Healthcare Providers' Education, Knowledge, Opinions, Preferences, Roles in Provision of/Referral to Genetic Services for HBOC. Also includes reviews, education papers, and other papers that are focused on or specifically written for the given provider group.
This subcategory includes references pertaining to or intended for healthcare providers generally, or including two or more of the other provider subcategories.
List was last updated on
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- EBCC-13 manifesto: Balancing pros and cons for contralateral prophylactic mastectomy.
- Schmidt MK, Kelly JE, Brédart A, Cameron DA, de Boniface J, Easton DF, Offersen BV, Poulakaki F, Rubio IT, Sardanelli F, Schmutzler R, Spanic T, Weigelt B, Rutgers EJT.
- Eur J Cancer. 2022 Dec 13 [2023 Mar];181:79-91. doi: 10.1016/j.ejca.2022.11.036. Epub ahead of print.
- PMID: 36641897
- PubMed abstract
- Review, Guideline
- Free Full Text
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- Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk-reducing surgical decision-making practices: A mixed-methods study.
- Casalino S, Bruce S, Serfas K, Altman AD, Kean S, Lambert P, McManus KJ, Hartley JN, Nachtigal MW.
- J Genet Couns. 2023 Feb 20. doi: 10.1002/jgc4.1684. Epub ahead of print.
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- The Psychosocial Impact of the Decision to Undergo Risk-Reducing Salpingo-Oophorectomy Surgery in BRCA Mutation Carriers and the Role of Physician-Patient Communication.
- Alves-Nogueira AC, Melo D, Carona C, Figueiredo-Dias M.
- Curr Oncol. 2023 Feb 18;30(2):2429-2440. doi: 10.3390/curroncol30020185.
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- Breast Cancer Screening Utilization and Outcomes in Women with Neurofibromatosis Type 1.
- Yan K, Gao Y, Heller SL.
- Clin Breast Cancer. 2023 Feb 12:S1526-8209(23)00035-6. doi: 10.1016/j.clbc.2023.02.005. Epub ahead of print.
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- Socioeconomic Factors Are Associated With Disparities in Germline Testing in Pancreatic Cancer.
- King D, Scott R.
- OncLive. 2023 Feb 5.
- Conference report, Interview
- Free Full Text
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- Video telehealth to manage menopausal symptoms after cancer: a prospective study of clinicians and patient satisfaction.
- Rachagan N, Szabo RA, Rio I, Rees F, Hiscock HM, Hickey M.
- Menopause. 2023 Feb 1;30(2):143-148. doi: 10.1097/GME.0000000000002101. Epub 2022 Dec 13.
- PMID: 36696638
- PubMed abstract
- Source abstract
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- Survey Reveals Changing Genetic Testing Patterns, Persistent Disparities in Precision Oncology.
- Ray T.
- Precision Oncology News. 2023 Feb 1.
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- Implementation of a multi modal best practice bundle to improve genetic testing referral for pancreatic cancer patients. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Blazey M, Lee T, Hendershot A, Bartell N, Marino D.
- Fam Cancer. [P-20: Research Categories» Delivery of Care and Alternative Models.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Genetic Testing Challenges in Oncology: Patient With Pending Bill Has BRCA1 Result Withheld.
- Ray T.
- Precision Oncology News. 2023 Jan 23.
- Case report
- Free Full Text
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- Approaches to fertility preservation for young women with breast cancer.
- Razeti MG, Soldato D, Arecco L, Levaggi A, Puglisi S, Solinas C, Agostinetto E, Spinaci S, Lapuchesky L, Genova C, Massarotti C, Lambertini M.
- Clin Breast Cancer. 2023 Jan 13:S1526-8209(23)00006-X. doi: 10.1016/j.clbc.2023.01.006. Epub ahead of print.
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- Assessing Breast and Ovarian Cancer Risk Prior to Gender-Affirming Surgery.
- Cortina CS.
- JAMA Surg. 2023 Jan 11. doi: 10.1001/jamasurg.2022.5447. Epub ahead of print.
- PMID: 36630117
- PubMed abstract
- Source abstract
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- Klinisch relevante molekularpathologische Diagnostik beim Mammakarzinom [Clinically relevant molecular pathological diagnostics in breast cancer].
- Rodepeter FR, Teply-Szymanski J, Romey M, Grass A, Erber R, Lebeau A, Mack EKM, Tarawneh TS, Gremke N, Boekhoff J, Wündisch T, Wagner U, Jank P, Denkert C.
- Pathologie (Heidelb). 2023 Jan 11. German. doi: 10.1007/s00292-022-01175-0. Epub ahead of print.
- PMID: 36629894
- PubMed abstract
- Source abstract
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- High-dose chemotherapy with stem cell rescue to treat stage III homologous deficient breast cancer: factors influencing clinical implementation.
- Verbeek JGE, de Jong VMT, Wijnja HM, Jager A, Linn SC, Retèl VP, van Harten WH.
- BMC Cancer. 2023 Jan 7;23(1):26. doi: 10.1186/s12885-022-10412-x.
- PMID: 36611165
- PubMed abstract
- Guideline
- Free Full Text
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- Missed opportunities in the real-world genetic testing in BRCA gene variant carriers with cancers meeting NCCN criteria.
- Lee SS, Rajeev P, Finning S, Oh C, Pothuri B.
- Gynecol Oncol. 2023 Jan 5;170:32-37. doi: 10.1016/j.ygyno.2022.12.015. Epub ahead of print.
- PMID: 36610379
- PubMed abstract
- Source abstract
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- Effectiveness of Secondary Risk-Reducing Strategies in Patients With Unilateral Breast Cancer With Pathogenic Variants of BRCA1 and BRCA2 Subjected to Breast-Conserving Surgery: Evidence-Based Simulation Study.
- Maksimenko J, Rodrigues PP, Nakazawa-Miklaševiča M, Pinto D, Miklaševičs E, Trofimovičs G, Gardovskis J, Cardoso F, Cardoso MJ.
- JMIR Form Res. 2022 Dec 29;6(12):e37144. doi: 10.2196/37144.
- PMID: 36580360
- PubMed abstract
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- Australasian Genetic Counselors’ Perceptions of Their Role in Supporting Clients’ Behavior Change.
- Jacobs C, Turbitt E, McEwen A, Atkins L.
- J Pers Med. 2022 Dec 23;13(1):30. doi: 10.3390/jpm13010030.
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- Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model.
- Etchegary H, Pike A, Puddester R, Watkins K, Warren M, Francis V, Woods M, Green J, Savas S, Seal M, Gao Z, Avery S, Curtis F, McGrath J, MacDonald D, Burry TN, Dawson L.
- PLoS One. 2022 Dec 22;17(12):e0279317. doi: 10.1371/journal.pone.0279317.
- PMID: 36548287
- PubMed abstract
- Study protocol
- Free PMC article
- Free Full Text
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- Psychological factors and the uptake of preventative measures in BRCA1/2 pathogenic variant carriers: results of a prospective cohort study.
- Dick J, Tüchler A, Brédart A, Vitinius F, Wassermann K, Rhiem K, Schmutzler RK.
- Hered Cancer Clin Pract. 2022 Dec 19;20(1):38. doi: 10.1186/s13053-022-00244-y.
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- Informational needs of individuals from BRCA-harboring families: a systematic review and content analysis.
- Park SY, Kim Y, Kim S, Katapodi MC.
- Genet Med. 2022 Dec 18:S1098-3600(22)01068-1. doi: 10.1016/j.gim.2022.100001. Epub ahead of print.
- Review
- Free Full Text
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- Providers' perspectives on the reproductive decision-making of BRCA-positive women.
- Dason ES, Drost L, Greenblatt EM, Scheer AS, Han J, Sobel M, Allen L, Jacobson M, Doshi T, Wolff E, McMahon E, Jones CA.
- BMC Womens Health. 2022 Dec 8;22(1):506. doi: 10.1186/s12905-022-02093-2.
- PMID: 36482357
- PubMed abstract
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- Does mainstream BRCA testing affect surgical decision-making in newly-diagnosed breast cancer patients?
- Ain Q, Richardson C, Mutebi M, George A, Kemp Z, Rusby JE.
- Breast. 2022 Dec 6:S0960-9776(22)00193-X. doi: 10.1016/j.breast.2022.12.001. Epub ahead of print.
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- The neglected role of preimplantation genetic testing for Lynch syndrome.
- Dallagiovanna C, Filippi F, Riccaboni A, Vigano' P, Martinelli F, Somigliana E, Ricci MT, Vitellaro M.
- Reprod Biomed Online. 2022 Dec 5:S1472-6483(22)00832-X. doi: 10.1016/j.rbmo.2022.12.001. Epub ahead of print.
- PMID: 36566148
- PubMed abstract
- Commentary
- Free Full Text
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- Long-term response to olaparib in a patient with metastatic pancreatic cancer associated with hereditary breast and ovarian cancer syndrome.
- Tsuneizumi M, Terada S, Usui T, Yamaguchi K, Hayami R, Matsunuma R.
- Oxf Med Case Reports. 2022 Nov 24;2022(11):omac124. doi: 10.1093/omcr/omac124.
- PMID: 36447463
- PubMed abstract
- Case report
- Free PMC article
- Free Full Text
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- Stellenwert der genetischen Testung beim Prostatakarzinom [Importance of genetic testing in prostate cancer].
- Steinkellner L, Luger F, Loidl W.
- Urologie. 2022 Nov 15. German. doi: 10.1007/s00120-022-01977-3. Epub ahead of print.
- PMID: 36378280
- PubMed abstract
- Source abstract
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- Genetic Testing Proves Significant in Identifying Somatic and Germline Mutations in Prostate Cancer.
- Hollasch M, Antonarakis ES.
- OncLive. 2022 Nov 11.
- Review
- Free Full Text
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- Testing a deliberative democracy method with citizens of African ancestry to weigh pros and cons of targeted screening for hereditary breast and ovarian cancer risk.
- Guan Y, Pathak S, Ballard D, Veluswamy JK, McCullough LE, McBride CM, Gornick MC.
- Front Public Health. 2022 Nov 8;10:984926. doi: 10.3389/fpubh.2022.984926.
- PMID: 36424974
- PubMed abstract
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- Genetic Testing Among Patients with High-Risk Breast, Ovarian, Pancreatic, and Prostate Cancers.
- Clark NM, Roberts EA, Fedorenko C, Sun Q, Dubard-Gault M, Handford C, Yung R, Cheng HH, Sham JG, Norquist BM, Flanagan MR.
- Ann Surg Oncol. 2022 Nov 5. doi: 10.1245/s10434-022-12755-y. Epub ahead of print.
- PMID: 36335273
- PubMed abstract
- Source abstract
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- Reducing the risk of breast cancer.
- Pederson HJ, Al-Hilli Z, Kurian AW.
- Cleve Clin J Med. 2022 Nov 1;89(11):643-652. doi: 10.3949/ccjm.89a.21113.
- PMID: 36319046
- PubMed abstract
- Review
- Free Full Text
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- Expert consensus of the Spanish Society of Pathology and the Spanish Society of Medical Oncology on the determination of biomarkers in pancreatic and biliary tract cancer.
- Vera R, Ibarrola-de-Andrés C, Adeva J, Pérez-Rojas J, García-Alfonso P, Rodríguez-Gil Y, Macarulla T, Serrano-Piñol T, Mondéjar R, Madrigal-Rubiales B.
- Clin Transl Oncol. 2022 Nov;24(11):2107-2119. doi: 10.1007/s12094-022-02873-0. Epub 2022 Aug 25.
- PMID: 36008616
- PubMed abstract
- Guideline
- Free PMC article
- Free Full Text
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- Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review.
- Dron HA, Bucio D, Young JL, Tabor HK, Cho MK.
- J Genet Couns. 2022 Oct 27. doi: 10.1002/jgc4.1632. Epub ahead of print.
- PMID: 36301246
- PubMed abstract
- Review
- Free Full Text
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- Nest Genomics Building EHR-Integrated Clinical Decision Support for Genetics-Informed Care.
- Cohen JK.
- GenomeWeb. Disease Areas. Cancer. 2022 Oct 25.
- News
- Source abstract
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- From the patient to the population: Use of genomics for population screening.
- Mighton C, Shickh S, Aguda V, Krishnapillai S, Adi-Wauran E, Bombard Y.
- Front Genet. 2022 Oct 24;13:893832. doi: 10.3389/fgene.2022.893832.
- PMID: 36353115
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- Risk reduction and screening of cancer in hereditary breast-ovarian cancer syndromes: ESMO Clinical Practice Guideline.
- Sessa C, Balmaña J, Bober SL, Cardoso MJ, Colombo N, Curigliano G, Domchek SM, Evans DG, Fischerova D, Harbeck N, Kuhl C, Lemley B, Levy-Lahad E, Lambertini M, Ledermann JA, Loibl S, Phillips KA, Shimon P; ESMO Guidelines Committee.
- Ann Oncol. 2022 Oct 19:S0923-7534(22)04193-X. doi: 10.1016/j.annonc.2022.10.004. Epub ahead of print.
- PMID: 36307055
- PubMed abstract
- Guideline
- Free Full Text
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- Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort.
- Sarki M, Ming C, Aceti M, Fink G, Aissaoui S, Bürki N, Graffeo R, Heinimann K, Zufferey MC, Monnerat C, Rabaglio M, Zürrer-Härdi U, Chappuis PO, Katapodi MC.
- J Pers Med. 2022 Oct 19;12(10):1740. doi: 10.3390/jpm12101740.
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- Hereditary Breast and Ovarian Cancer Service in Sparsely Populated Western Pomerania.
- Felbor U, Bülow R, Schmutzler RK, Rath M.
- Healthcare (Basel). 2022 Oct 13;10(10):2021. doi: 10.3390/healthcare10102021.
- PMID: 36292468
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: Missed Variant Update Delays Li-Fraumeni Diagnosis.
- Ray T.
- Precision Oncology News. 2022 Oct 12.
- Case report
- Free Full Text
Special article:
Is there a duty to reinterpret genetic data? The ethical dimensions.
- PMID: 31616070
- PubMed abstract
- Free Full Text
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- Provider discussion of genetic counseling among high-risk Spanish-preferring Latina breast cancer survivors.
- Conley CC, Rivera Rivera JN, Castro-Figueroa EM, Moreno L, Dutil J, García JD, Ricker C, Quinn GP, Soliman H, Vadaparampil ST.
- Transl Behav Med. 2022 Oct 7;12(9):900-908. doi: 10.1093/tbm/ibac031.
- PMID: 36205471
- PubMed abstract
- Source abstract
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- Updates on Management of Hereditary Breast Cancer: New Data on PARP Inhibitors Change Recommendations Regarding the Multidisciplinary Care of Breast Cancer Patients with BRCA Mutations.
- McGuire KP, Arthur DW, Mamounas EP.
- Ann Surg Oncol. 2022 Oct;29(11):6504-6507. doi: 10.1245/s10434-022-12048-4. Epub 2022 Jun 18.
- PMID: 35717518
- PubMed abstract
- Commentary, Review
- Free Full Text
Guideline:
Management of Hereditary Breast Cancer: American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology Guideline.
- PMID: 32243226
- PubMed abstract
- Free Full Text
Summary, Review:
Management of Hereditary Breast Cancer: ASCO, ASTRO, and SSO Guideline.
- PMID: 32246307
- PubMed abstract
- Free Full Text
Guideline:
Adjuvant PARP Inhibitors in Patients With High-Risk Early-Stage HER2-Negative Breast Cancer and Germline BRCA Mutations: ASCO Hereditary Breast Cancer Guideline Rapid Recommendation Update.
- PMID: 34343058
- PubMed abstract
- Free Full Text
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- Talking about Risk, UncertaintieS of Testing IN Genetics (TRUSTING): development and evaluation of an educational programme for healthcare professionals about BRCA1 & BRCA2 testing.
- Fallowfield L, Solis-Trapala I, Starkings R, May S, Matthews L, Eccles D, Evans DG, Turnbull C, Crawford G, Jenkins V.
- Br J Cancer. 2022 Oct;127(6):1116-1122. doi: 10.1038/s41416-022-01871-x. Epub 2022 Jun 17.
- PMID: 35715636
- PubMed abstract
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- Integrating hereditary breast and ovarian cancer genetic counselling and testing into mainstream clinical practice: Legal and ethical challenges.
- Charron M, Kaiser B, Dauge A, Gallois H, Lapointe J, Dorval M, Nabi H, Joly Y.
- Crit Rev Oncol Hematol. 2022 Oct;178:103797. doi: 10.1016/j.critrevonc.2022.103797. Epub 2022 Aug 27.
- PMID: 36031172
- PubMed abstract
- Source abstract
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- Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country.
- Lee YQ, Yoon SY, Hassan T, Padmanabhan H, Yip CH, Keng WT, Thong MK, Ahmad Annuar MA, Mohd Taib NA, Teo SH.
- J Genet Couns. 2022 Oct;31(5):1080-1089. doi: 10.1002/jgc4.1579. Epub 2022 Apr 28.
- PMID: 35481858
- PubMed abstract
- Source abstract
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- Patient Understanding of Tumor Genomic Testing: A Quality Improvement Effort.
- Senter L, Veney D, Surplus T, Haynam M, Adams EJ, Hampel H, Toland AE, Presley CJ, Padamsee TJ, Lee CN, Hovick SR, Stover DG.
- JCO Oncol Pract. 2022 Sep 21:OP2200316. doi: 10.1200/OP.22.00316. Epub ahead of print.
- PMID: 36130146
- PubMed abstract
- Source abstract
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- Genetic Tests Create Treatment Opportunities and Confusion for Breast Cancer Patients.
- Andrews M.
- KHN [Kaiser Health News]. 2022 Sep 21.
- Press
- Free Full Text
Press: Genetic Tests Create Treatment Opportunities and Confusion for Breast Cancer Patients. (Medscape)
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- Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing.
- Bokkers K, Bleiker EMA, Hoogendam JP, Velthuizen ME, Schreuder HWR, Gerestein CG, Lange JG, Louwers JA, Koudijs MJ, Ausems MGEM, Zweemer RP.
- Hered Cancer Clin Pract. 2022 Sep 8;20(1):33. doi: 10.1186/s13053-022-00238-w.
- PMID: 36076240
- PubMed abstract
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- Polygenic risk scores and risk-stratified breast cancer screening: Familiarity and perspectives of health care professionals.
- Lapointe J, Buron AC, Mbuya-Bienge C, Dorval M, Pashayan N, Brooks JD, Walker MJ, Chiquette J, Eloy L, Blackmore K, Turgeon A, Lambert-Côté L, Leclerc L, Dalpé G, Joly Y, Knoppers BM, Chiarelli AM, Simard J, Nabi H.
- Genet Med. 2022 Sep 3:S1098-3600(22)00892-9. doi: 10.1016/j.gim.2022.08.001. Epub ahead of print.
- PMID: 36057905
- PubMed abstract
- Source abstract
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- Novel germline mutations for active surveillance and imaging strategies in prostate cancer.
- Mondschein R, Taylor R, Thorne H, Bolton D.
- Curr Opin Urol. 2022 Sep 1;32(5):456-461. doi: 10.1097/MOU.0000000000001024. Epub 2022 Jul 18.
- PMID: 35855555
- PubMed abstract
- Source abstract
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- 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.
- McVeigh TP, Sweeney KJ, Brennan DJ, McVeigh UM, Ward S, Strydom A, Seal S, Astbury K, Donnellan P, Higgins J, Keane M, Kerin MJ, Malone C, McGough P, McLaughlin R, O'Leary M, Rushe M, Barry MK, MacGregor G, Sugrue M, Yousif A, Al-Azawi D, Berkeley E, Boyle TJ, Connolly EM, Nolan C, Richardson E, Giffney C, Doyle SB, Broderick S, Boyd W, McVey R, Walsh T, Farrell M, Gallagher DJ, Rahman N, George AJ.
- Fam Cancer. 2022 Aug 27. doi: 10.1007/s10689-022-00313-0. Epub ahead of print.
- PMID: 36029389
- PubMed abstract
- Source abstract
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- How do women who are informed that they are at increased risk of breast cancer appraise their risk? A systematic review of qualitative research.
- Woof VG, Howell A, McWilliams L, Gareth Evans D, French DP.
- Br J Cancer. 2022 Aug 24. doi: 10.1038/s41416-022-01944-x. Epub ahead of print.
- PMID: 36002751
- PubMed abstract
- Review
- Free Full Text
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- GeneHome - a Novel Model to Deliver Care to Individuals with Genetic Predisposition to Cancer.
- Nocera Zachariah N, Lee MC, Chang MD, Moore C, Wang X.
- Cancer Control. 2022 Jan-Dec [First published 2022 Aug 17];29:10732748221109951. doi: 10.1177/10732748221109951.
- PMID: 35976772
- PubMed abstract
- Source abstract
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- BRCA mutation carriers' perception about benefits and risks associated with combined hormonal contraceptives use.
- Grandi G, Monari F, Boggio Sola V, Cortesi L, Toss A, Del Savio MC, Melotti C, Centurioni MG, Gustavino C, Varesco L, Facchinetti F, Barra F.
- Eur J Contracept Reprod Health Care. 2022 Aug 10:1-6. doi: 10.1080/13625187.2022.2107199. Epub ahead of print.
- PMID: 35946412
- PubMed abstract
- Source abstract
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- A qualitative reflexive thematic analysis into the experiences of being identified with a BRCA1/2 gene alteration: "So many little, little traumas could have been avoided".
- Warner NZ, Groarke A.
- BMC Health Serv Res. 2022 Aug 6;22(1):1007. doi: 10.1186/s12913-022-08372-w.
- PMID: 35933387
- PubMed abstract
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- A Woman Needs to Know She Is a BRCA Carrier Before She Develops Breast Cancer.
- Hughes KS, Yin K.
- Ann Surg Oncol. 2022 Aug;29(8):4667-4669. doi: 10.1245/s10434-022-11860-2. Epub 2022 May 12.
- PMID: 35552928
- PubMed abstract
- Commentary
- Free Full Text
Original research:
Comparison of Outcomes Between BRCA Pathogenic Variant Carriers Undergoing Breast-Conserving Surgery Versus Mastectomy.
- PMID: 35585432
- PubMed abstract
- Source abstract
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- Making BRCA1 genetic test reports easier to understand through user-centered design: A randomized trial.
- Recchia G, Lawrence ACE, Capacchione L, Freeman ALJ.
- Genet Med. 2022 Aug;24(8):1684-1696. doi: 10.1016/j.gim.2022.04.016. Epub 2022 May 6.
- PMID: 35522238
- PubMed abstract
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- Experiences of individuals with a variant of uncertain significance on genetic testing for hereditary cancer risks: a mixed method systematic review.
- Gould D, Walker R, Makari-Judson G, Seven M.
- J Community Genet. 2022 Aug;13(4):371-379. doi: 10.1007/s12687-022-00600-4. Epub 2022 Jul 12.
- PMID: 35819584
- PubMed abstract
- Source abstract
- Review
- Free PMC article
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- Comparing the attitudes of physicians and non-physicians toward communicating a patient's BRCA1 mutation to a first-degree relative against a patient's wishes.
- Zebrack JE, Yang W, Milone M, Coppes MJ.
- J Community Genet. 2022 Aug;13(4):403-410. doi: 10.1007/s12687-022-00591-2. Epub 2022 May 21.
- PMID: 35596048
- PubMed abstract
- Source abstract
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- Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients.
- Levin Fridman A, Raz A, Timmermans S, Shkedi-Rafid S.
- J Genet Couns. 2022 Aug;31(4):912-921. doi: 10.1002/jgc4.1560. Epub 2022 Feb 4.
- PMID: 35122362
- PubMed abstract
- Source abstract
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- Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low-middle income country.
- Ehsan L, Waheed MT, Akbar F, Siddiqui Z, Sattar AK, Kirmani S.
- J Genet Couns. 2022 Aug;31(4):998-1002. doi: 10.1002/jgc4.1555. Epub 2022 Jan 31.
- PMID: 35099095
- PubMed abstract
- Source abstract
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- The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband–Provider and Proband–Family Communication in Hereditary Breast and Ovarian Cancer.
- Pedrazzani C, Aceti M, Schweighoffer R, Kaiser-Grolimund A, Bürki N, Chappuis PO, Graffeo R, Monnerat C, Pagani O, Rabaglio M, Katapodi MC, Caiata-Zufferey M.
- J Pers Med. 2022 Jul 29;12(8):1249. doi: 10.3390/jpm12081249.
- PMID: 36013197
- PubMed abstract
- Source abstract
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- Survey on implementation of molecular testing in ovarian cancer and PARP inhibitor: a national North-Eastern German Society of Gynecologic Oncology/Young Academy of Gynecologic Oncology/Arbeitsgemeinschaft Gynäkologische Onkologie intergroup analysis.
- Nguyen-Sträuli BD, Baum J, Meyer-Wilmes P, Kreklau A, Buschmann C, El Ouardi N, Fotopoulou C, Hummel M, Chekerov R, Braicu E, Sehouli J, Pietzner K.
- Int J Gynecol Cancer. 2022 Jul 27:ijgc-2022-003637. doi: 10.1136/ijgc-2022-003637. Epub ahead of print.
- PMID: 35896275
- PubMed abstract
- Source abstract
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- Contraception and Hormone Replacement Therapy in Healthy Carriers of Germline BRCA1/2 Genes Pathogenic Variants: Results from an Italian Survey.
- Massarotti C, Buonomo B, Dellino M, Campanella M, De Stefano C, Ferrari A, Anserini P, Lambertini M, Peccatori FA.
- Cancers (Basel). 2022 Jul 15;14(14):3457. doi: 10.3390/cancers14143457.
- PMID: 35884518
- PubMed abstract
- Source abstract
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- Genetic clinicians' confidence in BOADICEA comprehensive breast cancer risk estimates and counselees' psychosocial outcomes: a prospective study.
- Brédart A, De Pauw A, Tüchler A, Lakeman IMM, Anota A, Rhiem K, Schmutzler R, van Asperen CJ, Devilee P, Stoppa-Lyonnet D, Kop JL, Dolbeault S.
- Clin Genet. 2022 Jul;102(1):30-39. doi: 10.1111/cge.14147. Epub 2022 May 16.
- PMID: 35508697
- PubMed abstract
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- Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer.
- Bokkers K, Zweemer RP, Koudijs MJ, Stehouwer S, Velthuizen ME, Bleiker EMA, Ausems MGEM.
- Fam Cancer. 2022 Jul;21(3):295-304. doi: 10.1007/s10689-021-00277-7. Epub 2021 Oct 7.
- PMID: 34617209
- PubMed abstract
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- Patients' challenges, competencies, and perceived support in dealing with information needs - A qualitative analysis in patients with breast and gynecological cancer.
- Fahmer N, Faller H, Engehausen D, Hass HG, Reuss-Borst M, Duelli K, Wöckel A, Heuschmann PU, Meng K.
- Patient Educ Couns. 2022 Jul;105(7):2382-2390. doi: 10.1016/j.pec.2021.12.006. Epub 2021 Dec 9.
- PMID: 34930628
- PubMed abstract
- Source abstract
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- Survey on Physicians' Knowledge and Training Needs in Genetic Counseling in Germany.
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- 'Steep learning curves' to 'Smooth Sailing': A reappraisal of telegenetics amidst the COVID-19 pandemic.
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- Development and pilot testing of a training for bilingual community education professionals about hereditary breast and ovarian cancer among Latinas: ÁRBOLES Familiares.
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- Influence of payer coverage and out-of-pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings.
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- Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma.
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- Knowledge and perceptions of BRCA1/2 genetic testing and needs of diverse women with a personal or family history of breast cancer in South Florida.
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- Genetic Testing Challenges in Oncology: Inaccurate Patient Claims Complicate Cancer Risk Management.
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- The evolving role of germline genetic testing and management in prostate cancer: Report from the Princess Margaret Cancer Centre International Retreat.
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- Pancreas in Hereditary Syndromes: Cross-sectional Imaging Spectrum.
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- A Retrospective 5-Year Single Center Study Highlighting the Risk of Cancer Predisposition in Adolescents and Young Adults.
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- Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I).
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- Development and Pilot Implementation of the Genomic Risk Assessment for Cancer Implementation and Sustainment (GRACIAS) Intervention in Mexico.
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- A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.
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- Cancers (Basel). 2021 May 31;13(11):2729. doi: 10.3390/cancers13112729.
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- Genetic Testing Challenges in Oncology: Immigrant Mislabeled as BRCA-Positive, Regrets Ovary Removal.
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- Modernizing family health history: achievable strategies to reduce implementation gaps.
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- OHSU to Expand Tumor Board Program After Seeing Benefits in Breast Cancer Patients.
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- Health system interventions to integrate genetic testing in routine oncology services: A systematic review.
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- Making Sense of a Health Threat: Illness Representations, Coping, and Psychological Distress among BRCA1/2 Mutation Carriers.
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- Testing a best practices risk result format to communicate genetic risks.
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- Germline Genetics of Prostate Cancer: Prevalence of Risk Variants and Clinical Implications for Disease Management.
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- Genetic Testing Challenges in Oncology: BRCA1-Positive Patient Told Paternal Cancer Risk Unimportant.
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- Family planning in carriers of BRCA1 and BRCA2 pathogenic variants.
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- Management of patients with BRCA mutation from the point of view of a breast surgeon.
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- Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice.
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- Controversies in Hereditary Cancer Management.
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- Assessment of Clinical Benefit of Integrative Genomic Profiling in Advanced Solid Tumors.
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- Patients' and professionals' perspective of non-in-person visits in hereditary cancer: predictors and impact of the COVID-19 pandemic.
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- Genetic Testing Challenges in Oncology: BRCA1-Positive Breast Cancer Patient Told She's Negative.
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- Health care professionals' attitudes toward cancer gene panel testing.
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- The Knowledge and Attitude of Patients Diagnosed with Epithelial Ovarian Cancer towards Genetic Testing.
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- Barriers and Facilitators to Genetic Service Delivery Models: Scoping Review.
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- Globally Rare BRCA2 Variants With Founder Haplotypes in the South African Population: Implications for Point-of-Care Testing Based on a Single-Institution BRCA1/2 Next-Generation Sequencing Study.
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- Gene Screenings Hold Disease Clues, but Unexplained Anomalies Often Raise Fears.
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- Male Breast Cancer Risk Assessment and Screening Recommendations in High-Risk Men Who Undergo Genetic Counseling and Multigene Panel Testing.
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- The impact of the number of tests presented and a provider recommendation on decisions about genetic testing for cancer risk.
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- Breast Cancer Chemoprevention: Use and Views of Australian Women and their Clinicians.
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- Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England.
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- Factors associated with the decision to undergo risk-reducing salpingo-oophorectomy among women at high risk for hereditary breast and ovarian cancer: a systematic review.
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- My Gene Counsel and Genomet Announce Product Partnership to Transform Cancer Care Around the Globe.
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- Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals.
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- Genetic counseling in prostate cancer: How to implement it in daily clinical practice?
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- Current Genetic Service Delivery Models for the Provision of Genetic Testing in Europe: A Systematic Review of the Literature.
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No 366 - Prise en charge gynécologique du cancer du sein et de l'ovaire héréditaire.
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- Genetic Counselors: Don’t Wait for an Invitation. Crash the Party.
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- Involvement and Influence of Healthcare Providers, Family Members, and Other Mutation Carriers in the Cancer Risk Management Decision-Making Process of BRCA1 and BRCA2 Mutation Carriers.
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- Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap.
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- A comparison of patient satisfaction (using the BREAST-Q questionnaire) with bilateral breast reconstruction following risk-reducing or therapeutic mastectomy.
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- BRCA1 and BRCA2 Testing in Medically Underserved Medicare Beneficiaries With Breast or Ovarian Cancer.
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- Patients' perspectives and experiences concerning barriers to accessing information about bilateral prophylactic mastectomy.
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- “Second-Class Status?” Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome.
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- Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists.
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- Breast Cancer Genetics and Indications for Prophylactic Mastectomy.
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- Clinical Cancer Genetics in a Lower-Middle Income Country: Considerations for Policymaking.
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- Support needs of couples with hereditary breast and ovarian cancer during reproductive decision-making.
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- Gynecol Oncol. 2018 Jun;149(3):565-569. doi: 10.1016/j.ygyno.2018.03.059. Epub 2018 Apr 10.
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- Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
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Blog post, News: NSGC Responds to U.S. Food and Drug Administration Approval of Direct-to-Consumer Cancer Test that Reports Three BRCA Mutations (NSGC Blog)
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- Genetic assessment wait time indicators in the High Risk Ontario Breast Screening Program.
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Comments on NSGC Discussion Forum Cancer SIG
Subject: Dr. Narod's commentary on pre-test genetic counseling
Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
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Press: Too Few Women Get Counseling Before Breast Cancer Gene Test: Study (MedlinePlus)
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Subject: New England Journal of Medicine article/discussion on Screening an Asymptomatic Person for Genetic R
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Comments on NSGC Discussion Forum Cancer SIG
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Comments on NSGC Discussion Forum Cancer SIG
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- Star Power.
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