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Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report

BACKGROUND: We previously reported that in pathogenic mismatch repair (path_MMR) variant carriers, the incidence of colorectal cancer (CRC) was not reduced when colonoscopy was undertaken more frequently than once every 3 years, and that CRC stage and interval since last colonoscopy were not correla...

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Autores principales: Dominguez-Valentin, Mev, Seppälä, Toni T., Sampson, Julian R., Macrae, Finlay, Winship, Ingrid, Evans, D. Gareth, Scott, Rodney J., Burn, John, Möslein, Gabriela, Bernstein, Inge, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, 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, Rønlund, 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, Knebel Doeberitz, Magnus v, Ahadova, Aysel, Lindor, Noralane, Steinke-Lange, Verena, Holinski-Feder, Elke, Mecklin, Jukka-Pekka, Møller, Pål
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792227/
https://www.ncbi.nlm.nih.gov/pubmed/31636762
http://dx.doi.org/10.1186/s13053-019-0127-3
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author Dominguez-Valentin, Mev
Seppälä, Toni T.
Sampson, Julian R.
Macrae, Finlay
Winship, Ingrid
Evans, D. Gareth
Scott, Rodney J.
Burn, John
Möslein, Gabriela
Bernstein, Inge
Pylvänäinen, Kirsi
Renkonen-Sinisalo, Laura
Lepistö, 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
Rønlund, 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
Knebel Doeberitz, Magnus v
Ahadova, Aysel
Lindor, Noralane
Steinke-Lange, Verena
Holinski-Feder, Elke
Mecklin, Jukka-Pekka
Møller, Pål
author_facet Dominguez-Valentin, Mev
Seppälä, Toni T.
Sampson, Julian R.
Macrae, Finlay
Winship, Ingrid
Evans, D. Gareth
Scott, Rodney J.
Burn, John
Möslein, Gabriela
Bernstein, Inge
Pylvänäinen, Kirsi
Renkonen-Sinisalo, Laura
Lepistö, 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
Rønlund, 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
Knebel Doeberitz, Magnus v
Ahadova, Aysel
Lindor, Noralane
Steinke-Lange, Verena
Holinski-Feder, Elke
Mecklin, Jukka-Pekka
Møller, Pål
author_sort Dominguez-Valentin, Mev
collection PubMed
description BACKGROUND: We previously reported that in pathogenic mismatch repair (path_MMR) variant carriers, the incidence of colorectal cancer (CRC) was not reduced when colonoscopy was undertaken more frequently than once every 3 years, and that CRC stage and interval since last colonoscopy were not correlated. METHODS: The Prospective Lynch Syndrome Database (PLSD) that records outcomes of surveillance was examined to determine survival after colon cancer in relation to the time since previous colonoscopy and pathological stage. Only path_MMR variants scored by the InSiGHT variant database as class 4 or 5 (clinically actionable) were included in the analysis. RESULTS: Ninety-nine path_MMR carriers had no cancer prior to or at first colonoscopy, but subsequently developed colon cancer. Among these, 96 were 65 years of age or younger at diagnosis, and included 77 path_MLH1, 17 path_MSH2, and 2 path_MSH6 carriers. The number of cancers detected within < 1.5, 1.5–2.5, 2.5–3.5 and at > 3.5 years after previous colonoscopy were 9, 43, 31 and 13, respectively. Of these, 2, 8, 4 and 3 were stage III, respectively, and only one stage IV (interval 2.5–3.5 years) disease. Ten-year crude survival after colon cancer were 93, 94 and 82% for stage I, II and III disease, respectively (p < 0.001). Ten-year crude survival when the last colonoscopy had been < 1.5, 1.5–2.5, 2.5–3.5 or > 3.5 years before diagnosis, was 89, 90, 90 and 92%, respectively (p = 0.91). CONCLUSIONS: In path_MLH1 and path_MSH2 carriers, more advanced colon cancer stage was associated with poorer survival, whereas time since previous colonoscopy was not. Although the numbers are limited, together with our previously reported findings, these results may be in conflict with the view that follow-up of path_MMR variant carriers with colonoscopy intervals of less than 3 years provides significant benefit.
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spelling pubmed-67922272019-10-21 Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report Dominguez-Valentin, Mev Seppälä, Toni T. Sampson, Julian R. Macrae, Finlay Winship, Ingrid Evans, D. Gareth Scott, Rodney J. Burn, John Möslein, Gabriela Bernstein, Inge Pylvänäinen, Kirsi Renkonen-Sinisalo, Laura Lepistö, 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 Rønlund, 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 Knebel Doeberitz, Magnus v Ahadova, Aysel Lindor, Noralane Steinke-Lange, Verena Holinski-Feder, Elke Mecklin, Jukka-Pekka Møller, Pål Hered Cancer Clin Pract Research BACKGROUND: We previously reported that in pathogenic mismatch repair (path_MMR) variant carriers, the incidence of colorectal cancer (CRC) was not reduced when colonoscopy was undertaken more frequently than once every 3 years, and that CRC stage and interval since last colonoscopy were not correlated. METHODS: The Prospective Lynch Syndrome Database (PLSD) that records outcomes of surveillance was examined to determine survival after colon cancer in relation to the time since previous colonoscopy and pathological stage. Only path_MMR variants scored by the InSiGHT variant database as class 4 or 5 (clinically actionable) were included in the analysis. RESULTS: Ninety-nine path_MMR carriers had no cancer prior to or at first colonoscopy, but subsequently developed colon cancer. Among these, 96 were 65 years of age or younger at diagnosis, and included 77 path_MLH1, 17 path_MSH2, and 2 path_MSH6 carriers. The number of cancers detected within < 1.5, 1.5–2.5, 2.5–3.5 and at > 3.5 years after previous colonoscopy were 9, 43, 31 and 13, respectively. Of these, 2, 8, 4 and 3 were stage III, respectively, and only one stage IV (interval 2.5–3.5 years) disease. Ten-year crude survival after colon cancer were 93, 94 and 82% for stage I, II and III disease, respectively (p < 0.001). Ten-year crude survival when the last colonoscopy had been < 1.5, 1.5–2.5, 2.5–3.5 or > 3.5 years before diagnosis, was 89, 90, 90 and 92%, respectively (p = 0.91). CONCLUSIONS: In path_MLH1 and path_MSH2 carriers, more advanced colon cancer stage was associated with poorer survival, whereas time since previous colonoscopy was not. Although the numbers are limited, together with our previously reported findings, these results may be in conflict with the view that follow-up of path_MMR variant carriers with colonoscopy intervals of less than 3 years provides significant benefit. BioMed Central 2019-10-14 /pmc/articles/PMC6792227/ /pubmed/31636762 http://dx.doi.org/10.1186/s13053-019-0127-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dominguez-Valentin, Mev
Seppälä, Toni T.
Sampson, Julian R.
Macrae, Finlay
Winship, Ingrid
Evans, D. Gareth
Scott, Rodney J.
Burn, John
Möslein, Gabriela
Bernstein, Inge
Pylvänäinen, Kirsi
Renkonen-Sinisalo, Laura
Lepistö, 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
Rønlund, 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
Knebel Doeberitz, Magnus v
Ahadova, Aysel
Lindor, Noralane
Steinke-Lange, Verena
Holinski-Feder, Elke
Mecklin, Jukka-Pekka
Møller, Pål
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title_full Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title_fullStr Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title_full_unstemmed Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title_short Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
title_sort survival by colon cancer stage and screening interval in lynch syndrome: a prospective lynch syndrome database report
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792227/
https://www.ncbi.nlm.nih.gov/pubmed/31636762
http://dx.doi.org/10.1186/s13053-019-0127-3
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