How to structure an oncogenetics service for the public health system: Report of the implementation of the first service in Northeastern Brazil
Identifying carriers of genetic mutations that increase the risk of developing cancer allows to adopt timely risk-reducing strategies. However, due to the elevated cost of genetic testing, few oncogenetics services are available in the Brazilian public health care system, especially in economically...
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Published in: | Cancer genetics Vol. 250-251; pp. 6 - 11 |
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Abstract | Identifying carriers of genetic mutations that increase the risk of developing cancer allows to adopt timely risk-reducing strategies. However, due to the elevated cost of genetic testing, few oncogenetics services are available in the Brazilian public health care system, especially in economically disadvantaged areas.
To describe the implementation of an oncogenetics service for patients suspected of hereditary cancer syndromes (HBOC and HNPCC) at a philanthropic referral oncology hospital in Northeastern Brazil, funded by the Ministry of Health's National Oncology Care Support Program (PRONON).
The service was implemented with the PDCA method (Plan, Do, Check and Act).
During the first year of operation (starting in August 2018), 675 individuals were examined, of whom 272 patients and 98 family members were submitted to genetic testing. This included the collection of 338 DNA samples of which 300 were sequenced. The analysis identified 48 (17.1%) mutations for HBOC and 19 (6.8%) for HNPCC.
In one year, the oncogenetics service was able to benefit over 300 families by generating advanced molecular data which may be used for tailoring cancer prevention and management. |
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AbstractList | Identifying carriers of genetic mutations that increase the risk of developing cancer allows to adopt timely risk-reducing strategies. However, due to the elevated cost of genetic testing, few oncogenetics services are available in the Brazilian public health care system, especially in economically disadvantaged areas.
To describe the implementation of an oncogenetics service for patients suspected of hereditary cancer syndromes (HBOC and HNPCC) at a philanthropic referral oncology hospital in Northeastern Brazil, funded by the Ministry of Health's National Oncology Care Support Program (PRONON).
The service was implemented with the PDCA method (Plan, Do, Check and Act).
During the first year of operation (starting in August 2018), 675 individuals were examined, of whom 272 patients and 98 family members were submitted to genetic testing. This included the collection of 338 DNA samples of which 300 were sequenced. The analysis identified 48 (17.1%) mutations for HBOC and 19 (6.8%) for HNPCC.
In one year, the oncogenetics service was able to benefit over 300 families by generating advanced molecular data which may be used for tailoring cancer prevention and management. |
Author | Lima, Marcos Venício Alves Nogueira, Camila Sampaio de Albuquerque, Clarissa Gondim Picanço Wong, Deysi Viviana Tenazoa Silva-Fernandes, Isabelle Joyce de Lima Oliveira, Francisca Fernanda Barbosa Silva, Paulo Goberlânio de Barros Bitencourt, Flávio da Silveira |
Author_xml | – sequence: 1 givenname: Camila Sampaio orcidid: 0000-0002-2888-2039 surname: Nogueira fullname: Nogueira, Camila Sampaio organization: Federal University of Ceará, Rua Alexandre Baraúna 994, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 2 givenname: Isabelle Joyce de Lima surname: Silva-Fernandes fullname: Silva-Fernandes, Isabelle Joyce de Lima email: isabellejoyce@gmail.com organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 3 givenname: Clarissa Gondim Picanço surname: de Albuquerque fullname: de Albuquerque, Clarissa Gondim Picanço organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 4 givenname: Francisca Fernanda Barbosa surname: Oliveira fullname: Oliveira, Francisca Fernanda Barbosa organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 5 givenname: Deysi Viviana Tenazoa orcidid: 0000-0002-9741-7560 surname: Wong fullname: Wong, Deysi Viviana Tenazoa organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 6 givenname: Paulo Goberlânio de Barros surname: Silva fullname: Silva, Paulo Goberlânio de Barros organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 7 givenname: Flávio da Silveira orcidid: 0000-0001-8985-4579 surname: Bitencourt fullname: Bitencourt, Flávio da Silveira organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil – sequence: 8 givenname: Marcos Venício Alves surname: Lima fullname: Lima, Marcos Venício Alves organization: Ceará Cancer Institute, Rua Papi Junior 1222, Rodolfo Teófilo, Fortaleza, Ceará, Brazil |
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Keywords | Breast neoplasms Colorectal neoplasms Mutagenicity testing Ovarian neoplasms Lynch syndrome |
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SubjectTerms | Breast neoplasms Colorectal neoplasms Lynch syndrome Mutagenicity testing Ovarian neoplasms |
Title | How to structure an oncogenetics service for the public health system: Report of the implementation of the first service in Northeastern Brazil |
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