Literature DB >> 24461199

Familial melanoma by histology and age: joint data from five Nordic countries.

Mahdi Fallah1, Eero Pukkala2, Kristina Sundquist3, Steinar Tretli4, Jörgen H Olsen5, Laufey Tryggvadottir6, Kari Hemminki7.   

Abstract

BACKGROUND: We aimed to estimate lifetime cumulative risk of melanoma (CRM) in relatives of patients with melanoma by histology and age at diagnosis in patients and relatives.
METHODS: A population-based cohort of 238724 first-degree relatives of 46091 melanoma patients diagnosed in 1955-2010 in Nordic countries was followed for cancer incidence.
FINDINGS: The CRM (0-79 years) in first-degree relatives of a patient with superficial spreading (SSM), nodular (NM), or lentigo maligna melanoma was quite similar, ranging from 2.5% to about 3%, which represents about 2-fold increase over the general population risk. When one melanoma patient in the family was diagnosed before age 30, the CRM was about 3%. When there were > or =2 melanoma patients diagnosed before age 30 in a family, CRM for relatives was about 14%, 6% for diagnoses at age 30-59, and 5% for diagnoses at age 60 or older. Depending on age at diagnosis of same-sex twins (not known whether monozygotic/dizygotic), their CRM was about 7-21%. Although no familial case of concordant histological types of acral lentiginous/desmoplastic/compound nevus/spindle cell melanomas or malignant blue nevus was found, familial risks of discordant histological types of melanoma were interchangeably high for most of the types, e.g. higher risk of SSM when a first-degree relative had NM [standardized incidence ratios (SIR)=2.6, 95% confidence interval (CI)=2.1-3.3, n=72] or acral lentiginous (4.0, 95% CI=1.5-8.8, n=6) and vice versa. There was a tendency toward concordant age at diagnosis of melanoma among relatives of melanoma patients.
INTERPRETATION: Findings of this study may help clinicians to find subjects at high melanoma risk for the genetic counseling. The risk was highest when melanoma occurred in a same-sex twin, one first-degree relative diagnosed at young age (<30), or > or =2 first-degree relatives. Histological type of melanoma does not seem to play an important role in familial melanoma. FUNDING: This work was supported by the Nordic Cancer Union, Swedish Council for Working Life and Social Research, and German Cancer Aid.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Familial risk; Histology-specific; Melanoma; Nordic countries; Skin cancer; Standardized incidence ratio

Mesh:

Year:  2014        PMID: 24461199     DOI: 10.1016/j.ejca.2013.12.023

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  8 in total

1.  Absence of germline CDKN2A mutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?

Authors:  Sara Di Lorenzo; Daniele Fanale; Bartolo Corradino; Valentina Caló; Gaetana Rinaldi; Viviana Bazan; Antonio Giordano; Adriana Cordova; Antonio Russo
Journal:  Cancer Biol Ther       Date:  2016       Impact factor: 4.742

2.  Framing recommendations to promote prevention behaviors among people at high risk: A simulation study of responses to melanoma genetic test reporting.

Authors:  Jennifer M Taber; Lisa G Aspinwall
Journal:  J Genet Couns       Date:  2015-01-14       Impact factor: 2.537

3.  Melanoma risk assessment based on relatives' age at diagnosis.

Authors:  Yelena P Wu; Wendy Kohlmann; Karen Curtin; Zhe Yu; Heidi A Hanson; Mia Hashibe; Bridget G Parsons; Jathine Wong; Joshua D Schiffman; Douglas Grossman; Sancy A Leachman
Journal:  Cancer Causes Control       Date:  2017-12-14       Impact factor: 2.506

4.  Correlates of Sun Protection and Sunburn in Children of Melanoma Survivors.

Authors:  Mary K Tripp; Susan K Peterson; Alexander V Prokhorov; Sanjay S Shete; Jeffrey E Lee; Jeffrey E Gershenwald; Ellen R Gritz
Journal:  Am J Prev Med       Date:  2016-04-07       Impact factor: 5.043

5.  Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.

Authors:  Karin A W Wadt; Lauren G Aoude; Lotte Krogh; Lone Sunde; Anders Bojesen; Karen Grønskov; Nine Wartacz; Jakob Ek; Morten Tolstrup-Andersen; Mette Klarskov-Andersen; Åke Borg; Steffen Heegaard; Jens F Kiilgaard; Thomas V O Hansen; Kerenaftali Klein; Göran Jönsson; Krzysztof T Drzewiecki; Morten Dunø; Nicholas K Hayward; Anne-Marie Gerdes
Journal:  PLoS One       Date:  2015-03-24       Impact factor: 3.240

6.  The surprising implications of familial association in disease risk.

Authors:  Morten Valberg; Mats Julius Stensrud; Odd O Aalen
Journal:  BMC Public Health       Date:  2018-01-15       Impact factor: 3.295

7.  Familial aggregation of early-onset cancers.

Authors:  Sanna M M Heikkinen; Laura-Maria Madanat-Harjuoja; Karri J M Seppä; Matti E Rantanen; Elli M Hirvonen; Nea K Malila; Janne M Pitkäniemi
Journal:  Int J Cancer       Date:  2019-06-27       Impact factor: 7.396

Review 8.  Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease.

Authors:  Patricia Basurto-Lozada; Christian Molina-Aguilar; Carolina Castaneda-Garcia; Martha Estefania Vázquez-Cruz; Omar Isaac Garcia-Salinas; Alethia Álvarez-Cano; Héctor Martínez-Said; Rodrigo Roldán-Marín; David J Adams; Patricia A Possik; Carla Daniela Robles-Espinoza
Journal:  Pigment Cell Melanoma Res       Date:  2020-06-17       Impact factor: 4.693

  8 in total

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