Premature menopause in survivors of childhood cancer: A report from the childhood cancer survivor study

被引:383
作者
Sklar, Charles A.
Mertens, Ann C.
Mitby, Pauline
Whitton, John
Stovall, Marilyn
Kasper, Catherine
Mulder, Jean
Green, Daniel
Nicholson, H. Stacy
Tasui, Yutaka
Robison, Leslie L.
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
[2] Univ Minnesota, Sch Med, Dept Pediat, Minneapolis, MN 55455 USA
[3] Fred Hutchinson Canc Res Ctr, Canc Prevent Res Program, Seattle, WA 98104 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Phys, Houston, TX 77030 USA
[5] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[6] Roswell Pk Canc Inst, Dept Pediat, Buffalo, NY 14263 USA
[7] Oregon Hlth Sci Univ, Dept Pediat, Portland, OR 97201 USA
[8] Univ Alberta, Dept Publ Hlth Sci, Edmonton, AB T6G 2M7, Canada
[9] St Jude Childrens Hosp, Dept Epidemiol & Canc Control, Memphis, TN 38105 USA
关键词
D O I
10.1093/jnci/djj243
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Childhood cancer survivors who retain ovarian function after completing cancer treatment are at increased risk of developing premature menopause, defined as cessation of menses before age 40 years. However, published data pertaining to the risk and frequency of premature menopause are limited. Methods: We assessed the incidence of and risk factors for premature menopause in 2819 survivors of childhood cancer who were older than 18 years and were participants in the multicenter Childhood Cancer Survivor Study (CCSS). The comparison group was 1065 female siblings of participants in the CCSS. A multiple Poisson regression model was constructed to determine risk factors for nonsurgical premature menopause. All statistical tests were two-sided. Results: A total of 126 childhood cancer survivors and 33 control siblings developed premature menopause. Of these women, 61 survivors (48%) and 31 siblings (94%) had surgically induced menopause (rate ratio [RR] = 0.8, 95% confidence interval [CI] = 0.52 to 1.23). However, the cumulative incidence of nonsurgical premature menopause was higher for survivors than for siblings (8% versus 0.8%; RR = 13.21, 95% CI = 3.26 to 53.51; P <.001). A multiple Poisson regression model showed that risk factors for nonsurgical premature menopause included attained age, exposure to increasing doses of radiation to the ovaries, increasing alkylating agent score (based on number of alkylating agents and cumulative dose), and a diagnosis of Hodgkin lymphoma. For survivors who were treated with alkylating agents plus abdominopelvic radiation, the cumulative incidence of nonsurgical premature menopause approached 30%. Conclusions: The results of this study will facilitate counseling current survivors about their future risk of premature menopause and aid in designing new regimens that seek to diminish late ovarian toxicity.
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页码:890 / 896
页数:7
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