Abstract
The first International Workshop of the ATM and Cancer Risk group focusing on the role of Ataxia-Telangiectasia Mutated (ATM) gene in cancer was held on December 4 and 5, 2019 at Institut Curie in Paris, France. It was motivated by the fact that germline ATM pathogenic variants have been found to be associated with different cancer types. However, due to the lack of precise age-, sex-, and site-specific risk estimates, no consensus on management guidelines for variant carriers exists, and the clinical utility of ATM variant testing is uncertain. The meeting brought together epidemiologists, geneticists, biologists and clinicians to review current knowledge and on-going challenges related to ATM and cancer risk. This report summarizes the meeting sessions content that covered the latest results in family-based and population-based studies, the importance of accurate variant classification, the effect of radiation exposures for ATM variant carriers, and the characteristics of ATM-deficient tumors. The report concludes that ATM variant carriers outside of the context of Ataxia-Telangiectasia may benefit from effective cancer risk management and therapeutic strategies and that efforts to set up large-scale studies in the international framework to achieve this goal are necessary.
Original language | English (US) |
---|---|
Pages (from-to) | 211-227 |
Number of pages | 17 |
Journal | Familial Cancer |
Volume | 21 |
Issue number | 2 |
DOIs | |
State | Published - Apr 2022 |
Keywords
- ATM
- Cancer risk
- Cancer spectrum
- Tumor profiles
- Variants classification
ASJC Scopus subject areas
- Genetics
- Oncology
- Genetics(clinical)
- Cancer Research
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In: Familial Cancer, Vol. 21, No. 2, 04.2022, p. 211-227.
Research output: Contribution to journal › Review article › peer-review
}
TY - JOUR
T1 - First international workshop of the ATM and cancer risk group (4-5 December 2019)
AU - Spanish ATM working group
AU - GC-HBOC
AU - CARRIERS and Ambry Groups
AU - Lesueur, Fabienne
AU - Easton, Douglas F.
AU - Renault, Anne Laure
AU - Tavtigian, Sean V.
AU - Bernstein, Jonine L.
AU - Kote-Jarai, Zsofia
AU - Eeles, Rosalind A.
AU - Plaseska-Karanfia, Dijana
AU - Feliubadaló, Lidia
AU - Moles-Fernández, Alejandro
AU - Santamariña-Pena, Marta
AU - Sánchez, Alysson T.
AU - López-Novo, Anael
AU - Porras, Luz Marina
AU - Blanco, Ana
AU - Capellá, Gabriel
AU - de la Hoya, Miguel
AU - Molina, Ignacio J.
AU - Osorio, Ana
AU - Pineda, Marta
AU - Rueda, Daniel
AU - de la Cruz, Xavier
AU - Diez, Orland
AU - Ruiz-Ponte, Clara
AU - Gutiérrez-Enríquez, Sara
AU - Vega, Ana
AU - Lázaro, Conxi
AU - Arun, Banu
AU - Herold, Natalie
AU - Versmold, Beatrix
AU - Schmutzler, Rita Katharina
AU - Nguyen-Dumont, Tú
AU - Southey, Melissa C.
AU - Dorling, Leila
AU - Dunning, Alison M.
AU - Ghiorzo, Paola
AU - Dalmasso, Bruna Samia
AU - Cavaciuti, Eve
AU - Le Gal, Dorothée
AU - Roberts, Nicholas J.
AU - Dominguez-Valentin, Mev
AU - Rookus, Matti
AU - Taylor, Alexander M.R.
AU - Goldstein, Alisa M.
AU - Goldgar, David E.
AU - Couch, Fergus
AU - Kraft, Peter
AU - Weitzel, Jeffrey
AU - Nathanson, Kate
AU - Domchek, Susan
N1 - Funding Information: We thank AT EUROPE, Association Pour la Recherche sur l’Ataxie-Télangiectasie (APRAT), GENETICANCER, Association pour la Recherche sur le Cancer (ARC), ROCHE, DNA GenoTek, Agilent and Institut Curie for supporting this workshop. We also thank Janet Hall, Juliette Coignard, Gaëlle Bellière-Dahan and the staff from the Genetic Epidemiology of Cancer team (U900) for their help in preparing it. TN-D acknowledges the National Breast Cancer Foundation (Australia) Career Development Fellow (ECF-17-001). MCS is a National Health and Medical Research Council (NMHRC, Australia) Senior Research Fellow (APP1155163). AMG’s participation was supported by the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics. MD-V acknowledges The Norwegian Cancer Society, contract 194751-2017, for funding. RE and ZKJ acknowledge the support of the NIHR to the Biomedical Research Centre at The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, UK. PG and BD thank the LILT; Lega Italiana per la Lotta Contro I Tumori, IG2019, for funding. LF was supported by the Carlos III National Institute of Health funded by 19 FEDER funds – a way to build Europe – [PI19/00553; PI16/00563; PI16/01898; SAF2015-68016-R and CIBERONC] and by the Government of Catalonia [Pla estratègic de recerca i innovació en salut (PERIS_MedPerCan and URDCat projects), 2017SGR1282, 2017SGR496 and CERCA Program (institutional support)]. Spanish ATM working group: Lidia Feliubadaló, Alejandro Moles‐Fernández, Marta Santamariña-Pena, Alysson T. Sánchez, Anael López-Novo, Luz-Marina Porras, Ana Blanco, Gabriel Capellá, Miguel de la Hoya, Ignacio J. Molina, Ana Osorio, Marta Pineda, Daniel Rueda, Xavier de la Cruz, Orland Diez, Clara Ruiz-Ponte, Sara Gutiérrez-Enríquez, Ana Vega, Conxi Lázaro. Norwegian working group: Sigve Nakken, Pål Moller, Eivind Hovig Ambry Group: Holly LaDuca. CARRIERS Group: Fergus Couch, Peter Kraft, Jeffrey Weitzel, Kate Nathanson, Susan Domchek German Consortium of Hereditary Breast- and Ovarian Cancer (GC-HBOC): Rita Katharina Schmutzler, Ulrich Bick, Dorothee Speiser, Dieter Niederacher, Tanja Fehm, Cornelia Meisel, Evelin Schröck, Matthias W. Beckmann, Christine Solbach, Judith Fischer, Julia Gallwas, Ute Felbor, Christoph Thomssen, Isabell Witzel, Gunnar Schmidt, Christian P. Schaaf, Norbert Arnold, Susanne Briest, Susann Schweiger, Marion Kiechle, Anne Quante, Nadia Harbeck, Sven Mahner, Ulrike Siebers-Renelt, Bernhard H. F. Weber, Olaf Rieß, Wolfgang Janni, Thomas Haaf, Reinhard Büttner, Christoph Engel. List of workshop attendees Aissaoui Hanaa (Agilent, France), Anchisi Cédric (AT Europe, France), Andreassen Paul R. (Cincinnati Children’s Hospital Medical Center, USA), Andrieu Nadine (Inserm U900 - Institut Curie, Paris, France), Arun Banu (The University of Texas MD Anderson Cancer Center, Houston, USA), Balmaña Gelpi Judith (Vall d’Hebron University Hospital, Barcelona, Spain), Beauvallet Juana (Inserm U900 - Institut Curie, Paris, France), Bellière Dahan Gaëlle (Inserm U900 - Institut Curie, Paris, France), Béra Odile (CHUM, Fort de France, Martinique), Bernstein L. Jonine (Memorial Sloan Kettering Cancer Center, New York, USA), Bonnet-Boissinot Sarah (Inserm U900 - Institut Curie, Paris, France), Brayotel Fanny (Institut Godinot, Reims, France), Bressac-de Paillerets Brigitte (Gustave Roussy, Villejuif, France), Caldes Trinidad (Spanish Ministery of Health, Madrid, Spain), Caputo Sandrine (Institut Curie, Paris, France), Caron Olivier (Gustave Roussy Hôpital Universitaire, Villejuif, France), Cavaciuti Eve (Inserm U900 - Institut Curie, Paris, France), Chen-Shtoyerman Rakefet (Kaplan Medical Center; Barzilai Medical Center; Herzelia Medical Center, Rehovot, Israel), Cohen-Haguenauer Odile (APHP-Paris University, Paris, France), Coignard Juliette (Inserm U900 - Institut Curie, Paris, France), Colas Chrystelle (Institut Curie, Paris, France), Collée Margriet (Eramus University Medical Center, Rotterdam, Netherlands), Corsini Carole (Montpellier Hospital, France), Couch Fergus (Mayo clinic, Rochester, USA), Coupier Isabelle (CHU, Montpellier, France), Cusin Veronica (Hôpital Pitié-Salpêtrière, Paris, France), Dalmasso Bruna Samia (University of Genoa, Liguria, Italy), De la Hoya Miguel (Academic Hospital San Carlos, Madrid, Spain), De Pauw Antoine (Institut Curie, Paris, France), Delhomelle Hélène (Institut Curie, Paris, France), Denkey Fafa (Inserm U900 - Institut Curie, Paris, France), Dominguez Valentin Mev (Oslo University Hospital, Norway), Dondon Marie-Gabrielle (Inserm U900 - Institut Curie, Paris, France), Dorling Leila (University of Cambridge, United Kingdom), Dunning Alison (University of Cambridge, United Kingdom), Easton Douglas (University of Cambridge, United Kingdom), Eeles Rosalind (The Institute of Cancer Research, Sutton, United Kingdom), Eon-Marchais Séverine (Inserm U900 - Institut Curie, Paris, France ), Feliubadaló Lidia (Catalan Institute of Oncology, Madrid, Spain), Ghiorzo Paola (University of Genoa and Ospedale, Policlinico San Martino, Genoa), Goldgar David (Huntsman Cancer Institute, Salt Lake City, USA), Goldstein Alisa (National Institute of Health, Bethesda, USA), Grangier Anaïs (CHU Limoges, France), Gutierrez-Enriquez Sara (Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain), Hall Janet (Inserm, Lyon, France), Herold Natalie (University Hospital Cologne, Center for Hereditary Breast and Ovarian Cancer, Germany), Hirasawa Akira (Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Japan), Imbert-Bouteille Marion (CHU Montpellier, Herault, France), Ingster Olivier (CHU Angers, France), Jiao Yue (Inserm U900 - Institut Curie, Paris, France), Kets C. Marleen (Antoni van Leeuwenhoek Hospital, Amsterdam, Netherlands), Konstantopoulou Irene (NCSR Demokritos, Attika, Greece), Kote-Jarai Zsofia (The Institute of Cancer Research, Sutton, United Kingdom), Lázaro Conxi (Catalan Institute of Oncology, L’Hospitalet de Llobregat, Spain), Le Gal Dorothée (Inserm U900 - Institut Curie, Paris, France ), Le Mentec Marine (Institut Curie, Paris, France), Leman Raphaël (Centre François Baclesse, Caen), Lenoir Gilbert (Cancer Campus, Villejuif, France), Lesueur Fabienne (Inserm U900 - Institut Curie, Paris, France), Longy Michel (Institut Bergonié - CLCC Bordeaux, France), Macquere Pierre (Institut Bergonié, Bordeaux, France), Martins Alexandra (Inserm, Rouen, France), Mebirouk Noura (Inserm U900 - Institut Curie, Paris, France), Michailidou Kyriaki (The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus), Moghadasi Setareh (Leiden University Medical Center, Zuid Holland, Netherlands), Mouret-Fourme Emmanuelle (Institut Curie, Paris, France), Nambot Sophie (CHU Dijon, Bourgogne, France), Nguyen Tan Dat (Institut de cancérologie Godinot, Reims, France), Nguyen-Dumont Tú (Monash University, Clayton, Australia), Nicolas Alain (Institut Curie, Paris, France), Nogues Catherine (Institut Paoli Calmettes, Marseille, France), Petrilli Virginie (CNRS, Lyon, France), Plaseska-Karanfilska Dijana (Macedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia), Popovici Cornel (Institut Paoli-Calmettes, Marseille, France), Renault Anne-Laure (Monash University, Clayton, Australia), Revel Claude (Agilent, France), Roberts Nicholas (The Johns Hopkins University, Maryland, USA), Rookus Matti (Netherlands Cancer Institute NKI, Amsterdam, The Netherlands), Rouleau Etienne (Gustave Roussy, Villejuif, France), Sabraoui Dany (DNA GENOTEK, Ottawa, Canada), Santana Elizabeth (Hospital Sirio-Libanes, Sao Paulo, Brazil), Saule Claire (Institut Curie, Paris, France), Sevenet Nicolas (Université de Bordeaux et Institut Bergonié, France, Bordeaux), Southey Melissa (Monash University, Clayton, Australia), Stoppa-Lyonnet Dominique (Institut Curie, Paris, France), T’Kint Daphné (Jules Bordet Institute, Bruxelles, Belgium), Tan Yen (Medical University of Vienna / Prof Christian Singer, Vienna, Austria), Tavtigian Sean (Huntsman Cancer Institute, Salt Lake City, USA), Taylor Malcolm (Institute of Cancer and Genomic Sciences, University of Birmingham, United Kingdom), Teixeira Manuel (Portuguese Oncology Institute of Porto (IPO Porto), Porto, Portugal), Under Sheila (Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland), Van Asperen Christi (Leiden University Medical Center, Leiden, Netherlands), Vega Ana (Galician Health Service, Santiago de Compostela, A Coruña, Spain), Versmold Beatrix (University Hospital Cologne, Center for Hereditary Breast and Ovarian Cancer, Cologne, Germany), Yannoukakos Drakoulis (National Center for Scientific Research Demokritos, Attiki, Greece). Funding Information: We thank AT EUROPE, Association Pour la Recherche sur l’Ataxie-Télangiectasie (APRAT), GENETICANCER, Association pour la Recherche sur le Cancer (ARC), ROCHE, DNA GenoTek, Agilent and Institut Curie for supporting this workshop. We also thank Janet Hall, Juliette Coignard, Gaëlle Bellière-Dahan and the staff from the Genetic Epidemiology of Cancer team (U900) for their help in preparing it. TN-D acknowledges the National Breast Cancer Foundation (Australia) Career Development Fellow (ECF-17-001). MCS is a National Health and Medical Research Council (NMHRC, Australia) Senior Research Fellow (APP1155163). AMG’s participation was supported by the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics. MD-V acknowledges The Norwegian Cancer Society, contract 194751-2017, for funding. RE and ZKJ acknowledge the support of the NIHR to the Biomedical Research Centre at The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, UK. PG and BD thank the LILT; Lega Italiana per la Lotta Contro I Tumori, IG2019, for funding. LF was supported by the Carlos III National Institute of Health funded by 19 FEDER funds – a way to build Europe – [PI19/00553; PI16/00563; PI16/01898; SAF2015-68016-R and CIBERONC] and by the Government of Catalonia [Pla estratègic de recerca i innovació en salut (PERIS_MedPerCan and URDCat projects), 2017SGR1282, 2017SGR496 and CERCA Program (institutional support)]. Spanish ATM working group: Lidia Feliubadaló, Alejandro Moles‐Fernández, Marta Santamariña-Pena, Alysson T. Sánchez, Anael López-Novo, Luz-Marina Porras, Ana Blanco, Gabriel Capellá, Miguel de la Hoya, Ignacio J. Molina, Ana Osorio, Marta Pineda, Daniel Rueda, Xavier de la Cruz, Orland Diez, Clara Ruiz-Ponte, Sara Gutiérrez-Enríquez, Ana Vega, Conxi Lázaro. Norwegian working group: Sigve Nakken, Pål Moller, Eivind Hovig Ambry Group: Holly LaDuca. CARRIERS Group: Fergus Couch, Peter Kraft, Jeffrey Weitzel, Kate Nathanson, Susan Domchek German Consortium of Hereditary Breast- and Ovarian Cancer (GC-HBOC): Rita Katharina Schmutzler, Ulrich Bick, Dorothee Speiser, Dieter Niederacher, Tanja Fehm, Cornelia Meisel, Evelin Schröck, Matthias W. Beckmann, Christine Solbach, Judith Fischer, Julia Gallwas, Ute Felbor, Christoph Thomssen, Isabell Witzel, Gunnar Schmidt, Christian P. Schaaf, Norbert Arnold, Susanne Briest, Susann Schweiger, Marion Kiechle, Anne Quante, Nadia Harbeck, Sven Mahner, Ulrike Siebers-Renelt, Bernhard H. F. Weber, Olaf Rieß, Wolfgang Janni, Thomas Haaf, Reinhard Büttner, Christoph Engel. List of workshop attendees Aissaoui Hanaa (Agilent, France), Anchisi Cédric (AT Europe, France), Andreassen Paul R. (Cincinnati Children’s Hospital Medical Center, USA), Andrieu Nadine (Inserm U900 - Institut Curie, Paris, France), Arun Banu (The University of Texas MD Anderson Cancer Center, Houston, USA), Balmaña Gelpi Judith (Vall d’Hebron University Hospital, Barcelona, Spain), Beauvallet Juana (Inserm U900 - Institut Curie, Paris, France), Bellière Dahan Gaëlle (Inserm U900 - Institut Curie, Paris, France), Béra Odile (CHUM, Fort de France, Martinique), Bernstein L. Jonine (Memorial Sloan Kettering Cancer Center, New York, USA), Bonnet-Boissinot Sarah (Inserm U900 - Institut Curie, Paris, France), Brayotel Fanny (Institut Godinot, Reims, France), Bressac-de Paillerets Brigitte (Gustave Roussy, Villejuif, France), Caldes Trinidad (Spanish Ministery of Health, Madrid, Spain), Caputo Sandrine (Institut Curie, Paris, France), Caron Olivier (Gustave Roussy Hôpital Universitaire, Villejuif, France), Cavaciuti Eve (Inserm U900 - Institut Curie, Paris, France), Chen-Shtoyerman Rakefet (Kaplan Medical Center; Barzilai Medical Center; Herzelia Medical Center, Rehovot, Israel), Cohen-Haguenauer Odile (APHP-Paris University, Paris, France), Coignard Juliette (Inserm U900 - Institut Curie, Paris, France), Colas Chrystelle (Institut Curie, Paris, France), Collée Margriet (Eramus University Medical Center, Rotterdam, Netherlands), Corsini Carole (Montpellier Hospital, France), Couch Fergus (Mayo clinic, Rochester, USA), Coupier Isabelle (CHU, Montpellier, France), Cusin Veronica (Hôpital Pitié-Salpêtrière, Paris, France), Dalmasso Bruna Samia (University of Genoa, Liguria, Italy), De la Hoya Miguel (Academic Hospital San Carlos, Madrid, Spain), De Pauw Antoine (Institut Curie, Paris, France), Delhomelle Hélène (Institut Curie, Paris, France), Denkey Fafa (Inserm U900 - Institut Curie, Paris, France), Dominguez Valentin Mev (Oslo University Hospital, Norway), Dondon Marie-Gabrielle (Inserm U900 - Institut Curie, Paris, France), Dorling Leila (University of Cambridge, United Kingdom), Dunning Alison (University of Cambridge, United Kingdom), Easton Douglas (University of Cambridge, United Kingdom), Eeles Rosalind (The Institute of Cancer Research, Sutton, United Kingdom), Eon-Marchais Séverine (Inserm U900 - Institut Curie, Paris, France), Feliubadaló Lidia (Catalan Institute of Oncology, Madrid, Spain), Ghiorzo Paola (University of Genoa and Ospedale, Policlinico San Martino, Genoa), Goldgar David (Huntsman Cancer Institute, Salt Lake City, USA), Goldstein Alisa (National Institute of Health, Bethesda, USA), Grangier Anaïs (CHU Limoges, France), Gutierrez-Enriquez Sara (Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain), Hall Janet (Inserm, Lyon, France), Herold Natalie (University Hospital Cologne, Center for Hereditary Breast and Ovarian Cancer, Germany), Hirasawa Akira (Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Japan), Imbert-Bouteille Marion (CHU Montpellier, Herault, France), Ingster Olivier (CHU Angers, France), Jiao Yue (Inserm U900 - Institut Curie, Paris, France), Kets C. Marleen (Antoni van Leeuwenhoek Hospital, Amsterdam, Netherlands), Konstantopoulou Irene (NCSR Demokritos, Attika, Greece), Kote-Jarai Zsofia (The Institute of Cancer Research, Sutton, United Kingdom), Lázaro Conxi (Catalan Institute of Oncology, L’Hospitalet de Llobregat, Spain), Le Gal Dorothée (Inserm U900 - Institut Curie, Paris, France), Le Mentec Marine (Institut Curie, Paris, France), Leman Raphaël (Centre François Baclesse, Caen), Lenoir Gilbert (Cancer Campus, Villejuif, France), Lesueur Fabienne (Inserm U900 - Institut Curie, Paris, France), Longy Michel (Institut Bergonié - CLCC Bordeaux, France), Macquere Pierre (Institut Bergonié, Bordeaux, France), Martins Alexandra (Inserm, Rouen, France), Mebirouk Noura (Inserm U900 - Institut Curie, Paris, France), Michailidou Kyriaki (The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus), Moghadasi Setareh (Leiden University Medical Center, Zuid Holland, Netherlands), Mouret-Fourme Emmanuelle (Institut Curie, Paris, France), Nambot Sophie (CHU Dijon, Bourgogne, France), Nguyen Tan Dat (Institut de cancérologie Godinot, Reims, France), Nguyen-Dumont Tú (Monash University, Clayton, Australia), Nicolas Alain (Institut Curie, Paris, France), Nogues Catherine (Institut Paoli Calmettes, Marseille, France), Petrilli Virginie (CNRS, Lyon, France), Plaseska-Karanfilska Dijana (Macedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia), Popovici Cornel (Institut Paoli-Calmettes, Marseille, France), Renault Anne-Laure (Monash University, Clayton, Australia), Revel Claude (Agilent, France), Roberts Nicholas (The Johns Hopkins University, Maryland, USA), Rookus Matti (Netherlands Cancer Institute NKI, Amsterdam, The Netherlands), Rouleau Etienne (Gustave Roussy, Villejuif, France), Sabraoui Dany (DNA GENOTEK, Ottawa, Canada), Santana Elizabeth (Hospital Sirio-Libanes, Sao Paulo, Brazil), Saule Claire (Institut Curie, Paris, France), Sevenet Nicolas (Université de Bordeaux et Institut Bergonié, France, Bordeaux), Southey Melissa (Monash University, Clayton, Australia), Stoppa-Lyonnet Dominique (Institut Curie, Paris, France), T’Kint Daphné (Jules Bordet Institute, Bruxelles, Belgium), Tan Yen (Medical University of Vienna / Prof Christian Singer, Vienna, Austria), Tavtigian Sean (Huntsman Cancer Institute, Salt Lake City, USA), Taylor Malcolm (Institute of Cancer and Genomic Sciences, University of Birmingham, United Kingdom), Teixeira Manuel (Portuguese Oncology Institute of Porto (IPO Porto), Porto, Portugal), Under Sheila (Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland), Van Asperen Christi (Leiden University Medical Center, Leiden, Netherlands), Vega Ana (Galician Health Service, Santiago de Compostela, A Coruña, Spain), Versmold Beatrix (University Hospital Cologne, Center for Hereditary Breast and Ovarian Cancer, Cologne, Germany), Yannoukakos Drakoulis (National Center for Scientific Research Demokritos, Attiki, Greece). Publisher Copyright: © 2021, The Author(s), under exclusive licence to Springer Nature B.V.
PY - 2022/4
Y1 - 2022/4
N2 - The first International Workshop of the ATM and Cancer Risk group focusing on the role of Ataxia-Telangiectasia Mutated (ATM) gene in cancer was held on December 4 and 5, 2019 at Institut Curie in Paris, France. It was motivated by the fact that germline ATM pathogenic variants have been found to be associated with different cancer types. However, due to the lack of precise age-, sex-, and site-specific risk estimates, no consensus on management guidelines for variant carriers exists, and the clinical utility of ATM variant testing is uncertain. The meeting brought together epidemiologists, geneticists, biologists and clinicians to review current knowledge and on-going challenges related to ATM and cancer risk. This report summarizes the meeting sessions content that covered the latest results in family-based and population-based studies, the importance of accurate variant classification, the effect of radiation exposures for ATM variant carriers, and the characteristics of ATM-deficient tumors. The report concludes that ATM variant carriers outside of the context of Ataxia-Telangiectasia may benefit from effective cancer risk management and therapeutic strategies and that efforts to set up large-scale studies in the international framework to achieve this goal are necessary.
AB - The first International Workshop of the ATM and Cancer Risk group focusing on the role of Ataxia-Telangiectasia Mutated (ATM) gene in cancer was held on December 4 and 5, 2019 at Institut Curie in Paris, France. It was motivated by the fact that germline ATM pathogenic variants have been found to be associated with different cancer types. However, due to the lack of precise age-, sex-, and site-specific risk estimates, no consensus on management guidelines for variant carriers exists, and the clinical utility of ATM variant testing is uncertain. The meeting brought together epidemiologists, geneticists, biologists and clinicians to review current knowledge and on-going challenges related to ATM and cancer risk. This report summarizes the meeting sessions content that covered the latest results in family-based and population-based studies, the importance of accurate variant classification, the effect of radiation exposures for ATM variant carriers, and the characteristics of ATM-deficient tumors. The report concludes that ATM variant carriers outside of the context of Ataxia-Telangiectasia may benefit from effective cancer risk management and therapeutic strategies and that efforts to set up large-scale studies in the international framework to achieve this goal are necessary.
KW - ATM
KW - Cancer risk
KW - Cancer spectrum
KW - Tumor profiles
KW - Variants classification
UR - http://www.scopus.com/inward/record.url?scp=85107970671&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85107970671&partnerID=8YFLogxK
U2 - 10.1007/s10689-021-00248-y
DO - 10.1007/s10689-021-00248-y
M3 - Review article
C2 - 34125377
AN - SCOPUS:85107970671
SN - 1389-9600
VL - 21
SP - 211
EP - 227
JO - Familial Cancer
JF - Familial Cancer
IS - 2
ER -