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Duration of tamoxifen use and the risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers

Authors :
Eitan Friedman
Peter Ainsworth
Ava Kwong
Jacek Gronwald
Sofia D. Merajver
John Lunn
Andrea Eisen
Talia Donenberg
Wendy S. Meschino
Rochelle Demsky
Taya Fallen
Fergus J. Couch
Joanne L. Blum
Albert E. Chudley
Charis Eng
Raluca N. Kurz
Kelly A. Metcalfe
Mary B. Daly
Aletta Poll
Howard M. Saal
Louise Bordeleau
André Robidoux
A Jakubowska
Steven A. Narod
Tomasz Byrski
Claudine Isaacs
Charmaine Kim-Sing
Jane McLennan
Kenneth Offit
Dominique Stoppa-Lyonnet
Nadine Tung
Robert E. Reilly
Daniel Rayson
Edmond G. Lemire
Marie E. Wood
Jan Klijn
Siranoush Manoukian
Barry P. Rosen
Gad Rennert
Gareth Evans
Susan Armel
Ruth Gershoni-Baruch
Pål Møller
Jan Lubinski
Mark E. Robson
Sonia Nanda
Beth Y. Karlan
Barbara Pasini
Henry T. Lynch
Kevin Sweet
Leigha Senter
Christian F. Singer
Ping Sun
Judy Garber
Lovise Maehle
Josephine Wagner Costalas
Ophira Ginsburg
Dawna Gilchrist
Tomasz Huzarski
Wendy McKinnon
Jeffrey N. Weitzel
William D. Foulkes
Susan L. Neuhausen
Noah D. Kauff
Christine Rappaport
Carey A. Cullinane
David M. Euhus
Tuya Pal
Dana Zakalik
Olufunmilayo I. Olopade
Seema Panchal
Cezary Cybulski
Susan T. Vadaparampil
Source :
Breast Cancer Research and Treatment. 146:421-427
Publication Year :
2014
Publisher :
Springer Science and Business Media LLC, 2014.

Abstract

Women with a mutation in BRCA1 or BRCA2 face a lifetime risk of breast cancer of approximately 80 %. Tamoxifen treatment of the first cancer has been associated with a reduction in the risk of a subsequent contralateral cancer. We studied 1,504 women with a known BRCA1 or BRCA2 mutation, 411 women with bilateral breast cancer (cases) and 1,093 women with unilateral breast cancer (controls) in a matched case-control study. Control women were of similar age and had a similar age of diagnosis of first breast cancer as the cases. For each woman who used tamoxifen, the starting and stopping dates were abstracted and the duration of tamoxifen use was calculated. Three hundred and thirty-one women had used tamoxifen (22 %); of these 84 (25 %) had completed four or more years of tamoxifen, the remainder stopped prematurely or were current users. For women with up to 1 year of tamoxifen use, the odds ratio for contralateral breast cancer was 0.37 (95 % CI 0.20-0.69; p = 0.001) compared to women with no tamoxifen use. Among women with 1-4 years of tamoxifen use the odds ratio was 0.53 (95 % CI 0.32-0.87; p = 0.01). Among women with four or more years of tamoxifen use the odds ratio was 0.83 (95 % CI 0.44-1.55; p = 0.55). Short-term use of tamoxifen for chemoprevention in BRCA1 and BRCA2 mutation carriers may be as effective as a conventional 5-year course of treatment.

Details

ISSN :
15737217 and 01676806
Volume :
146
Database :
OpenAIRE
Journal :
Breast Cancer Research and Treatment
Accession number :
edsair.doi.dedup.....ce7b5df22a2dfdec890e6aaef924df2a