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    المؤلفون: Purdue, Mark P., Dutta, Diptavo, Machiela, Mitchell J., Gorman, Bryan R., Winter, Timothy, Okuhara, Dayne, Cleland, Sara, Ferreiro-Iglesias, Aida, Scheet, Paul, Liu, Aoxing, Wu, Chao, Antwi, Samuel O., Larkin, James, Zequi, Stênio C., Sun, Maxine, Hikino, Keiko, Hajiran, Ali, Lawson, Keith A., Cárcano, Flavio, Blanchet, Odile, Shuch, Brian, Nepple, Kenneth G., Margue, Gaëlle, Sundi, Debasish, Diver, W. Ryan, Folgueira, Maria A. A. K., van Bokhoven, Adrie, Neffa, Florencia, Brown, Kevin M., Hofmann, Jonathan N., Rhee, Jongeun, Yeager, Meredith, Cole, Nathan R., Hicks, Belynda D., Manning, Michelle R., Hutchinson, Amy A., Rothman, Nathaniel, Huang, Wen-Yi, Linehan, W. Marston, Lori, Adriana, Ferragu, Matthieu, Zidane-Marinnes, Merzouka, Serrano, Sérgio V., Magnabosco, Wesley J., Vilas, Ana, Decia, Ricardo, Carusso, Florencia, Graham, Laura S., Anderson, Kyra, Bilen, Mehmet A., Arciero, Cletus, Pellegrin, Isabelle, Ricard, Solène, Scelo, Ghislaine, Banks, Rosamonde E., Vasudev, Naveen S., Soomro, Naeem, Stewart, Grant D., Adeyoju, Adebanji, Bromage, Stephen, Hrouda, David, Gibbons, Norma, Patel, Poulam, Sullivan, Mark, Protheroe, Andrew, Nugent, Francesca I., Fournier, Michelle J., Zhang, Xiaoyu, Martin, Lisa J., Komisarenko, Maria, Eisen, Timothy, Cunningham, Sonia A., Connolly, Denise C., Uzzo, Robert G., Zaridze, David, Mukeria, Anush, Holcatova, Ivana, Hornakova, Anna, Foretova, Lenka, Janout, Vladimir, Mates, Dana, Jinga, Viorel, Rascu, Stefan, Mijuskovic, Mirjana, Savic, Slavisa, Milosavljevic, Sasa, Gaborieau, Valérie, Abedi-Ardekani, Behnoush, McKay, James, Johansson, Mattias, Phouthavongsy, Larry, Hayman, Lindsay, Li, Jason, Lungu, Ilinca, Bezerra, Stephania M., Souza, Aline G., Sares, Claudia T. G., Reis, Rodolfo B., Gallucci, Fabio P., Cordeiro, Mauricio D., Pomerantz, Mark, Lee, Gwo-Shu M., Freedman, Matthew L., Jeong, Anhyo, Greenberg, Samantha E., Sanchez, Alejandro, Thompson, R. Houston, Sharma, Vidit, Thiel, David D., Ball, Colleen T., Abreu, Diego, Lam, Elaine T., Nahas, William C., Master, Viraj A., Patel, Alpa V., Bernhard, Jean-Christophe, Freedman, Neal D., Bigot, Pierre, Reis, Rui M., Colli, Leandro M., Finelli, Antonio, Manley, Brandon J., Terao, Chikashi, Choueiri, Toni K., Carraro, Dirce M., Houlston, Richard, Eckel-Passow, Jeanette E., Abbosh, Philip H., Ganna, Andrea, Brennan, Paul, Gu, Jian, Chanock, Stephen J.

    المصدر: Nature Genetics; 20240101, Issue: Preprints p1-10, 10p

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    وصف الملف: application/pdf

    العلاقة: Bratslavsky, Gennady; Mendhiratta, Neil; Daneshvar, Michael; Brugarolas, James; Ball, Mark W.; Metwalli, Adam; Nathanson, Katherine L.; Pierorazio, Phillip M.; Boris, Ronald S.; Singer, Eric A.; Carlo, Maria I.; Daly, Mary B.; Henske, Elizabeth P.; Hyatt, Colette; Middleton, Lindsay; Morris, Gloria; Jeong, Anhyo; Narayan, Vivek; Rathmell, W. Kimryn; Vaishampayan, Ulka; Lee, Bruce H.; Battle, Dena; Hall, Michael J.; Hafez, Khaled; Jewett, Michael A. S.; Karamboulas, Christina; Pal, Sumanta K.; Hakimi, A. Ari; Kutikov, Alexander; Iliopoulos, Othon; Linehan, W. Marston; Jonasch, Eric; Srinivasan, Ramaprasad; Shuch, Brian (2021). "Genetic risk assessment for hereditary renal cell carcinoma: Clinical consensus statement." Cancer (21): 3957-3966.; https://hdl.handle.net/2027.42/170869Test; Cancer; Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019; 69: 7 ‐ 34. doi:10.3322/caac.21551; Isla D, de Castro J, Garcia‐Campelo R, et al. Treatment options beyond immunotherapy in patients with wild‐type lung adenocarcinoma: a Delphi consensus. Clin Transl Oncol. 2020; 22: 759 ‐ 771. doi:10.1007/s12094‐019‐02191‐y; Linehan WM, Ricketts CJ. The Cancer Genome Atlas of renal cell carcinoma: findings and clinical implications. Nat Rev Urol. 2019; 16: 539 ‐ 552. doi:10.1038/s41585‐019‐0211‐5; Carlo MI, Mukherjee S, Mandelker D, et al. Prevalence of germline mutations in cancer susceptibility genes in patients with advanced renal cell carcinoma. JAMA Oncol. 2018; 4: 1228 ‐ 1235. doi:10.1001/jamaoncol.2018.1986; Huang KL, Mashl RJ, Wu Y, et al. Pathogenic germline variants in 10,389 adult cancers. Cell. 2018; 173: 355 ‐ 370.e14. doi:10.1016/j.cell.2018.03.039; Shuch B, Vourganti S, Ricketts CJ, et al. Defining early‐onset kidney cancer: implications for germline and somatic mutation testing and clinical management genetic counseling. J Clin Oncol. 2014; 32: 431 ‐ 437.; Adeniran AJ, Shuch B, Humphrey PA. 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Eur Urol. 2019; 76: 790 ‐ 813. doi:10.1016/j.eururo.2019.09.020; Lapini A, Caffo O, Pappagallo G, et al. Monitoring patients with metastatic hormone‐sensitive and metastatic castration‐resistant prostate cancer: a multidisciplinary consensus document. Cancers (Basel). 2019; 11: 1908.; Hall MJ, Patrick‐Miller LJ, Egleston BL, et al. Use and patient‐reported outcomes of clinical multigene panel testing for cancer susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study. JCO Precis Oncol. 2018; 2: PO.18.00199. doi:10.1200/po.18.00199; Cohen SA, Bradbury A, Henderson V, Hoskins K, Bednar E, Arun BK. Genetic counseling and testing in a community setting: quality, access, and efficiency. Am Soc Clin Oncol Educ Book. 2019; 39: e34 ‐ e44. doi:10.1200/edbk_238937; Hilgart JS, Hayward JA, Coles B, Iredale R. Telegenetics: a systematic review of telemedicine in genetics services. Genet Med. 2012; 14: 765 ‐ 776. doi:10.1038/gim.2012.40; Hoskovec JM, Bennett RL, Carey ME, et al. Projecting the supply and demand for certified genetic counselors: a workforce study. J Genet Couns. 2018; 27: 16 ‐ 20. doi:10.1007/s10897‐017‐0158‐8; Green BB, Coronado GD, Devoe JE, Allison J. Navigating the murky waters of colorectal cancer screening and health reform. Am J Public Health. 2014; 104: 982 ‐ 986. doi:10.2105/AJPH.2014.301877; Robson ME, Bradbury AR, Arun B, et al. American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. J Clin Oncol. 2015; 33: 3660 ‐ 3667. doi:10.1200/JCO.2015.63.0996; Easton DF, Pharoah PDP, Antoniou AC, et al. Gene‐panel sequencing and the prediction of breast‐cancer risk. N Engl J Med. 2015; 372: 2243 ‐ 2257. doi:10.1056/NEJMsr1501341; Lynce F, Isaacs C. How far do we go with genetic evaluation? Gene, panel, and tumor testing. Am Soc Clin Oncol Educ Book. 2016; 35: e72 ‐ e78. doi:10.14694/edbk_160391; Shuch B, Singer EA, Bratslavsky G. The surgical approach to multifocal renal cancers: hereditary syndromes, ipsilateral multifocality, and bilateral tumors. Urol Clin North Am. 2012; 39: 133 ‐ 148. doi:10.1016/j.ucl.2012.01.006; Hampel H, Bennett RL, Buchanan A, Pearlman R, Wiesner GL. A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. Genet Med. 2015; 17: 70 ‐ 87. doi:10.1038/gim.2014.147; Motzer RJ, Jonasch E, Boyle S, et al. NCCN Guidelines Insights: Kidney Cancer, Version 1.2021. J Natl Compr Cancer Netw. 2020; 18: 1160 ‐ 1170. doi:10.6004/jnccn.2020.0043; Campbell S, Uzzo RG, Allaf ME, et al. Renal mass and localized renal cancer: AUA guideline. J Urol. 2017; 198: 520 ‐ 529. doi:10.1016/j.juro.2017.04.100; Ljungberg B, Bensalah K, Canfield S, et al. EAU guidelines on renal cell carcinoma: 2014 update. Eur Urol. 2015; 67: 913 ‐ 924. doi:10.1016/j.eururo.2015.01.005; Brierley KL, Campfield D, Ducaine W, et al. Errors in delivery of cancer genetics services: implications for practice. Conn Med. 2010; 74: 413 ‐ 423.; Brierley KL, Blouch E, Cogswell W, et al. Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications. Cancer J. 2012; 18: 303 ‐ 309. doi:10.1097/PPO.0b013e3182609490; Laforest F, Mann B, Edwards A, Kirkegaard P. Genetic cancer risk assessment in general practice: systematic review of tools available, clinician attitudes, and patient outcomes. Br J Gen Pract. 2019; 69: e97 ‐ e105. doi:10.3399/bjgp18X700265; Shuch B, Zhang J. Genetic predisposition to renal cell carcinoma: implications for counseling, testing, screening, and management. J Clin Oncol. 2018; 36: 3560 ‐ 3566. doi:10.1200/JCO.2018.79.2523; National Comprehensive Cancer Network (NCCN). NCCN Guidelines and Clinical Resources. NCCN; 2020. https://www.nccn.org/professionals/development.aspxTest. Accessed May 14, 2020.; Nguyen KA, Syed JS, Espenschied CR, et al. Advances in the diagnosis of hereditary kidney cancer: initial results of a multigene panel test. Cancer. 2017; 123: 4363 ‐ 4371. doi:10.1002/cncr.30893; Mucci LA, Hjelmborg JB, Harris JR, et al. Familial risk and heritability of cancer among twins in Nordic countries. JAMA. 2016; 315: 68 ‐ 76. doi:10.1001/jama.2015.17703; Haas NB, Nathanson KL. Hereditary kidney cancer syndromes. Adv Chronic Kidney Dis. 2014; 21: 81 ‐ 90. doi:10.1053/j.ackd.2013.10.001

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