Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/19400
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Davis, Susan R | - |
dc.contributor.author | Robinson, Penelope J | - |
dc.contributor.author | Jane, Fiona | - |
dc.contributor.author | White, Shane | - |
dc.contributor.author | Brown, Kristy A | - |
dc.contributor.author | Piessens, Sofie | - |
dc.contributor.author | Edwards, Andrew | - |
dc.contributor.author | McNeilage, Jane | - |
dc.contributor.author | Woinarski, Jillian | - |
dc.contributor.author | Chipman, Mitchell | - |
dc.contributor.author | Bell, Robin J | - |
dc.date | 2018-08-14 | - |
dc.date.accessioned | 2018-09-17T01:47:05Z | - |
dc.date.available | 2018-09-17T01:47:05Z | - |
dc.date.issued | 2018-11 | - |
dc.identifier.citation | Clinical Endocrinology 2018; 89(5): 605-612 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/19400 | - |
dc.description.abstract | We investigated whether metformin prevents tamoxifen-induced endometrial changes and insulin resistance (IR) after a diagnosis of breast cancer. This was a single centre, randomized, double-blind, placebo-controlled, parallel group trial. Postmenopausal women with hormone receptor-positive breast cancer taking tamoxifen were randomly allocated to metformin 850mg or identical placebo, twice daily, for 52 weeks. Outcome measures included double endometrial thickness (ET) measured by transvaginal ultrasound, fasting insulin, glucose and IR estimated by the homeostasis model of assessment (HOMA-IR). 112 women were screened and 102 randomized. Results are presented as median (range). The 101 women who took at least one dose of medication were aged 56 (43-72) years, 5(0.5-28) years post menopause and had taken tamoxifen for 28.9 (0-367.4) weeks. The baseline ET was 2.9mm (1.4-21.9) for the placebo group (n=52) and 2.5mm (1.3-14.8) for the metformin group (n=50). At 52 weeks, the median ET was statistically significantly lower for the metformin (n=36) than the placebo group (n=45), (2.3 mm (1.4-7.8) vs 3.0 (1.2-11.3); p=0.05). 13.3% allocated to placebo had an ET greater than 4mm vs 5.7% for metformin (p=0.26). There was no endometrial atypia or cancer. Compared with placebo, metformin resulted in significantly greater baseline adjusted reductions in weight (p<0.001), waist circumference (0.03) and HOMA-IR (p<0.001). Metformin appears to inhibit tamoxifen-induced endometrial changes and has favourable metabolic effects. Further research into the adjuvant use of metformin after breast cancer and to prevent, EH and cancer is warranted. This article is protected by copyright. All rights reserved. | - |
dc.language.iso | eng | - |
dc.title | The benefits of adding metformin to tamoxifen to protect the endometrium- a randomized placebo-controlled trial. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Clinical Endocrinology | - |
dc.identifier.affiliation | Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | Weill Cornell Medicine, NY, NY, USA | - |
dc.identifier.affiliation | Camberwell Ultrasound for Women, Melbourne, Malvern, Vic, Australia | - |
dc.identifier.affiliation | Epworth Healthcare, East Melbourne, Vic, Australia | - |
dc.identifier.affiliation | Victorian Breast & Oncology Care, East Melbourne, Vic, Australia | - |
dc.identifier.affiliation | Women's Health Research Program, School of Public Health and Preventive Medicine, Monash University, Melbourne, Vic, Australia | - |
dc.identifier.doi | 10.1111/cen.13830 | - |
dc.identifier.pubmedid | 30107043 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | White, Shane | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
Appears in Collections: | Journal articles |
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.