSE National Cancer Control Programme BRCA Testing (PARP Inhibitors). 2021 08 July 2022

  88. Kalachand R, Hennessy B, Byrne A, Casey O. (2019) Cancer trials ireland opens study to enable upfront and streamlined germline and somatic BRCA1/2 mutation testing in women with ovarian cancer

  89. HSE, HSE initiates a National Genetics and Genomics Strategy for Ireland (Press Release) 2022, available from https://www.hse.ie/eng/services/news/media/pressrel/hse-initiates-a-national-genetics-and-genomics-strategy-for-ireland.html. Accessed 1 Jun 2022.

  90. NICE, Familial breast cancer: Classification and care of people at risk of familial breast cancer and management of breast cancer and related risks in people with a family history of breast cancer (Update of clinical guideline 14 and 41). 2017. Accessed 1 Jun 2022

Download references

Acknowledgements

With thanks to Ms Judith McLucas, Ms Caoimhe Ní Mhuircheartaigh and Dr Oliver O’Brien for their assistance. MCG-Ireland Collaborators: Terri P. McVeigh, Angela J. George, Simon Ward, (Royal Marsden NHS Trust), Ann Strydom, Sheila Seal, Nazneen Rahman, (TGL Clinical Laboratory), Una M. McVeigh, Karl J. Sweeney, Ray McLaughlin, Carmel Malone, Michael J. Kerin, Kevin Barry, Michael Sugrue, Geraldine MacGregor, Pauline McGough, Judith McLucas, Margaret Rushe, Maccon Keane, Paul Donnellan, Ala Yousif, Michael O’Leary, Katherine Astbury, Joanne Higgins, Caoimhe Ní Mhuircheartaigh, (Soalta University Hospital Group), David J. Gallagher, Eileen Berkeley, Carmel Nolan, Elizabeth Connolly, Terry Boyle, Dhafir Al-Azawi, Elaine Richardson, Samantha Doyle, (St James’s University Hospital), Claire Giffney, Donal Brennan, Ruaidhri McVey, Thomas Walsh, Oliver O’Brien, Sheila Broderick, (Mater Misericordiae University Hospital), Michael Farrell, (Mater Private Hospital).

Funding

This pilot was supported by the Royal Marsden/ICR NIHR Specialist Biomedical Research Centre for Cancer and Wellcome grant 098518, and Health Research Board grants HRB/HSE NSAFP 2014/1 and HRB KEDS-2017-043. Constitutional genetic tests were funded by TGLclinical.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Terri Patricia McVeigh.

Ethics declarations

Conflict of interest

Dr Nazneen Rahman is a Non-executive Director of AstraZeneca.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 149 KB)

Supplementary file2 (PDF 60 KB)

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

McVeigh, T.P., Sweeney, K.J., Brennan, D.J. et al. A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland. Familial Cancer 22, 135–149 (2023). https://doi.org/10.1007/s10689-022-00313-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10689-022-00313-0

Keywords

Navigation