Literature DB >> 22324859

Higher than expected estradiol levels in aromatase inhibitor-treated, postmenopausal breast cancer patients.

T Kunovac Kallak1, J Baumgart, A Stavreus Evers, I Sundström Poromaa, L Moby, K Kask, E Norjavaara, M M Kushnir, J Bergquist, K Nilsson.   

Abstract

OBJECTIVE: Vaginal estradiol is considered contraindicated in aromatase inhibitor (AI)-treated patients because of the risk of elevated estrogen levels. This leaves limited treatment options for patients experiencing gynecological symptoms. However, in clinical practice, no precise estimation has been performed of circulating estrogens and aromatase index in postmenopausal breast cancer patients on long-lasting AI or tamoxifen treatment.
METHODS: Steroid hormones were measured using liquid chromatography tandem mass spectrometry (LC-MS/MS) and extraction radioimmunoassay (RIA). Postmenopausal AI-treated patients (n =33) were compared with tamoxifen-treated patients (n =34) and controls without vaginal treatment (n =56), with vaginal estradiol (n =25), or with estriol (n =11) treatment.
RESULTS: By use of LC-MS/MS, median (range) estradiol plasma concentrations were 16.7 (2.4-162.6), 31.0 (13.4-77.1), 27.2 (7.8-115.8) and 33.3 (20.3-340.1) pmol/l in AI-treated breast cancer patients, tamoxifen-treated breast cancer patients, postmenopausal controls and postmenopausal controls on vaginal estradiol, respectively. The AI-treated group and subgroups had significantly lower estradiol and estrone concentrations than all other groups (p <0.05). There was extensive interindividual variation in estradiol concentration within the AI-treated group, measured using both LC-MS/MS (2.3-182.0 pmol/l) and extraction RIA (2.4-162.6 pmol/l). The AI-treated group had lower aromatase index compared to all other groups (p <0.05-0.001).
CONCLUSION: Circulating estrogen levels may have been underestimated in previous longitudinal studies of AI-treated breast cancer patients. Additional studies are required to further evaluate the role of circulating estrogens in breast cancer patients suffering from gynecological symptoms.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22324859     DOI: 10.3109/13697137.2011.642427

Source DB:  PubMed          Journal:  Climacteric        ISSN: 1369-7137            Impact factor:   3.005


  2 in total

1.  Breast cancer, endometrial cancer, and cardiovascular events in participants who used vaginal estrogen in the Women's Health Initiative Observational Study.

Authors:  Carolyn J Crandall; Kathleen M Hovey; Christopher A Andrews; Rowan T Chlebowski; Marcia L Stefanick; Dorothy S Lane; Jan Shifren; Chu Chen; Andrew M Kaunitz; Jane A Cauley; JoAnn E Manson
Journal:  Menopause       Date:  2018-01       Impact factor: 2.953

2.  Low levels of circulating estrogen sensitize PTEN-null endometrial tumors to PARP inhibition in vivo.

Authors:  Deanna M Janzen; Daniel Y Paik; Miguel A Rosales; Brian Yep; Donghui Cheng; Owen N Witte; Huseyin Kayadibi; Christopher M Ryan; Michael E Jung; Kym Faull; Sanaz Memarzadeh
Journal:  Mol Cancer Ther       Date:  2013-11-12       Impact factor: 6.261

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.