Impact of tamoxifen therapy on fertility in breast cancer survivors.
Impact of tamoxifen therapy on fertility in breast cancer survivors.
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DOI:
10.1016/j.fertnstert.2016.10.020
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发表时间:
2017-01
影响因子:
6.7
通讯作者:
Howards, Penelope P.
中科院分区:
文献类型:
--
作者:
Shandley, Lisa M.;Spencer, Jessica B.;Fothergill, Amy;Mertens, Ann C.;Manatunga, Amita;Paplomata, Elisavet;Howards, Penelope P.
To determine if tamoxifen use is associated with decreased ovarian reserve and decreased likelihood of having a child following breast cancer diagnosis. Furthering Understanding of Cancer, Health, and Survivorship in Adult (FUCHSIA) Women Study–a population-based cohort study Not applicable. Three hundred ninety-seven female breast cancer survivors aged 22–45 years who were diagnosed between ages 20–35 years and were at least 2 years post-diagnosis; 108 survivors also participated in a clinic visit. None Time to first child after cancer diagnosis, clinical measures of ovarian reserve (anti-Müllerian hormone [AMH] and antral follicle count [AFC]) after cancer Women who ever used tamoxifen were substantially less likely to have a child following breast cancer diagnosis (hazard ratio [HR]=0.29, 95% confidence interval [CI]: 0.16, 0.54) than women who had never used tamoxifen. After adjusting for age at diagnosis, exposure to an alkylating agent, and race, the HR was 0.25 (95% CI: 0.14, 0.47). However, after adjusting for potential confounders, women who had used tamoxifen had an estimated geometric mean AMH level 2.47 (95% CI: 1.08, 5.65) times higher than women who had never taken tamoxifen. AFC was also higher in the tamoxifen group compared to tamoxifen non-users when adjusted for the same variables (risk ratio=1.21, 95% CI: 0.84, 1.73). Breast cancer survivors who used tamoxifen were less likely to have a child following cancer diagnosis compared to survivors who never used tamoxifen. However, tamoxifen users did not have decreased ovarian reserve compared to tamoxifen non-users.
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影响因子:
2.9
作者:
Quinn, Molly M.;Letourneau, Joseph M.;Rosen, Mitchell P.
通讯作者:
Rosen, Mitchell P.
影响因子:
168.9
作者:
Davies, Christina;Pan, Hongchao;Godwin, Jon;Gray, Richard;Arriagada, Rodrigo;Raina, Vinod;Abraham, Mirta;Medeiros Alencar, Victor Hugo;Badran, Atef;Bonfill, Xavier;Bradbury, Joan;Clarke, Michael;Collins, Rory;Davis, Susan R.;Delmestri, Antonella;Forbes, John F.;Haddad, Peiman;Hou, Ming-Feng;Inbar, Moshe;Khaled, Hussein;Kielanowska, Joanna;Kwan, Wing-Hong;Mathew, Beela S.;Mittra, Indraneel;Mueller, Bettina;Nicolucci, Antonio;Peralta, Octavio;Pernas, Fany;Petruzelka, Lubos;Pienkowski, Tadeusz;Radhika, Ramachandran;Rajan, Balakrishnan;Rubach, Maryna T.;Tort, Sera;Urrutia, Gerard;Valentini, Miriam;Wang, Yaochen;Peto, Richard
通讯作者:
Peto, Richard
DOI:
10.2147/dddt.s75266
发表时间:
2015
期刊:
Drug design, development and therapy
影响因子:
--
作者:
Pala Ş;Atilgan R;Ozkan ZS;Kavak SB;Ilhan N;Akpolat N;Sapmaz E
通讯作者:
Sapmaz E
影响因子:
168.9
作者:
Davies, C.;Godwin, J.;Gray, R.;Clarke, M.;Darby, S.;McGale, P.;Wang, Y. C.;Peto, R.;Pan, H. C.;Cutter, D.;Taylor, C.;Ingle, J.
通讯作者:
Ingle, J.
影响因子:
2.4
作者:
Metindir, J;Aslan, S;Bilir, G
通讯作者:
Bilir, G