The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study
To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Women known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline q...
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Published in | Gynecologic oncology Vol. 104; no. 1; pp. 7 - 10 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.01.2007
|
Subjects | |
Online Access | Get full text |
ISSN | 0090-8258 1095-6859 |
DOI | 10.1016/j.ygyno.2006.08.004 |
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Abstract | To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the
BRCA1 or
BRCA2 genes.
Women known to carry a
BRCA1 or
BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates.
After an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR
=
5.3,
p
=
0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR
=
2.7,
p
=
0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (
p
=
0.0004).
The main contributor to the increased risk of endometrial cancer among
BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. |
---|---|
AbstractList | To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the
BRCA1 or
BRCA2 genes.
Women known to carry a
BRCA1 or
BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates.
After an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR
=
5.3,
p
=
0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR
=
2.7,
p
=
0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (
p
=
0.0004).
The main contributor to the increased risk of endometrial cancer among
BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes.OBJECTIVETo evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes.Women known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates.PATIENTS AND METHODSWomen known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates.After an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR=5.3, p=0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR=2.7, p=0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (p=0.0004).RESULTSAfter an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR=5.3, p=0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR=2.7, p=0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (p=0.0004).The main contributor to the increased risk of endometrial cancer among BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy.CONCLUSIONThe main contributor to the increased risk of endometrial cancer among BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. AbstractObjectiveTo evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Patients and methodsWomen known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates. ResultsAfter an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR = 5.3, p= 0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR = 2.7, p= 0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 ( p= 0.0004). ConclusionThe main contributor to the increased risk of endometrial cancer among BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Women known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates. After an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR=5.3, p=0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR=2.7, p=0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (p=0.0004). The main contributor to the increased risk of endometrial cancer among BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. |
Author | Moller, Pal Ghadirian, Parviz Lubinski, Jan Lynch, Henry T. Friedman, Eitan Sun, Ping Beiner, Mario E. Rosen, Barry Finch, Amy Narod, Steven A. |
Author_xml | – sequence: 1 givenname: Mario E. surname: Beiner fullname: Beiner, Mario E. organization: Centre for Research in Women’s Health, 790 Bay Street, Toronto, ON, Canada M5G 1N8 – sequence: 2 givenname: Amy surname: Finch fullname: Finch, Amy organization: Centre for Research in Women’s Health, 790 Bay Street, Toronto, ON, Canada M5G 1N8 – sequence: 3 givenname: Barry surname: Rosen fullname: Rosen, Barry organization: Division of Gynecologic Oncology, Princess Margaret Hospital and University of Toronto, Toronto, ON, Canada – sequence: 4 givenname: Jan surname: Lubinski fullname: Lubinski, Jan organization: Pomeranian Medical University, Szczecin, Poland – sequence: 5 givenname: Pal surname: Moller fullname: Moller, Pal organization: Department of Cancer Genetics, Norwegian Radium Hospital, Oslo, Norway – sequence: 6 givenname: Parviz surname: Ghadirian fullname: Ghadirian, Parviz organization: Epidemiology Research Unit, CHUM Hôtel-Dieu, University of Montreal, Montreal, QC, Canada – sequence: 7 givenname: Henry T. surname: Lynch fullname: Lynch, Henry T. organization: Department of Preventive Medicine and Public Health, Creighton University School of Medicine, Omaha, NE 68178, USA – sequence: 8 givenname: Eitan surname: Friedman fullname: Friedman, Eitan organization: Oncogenetics Unit, Chaim Sheba Medical Center, Tel-Hashomer, Israel – sequence: 9 givenname: Ping surname: Sun fullname: Sun, Ping organization: Centre for Research in Women’s Health, 790 Bay Street, Toronto, ON, Canada M5G 1N8 – sequence: 10 givenname: Steven A. surname: Narod fullname: Narod, Steven A. email: steven.narod@sw.ca organization: Centre for Research in Women’s Health, 790 Bay Street, Toronto, ON, Canada M5G 1N8 |
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Snippet | To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the
BRCA1 or
BRCA2 genes.
Women known to carry a
BRCA1 or
BRCA2... AbstractObjectiveTo evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Patients and methodsWomen... To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Women known to carry a BRCA1 or BRCA2... To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes.OBJECTIVETo evaluate the risk of endometrial... |
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SubjectTerms | Adult Aged Antineoplastic Agents, Hormonal - adverse effects Association BRCA1 BRCA2 Breast Neoplasms - drug therapy Endometrial cancer Endometrial Neoplasms - genetics Female Follow-Up Studies Genes, BRCA1 Genes, BRCA2 Germ-Line Mutation Hematology, Oncology, and Palliative Medicine Humans Middle Aged Obstetrics and Gynecology Prospective Studies Tamoxifen - adverse effects |
Title | The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study |
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