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

被引：0

作者：

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

机构：

[1] Helsinki University Central Hospital,Department of Surgery

[2] University of Helsinki,Department of Tumor Biology, Institute of Cancer Research

[3] Heidelberg University Hospital and DKFZ,Department of Medical Genetics, The Norwegian Radium Hospital

[4] The Norwegian Radium Hospital,Medical Genetics

[5] part of Oslo University Hospital,Dept. of Surgical Gastroenterology

[6] Oslo University Hospital,Department of Clinical Genetics

[7] The Royal Melbourne Hospital,Institute of Human Genetics

[8] University of Melbourne,Department of Internal Medicine I

[9] University of Manchester & Manchester University Hospitals Foundation Trust,Center for Hereditary Tumor Syndromes

[10] The Danish HNPCC Register,Institute for Medical Genetics and Pathology

[11] Clinical Research Centre,Department of Gastroenterology and Hepatology

[12] Copenhagen University Hospital,Department of Gastroenterology and Hepatology

[13] Cardiff University,Institute for Medical Informatics, Statistics and Epidemiology

[14] University of Newcastle and the Hunter Medical Research Institute,Medical School, Institute of Human Genetics

[15] University of Newcastle,Department of Medicine, Knappschaftskrankenhaus

[16] University Witten-Herdecke,St Mark’s Hospital, Department of Surgery and Cancer

[17] Aalborg University Hospital,Department of Surgical Gastroenterology

[18] Medizinische Klinik und Poliklinik IV,Department of Health Sciences Research

[19] Campus Innenstadt,Center for Bioinformatics, Department of Informatics

[20] Klinikum der Universität München,Department of Medical Genetics

[21] MGZ- Medical Genetics Center,Department of Surgery

[22] Central Finland Central Hospital,Faculty of Sport and Health Sciences

[23] Education and Research,undefined

[24] Aalborg University Hospital,undefined

[25] Karolinska Institutet,undefined

[26] Hadassah Medical Center,undefined

[27] Jerusalem,undefined

[28] and Sheba Medical Center,undefined

[29] University of Bonn,undefined

[30] University Hospital Bonn,undefined

[31] University Hospital Bonn,undefined

[32] University Hospital Basel,undefined

[33] Hospital Fuerzas Armadas,undefined

[34] Grupo Colaborativo Uruguayo,undefined

[35] Investigación de Afecciones Oncológicas Hereditarias (GCU),undefined

[36] Tel-Aviv Soursky Medical Center,undefined

[37] Isala Clinics,undefined

[38] Leiden University Medical Centre,undefined

[39] University of Leipzig,undefined

[40] Heinrich-Heine-University,undefined

[41] Ruhr-University Bochum,undefined

[42] Imperial College London,undefined

[43] University of Manchester and St Mary’s Hospital,undefined

[44] Hereditary Cancer Program,undefined

[45] Catalan Institute of Oncology,undefined

[46] Insititut d’Investigació Biomèdica de Bellvitge (IDIBELL),undefined

[47] ONCOBELL Program,undefined

[48] L’Hospitalet de Llobregat,undefined

[49] Centro de Investigación Biomédica en Red de Cáncer (CIBERONC),undefined

[50] University Medical Center Groningen,undefined

来源：

Hereditary Cancer in Clinical Practice | / 17卷

关键词：

Mismatch repair; Microsatellite instability; Lynch syndrome; Hereditary cancer; Colorectal cancer; Hereditary nonpolyposis colorectal cancer; Colonoscopy; Endoscopy; Surveillance; Screening; Over-diagnosis;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

共 50 条

[1] 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
Seppala, Toni T.
Ahadova, Aysel
Dominguez-Valentin, Mev
Macrae, Finlay
Evans, D. Gareth
Therkildsen, Christina
Sampson, Julian
Scott, Rodney
Burn, John
Moeslein, Gabriela
Bernstein, Inge
Holinski-Feder, Elke
Pylvanainen, Kirsi
Renkonen-Sinisalo, Laura
Lepisto, Anna
Lautrup, Charlotte Kvist
Lindblom, Annika
Plazzer, John-Paul
Winship, Ingrid
Tjandra, Douglas
Katz, Lior H.
Aretz, Stefan
Hueneburg, Robert
Holzapfel, Stefanie
Heinimann, Karl
Della Valle, Adriana
Neffa, Florencia
Gluck, Nathan
Cappel, Wouter H. de Vos Tot Nederveen
Vasen, Hans
Morak, Monika
Steinke-Lange, Verena
Engel, Christoph
Rahner, Nils
Schmiegel, Wolff
Vangala, Deepak
Thomas, Huw
Green, Kate
Lalloo, Fiona
Crosbie, Emma J.
Hill, James
Capella, Gabriel
Pineda, Marta
Navarro, Matilde
Blanco, Ignacio
ten Broeke, Sanne
Nielsen, Maartje
Ljungmann, Ken
Nakken, Sigve
Lindor, Noralane
HEREDITARY CANCER IN CLINICAL PRACTICE, 2019, 17 (1)
[2] Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
Mev Dominguez-Valentin
Toni T. Seppälä
Julian R. Sampson
Finlay Macrae
Ingrid Winship
D. Gareth Evans
Rodney J. Scott
John Burn
Gabriela Möslein
Inge Bernstein
Kirsi Pylvänäinen
Laura Renkonen-Sinisalo
Anna Lepistö
Annika Lindblom
John-Paul Plazzer
Douglas Tjandra
Huw Thomas
Kate Green
Fiona Lalloo
Emma J. Crosbie
James Hill
Gabriel Capella
Marta Pineda
Matilde Navarro
Joan Brunet Vidal
Karina Rønlund
Randi Thyregaard Nielsen
Mette Yilmaz
Louise Laurberg Elvang
Lior Katz
Maartje Nielsen
Sanne W. ten Broeke
Sigve Nakken
Eivind Hovig
Lone Sunde
Matthias Kloor
Magnus v Knebel Doeberitz
Aysel Ahadova
Noralane Lindor
Verena Steinke-Lange
Elke Holinski-Feder
Jukka-Pekka Mecklin
Pål Møller
Hereditary Cancer in Clinical Practice, 17
[3] Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
Dominguez-Valentin, Mev
Seppala, Toni T.
Sampson, Julian R.
Macrae, Finlay
Winship, Ingrid
Evans, D. Gareth
Scott, Rodney J.
Burn, John
Moeslein, Gabriela
Bernstein, Inge
Pylvanainen, Kirsi
Renkonen-Sinisalo, Laura
Lepistoe, Anna
Lindblom, Annika
Plazzer, John-Paul
Tjandra, Douglas
Thomas, Huw
Green, Kate
Lalloo, Fiona
Crosbie, Emma J.
Hill, James
Capella, Gabriel
Pineda, Marta
Navarro, Matilde
Vidal, Joan Brunet
Ronlund, Karina
Nielsen, Randi Thyregaard
Yilmaz, Mette
Elvang, Louise Laurberg
Katz, Lior
Nielsen, Maartje
ten Broeke, Sanne W.
Nakken, Sigve
Hovig, Eivind
Sunde, Lone
Kloor, Matthias
Doeberitz, Magnus von Knebel
Ahadova, Aysel
Lindor, Noralane
Steinke-Lange, Verena
Holinski-Feder, Elke
Mecklin, Jukka-Pekka
Moller, Pal
HEREDITARY CANCER IN CLINICAL PRACTICE, 2019, 17 (01)
[4] Screening and diagnosis of endometrial cancer in Lynch syndrome
Caroline Cornou
Anne Sophie Bats
Charlotte Ngo
Léa Rossi
Perrine Capmas
Pierre Laurent-Puig
Chérazade Bensaid
Claude Nos
Marie Aude Lefrère-Belda
Fabrice Lécuru
World Journal of Obstetrics and Gynecology, 2016, (04) : 218 - 225
[5] Interval between the First Cancer and the Genetic Diagnosis in Lynch Syndrome Probands
Yamashita, Kentaro
Fukushima, Hisayo
Teramoto, Mizue
Okita, Kenji
Ishikawa, Aki
Sakurai, Akihiro
Akagi, Kiwamu
Nakase, Hiroshi
INTERNAL MEDICINE, 2021, 60 (17) : 2719 - 2724
[6] Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
Moller, Pal
Seppala, Toni
Bernstein, Inge
Holinski-Feder, Elke
Sala, Paola
Evans, D. Gareth
Lindblom, Annika
Macrae, Finlay
Blanco, Ignacio
Sijmons, Rolf
Jeffries, Jacqueline
Vasen, Hans
Burn, John
Nakken, Sigve
Hovig, Eivind
Rodland, Einar Andreas
Tharmaratnam, Kukatharmini
Cappel, Wouter H. de Vos Tot Nederveen
Hill, James
Wijnen, Juul
Green, Kate
Lalloo, Fiona
Sunde, Lone
Mints, Miriam
Bertario, Lucio
Pineda, Marta
Navarro, Matilde
Morak, Monika
Renkonen-Sinisalo, Laura
Frayling, Ian M.
Plazzer, John-Paul
Pylvanainen, Kirsi
Sampson, Julian R.
Capella, Gabriel
Mecklin, Jukka-Pekka
Moslein, Gabriela
GUT, 2017, 66 (03) : 464 - 472
[7] The "scope" of colorectal cancer screening in Lynch syndrome: is there an optimal interval?
Biller, Leah H.
Ng, Kimmie
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2023, 115 (07): : 775 - 777
[8] Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Pål Møller
Toni Seppälä
James G. Dowty
Saskia Haupt
Mev Dominguez-Valentin
Lone Sunde
Inge Bernstein
Christoph Engel
Stefan Aretz
Maartje Nielsen
Gabriel Capella
Dafydd Gareth Evans
John Burn
Elke Holinski-Feder
Lucio Bertario
Bernardo Bonanni
Annika Lindblom
Zohar Levi
Finlay Macrae
Ingrid Winship
John-Paul Plazzer
Rolf Sijmons
Luigi Laghi
Adriana Della Valle
Karl Heinimann
Elizabeth Half
Francisco Lopez-Koestner
Karin Alvarez-Valenzuela
Rodney J. Scott
Lior Katz
Ido Laish
Elez Vainer
Carlos Alberto Vaccaro
Dirce Maria Carraro
Nathan Gluck
Naim Abu-Freha
Aine Stakelum
Rory Kennelly
Des Winter
Benedito Mauro Rossi
Marc Greenblatt
Mabel Bohorquez
Harsh Sheth
Maria Grazia Tibiletti
Leonardo S. Lino-Silva
Karoline Horisberger
Carmen Portenkirchner
Ivana Nascimento
Norma Teresa Rossi
Leandro Apolinário da Silva
Hereditary Cancer in Clinical Practice, 20
[9] Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Moller, Pal
Seppala, Toni
Dowty, James G.
Haupt, Saskia
Dominguez-Valentin, Mev
Sunde, Lone
Bernstein, Inge
Engel, Christoph
Aretz, Stefan
Nielsen, Maartje
Capella, Gabriel
Evans, Dafydd Gareth
Burn, John
Holinski-Feder, Elke
Bertario, Lucio
Bonanni, Bernardo
Lindblom, Annika
Levi, Zohar
Macrae, Finlay
Winship, Ingrid
Plazzer, John-Paul
Sijmons, Rolf
Laghi, Luigi
Della Valle, Adriana
Heinimann, Karl
Half, Elizabeth
Lopez-Koestner, Francisco
Alvarez-Valenzuela, Karin
Scott, Rodney J.
Katz, Lior
Laish, Ido
Vainer, Elez
Vaccaro, Carlos Alberto
Carraro, Dirce Maria
Gluck, Nathan
Abu-Freha, Naim
Stakelum, Aine
Kennelly, Rory
Winter, Des
Rossi, Benedito Mauro
Greenblatt, Marc
Bohorquez, Mabel
Sheth, Harsh
Tibiletti, Maria Grazia
Lino-Silva, Leonardo S.
Horisberger, Karoline
Portenkirchner, Carmen
Nascimento, Ivana
Rossi, Norma Teresa
da Silva, Leandro Apolinario
HEREDITARY CANCER IN CLINICAL PRACTICE, 2022, 20 (01)
[10] Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤70 years
Leenen, Celine H. M.
van Lier, Margot G. F.
van Doorn, Helena C.
van Leerdam, Monique E.
Kooi, Sjarlot G.
de Waard, Judith
Hoedemaeker, Robert F.
van den Ouweland, Ans M. W.
Hulspas, Sanne M.
Dubbink, Hendrikus J.
Kuipers, Ernst J.
Wagner, Anja
Dinjens, Winand N. M.
Steyerberg, Ewout W.
GYNECOLOGIC ONCOLOGY, 2012, 125 (02) : 414 - 420

← 1 2 3 4 5 →