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ORIGINAL ARTICLE

Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer

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Pages 611-617 | Received 08 May 2006, Published online: 08 Jul 2009

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Anna Forsberg, Lars Kjellström, Anna Andreasson, Edgar Jaramillo, Carlos A. Rubio, Erik Björck, Lars Agréus, Nicholas J. Talley & Annika Lindblom. (2015) Colonoscopy findings in high-risk individuals compared to an average-risk control population. Scandinavian Journal of Gastroenterology 50:7, pages 866-874.
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Joseph Sleiman, Natalie Farha, Jonathan Beard, James Bena, Shannon Morrison, Susan Milicia, Brandie Heald, Matthew F. Kalady, James Church, David Liska, Gautam Mankaney & Carol A. Burke. (2023) Incidence and prevalence of advanced colorectal neoplasia in Lynch syndrome. Gastrointestinal Endoscopy 98:3, pages 412-419.e8.
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Alexandra Kavun, Egor Veselovsky, Alexandra Lebedeva, Ekaterina Belova, Olesya Kuznetsova, Valentina Yakushina, Tatiana Grigoreva, Vladislav Mileyko, Mikhail Fedyanin & Maxim Ivanov. (2023) Microsatellite Instability: A Review of Molecular Epidemiology and Implications for Immune Checkpoint Inhibitor Therapy. Cancers 15:8, pages 2288.
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Gergely Buglyó, Jakub Styk, Ondrej Pös, Ádám Csók, Vanda Repiska, Beáta Soltész, Tomas Szemes & Bálint Nagy. (2022) Liquid Biopsy as a Source of Nucleic Acid Biomarkers in the Diagnosis and Management of Lynch Syndrome. International Journal of Molecular Sciences 23:8, pages 4284.
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Xi Li, Guodong Liu & Wei Wu. (2021) Recent advances in Lynch syndrome. Experimental Hematology & Oncology 10:1.
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Aysel Ahadova, Pauline Luise Pfuderer, Maarit Ahtiainen, Alexej Ballhausen, Lena Bohaumilitzky, Svenja Kösegi, Nico Müller, Yee Lin Tang, Kosima Kosmalla, Johannes Witt, Volker Endris, Albrecht Stenzinger, Magnus von Knebel Doeberitz, Hendrik Bläker, Laura Renkonen-Sinisalo, Anna Lepistö, Jan Böhm, Jukka-Pekka Mecklin, Toni T. Seppälä & Matthias Kloor. (2021) Distinct Mutational Profile of Lynch Syndrome Colorectal Cancers Diagnosed under Regular Colonoscopy Surveillance. Journal of Clinical Medicine 10:11, pages 2458.
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Pål Møller. (2020) The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health care. Hereditary Cancer in Clinical Practice 18:1.
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Toni T. Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, Finlay Macrae, D. Gareth Evans, Christina Therkildsen, Julian Sampson, Rodney Scott, John Burn, Gabriela Möslein, Inge Bernstein, Elke Holinski-Feder, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepistö, Charlotte Kvist Lautrup, Annika Lindblom, John-Paul Plazzer, Ingrid Winship, Douglas Tjandra, Lior H. Katz, Stefan Aretz, Robert Hüneburg, Stefanie Holzapfel, Karl Heinimann, Adriana Della Valle, Florencia Neffa, Nathan Gluck, Wouter H. de Vos tot Nederveen Cappel, Hans Vasen, Monika Morak, Verena Steinke-Lange, Christoph Engel, Nils Rahner, Wolff Schmiegel, Deepak Vangala, Huw Thomas, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Gabriel Capella, Marta Pineda, Matilde Navarro, Ignacio Blanco, Sanne ten Broeke, Maartje Nielsen, Ken Ljungmann, Sigve Nakken, Noralane Lindor, Ian Frayling, Eivind Hovig, Lone Sunde, Matthias Kloor, Jukka-Pekka Mecklin, Mette Kalager & Pål Møller. (2019) Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report. Hereditary Cancer in Clinical Practice 17:1.
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Toni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, Heikki Järvinen, Laura Renkonen-Sinisalo, Inge Bernstein, Elke Holinski-Feder, Paola Sala, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons, Jacqueline Jeffries, Hans Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark Jenkins, Maurizio Genuardi, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Ian M. Frayling, John-Paul Plazzer, Julian R. Sampson, Gabriel Capella, Gabriela Möslein, Jukka-Pekka Mecklin & Pål Møller. (2017) Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report. Hereditary Cancer in Clinical Practice 15:1.
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Pål Møller, Toni Seppälä, Inge Bernstein, Elke Holinski-Feder, Paola Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons, Jacqueline Jeffries, Hans Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Laura Renkonen-Sinisalo, Ian M Frayling, John-Paul Plazzer, Kirsi Pylvanainen, Julian R Sampson, Gabriel Capella, Jukka-Pekka Mecklin & Gabriela Möslein. (2017) Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. Gut 66:3, pages 464-472.
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Stephanie A. Cohen. (2013) Current Lynch Syndrome Tumor Screening Practices: A Survey of Genetic Counselors. Journal of Genetic Counseling 23:1, pages 38-47.
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O. Caron, E. Consolino & D. Malka. (2011) Consultation d'oncogénétique digestive. EMC - Gastro-entérologie 6:1, pages 1-12.
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Ilaria Esposito, Mario de Bellis, Annalisa de Leone, Giovan Battista Rossi, Francesco Selvaggi, Massimo Di Maio, Dario Musto, Maura C. Tracey, Pietro Marone, Pasquale Esposito, Alfonso Tempesta & Gabriele Riegler. (2010) Endoscopic surveillance for hereditary non-polyposis colorectal cancer (HNPCC) family members in a Southern Italian region. Digestive and Liver Disease 42:10, pages 698-703.
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Steffen Bülow & Inge Bernstein. 2010. Hereditary Colorectal Cancer. Hereditary Colorectal Cancer 595 612 .
Hans F. A. Vasen & J. C. H. Hardwick. 2010. Hereditary Colorectal Cancer. Hereditary Colorectal Cancer 271 299 .
Eli Marie Grindedal, Pål Møller, Ros Eeles, Astrid Tenden Stormorken, Inger Marie Bowitz-Lothe, Stefan Magnus Landrø, Neal Clark, Rune Kvåle, Susan Shanley & Lovise Mæhle. (2009) Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer. Cancer Epidemiology, Biomarkers & Prevention 18:9, pages 2460-2467.
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Eli Marie Grindedal, Ignacio Blanco, Astrid Stormorken, Lovise Maehle, Neal Clark, Sara González, Gabriel Capella, Hans Vasen, John Burn & Pål Møller. (2008) High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers. Familial Cancer 8:2, pages 145-151.
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