Title | PMS2 monoallelic mutation carriers: the known unknown. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Goodenberger, MKL, Thomas, BC, Riegert-Johnson, D, C Boland, R, Plon, SE, Clendenning, M, Win, AKo, Senter, L, Lipkin, SM, Stadler, ZK, Macrae, FA, Lynch, HT, Weitzel, JN, de la Chapelle, A, Syngal, S, Lynch, P, Parry, S, Jenkins, MA, Gallinger, S, Holter, S, Aronson, M, Newcomb, PA, Burnett, T, Le Marchand, L, Pichurin, P, Hampel, H, Terdiman, JP, Lu, KH, Thibodeau, S, Lindor, NM |
Journal | Genet Med |
Volume | 18 |
Issue | 1 |
Pagination | 13-9 |
Date Published | 2016 Jan |
ISSN | 1530-0366 |
Keywords | Adenosine Triphosphatases, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA Repair Enzymes, DNA-Binding Proteins, Early Detection of Cancer, Germ-Line Mutation, Heterozygote, Humans, Mismatch Repair Endonuclease PMS2, Penetrance |
Abstract | Germ-line mutations in MLH1, MSH2, MSH6, and PMS2 have been shown to cause Lynch syndrome. The penetrance of the cancer and tumor spectrum has been repeatedly studied, and multiple professional societies have proposed clinical management guidelines for affected individuals. Several studies have demonstrated a reduced penetrance for monoallelic carriers of PMS2 mutations compared with the other mismatch repair (MMR) genes, but clinical management guidelines have largely proposed the same screening recommendations for all MMR gene carriers. The authors considered whether enough evidence existed to propose new screening guidelines specific to PMS2 mutation carriers with regard to age at onset and frequency of colonic screening. Published reports of PMS2 germ-line mutations were combined with unpublished cases from the authors' research registries and clinical practices, and a discussion of potential modification of cancer screening guidelines was pursued. A total of 234 monoallelic PMS2 mutation carriers from 170 families were included. Approximately 8% of those with colorectal cancer (CRC) were diagnosed before age 30, and each of these tumors presented on the left side of the colon. As it is currently unknown what causes the early onset of CRC in some families with monoallelic PMS2 germline mutations, the authors recommend against reducing cancer surveillance guidelines in families found having monoallelic PMS2 mutations in spite of the reduced penetrance.Genet Med 18 1, 13-19. |
DOI | 10.1038/gim.2015.27 |
Alternate Journal | Genet. Med. |
PubMed ID | 25856668 |
PubMed Central ID | PMC4834863 |
Grant List | R01 CA067941 / CA / NCI NIH HHS / United States P30 CA016672 / CA / NCI NIH HHS / United States RC4 CA153828 / CA / NCI NIH HHS / United States U01 CA074799 / CA / NCI NIH HHS / United States U01/U24 CA074799 / CA / NCI NIH HHS / United States U24 CA074783 / CA / NCI NIH HHS / United States U24 CA074794 / CA / NCI NIH HHS / United States U24 CA074806 / CA / NCI NIH HHS / United States U24 CA097735 / CA / NCI NIH HHS / United States U01 CA074794 / CA / NCI NIH HHS / United States P30 CA008748 / CA / NCI NIH HHS / United States U01/U24 CA074783 / CA / NCI NIH HHS / United States U01/U24 CA074794 / CA / NCI NIH HHS / United States U01 CA097735 / CA / NCI NIH HHS / United States P30 CA016058 / CA / NCI NIH HHS / United States UM1 CA167551 / CA / NCI NIH HHS / United States R01 CA072851 / CA / NCI NIH HHS / United States U01 CA074783 / CA / NCI NIH HHS / United States U01/U24 CA097735 / CA / NCI NIH HHS / United States U24 CA074799 / CA / NCI NIH HHS / United States U01 CA074806 / CA / NCI NIH HHS / United States U24 CA074800 / CA / NCI NIH HHS / United States U01/U24 CA074806 / CA / NCI NIH HHS / United States U01 CA074800 / CA / NCI NIH HHS / United States U01/U24 CA074800 / CA / NCI NIH HHS / United States |