Predictive testing for BRCA1 and 2 mutations: a male contribution

被引:30
作者
Daly, PA
Nolan, C
Green, A
Ormiston, W
Cody, N
McDevitt, T
O'hIci, B
Byrne, D
McDermott, E
Carney, DN
O'Higgins, N
Barton, DE
机构
[1] St James Hosp, Dept Haematol & Oncol, Dublin 8, Ireland
[2] Trinity Coll Dublin, Dublin, Ireland
[3] Natl Ctr Med Genet, Dublin, Ireland
[4] Univ Coll, Dublin, Ireland
[5] St Vincents Univ Hosp, Dublin, Ireland
[6] Mater Misericordiae Univ Hosp, Dublin, Ireland
关键词
BRCA1; BRCA2; cancer genetics; predictive testing in men;
D O I
10.1093/annonc/mdg164
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Management strategies for women carrying BRCA1 and 2 mutations are becoming clearer and predictive testing for a known family mutation is commonly undertaken. Implications for men are not as clear and they participate less frequently. Patients and methods: Twenty-six men from 10 extended families underwent predictive testing. Their motivation, reaction and outcome were studied. Subjects had appropriate pre- and post-test counselling. Informed consent was obtained before predictive testing for known deleterious mutations. DNA analysis followed standard procedures. Results: Eighteen tested positive and eight negative. Four had adverse psychological reactions and three reneged on their commitments to impart results. The spouse of another man had an adverse psychological reaction to the disclosure of his positive result. Two, already suffering from prostate cancer, were phenocopies and paternal lineage transmission was unexpectedly determined in another. Risk was removed from 33 offspring and confirmed for 56. Conclusions: Complex themes associated with genetic testing are confirmed and the spectrum extended. Men appear to understand the importance of participating in this process. Methods of avoiding adverse reactions merit further study along with other aspects of the process.
引用
收藏
页码:549 / 553
页数:5
相关论文
共 27 条
[1]   Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members [J].
Bleiker, EMA ;
Aaronson, NK ;
Menko, FH ;
Hahn, DEE ;
vanAsperen, CJ ;
Rutgers, EJT ;
tenKate, LP ;
Leschot, NJ .
PATIENT EDUCATION AND COUNSELING, 1997, 32 (1-2) :107-116
[2]  
Breast Canc Linkage Consortium, 1999, JNCI-J NATL CANCER I, V91, P1310
[3]   Recommendations for follow-up care of individuals with an inherited predisposition to cancer .2. BRCA1 and BRCA2 [J].
Burke, W ;
Daly, M ;
Garber, J ;
Botkin, J ;
Kahn, MJE ;
Lynch, P ;
McTierman, A ;
Offit, K ;
Perlman, J ;
Petersen, G ;
Thomson, E ;
Varricchio, C .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (12) :997-1003
[4]   Anticipated versus actual emotional reactions to disclosure of results of genetic tests for cancer susceptibility:: Findings from p53 and BRCA1 testing programs [J].
Dorval, M ;
Patenaude, AF ;
Schneider, KA ;
Kieffer, SA ;
DiGianni, L ;
Kalkbrenner, KJ ;
Bromberg, JI ;
Basili, LA ;
Calzone, K ;
Stopfer, J ;
Weber, BL ;
Garber, JE .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (10) :2135-2142
[5]   Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13 [J].
Easton, DF ;
Steele, L ;
Fields, P ;
Ormiston, W ;
Averill, D ;
Daly, PA ;
McManus, R ;
Neuhausen, SL ;
Ford, D ;
Wooster, R ;
CannonAlbright, LA ;
Stratton, MR ;
Goldgar, DE .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (01) :120-128
[6]   Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families [J].
Ford, D ;
Easton, DF ;
Stratton, M ;
Narod, S ;
Goldgar, D ;
Devilee, P ;
Bishop, DT ;
Weber, B ;
Lenoir, G ;
Chang-Claude, J ;
Sobol, H ;
Teare, MD ;
Struewing, J ;
Arason, A ;
Scherneck, S ;
Peto, J ;
Rebbeck, TR ;
Tonin, P ;
Neuhausen, S ;
Barkardottir, R ;
Eyfjord, J ;
Lynch, H ;
Ponder, BAJ ;
Gayther, SA ;
Birch, JM ;
Lindblom, A ;
Stoppa-Lyonnet, D ;
Bignon, Y ;
Borg, A ;
Hamann, U ;
Haites, N ;
Scott, RJ ;
Maugard, CM ;
Vasen, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) :676-689
[7]   Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2:: Analysis of 10,000 individuals [J].
Frank, TS ;
Deffenbaugh, AM ;
Reid, JE ;
Hulick, M ;
Ward, BE ;
Lingenfelter, B ;
Gumpper, KL ;
Scholl, T ;
Tavtigian, SV ;
Pruss, DR ;
Critchfield, GC .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1480-1490
[8]   Breast cancer in carriers of BRCA1 and BRCA2 mutations:: Tackling a molecular and clinical conundrum [J].
Haber, DA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3367-3370
[9]   RAPID DETECTION OF BRCA1 MUTATIONS BY THE PROTEIN TRUNCATION TEST [J].
HOGERVORST, FBL ;
CORNELIS, RS ;
BOUT, M ;
VANVLIET, M ;
OOSTERWIJK, JC ;
OLMER, R ;
BAKKER, B ;
KLIJN, JGM ;
VASEN, HFA ;
MEIJERSHEIJBOER, H ;
MENKO, FH ;
CORNELISSE, CJ ;
DENDUNNEN, JT ;
DEVILEE, P ;
VANOMMEN, GJB .
NATURE GENETICS, 1995, 10 (02) :208-212
[10]   Pitfalls of genetic testing [J].
Hubbard, R ;
Lewontin, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (18) :1192-1194