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Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Tischkowitz, Marc; Balmaña, Judith; Foulkes, William D; James, Paul; Ngeow, Joanne; Schmutzler, Rita; Voian, Nicoleta; Wick, Myra J; Stewart, Douglas R; Pal, Tuya.
Afiliação
  • Tischkowitz M; Department of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, UK.
  • Balmaña J; Hereditary Cancer Genetics Group, Vall d'Hebron Institute of Oncology (VHIO) and Medical Oncology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Hospital Campus, Barcelona, Spain.
  • Foulkes WD; Departments of Human Genetics, Oncology and Medicine, McGill University, Montréal, QC, Canada.
  • James P; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia.
  • Ngeow J; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
  • Schmutzler R; Genomic Medicine, Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
  • Voian N; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
  • Wick MJ; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
  • Stewart DR; University Hospital of Cologne, Center of Integrated Oncology, CIO and Center of Familial Breast and Ovarian Cancer, Cologne, Germany.
  • Pal T; Genetic Risk Clinic, Providence Cancer Institute, Portland, OR, USA.
Genet Med ; 23(8): 1416-1423, 2021 08.
Article em En | MEDLINE | ID: mdl-33976419
ABSTRACT

PURPOSE:

PALB2 germline pathogenic variants are associated with increased breast cancer risk and smaller increased risk of pancreatic and likely ovarian cancer. Resources for health-care professionals managing PALB2 heterozygotes are currently limited.

METHODS:

A workgroup of experts sought to outline management of PALB2 heterozygotes based on current evidence. Peer-reviewed publications from PubMed were identified to guide recommendations, which arose by consensus and the collective expertise of the authors.

RESULTS:

PALB2 heterozygotes should be offered BRCA1/2-equivalent breast surveillance. Risk-reducing mastectomy can be considered guided by personalized risk estimates. Pancreatic cancer surveillance should be considered, but ideally as part of a clinical trial. Typically, ovarian cancer surveillance is not recommended, and risk-reducing salpingo-oophorectomy should only rarely be considered before the age of 50. Given the mechanistic similarities, PALB2 heterozygotes should be considered for therapeutic regimens and trials as those for BRCA1/2.

CONCLUSION:

This guidance is similar to those for BRCA1/2. While the range of the cancer risk estimates overlap with BRCA1/2, point estimates are lower in PALB2 so individualized estimates are important for management decisions. Systematic prospective data collection is needed to determine as yet unanswered questions such as the risk of contralateral breast cancer and survival after cancer diagnosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Genética Médica Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Genética Médica Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article