Guidelines on all aspects of selecting patients for testing, risk assessment, evaluating risk factors, etc.
Not just clinical guidelines themselves, but any papers dealing with any aspect of guidelines, such as assessments of their effectiveness, assessments of providers' adherence to guidelines, press reports announcing new guideline's release, and so forth.
List was last updated on
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- Challenges in periodic revision of genetic testing results: comparison of the main classification guidelines and report of a retrospective analysis involving BRCA1/BRCA2 Variants of Uncertain Significance.
- Finger Andreis T, Isabel Weber de Souza K, Araujo Vieira I, Alemar B, Sinigaglia M, Marinho de Araújo Rocha Y, Artigalás O, Bittar C, Brinckmann Oliveira Netto C, Ashton-Prolla P, Rosset C.
- Gene. 2023 Feb 10:147281. doi: 10.1016/j.gene.2023.147281. Epub ahead of print.
- PMID: 36775216
- PubMed abstract
- Source abstract
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- Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels.
- Chang EY, Solomon I, Culver JO, Gorman N, Comeaux JG, Lerman C, Quinn EA, Ekstein T.
- J Genet Couns. 2023 Feb 6. doi: 10.1002/jgc4.1680. Epub ahead of print.
- PMID: 36747331
- PubMed abstract
- Source abstract
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- Mitigating fear of cancer recurrence.
- Sorscher S.
- Breast Cancer Res Treat. 2023 Feb 3. doi: 10.1007/s10549-022-06824-9. Epub ahead of print.
- PMID: 36737585
- PubMed abstract
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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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- Atypical ATMs: Broadening the Phenotypic Spectrum of ATM-associated Hereditary Cancer.
- Borja NA, Silva-Smith R, Huang M, Parekh DJ, Sussman D, Tekin M.
- Front Oncol. 2023 Feb 3;13:1068110. doi: 10.3389/fonc.2023.1068110.
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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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- 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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- Performance of INHERET® risk assessment tool for identifying pathogenic germline variants among individuals referred for cancer genetics evaluation. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Henry ML, Pialtos K, Fry S, Koeppe E, Osborne J, Cook A, Hulswitt B, Milliron KJ, Merajver S, Stoffel E.
- Fam Cancer. [P-21: 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 BRCA mutations testing in formalin-fixed paraffin-embedded (FFPE) samples of different cancer types.
- Zannini G, Facchini G, De Sio M, De Vita F, Ronchi A, Orditura M, Vietri MT, Ciardiello F, Franco R, Accardo M, Zito Marino F.
- Pathol Res Pract. 2023 Jan 23;243:154336. doi: 10.1016/j.prp.2023.154336. Epub ahead of print.
- PMID: 36736144
- 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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- 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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- Prevalence of Germline BRCA1/2 Variants in Ashkenazi and Non-Ashkenazi Prostate Cancer Populations: A Systematic Review and Meta-Analysis.
- Cioffi A, De Cobelli O, Veronesi P, La Vecchia C, Maisonneuve P, Corso G.
- Cancers (Basel). 2023 Jan 2;15(1):306. doi: 10.3390/cancers15010306.
- Meta-Analysis
- 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.
- Rev Esp Patol. 2023 Jan-Mar;56(1):32-44. doi: 10.1016/j.patol.2022.06.004. Epub 2022 Aug 26.
- PMID: 36599598
- 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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- All HER2-negative breast cancer patients need gBRCA testing: cost-effectiveness and clinical benefits.
- Wu HL, Luo ZY, He ZL, Gong Y, Mo M, Ming WK, Liu GY.
- Br J Cancer. 2022 Dec 23. doi: 10.1038/s41416-022-02111-y. Epub ahead of print.
- PMID: 36564566
- PubMed 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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- Real World Cost-Effectiveness Analysis of Population Screening for BRCA Variants among Ashkenazi Jews Compared with Family History-Based Strategies.
- Michaelson-Cohen R, Cohen MJ, Cohen C, Greenberg D, Shmueli A, Lieberman S, Tomer A, Levy-Lahad E, Lahad A.
- Cancers (Basel). 2022 Dec 12;14(24):6113. doi: 10.3390/cancers14246113.
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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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- Hereditary breast cancer: syndromes, tumour pathology and molecular testing.
- Sokolova A, Johnstone KJ, McCart Reed AE, Simpson PT, Lakhani SR.
- Histopathology. 2022 Dec 5. doi: 10.1111/his.14808. Epub ahead of print.
- PMID: 36468211
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Yes, We Can, But Should We? Ethical Considerations in Reporting Germline Findings From Paired Tumor-Normal Genomic Testing in Patients With Advanced Cancer.
- Hunter CL, Helft PR.
- J Clin Oncol. 2022 Dec 5:JCO2200796. doi: 10.1200/JCO.22.00796. Epub ahead of print.
- PMID: 36469841
- PubMed abstract
- Source abstract
- Commentary
- Free Full Text
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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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- Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
- Garcia-Pelaez J, Barbosa-Matos R, Lobo S, Dias A, Garrido L, Castedo S, Sousa S, Pinheiro H, Sousa L, Monteiro R, Maqueda JJ, Fernandes S, Carneiro F, Pinto N, Lemos C, Pinto C, Teixeira MR, Aretz S, Bajalica-Lagercrantz S, Balmaña J, Blatnik A, Benusiglio PR, Blanluet M, Bours V, Brems H, Brunet J, Calistri D, Capellá G, Carrera S, Colas C, Dahan K, de Putter R, Desseignés C, Domínguez-Garrido E, Egas C, Evans DG, Feret D, Fewings E, Fitzgerald RC, Coulet F, Garcia-Barcina M, Genuardi M, Golmard L, Hackmann K, Hanson H, Holinski-Feder E, Hüneburg R, Krajc M, Lagerstedt-Robinson K, Lázaro C, Ligtenberg MJL, Martínez-Bouzas C, Merino S, Michils G, Novakovic S, Patiño-García A, Ranzani GN, Schröck E, Silva I, Silveira C, Soto JL, Spier I, Steinke-Lange V, Tedaldi G, Tejada MI, Woodward ER, Tischkowitz M, Hoogerbrugge N, Oliveira C.
- Lancet Oncol. 2022 Nov 24:S1470-2045(22)00643-X. doi: 10.1016/S1470-2045(22)00643-X. Epub ahead of print.
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- Germline mutations in prostate cancer: a systematic review of the evidence for personalized medicine.
- Marino F, Totaro A, Gandi C, Bientinesi R, Moretto S, Gavi F, Pierconti F, Iacovelli R, Bassi P, Sacco E.
- Prostate Cancer Prostatic Dis. 2022 Nov 24. doi: 10.1038/s41391-022-00609-3. Epub ahead of print.
- PMID: 36434163
- PubMed abstract
- Source abstract
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- Editorial: Prostate Cancer Genomics: Application at Different Stages of a Patient's Journey.
- Poon DM, Azad A, Castro E, Kanesvaran R, Sartor O.
- Front Oncol. 2022 Nov 21;12:1101678. doi: 10.3389/fonc.2022.1101678.
- Commentary
- Free Full Text
•• Original research:
Genomic landscape of advanced prostate cancer patients with BRCA1 versus BRCA2 mutations as detected by comprehensive genomic profiling of cell-free DNA.
- PMID: 36185208
- PubMed abstract
- Free Full Text
•• Original research:
Genetic Testing and Its Clinical Application in Prostate Cancer Management: Consensus Statements from the Hong Kong Urological Association and Hong Kong Society of Uro-Oncology.
- PMID: 35924163
- PubMed abstract
- Free Full Text
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- Systematic mapping review of guidelines for BRCA1/2 genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer.
- Hughes BN, Jorgensen KA, Cummings S, Morah D, Krause K, Rauh-Hain JA, Herzog TJ.
- Int J Gynecol Cancer. 2022 Nov 11:ijgc-2022-003913. doi: 10.1136/ijgc-2022-003913. Epub ahead of print.
- PMID: 36368709
- PubMed abstract
- Source abstract
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- Prostate Cancer Has High Rate of Actionable Mutations, Underscoring Need for Testing.
- Rosa K, Antonarakis ES.
- OncLive. 2022 Nov 11.
- Review
- Free Full Text
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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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- 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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- Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy.
- Negri S, De Ponti E, Sina FP, Sala E, Dell'Oro C, Roversi G, Lazzarin S, Delle Marchette M, Inzoli A, Toso C, Fumagalli S, Campanella M, Kotsopoulos J, Fruscio R.
- Mol Genet Genomic Med. 2022 Oct 28:e2071. doi: 10.1002/mgg3.2071. Epub ahead of print.
- PMID: 36307994
- PubMed abstract
- Source abstract
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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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- 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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- Prevalence of pathogenic germline variants in the circulating tumor DNA testing.
- Yamamoto Y, Fukuyama K, Kanai M, Kondo T, Yoshioka M, Kou T, Quy PN, Kimura-Tsuchiya R, Yamada T, Matsumoto S, Kosugi S, Muto M.
- Int J Clin Oncol. 2022 Oct;27(10):1554-1561. doi: 10.1007/s10147-022-02220-x. Epub 2022 Jul 23.
- PMID: 35870019
- PubMed abstract
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- Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions.
- Saba LF, Sullivan CM, Solomon T, Huguenard S, Nassef SA.
- J Genet Couns. 2022 Oct;31(5):1062-1070. doi: 10.1002/jgc4.1577. Epub 2022 Apr 18.
- PMID: 35434961
- PubMed abstract
- Source abstract
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- Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients.
- Culver JO, Freiberg Y, Ricker C, Comeaux JG, Chang EY, Banerjee V, Sturgeon D, Solomon I, Kagey J, Dobre MG, Carey J, Carr A, Cho S, Lu J, Kang IM, Patel K, Terando A, Ye JC, Li M, Lerman C, Spicer D, Nelson M.
- Ann Surg Oncol. 2022 Sep 26. doi: 10.1245/s10434-022-12595-w. Epub ahead of print.
- PMID: 36161375
- PubMed abstract
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- Clinical Utility of Universal Germline Genetic Testing for Patients With Breast Cancer.
- Whitworth PW, Beitsch PD, Patel R, Rosen B, Compagnoni G, Baron PL, Simmons R, Brown EA, Gold L, Holmes D, Smith LA, Kinney M, Grady I, Clark P, Barbosa K, Lyons S, Riley L, Coomer C, Curcio L, Ruiz A, Khan S, MacDonald H, Hughes K, Hardwick MK, Heald B, Munro SB, Nielsen SM, Esplin ED.
- JAMA Netw Open. 2022 Sep 1 [2022 Sep 22];5(9):e2232787. doi: 10.1001/jamanetworkopen.2022.32787.
- PMID: 36136330
- PubMed abstract
Research news: Universal Genetic Testing in Breast Cancer Further Supported in New Invitae-Led Study. (GenomeWeb)
Research news: Time for Universal Germline Genetic Testing in Breast Cancer. (Medscape)
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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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- Biomarkers for Systemic Therapy in Metastatic Breast Cancer: ASCO Guideline Update.
- Henry NL, Somerfield MR, Dayao Z, Elias A, Kalinsky K, McShane LM, Moy B, Park BH, Shanahan KM, Sharma P, Shatsky R, Stringer-Reasor E, Telli M, Turner NC, DeMichele A.
- J Clin Oncol. 2022 Sep 20;40(27):3205-3221. doi: 10.1200/JCO.22.01063. Epub 2022 Jun 27.
- PMID: 35759724
- PubMed abstract
- Source abstract
- Guideline
- Free Full Text
Review:
Biomarkers for Systemic Therapy in Metastatic Breast Cancer: ASCO Guideline Update Q and A.
- PMID: 36122313
- PubMed abstract
- Free Full Text
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- Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer.
- Esplin ED, Nielsen SM, Bristow SL, Garber JE, Hampel H, Rana HQ, Samadder NJ, Shore ND, Nussbaum RL.
- JCO Precis Oncol. 2022 Sep [2022 Sep 15];6:e2100516. doi: 10.1200/PO.21.00516.
- PMID: 36108258
- PubMed abstract
- Source abstract
- Commentary
- Free Full Text
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- Addition of Germline Testing to Tumor-Only Sequencing Improves Detection of Pathogenic Germline Variants in Men With Advanced Prostate Cancer.
- Berchuck JE, Boiarsky D, Silver R, Sunkara R, McClure HM, Tsai HK, Siegmund S, Tewari AK, Nowak JA, Lindeman NI, Rana HQ, Choudhury AD, Pomerantz MM, Freedman ML, Van Allen EM, Taplin ME.
- JCO Precis Oncol. 2022 Aug [2022 Sep 14];6:e2200329. doi: 10.1200/PO.22.00329.
- PMID: 36103646
- PubMed abstract
- Source abstract
Identifier: NCT03328091: Genetic Counseling Processes and Outcomes Among Males With Prostate Cancer (ProGen) (ProGen). (ClinicalTrials.gov)
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- Biomarker Test Access for Precision Oncology Varies Widely in Europe, ESMO Survey Finds.
- Hopkins C.
- Precision Oncology News. 2022 Sep 14.
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- Somatic tumor mutations in moderate risk cancer genes: Targets for germline confirmatory testing.
- Llorin H, Graf M, Chun N, Ford J.
- Cancer Genet. 2022 Sep 6;268-269:22-27. doi: 10.1016/j.cancergen.2022.09.001. Epub ahead of print.
- PMID: 36116289
- PubMed abstract
- Source abstract
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- Who Should Consider BRCA Testing?
- [No author given]
- My Gene Counsel. Genetic Journal. 2022 Sep 6.
- Blog post
- Free Full Text
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- What can we learn from more than 1000 Brazilian patients at risk of hereditary cancer?
- Leite ACR, Suzuki DA, Pereira AAL, Machado NP, Barroso-Sousa R, Correa TS, Moura FC, Morbeck IAP, Gumz BP, Faria LDBB, Fernandes GDS, Sandoval RL.
- Front Oncol. 2022 Sep 5;12:963910. doi: 10.3389/fonc.2022.963910.
- PMID: 36132150
- PubMed abstract
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- Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK).
- Loong L, Garrett A, Allen S, Choi S, Durkie M, Callaway A, Drummond J, Burghel GJ, Robinson R, Torr B, Berry IR, Wallace AJ, Eccles DM, Ellard S, Baple E, Evans DG, Woodward ER, Kulkarni A, Lalloo F, Tischkowitz M, Lucassen A, Hanson H, Turnbull C; CanVIG-UK.
- Genet Med. 2022 Sep;24(9):1867-1877. doi: 10.1016/j.gim.2022.05.002. Epub 2022 Jun 3.
- PMID: 35657381
- PubMed abstract
- Guideline
- Free Full Text
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- Breast cancer in a teenage girl with BRCA mutation: A case report from a low middle-income country.
- Vohra LM, Ali D, Hashmi SA, Angez M.
- Int J Surg Case Rep. 2022 Sep;98:107513. doi: 10.1016/j.ijscr.2022.107513. Epub 2022 Aug 13.
- PMID: 36027825
- PubMed abstract
- Case report
- Free PMC article
- Free Full Text
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- An evidence-based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling.
- Green S, Hartzfeld D, Terry AB, Fissell K, Friedman S, Paolino N, Principe K, Sandbach J, Trzupek K, Winheld S, Malinowski J.
- J Genet Couns. 2022 Aug 30. doi: 10.1002/jgc4.1627. Epub ahead of print.
- PMID: 36054686
- PubMed abstract
- Source abstract
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- Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices.
- Lahiri S, Reys B, Wunder J, Pirzadeh-Miller S.
- J Genet Couns. 2022 Aug 17. doi: 10.1002/jgc4.1626. Epub ahead of print.
- PMID: 35978490
- PubMed abstract
- Source abstract
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- Oncologists Consider Germline Testing in Lung Cancer Patients Amid New Data Showing High Prevalence.
- Hopkins C.
- Precision Oncology News. Disease Areas. 2022 Aug 17.
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- Optimizing treatment selection and sequencing decisions for first-line maintenance therapy of newly diagnosed advanced ovarian cancer.
- Goh JCH, Gourley C, Tan DSP, Nogueira-Rodrigues A, Elghazaly H, Edy Pierre M, Giornelli G, Kim BG, Morales-Vasquez F, Tyulyandina A.
- Gynecol Oncol Rep. 2022 Jun 17 [eCollection 2022 Aug];42:101028. doi: 10.1016/j.gore.2022.101028.
- PMID: 35813356
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- Germline sequencing for presumed germline pathogenic variants via tumor-only comprehensive genomic profiling.
- Kondo T, Yamamoto Y, Fukuyama K, Kanai M, Yamada A, Matsubara J, Quy PN, Yoshioka M, Yamada T, Minamiguchi S, Matsumoto S, Kosugi S, Muto M.
- Int J Clin Oncol. 2022 Aug;27(8):1256-1263. doi: 10.1007/s10147-022-02176-y. Epub 2022 May 14.
- PMID: 35567649
- PubMed abstract
- Source abstract
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- Practice guidelines for BRCA1/2 tumour testing in ovarian cancer.
- Grafodatskaya D, O'Rielly DD, Bedard K, Butcher DT, Howlett CJ, Lytwyn A, McCready E, Parboosingh J, Spriggs EL, Vaags AK, Stockley TL.
- J Med Genet. 2022 Aug;59(8):727-736. doi: 10.1136/jmedgenet-2021-108238. Epub 2022 Apr 7.
- PMID: 35393334
- PubMed abstract
- Review
- Free Full Text
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- Germline genetics of prostate cancer.
- Khan HM, Cheng HH.
- Prostate. 2022 Aug;82 Suppl 1:S3-S12. doi: 10.1002/pros.24340.
- PMID: 35657157
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Clinical implications of homologous recombination repair mutations in prostate cancer.
- Cresta Morgado P, Mateo J.
- Prostate. 2022 Aug;82 Suppl 1:S45-S59. doi: 10.1002/pros.24352.
- PMID: 35657156
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Germline Testing of Patients With Non-small Cell Lung Cancers Demonstrating Incidentally Uncovered BRCA2 Apparent Pathogenic Germline Variants.
- Sorscher S.
- Clin Lung Cancer. 2022 Jul 21 [2022 Jul 20]:S1525-7304(22)00163-2. doi: 10.1016/j.cllc.2022.07.011. Epub ahead of print.
- PMID: 35977876
- PubMed abstract
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- Genetic Testing and Its Clinical Application in Prostate Cancer Management: Consensus Statements from the Hong Kong Urological Association and Hong Kong Society of Uro-Oncology.
- Chiu PKF, Lee EKC, Chan MTY, Chan WHC, Cheung MH, Lam MHC, Ma ESK, Poon DMC.
- Front Oncol. 2022 Jul 18;12:962958. doi: 10.3389/fonc.2022.962958.
- PMID: 35924163
- PubMed abstract
- Guideline
- Free PMC article
- Free Full Text
•• Commentary:
Editorial: Prostate Cancer Genomics: Application at Different Stages of a Patient's Journey.
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- BRCA1/2 in non-mucinous epithelial ovarian cancer: tumour with or without germline testing?
- Morgan RD, Burghel GJ, Flaum N, Bulman M, Smith P, Clamp AR, Hasan J, Mitchell CL, Salih Z, Woodward ER, Lalloo F, Crosbie EJ, Edmondson RJ, Wallace AJ, Jayson GC, Evans DGR.
- Br J Cancer. 2022 Jul;127(1):163-167. doi: 10.1038/s41416-022-01773-y. Epub 2022 Mar 8.
- PMID: 35260807
- PubMed abstract
- Source abstract
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- Genetic testing in prostate cancer management: Considerations informing primary care.
- Giri VN, Morgan TM, Morris DS, Berchuck JE, Hyatt C, Taplin ME.
- CA Cancer J Clin. 2022 Jul;72(4):360-371. doi: 10.3322/caac.21720. Epub 2022 Feb 24.
- PMID: 35201622
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients.
- de Oliveira JM, Zurro NB, Coelho AVC, Caraciolo MP, de Alexandre RB, Cervato MC, Minillo RM, de Vasconcelos Carvalho Neto G, Grivicich I, Oliveira JB.
- Eur J Hum Genet. 2022 Jul;30(7):818-823. doi: 10.1038/s41431-022-01098-7. Epub 2022 May 9.
- PMID: 35534704
- PubMed abstract
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Comments on NSGC Discussion Forum Cancer SIG
Subject: Slides for risk models
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