Papers dealing with demographics of testing, timing of testing, numbers of patients tested (or not tested) in given programs, overall population trends in testing, barriers to and facilitators of uptake/testing, etc.
List was last updated on
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- Improving Uptake of Cancer Genetic Risk Assessment in a Remote Tailored Risk Communication and Navigation Intervention: Large Effect Size but Room to Grow.
- Kinney AY, Walters ST, Lin Y, Lu SE, Kim A, Ani J, Heidt E, Le Compte CJG, O'Malley D, Stroup A, Paddock LE, Grumet S, Boyce TW, Toppmeyer DL, McDougall JA.
- J Clin Oncol. 2023 Feb 14:JCO2200751. doi: 10.1200/JCO.22.00751. Epub ahead of print.
- PMID: 36787512
- PubMed abstract
•• Identifier: NCT03326713: Genetic Risk Assessment for Cancer Education and Empowerment (GRACE) Project (GRACE). (ClinicalTrials.gov . Accessed 2023 Feb 14.)
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- Mainstream genetic testing for high-grade ovarian, tubal and peritoneal cancers: A tertiary referral centre experience.
- Srinivasa S, Bowman M, Titterton L, Harnett P, Brand A, Kirk J, Ragunathan A.
- Aust N Z J Obstet Gynaecol. 2023 Feb 13. doi: 10.1111/ajo.13650. Epub ahead of print.
- PMID: 36785489
- PubMed abstract
- Source abstract
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- Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: An observational study of four clinical workflows.
- Wang C, Lu H, Bowen DJ, Xuan Z.
- Genet Med. 2023 Feb 10:S1098-3600(23)00815-8. doi: 10.1016/j.gim.2023.100802. 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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- Proactive breast cancer risk assessment in primary care: a review based on the principles of screening.
- Usher-Smith JA, Hindmarch S, French DP, Tischkowitz M, Moorthie S, Walter FM, Dennison RA, Stutzin Donoso F, Archer S, Taylor L, Emery J, Morris S, Easton DF, Antoniou AC.
- Br J Cancer. 2023 Feb 3:1–11. doi: 10.1038/s41416-023-02145-w. Epub ahead of print.
- PMID: 36737659
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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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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- Testing for Inherited Susceptibility to Breast Cancer.
- Robson M.
- Hematol Oncol Clin North Am. 2023 Feb;37(1):17-31. doi: 10.1016/j.hoc.2022.08.003.
- PMID: 36435609
- PubMed abstract
- Source abstract
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- Dr. King on Delays in Access to Germline Testing in Pancreatic Cancer.
- King D.
- OncLive. OncLive TV. 2023 Jan 31.
- Conference report
- Free video
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- Implementing HRD Testing in Routine Clinical Practice on Patients with Primary High-Grade Advanced Ovarian Cancer.
- Heitz F, Ataseven B, Staniczok C, Denkert C, Rhiem K, Hahnen E, Heikaus S, Moubarak M, Welz J, Dagres T, Vrentas V, Bommert M, Schneider S, Concin N, Harter P.
- Cancers (Basel). 2023 Jan 29;15(3):818. doi: 10.3390/cancers15030818.
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- Financial toxicity in BRCA1 and BRCA2 carriers.
- Proussaloglou EM, Rosenthal AE, Raker CA, Wilbur JS, Stuckey AR, Robison KM.
- Gynecol Oncol. 2023 Jan 24;170:160-166. doi: 10.1016/j.ygyno.2023.01.007. Epub ahead of print.
- PMID: 36701836
- PubMed abstract
- Source abstract
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- Disparities in the uptake of cascade genetic testing among family members of mutation-positive lynch and HBOC syndrome patients. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Namey E, Dudley B, Horton C, Carraway C, Zhou J, Hatton W, Komala T, Milliard C, Namey T, Karloski E, Brand R.
- Fam Cancer. [O-05: Research Categories» Lynch syndrome.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Development of an EHR-integrated electronic tool for the identification of individuals at-risk for an inherited cancer syndrome. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Singh V, Rafter T, Sharbatji M, Brierley K, Healy C, Liu J, Brown Q, Xicola R, Kashyap N, Llor X.
- Fam Cancer. [O-06: Research Categories» Lynch syndrome.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Importance of timely genetics services and critical evaluation of diagnosis and reported family history when assessing for hereditary cancer syndromes. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Malca S.
- Fam Cancer. [P-08: Case Reports» Case Series on any topic.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Actionable pathogenic germline variants discovered by panel-based hereditary cancer testing in families with previously identified pathogenic variants. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Neumann C, Mcsweeny M, Rainey K, Campbell H, Nguyen C, Hall M.
- Fam Cancer. [P-13: Research Categories » Counseling, Behavioral Health, Psychosocial, and Survivorship.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Innovative approaches to expanding cancer genetic testing in Michigan (project might). [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Stoffel EM, Austin S, Koeppe E, Hanson EN, Delacroix E, Rizzo E, Griggs JJ, Resnicow K.
- Fam Cancer. [P-17: 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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- 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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- Attitudes about sharing genetic test results in families with hereditary cancer syndromes. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Guivatchian E, Koeppe E, Stoffel EM.
- Fam Cancer. [P-22: Research Categories » Other.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Oncologist knowledge of cost of genetic testing. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Weiner S, Austin SE, Carr G, Kidwell KM, Resnicow K, Martinez Stoffel E, Griggs J.
- Fam Cancer. [P-23: 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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- Decreased time from diagnosis to referral of PDAC patients: a quality improvement effort. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Cohen SA, Doran W, Harshbarger C, Nixon DM, Lichtenberg E, Cantafio A.
- Fam Cancer. [P-24: 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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- Pairing tumor testing with germline sequencing increases the number of pathogenic germline variants identified. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Nefeli Dimopoulos C, Brierly K, Gibson J, Walther Z, Llor X.
- Fam Cancer. [P-32: Research Categories» Gastric cancer-related syndromes.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Genetic Testing for Cancer Risk and Perceived Importance of Genetic Information Among US Population by Race and Ethnicity: a Cross-sectional Study.
- Hong YR, Yadav S, Wang R, Vadaparampil S, Bian J, George TJ, Braithwaite D.
- J Racial Ethn Health Disparities. 2023 Jan 23. doi: 10.1007/s40615-023-01526-4. Epub ahead of print.
- PMID: 36689121
- PubMed abstract
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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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- Impact of the coverage of risk-reducing salpingo-oophorectomy by the national insurance system for women with BRCA pathogenic variants in Japan.
- Nomura H, Abe A, Fusegi A, Yoshimitsu T, Misaka S, Murakami A, Matsumoto T, Tsumura S, Kanno M, Aoki Y, Netsu S, Omi M, Tanigawa T, Okamoto S, Omatsu K, Yunokawa M, Kanao H, Habano E, Arakawa H, Kaneko K, Ueki A, Haruyama Y, Inari H, Ueno T.
- Sci Rep. 2023 Jan 19;13(1):1018. doi: 10.1038/s41598-023-28304-w.
- PMID: 36658289
- PubMed abstract
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- Racial Differences in Germline Genetic Testing for Prostate Cancer: A Systematic Review.
- Briggs LG, Steele GL, Qian ZJ, Subbana S, Alkhatib KY, Labban M, Langbein BJ, Nguyen DD, Cellini J, Kilbridge K, Kibel AS, Trinh QD, Rana HQ, Cole AP.
- JCO Oncol Pract. 2023 Jan 12:OP2200634. doi: 10.1200/OP.22.00634. Epub ahead of print.
- PMID: 36649495
- PubMed abstract
- Source abstract
•• Commentary:
Germline Testing in Prostate Cancer: Implementation and Disparities of Care.
- PMID: 36720077
- PubMed abstract
- Free Full Text
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- Implementation of a Telehealth Genetic Testing Station to Deliver Germline Testing for Men With Prostate Cancer.
- Kwon DH, Gordon KM, Tong B, Borno HT, Beigh M, Fattah D, Schleicher A, Aggarwal RR, Blanco AM, Small EJ, Dhawan M.
- JCO Oncol Pract. 2023 Jan 12:OP2200638. doi: 10.1200/OP.22.00638. Epub ahead of print.
- PMID: 36649492
- PubMed abstract
- Source abstract
•• Commentary:
Germline Testing in Prostate Cancer: Implementation and Disparities of Care.
- PMID: 36720077
- PubMed abstract
- Free Full Text
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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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- January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey.
- Mechanic L, Helzlsouer K.
- Genet Med. GenePOD. 2023 Jan 9.
- Podcast
- Free Audio
•• Original research:
Awareness and use of genetic testing: An analysis of the Health Information National Trends Survey 2020.
- PMID: 36136089
- PubMed abstract
- Free Full Texts
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- Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience.
- Cohen SA, Nixon DM, Lichtenberg E.
- J Genet Couns. 2023 Jan 8. doi: 10.1002/jgc4.1671. Epub ahead of print.
- PMID: 36617522
- PubMed abstract
- Source abstract
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- Breast Cancer Advances in 2022 Showcase a Shifting Landscape.
- Sparano JA.
- OncLive. 2023 Jan 6.
- Commentary
- 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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- Current Issues in the Management of Patients With Newly Diagnosed Advanced-Stage High-Grade Serous Carcinoma of the Ovary.
- Penn CA, Alvarez RD.
- JCO Oncol Pract. 2023 Jan 5:OP2200461. doi: 10.1200/OP.22.00461. Epub ahead of print.
- PMID: 36603168
- PubMed abstract
- Review
- Free Full Text
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- Genetic Risk Prediction for Prostate Cancer: Implications for Early Detection and Prevention.
- Seibert TM, Garraway IP, Plym A, Mahal BA, Giri V, Jacobs MF, Cheng HH, Loeb S, Helfand BT, Eeles RA, Morgan TM.
- Eur Urol. 2023 Jan 4:S0302-2838(22)02870-6. doi: 10.1016/j.eururo.2022.12.021. Epub ahead of print.
- PMID: 36609003
- PubMed abstract
- Source abstract
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- Internet-Based Germline Genetic Testing for Men With Metastatic Prostate Cancer.
- Cheng HH, Sokolova AO, Gulati R, Bowen D, Knerr SA, Klemfuss N, Grivas P, Hsieh A, Lee JK, Schweizer MT, Yezefski T, Zhou A, Yu EY, Nelson PS, Montgomery B.
- JCO Precis Oncol. 2023 Jan;7:e2200104. doi: 10.1200/PO.22.00104.
- PMID: 36623239
- PubMed abstract
- Source abstract
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- Outcomes of Universal Point-of-Care Genetic Testing in Diverse Patients With Pancreatic Ductal Adenocarcinoma.
- Drogan CM, Kindler HL, Gao G, Kupfer SS.
- JCO Precis Oncol. 2023 Jan;7:e2200196. doi: 10.1200/PO.22.00196.
- PMID: 36689696
- PubMed abstract
- Source abstract
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- Genetic Testing in the Latinx community: Impact of acculturation and provider relationships.
- Ioffe YJ, Hong L, Joachim-Célestin M, Soret C, Montgomery S, Unternaehrer JJ.
- Gynecol Oncol. 2022 Dec 26;169:125-130. doi: 10.1016/j.ygyno.2022.12.001. Epub ahead of print.
- PMID: 36577267
- PubMed abstract
- Source abstract
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- Development of a comprehensive approach to adult hereditary cancer testing in Ontario.
- Bell KA, Kim R, Aronson M, Gillies B, Ali Awan A, Chun K, Hart J, Healey R, Kim L, Klaric G, Panabaker K, Sabatini PJB, Sadikovic B, Selvarajah S, Smith AC, Stockley TL, Vaags AK, Eisen A, Pollett A, Feilotter H.
- J Med Genet. 2022 Dec 23:jmg-2022-108945. doi: 10.1136/jmg-2022-108945. Epub ahead of print.
- PMID: 36564171
- PubMed abstract
- Source abstract
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- Promoters of BRCA testing under insurance coverage for non-metastatic breast cancer patients in Japan: a retrospective cohort study.
- Taji T, Odan N, Kataoka Y, Ikeda M, Yamaguchi A, Suzuki E, Suwa H.
- Breast Cancer. 2022 Dec 22. doi: 10.1007/s12282-022-01424-3. Epub ahead of print.
- PMID: 36547869
- PubMed abstract
- Source abstract
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- Genetic testing in privately insured women with surgically treated breast cancer.
- Dinan MA, Pitafi S, Greenup RA, Long JB, Gross CP.
- Breast Cancer Res Treat. 2022 Dec 21. doi: 10.1007/s10549-022-06829-4. Epub ahead of print.
- PMID: 36542252
- PubMed abstract
- Source abstract
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- Development and Psychometric Evaluation of Healthcare Access Measures among Women with Ovarian Cancer.
- Akinyemiju T, Joshi A, Deveaux A, Wilson LE, Chen D, Meernik C, Bevel M, Gathings J, Fish L, Barrett N, Worthy V, Boyce X, Martin K, Robinson C, Pisu M, Liang M, Potosky A, Huang B, Ward K, Schymura MJ, Berchuck A, Reeve BB.
- Cancers (Basel). 2022 Dec 19;14(24):6266. doi: 10.3390/cancers14246266.
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- Evaluation of out-of-pocket pay genetic testing in a publicly funded healthcare system.
- Grant P, Cook CB, Langlois S, Nuk J, Mung S, Zhang Q; GenCOUNSEL Study, Lynd LD, Austin J, Elliott AM.
- Clin Genet. 2022 Dec 11. doi: 10.1111/cge.14276. Epub ahead of print.
- PMID: 36504324
- PubMed abstract
- Source abstract
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- Understanding cancer genetic risk assessment motivations in a remote tailored risk communication and navigation intervention randomized controlled trial.
- Le Compte CG, Lu SE, Ani J, McDougall J, Walters ST, Toppmeyer D, Boyce TW, Stroup A, Paddock L, Grumet S, Lin Y, Heidt E, Kinney AY.
- Health Psychol Behav Med. 2022 Dec 9;10(1):1190-1215. doi: 10.1080/21642850.2022.2150623.
- PMID: 36518606
- PubMed abstract
- Source abstract
•• Identifier: NCT03326713: Genetic Risk Assessment for Cancer Education and Empowerment (GRACE) Project (GRACE). (ClinicalTrials.gov . Accessed 2022 Dec 16.)
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- Cancer Moonshot 2.0, health equity and BRCA1/2 testing.
- Sorscher S.
- J Cancer Policy. 2022 Dec 8:100379. doi: 10.1016/j.jcpo.2022.100379. Epub ahead of print.
- PMID: 36503104
- PubMed abstract
- Source abstract
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- Genetic medicine in companion diagnostics of germline BRCA testing of Japanese pancreatic cancer patients.
- Matsubayashi H, Todaka A, Kawakami T, Hamauchi S, Yokota T, Higashigawa S, Kiyozumi Y, Harada R, Kado N, Nishimura S, Ishiwatari H, Sato J, Niiya F, Ono H, Sugiura T, Sasaki K, Yasui H, Yamazaki K.
- J Hum Genet. 2022 Dec 8. doi: 10.1038/s10038-022-01097-y. Epub ahead of print.
- PMID: 36482120
- PubMed abstract
- Source abstract
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- Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results.
- Macklin-Mantia SK, Clift KE, Maimone S, Hodge DO, Riegert-Johnson D, Hines SL.
- J Genet Couns. 2022 Dec 7. doi: 10.1002/jgc4.1665. Epub ahead of print.
- PMID: 36478495
- PubMed abstract
- Source 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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- Sociodemographic, Clinical, and Variation Outcomes for Breast Cancer and Breast Cancer-Related Mutations in a Ten-Year Cohort From Neiva, Huila, Colombia.
- Olaya J, Sanjuan J, Torres-Lopez D, Olaya L, Gutierrez-Vargas M, Olaya G, Olaya JD.
- Cureus. 2022 Dec 6;14(12):e32257. doi: 10.7759/cureus.32257.
- PMID: 36620844
- PubMed abstract
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- Awareness and use of genetic testing: An analysis of the Health Information National Trends Survey 2020.
- Tiner JC, Mechanic LE, Gallicchio L, Gillanders EM, Helzlsouer KJ.
- Genet Med. 2022 Dec;24(12):2526-2534. doi: 10.1016/j.gim.2022.08.023. Epub 2022 Sep 22.
- PMID: 36136089
- PubMed abstract
•• Podcast: January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey. (Genetics in Medicine GenePOD)
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- A digital pathway for genetic testing in UK NHS patients with cancer: BRCA-DIRECT randomised study internal pilot.
- Torr B, Jones C, Choi S, Allen S, Kavanaugh G, Hamill M, Garrett A, MacMahon S, Loong L, Reay A, Yuan L, Valganon Petrizan M, Monson K, Perry N, Fallowfield L, Jenkins V, Gold R, Taylor A, Gabe R, Wiggins J, Lucassen A, Manchanda R, Gandhi A, George A, Hubank M, Kemp Z, Evans DG, Bremner S, Turnbull C.
- J Med Genet. 2022 Dec;59(12):1179-1188. doi: 10.1136/jmg-2022-108655. Epub 2022 Jul 22.
- PMID: 35868849
- PubMed abstract
•• Trial registration number: ISRCTN87845055: BRCA-DIRECT- Is digitally delivered information about genetic testing feasible, effective and acceptable to women with breast cancer?. (ISRCTN registry)
•• Press: UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer. (GenomeWeb)
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- Management of patients with advanced prostate cancer in Japan: 'real-world' consideration of the results from the Advanced Prostate Cancer Consensus Conference.
- Fujita K, Suzuki H, Hinata N, Miura Y, Edamura K, Tabata KI, Arai G, Matsubara N, Yasumizu Y, Kosaka T, Oya M, Sugimoto M.
- Transl Androl Urol. 2022 Dec;11(12):1771-1785. doi: 10.21037/tau-22-396.
- PMID: 36632151
- PubMed abstract
•• Commentary:
Assessment of real-world application of advanced prostate cancer management in Japan.
- PMID: 36632149
- PubMed abstract
- Free Full Text
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- Referral, Genetic Counselling, and BRCA Testing in the Manitoba High-Grade Serous Ovarian Cancer Population, 2004–2019.
- Winchar K, Lambert P, McManus KJ, Chodirker B, Kean S, Serfas K, Decker K, Nachtigal MW, Altman AD.
- Curr Oncol. 2022 Nov 30;29(12):9365-9376. doi: 10.3390/curroncol29120735.
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- BRCAShare-Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study.
- Aeilts AM, Carpenter KM, Hovick SR, Byrne L, Shoben AB, Senter L.
- J Genet Couns. 2022 Nov 25. doi: 10.1002/jgc4.1656. Epub ahead of print.
- PMID: 36426678
- PubMed abstract
- Source abstract
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- UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer.
- [No author given]
- GenomeWeb. The Scan. 2022 Nov 23.
- News
- Free Full Text
•• Original research:
A digital pathway for genetic testing in UK NHS patients with cancer: BRCA-DIRECT randomised study internal pilot.
- PMID: 35868849
- PubMed abstract
- Free Full Text
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- Four-in-Five Eligible Breast Cancer Patients Not Informed of Genomic Testing Options.
- [No author given]
- Inside Precision Medicine. Topics. Oncology. 2022 Nov 21.
- News
- Free Full Text
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- Fatalism and metaphor in Confucianism: A qualitative study of barriers to genetic testing among first-degree relatives of hereditary cancer patients from China.
- Jiang C, Liu L, Wang Y, Wu L, Zhang W, Wu X.
- Psychooncology. 2022 Nov 15. doi: 10.1002/pon.6068. Epub ahead of print.
- PMID: 36380559
- 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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- BRCA1/2 Mutation Testing in Patients with HER2-Negative Advanced Breast Cancer: Real-World Data from the United States, Europe, and Israel.
- Mahtani R, Niyazov A, Arondekar B, Lewis K, Rider A, Massey L, Lux MP.
- Cancers (Basel). 2022 Nov 2;14(21):5399. doi: 10.3390/cancers14215399.
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- Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants.
- Liu YL, Maio A, Kemel Y, Salo-Mullen EE, Sheehan M, Tejada PR, Trottier M, Arnold AG, Fleischut MH, Latham A, Carlo MI, Murciano-Goroff YR, Walsh MF, Mandelker D, Mehta N, Bandlamudi C, Arora K, Zehir A, Berger MF, Solit DB, Aghajanian C, Diaz LA Jr, Robson ME, Brown CL, Offit K, Hamilton JG, Stadler ZK.
- Cancer. 2022 Nov 1;128(21):3870-3879. doi: 10.1002/cncr.34434. Epub 2022 Aug 30.
- PMID: 36041233
- PubMed abstract
- Source abstract
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- The first Chinese National Union of Real-world Gynaecological Oncology Research and Patient Management Platform: A retrospective study.
- Zeng S, Chi J, Liu J, Jiao X, Liu X, Yu Y, Li R, Huo Y, Ma G, Zhao Y, Wang L, Zhou Q, Zou D, Cheng X, Li Q, Wang J, Yao S, Zhao W, Xia B, Chen Y, Fan J, Wang W, Hong L, Guo R, Liu Z, Gao Y, Li J, Zhang B, Yu J, Hu T, Zhang W, Shan W, Peng Z, Li M, Xie X, Ma D, Gao Q.
- BJOG. 2022 Nov;129 Suppl 2:60-69. doi: 10.1111/1471-0528.17328.
- PMID: 36485066
- PubMed abstract
- Source abstract
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- Real-World Study of Regional Differences in Patient Demographics, Clinical Characteristics, and BRCA1/2 Mutation Testing in Patients with Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer in the United States, Europe, and Israel.
- Mahtani R, Niyazov A, Lewis K, Rider A, Massey L, Arondekar B, Lux MP.
- Adv Ther. 2022 Oct 28. doi: 10.1007/s12325-022-02302-2. Epub ahead of print.
- PMID: 36333567
- PubMed abstract
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- Interdisciplinary risk counseling for hereditary breast and ovarian cancer: real-world data from a specialized center.
- Zang B, Helms M, Besch L, Kalmbach N, Stegen S, Blohmer JU, Speiser D.
- Arch Gynecol Obstet. 2022 Oct 28. doi: 10.1007/s00404-022-06819-3. Epub ahead of print.
- PMID: 36307613
- PubMed abstract
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- What happens in the long term: Uptake of cancer surveillance and prevention strategies among at-risk relatives with pathogenic variants detected via cascade testing.
- Frey MK, Ahsan MD, Badiner N, Lin J, Narayan P, Nitecki R, Rauh-Hain JA, Moss H, Fowlkes RK, Thomas C, Bergeron H, Christos P, Levi SR, Blank SV, Holcomb K, Cantillo E, Sharaf RN, Lipkin S, Offit K, Chapman-Davis E.
- Cancer. 2022 Oct 27. doi: 10.1002/cncr.34482. Epub ahead of print.
- PMID: 36305018
- PubMed abstract
- Source abstract
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- Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review.
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- Maximizing cancer prevention through genetic navigation for Lynch syndrome detection in women with newly diagnosed endometrial and nonserous/nonmucinous epithelial ovarian cancer.
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- "Being proactive, not reactive": exploring perceptions of genetic testing among White, Latinx, and Pacific Islander Populations.
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- Next-Generation Sequencing of Patients With Breast Cancer in Community Oncology Clinics.
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- Attitudes toward Risk-Reducing Mastectomy and Risk-Reducing Salpingo-oophorectomy among Young, Unmarried, Healthy Women in Korea.
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- Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States.
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- Novel Approach Using Administrative Claims to Evaluate Trends in Oncology Multigene Panel Testing for Patients Enrolled in Medicare Advantage Health Plans.
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- Use of a Standardized Tool to Identify Women at Risk for Hereditary Breast and Ovarian Cancer.
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- Real-world genetic testing patterns in metastatic castration-resistant prostate cancer.
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- Factors Influencing Discussion of Cancer Genetic Testing with Health-Care Providers in a Population-Based Survey.
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- The Screen Project: Guided Direct-To-Consumer Genetic Testing for Breast Cancer Susceptibility in Canada.
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- The Prevent Ovarian Cancer Program (POCP): Identification of women at risk for ovarian cancer using complementary recruitment approaches.
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- Management and outcomes of men diagnosed with primary breast cancer.
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- A Comparison of Patient-Reported Outcomes Following Consent for Genetic Testing Using an Oncologist- or Genetic Counselor-Mediated Model of Care.
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Letter, Comment:
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- Clinical and community genetics services in the Dutch Caribbean.
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- Clinical Utility of Next-Generation Sequencing-Based Panel Testing under the Universal Health-Care System in Japan: A Retrospective Analysis at a Single University Hospital.
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