From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America

Autores
Vaccaro, Carlos Alberto; López Kostner, Francisco; Adriana, Della Valle; Inez Palmero, Edenir; Rossi, Benedito Mauro; Antelo, Marina; Solano, Angela Rosario; Carraro, Dirce Maria; Forones, Nora Manoukian; Bohorquez, Mabel; Lino Silva, Leonardo S.; Buleje, Jose; Spirandelli, Florencia; Abe Sandes, Kiyoko; Nascimento, Ivana; Sullcahuaman, Yasser; Sarroca, Carlos; Gonzalez, Maria Laura; Herrando, Alberto Ignacio; Alvarez, Karin; Neffa, Florencia; Galvão, Henrique Camposreis; Esperon, Patricia; Golubicki, Mariano; Cisterna, Daniel; Cardoso, Florencia C.; Tardin Torrezan, Giovana; Aguiar Junior, Samuel; Aparecida Marques Pimenta, Célia; Nirvana da Cruz Formiga, María; Santos, Erika; Sá, Caroline U.; Oliveira, Edite P.; Fujita, Ricardo; Spirandelli, Enrique; Jimenez, Geiner; Santa Cruz Guindalini, Rodrigo; Gondim Meira Velame de Azevedo, Renata; Souza Mario Bueno, Larissa; dos Santos Nogueira, Sonia Tereza; Piñero, Tamara Alejandra
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndrome (LS) in the region. From the literature, we find that only nine (20%) of the Latin America and the Caribbean countries have developed guidelines for early detection of CRC, and also with a low adherence. We describe a genetic profile of LS, including a total of 2,685 suspected families, where confirmed LS ranged from 8% in Uruguay and Argentina to 60% in Peru. Among confirmed LS, path_MLH1 variants were most commonly identified in Peru (82%), Mexico (80%), Chile (60%), and path_MSH2/EPCAM variants were most frequently identified in Colombia (80%) and Argentina (47%). Path_MSH6 and path_PMS2 variants were less common, but they showed important presence in Brazil (15%) and Chile (10%), respectively. Important differences exist at identifying LS families in Latin American countries, where the spectrum of path_MLH1 and path_MSH2 variants are those most frequently identified. Our findings have an impact on the evaluation of the patients and their relatives at risk for LS, derived from the gene affected. Although the awareness of hereditary cancer and genetic testing has improved in the last decade, it is remains deficient, with 39%–80% of the families not being identified for LS among those who actually met both the clinical criteria for LS and showed MMR deficiency.
Fil: Vaccaro, Carlos Alberto. Hospital Italiano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: López Kostner, Francisco. No especifíca;
Fil: Adriana, Della Valle. Hospital Fuerzas Armadas; Uruguay
Fil: Inez Palmero, Edenir. Hospital de cáncer de Barretos, FACISB; Brasil
Fil: Rossi, Benedito Mauro. Hospital Sirio Libanes; Brasil
Fil: Antelo, Marina. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina. Universidad Nacional de Lanús; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Solano, Angela Rosario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas; Argentina
Fil: Carraro, Dirce Maria. No especifíca;
Fil: Forones, Nora Manoukian. Universidade Federal de Sao Paulo; Brasil
Fil: Bohorquez, Mabel. Universidad del Tolima; Colombia
Fil: Lino Silva, Leonardo S.. Instituto Nacional de Cancerologia; México
Fil: Buleje, Jose. Universidad de San Martín de Porres; Perú
Fil: Spirandelli, Florencia. No especifíca;
Fil: Abe Sandes, Kiyoko. Universidade Federal da Bahia; Brasil
Fil: Nascimento, Ivana. No especifíca;
Fil: Sullcahuaman, Yasser. Universidad Peruana de Ciencias Aplicadas; Perú. Instituto de Investigación Genomica; Perú
Fil: Sarroca, Carlos. Hospital Fuerzas Armadas; Uruguay
Fil: Gonzalez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
Fil: Herrando, Alberto Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
Fil: Alvarez, Karin. No especifíca;
Fil: Neffa, Florencia. Hospital Fuerzas Armadas; Uruguay
Fil: Galvão, Henrique Camposreis. Barretos Cancer Hospital; Brasil
Fil: Esperon, Patricia. Hospital Fuerzas Armadas; Uruguay
Fil: Golubicki, Mariano. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina
Fil: Cisterna, Daniel. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina
Fil: Cardoso, Florencia C.. Centro de Educación Medica E Invest.clinicas; Argentina
Fil: Tardin Torrezan, Giovana. No especifíca;
Fil: Aguiar Junior, Samuel. No especifíca;
Fil: Aparecida Marques Pimenta, Célia. Universidade Federal de Sao Paulo; Brasil
Fil: Nirvana da Cruz Formiga, María. No especifíca;
Fil: Santos, Erika. Hospital Sirio Libanes; Brasil
Fil: Sá, Caroline U.. Hospital Sirio Libanes; Brasil
Fil: Oliveira, Edite P.. Hospital Sirio Libanes; Brasil
Fil: Fujita, Ricardo. Universidad de San Martín de Porres; Perú
Fil: Spirandelli, Enrique. No especifíca;
Fil: Jimenez, Geiner. No especifíca;
Fil: Santa Cruz Guindalini, Rodrigo. Universidade de Sao Paulo; Brasil
Fil: Gondim Meira Velame de Azevedo, Renata. No especifíca;
Fil: Souza Mario Bueno, Larissa. Universidade Federal da Bahia; Brasil
Fil: dos Santos Nogueira, Sonia Tereza. No especifíca;
Fil: Piñero, Tamara Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
Materia
COLORECTAL CANCER
HEREDITARY
LATIN AMERICA
LYNCH SYNDROME
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/174711

id CONICETDig_f268a5f45de51ce33cafaaed773853a8
oai_identifier_str oai:ri.conicet.gov.ar:11336/174711
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin AmericaVaccaro, Carlos AlbertoLópez Kostner, FranciscoAdriana, Della ValleInez Palmero, EdenirRossi, Benedito MauroAntelo, MarinaSolano, Angela RosarioCarraro, Dirce MariaForones, Nora ManoukianBohorquez, MabelLino Silva, Leonardo S.Buleje, JoseSpirandelli, FlorenciaAbe Sandes, KiyokoNascimento, IvanaSullcahuaman, YasserSarroca, CarlosGonzalez, Maria LauraHerrando, Alberto IgnacioAlvarez, KarinNeffa, FlorenciaGalvão, Henrique CamposreisEsperon, PatriciaGolubicki, MarianoCisterna, DanielCardoso, Florencia C.Tardin Torrezan, GiovanaAguiar Junior, SamuelAparecida Marques Pimenta, CéliaNirvana da Cruz Formiga, MaríaSantos, ErikaSá, Caroline U.Oliveira, Edite P.Fujita, RicardoSpirandelli, EnriqueJimenez, GeinerSanta Cruz Guindalini, RodrigoGondim Meira Velame de Azevedo, RenataSouza Mario Bueno, Larissados Santos Nogueira, Sonia TerezaPiñero, Tamara AlejandraCOLORECTAL CANCERHEREDITARYLATIN AMERICALYNCH SYNDROMEhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndrome (LS) in the region. From the literature, we find that only nine (20%) of the Latin America and the Caribbean countries have developed guidelines for early detection of CRC, and also with a low adherence. We describe a genetic profile of LS, including a total of 2,685 suspected families, where confirmed LS ranged from 8% in Uruguay and Argentina to 60% in Peru. Among confirmed LS, path_MLH1 variants were most commonly identified in Peru (82%), Mexico (80%), Chile (60%), and path_MSH2/EPCAM variants were most frequently identified in Colombia (80%) and Argentina (47%). Path_MSH6 and path_PMS2 variants were less common, but they showed important presence in Brazil (15%) and Chile (10%), respectively. Important differences exist at identifying LS families in Latin American countries, where the spectrum of path_MLH1 and path_MSH2 variants are those most frequently identified. Our findings have an impact on the evaluation of the patients and their relatives at risk for LS, derived from the gene affected. Although the awareness of hereditary cancer and genetic testing has improved in the last decade, it is remains deficient, with 39%–80% of the families not being identified for LS among those who actually met both the clinical criteria for LS and showed MMR deficiency.Fil: Vaccaro, Carlos Alberto. Hospital Italiano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: López Kostner, Francisco. No especifíca;Fil: Adriana, Della Valle. Hospital Fuerzas Armadas; UruguayFil: Inez Palmero, Edenir. Hospital de cáncer de Barretos, FACISB; BrasilFil: Rossi, Benedito Mauro. Hospital Sirio Libanes; BrasilFil: Antelo, Marina. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina. Universidad Nacional de Lanús; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Solano, Angela Rosario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas; ArgentinaFil: Carraro, Dirce Maria. No especifíca;Fil: Forones, Nora Manoukian. Universidade Federal de Sao Paulo; BrasilFil: Bohorquez, Mabel. Universidad del Tolima; ColombiaFil: Lino Silva, Leonardo S.. Instituto Nacional de Cancerologia; MéxicoFil: Buleje, Jose. Universidad de San Martín de Porres; PerúFil: Spirandelli, Florencia. No especifíca;Fil: Abe Sandes, Kiyoko. Universidade Federal da Bahia; BrasilFil: Nascimento, Ivana. No especifíca;Fil: Sullcahuaman, Yasser. Universidad Peruana de Ciencias Aplicadas; Perú. Instituto de Investigación Genomica; PerúFil: Sarroca, Carlos. Hospital Fuerzas Armadas; UruguayFil: Gonzalez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; ArgentinaFil: Herrando, Alberto Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; ArgentinaFil: Alvarez, Karin. No especifíca;Fil: Neffa, Florencia. Hospital Fuerzas Armadas; UruguayFil: Galvão, Henrique Camposreis. Barretos Cancer Hospital; BrasilFil: Esperon, Patricia. Hospital Fuerzas Armadas; UruguayFil: Golubicki, Mariano. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; ArgentinaFil: Cisterna, Daniel. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; ArgentinaFil: Cardoso, Florencia C.. Centro de Educación Medica E Invest.clinicas; ArgentinaFil: Tardin Torrezan, Giovana. No especifíca;Fil: Aguiar Junior, Samuel. No especifíca;Fil: Aparecida Marques Pimenta, Célia. Universidade Federal de Sao Paulo; BrasilFil: Nirvana da Cruz Formiga, María. No especifíca;Fil: Santos, Erika. Hospital Sirio Libanes; BrasilFil: Sá, Caroline U.. Hospital Sirio Libanes; BrasilFil: Oliveira, Edite P.. Hospital Sirio Libanes; BrasilFil: Fujita, Ricardo. Universidad de San Martín de Porres; PerúFil: Spirandelli, Enrique. No especifíca;Fil: Jimenez, Geiner. No especifíca;Fil: Santa Cruz Guindalini, Rodrigo. Universidade de Sao Paulo; BrasilFil: Gondim Meira Velame de Azevedo, Renata. No especifíca;Fil: Souza Mario Bueno, Larissa. Universidade Federal da Bahia; BrasilFil: dos Santos Nogueira, Sonia Tereza. No especifíca;Fil: Piñero, Tamara Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; ArgentinaJohn Wiley & Sons Inc.2018-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/174711Vaccaro, Carlos Alberto; López Kostner, Francisco; Adriana, Della Valle; Inez Palmero, Edenir; Rossi, Benedito Mauro ; et al.; From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America; John Wiley & Sons Inc.; International Journal of Cancer. Journal International du Cancer; 145; 2; 10-2018; 318-3260020-7136CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/ijc.31920info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/ijc.31920info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:46:33Zoai:ri.conicet.gov.ar:11336/174711instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:46:33.54CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
title From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
spellingShingle From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
Vaccaro, Carlos Alberto
COLORECTAL CANCER
HEREDITARY
LATIN AMERICA
LYNCH SYNDROME
title_short From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
title_full From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
title_fullStr From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
title_full_unstemmed From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
title_sort From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
dc.creator.none.fl_str_mv Vaccaro, Carlos Alberto
López Kostner, Francisco
Adriana, Della Valle
Inez Palmero, Edenir
Rossi, Benedito Mauro
Antelo, Marina
Solano, Angela Rosario
Carraro, Dirce Maria
Forones, Nora Manoukian
Bohorquez, Mabel
Lino Silva, Leonardo S.
Buleje, Jose
Spirandelli, Florencia
Abe Sandes, Kiyoko
Nascimento, Ivana
Sullcahuaman, Yasser
Sarroca, Carlos
Gonzalez, Maria Laura
Herrando, Alberto Ignacio
Alvarez, Karin
Neffa, Florencia
Galvão, Henrique Camposreis
Esperon, Patricia
Golubicki, Mariano
Cisterna, Daniel
Cardoso, Florencia C.
Tardin Torrezan, Giovana
Aguiar Junior, Samuel
Aparecida Marques Pimenta, Célia
Nirvana da Cruz Formiga, María
Santos, Erika
Sá, Caroline U.
Oliveira, Edite P.
Fujita, Ricardo
Spirandelli, Enrique
Jimenez, Geiner
Santa Cruz Guindalini, Rodrigo
Gondim Meira Velame de Azevedo, Renata
Souza Mario Bueno, Larissa
dos Santos Nogueira, Sonia Tereza
Piñero, Tamara Alejandra
author Vaccaro, Carlos Alberto
author_facet Vaccaro, Carlos Alberto
López Kostner, Francisco
Adriana, Della Valle
Inez Palmero, Edenir
Rossi, Benedito Mauro
Antelo, Marina
Solano, Angela Rosario
Carraro, Dirce Maria
Forones, Nora Manoukian
Bohorquez, Mabel
Lino Silva, Leonardo S.
Buleje, Jose
Spirandelli, Florencia
Abe Sandes, Kiyoko
Nascimento, Ivana
Sullcahuaman, Yasser
Sarroca, Carlos
Gonzalez, Maria Laura
Herrando, Alberto Ignacio
Alvarez, Karin
Neffa, Florencia
Galvão, Henrique Camposreis
Esperon, Patricia
Golubicki, Mariano
Cisterna, Daniel
Cardoso, Florencia C.
Tardin Torrezan, Giovana
Aguiar Junior, Samuel
Aparecida Marques Pimenta, Célia
Nirvana da Cruz Formiga, María
Santos, Erika
Sá, Caroline U.
Oliveira, Edite P.
Fujita, Ricardo
Spirandelli, Enrique
Jimenez, Geiner
Santa Cruz Guindalini, Rodrigo
Gondim Meira Velame de Azevedo, Renata
Souza Mario Bueno, Larissa
dos Santos Nogueira, Sonia Tereza
Piñero, Tamara Alejandra
author_role author
author2 López Kostner, Francisco
Adriana, Della Valle
Inez Palmero, Edenir
Rossi, Benedito Mauro
Antelo, Marina
Solano, Angela Rosario
Carraro, Dirce Maria
Forones, Nora Manoukian
Bohorquez, Mabel
Lino Silva, Leonardo S.
Buleje, Jose
Spirandelli, Florencia
Abe Sandes, Kiyoko
Nascimento, Ivana
Sullcahuaman, Yasser
Sarroca, Carlos
Gonzalez, Maria Laura
Herrando, Alberto Ignacio
Alvarez, Karin
Neffa, Florencia
Galvão, Henrique Camposreis
Esperon, Patricia
Golubicki, Mariano
Cisterna, Daniel
Cardoso, Florencia C.
Tardin Torrezan, Giovana
Aguiar Junior, Samuel
Aparecida Marques Pimenta, Célia
Nirvana da Cruz Formiga, María
Santos, Erika
Sá, Caroline U.
Oliveira, Edite P.
Fujita, Ricardo
Spirandelli, Enrique
Jimenez, Geiner
Santa Cruz Guindalini, Rodrigo
Gondim Meira Velame de Azevedo, Renata
Souza Mario Bueno, Larissa
dos Santos Nogueira, Sonia Tereza
Piñero, Tamara Alejandra
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv COLORECTAL CANCER
HEREDITARY
LATIN AMERICA
LYNCH SYNDROME
topic COLORECTAL CANCER
HEREDITARY
LATIN AMERICA
LYNCH SYNDROME
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.2
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndrome (LS) in the region. From the literature, we find that only nine (20%) of the Latin America and the Caribbean countries have developed guidelines for early detection of CRC, and also with a low adherence. We describe a genetic profile of LS, including a total of 2,685 suspected families, where confirmed LS ranged from 8% in Uruguay and Argentina to 60% in Peru. Among confirmed LS, path_MLH1 variants were most commonly identified in Peru (82%), Mexico (80%), Chile (60%), and path_MSH2/EPCAM variants were most frequently identified in Colombia (80%) and Argentina (47%). Path_MSH6 and path_PMS2 variants were less common, but they showed important presence in Brazil (15%) and Chile (10%), respectively. Important differences exist at identifying LS families in Latin American countries, where the spectrum of path_MLH1 and path_MSH2 variants are those most frequently identified. Our findings have an impact on the evaluation of the patients and their relatives at risk for LS, derived from the gene affected. Although the awareness of hereditary cancer and genetic testing has improved in the last decade, it is remains deficient, with 39%–80% of the families not being identified for LS among those who actually met both the clinical criteria for LS and showed MMR deficiency.
Fil: Vaccaro, Carlos Alberto. Hospital Italiano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: López Kostner, Francisco. No especifíca;
Fil: Adriana, Della Valle. Hospital Fuerzas Armadas; Uruguay
Fil: Inez Palmero, Edenir. Hospital de cáncer de Barretos, FACISB; Brasil
Fil: Rossi, Benedito Mauro. Hospital Sirio Libanes; Brasil
Fil: Antelo, Marina. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina. Universidad Nacional de Lanús; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Solano, Angela Rosario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas; Argentina
Fil: Carraro, Dirce Maria. No especifíca;
Fil: Forones, Nora Manoukian. Universidade Federal de Sao Paulo; Brasil
Fil: Bohorquez, Mabel. Universidad del Tolima; Colombia
Fil: Lino Silva, Leonardo S.. Instituto Nacional de Cancerologia; México
Fil: Buleje, Jose. Universidad de San Martín de Porres; Perú
Fil: Spirandelli, Florencia. No especifíca;
Fil: Abe Sandes, Kiyoko. Universidade Federal da Bahia; Brasil
Fil: Nascimento, Ivana. No especifíca;
Fil: Sullcahuaman, Yasser. Universidad Peruana de Ciencias Aplicadas; Perú. Instituto de Investigación Genomica; Perú
Fil: Sarroca, Carlos. Hospital Fuerzas Armadas; Uruguay
Fil: Gonzalez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
Fil: Herrando, Alberto Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
Fil: Alvarez, Karin. No especifíca;
Fil: Neffa, Florencia. Hospital Fuerzas Armadas; Uruguay
Fil: Galvão, Henrique Camposreis. Barretos Cancer Hospital; Brasil
Fil: Esperon, Patricia. Hospital Fuerzas Armadas; Uruguay
Fil: Golubicki, Mariano. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina
Fil: Cisterna, Daniel. Gobierno de la Ciudad de Buenos Aires. Hospital de Gastroenterología "Dr. Carlos B. Udaondo"; Argentina
Fil: Cardoso, Florencia C.. Centro de Educación Medica E Invest.clinicas; Argentina
Fil: Tardin Torrezan, Giovana. No especifíca;
Fil: Aguiar Junior, Samuel. No especifíca;
Fil: Aparecida Marques Pimenta, Célia. Universidade Federal de Sao Paulo; Brasil
Fil: Nirvana da Cruz Formiga, María. No especifíca;
Fil: Santos, Erika. Hospital Sirio Libanes; Brasil
Fil: Sá, Caroline U.. Hospital Sirio Libanes; Brasil
Fil: Oliveira, Edite P.. Hospital Sirio Libanes; Brasil
Fil: Fujita, Ricardo. Universidad de San Martín de Porres; Perú
Fil: Spirandelli, Enrique. No especifíca;
Fil: Jimenez, Geiner. No especifíca;
Fil: Santa Cruz Guindalini, Rodrigo. Universidade de Sao Paulo; Brasil
Fil: Gondim Meira Velame de Azevedo, Renata. No especifíca;
Fil: Souza Mario Bueno, Larissa. Universidade Federal da Bahia; Brasil
Fil: dos Santos Nogueira, Sonia Tereza. No especifíca;
Fil: Piñero, Tamara Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Medicina Traslacional e Ingeniería Biomédica - Hospital Italiano. Instituto de Medicina Traslacional e Ingeniería Biomédica.- Instituto Universitario Hospital Italiano de Buenos Aires. Instituto de Medicina Traslacional e Ingeniería Biomédica; Argentina
description Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndrome (LS) in the region. From the literature, we find that only nine (20%) of the Latin America and the Caribbean countries have developed guidelines for early detection of CRC, and also with a low adherence. We describe a genetic profile of LS, including a total of 2,685 suspected families, where confirmed LS ranged from 8% in Uruguay and Argentina to 60% in Peru. Among confirmed LS, path_MLH1 variants were most commonly identified in Peru (82%), Mexico (80%), Chile (60%), and path_MSH2/EPCAM variants were most frequently identified in Colombia (80%) and Argentina (47%). Path_MSH6 and path_PMS2 variants were less common, but they showed important presence in Brazil (15%) and Chile (10%), respectively. Important differences exist at identifying LS families in Latin American countries, where the spectrum of path_MLH1 and path_MSH2 variants are those most frequently identified. Our findings have an impact on the evaluation of the patients and their relatives at risk for LS, derived from the gene affected. Although the awareness of hereditary cancer and genetic testing has improved in the last decade, it is remains deficient, with 39%–80% of the families not being identified for LS among those who actually met both the clinical criteria for LS and showed MMR deficiency.
publishDate 2018
dc.date.none.fl_str_mv 2018-10
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/174711
Vaccaro, Carlos Alberto; López Kostner, Francisco; Adriana, Della Valle; Inez Palmero, Edenir; Rossi, Benedito Mauro ; et al.; From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America; John Wiley & Sons Inc.; International Journal of Cancer. Journal International du Cancer; 145; 2; 10-2018; 318-326
0020-7136
CONICET Digital
CONICET
url http://hdl.handle.net/11336/174711
identifier_str_mv Vaccaro, Carlos Alberto; López Kostner, Francisco; Adriana, Della Valle; Inez Palmero, Edenir; Rossi, Benedito Mauro ; et al.; From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America; John Wiley & Sons Inc.; International Journal of Cancer. Journal International du Cancer; 145; 2; 10-2018; 318-326
0020-7136
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1002/ijc.31920
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/ijc.31920
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv John Wiley & Sons Inc.
publisher.none.fl_str_mv John Wiley & Sons Inc.
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1842268802786525184
score 13.13397