Improving treatment for obese women with early stage cancer of the uterus: Rationale and design of the levonorgestrel intrauterine device ± Metformin ± weight loss in endometrial cancer (feMME) trial

被引:52
作者
Hawkes, A. L. [1 ]
Quinn, M. [2 ]
Gebski, V. [3 ]
Armes, J. [4 ]
Brennan, D. [5 ]
Janda, M. [1 ]
Obermair, A. [1 ,5 ]
机构
[1] Queensland Univ Technol, Sch Publ Hlth & Social Work, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[2] Royal Womens Hosp, Melbourne, Vic, Australia
[3] Clin Trials Ctr, Natl Hlth & Med Res Council, Sydney, NSW, Australia
[4] Mater Adult Hosp, South Brisbane, Qld, Australia
[5] Royal Brisbane &Womens Hosp, Queensland Ctr Gynaecol Canc, Brisbane, Qld 4029, Australia
关键词
Endometrial cancer; Progestin/Progesterone; Levonorgestrel intrauterine device; Metformin; Weight loss; Physical activity; LIFE-STYLE INTERVENTION; HYPERPLASIA; PROGESTIN; RISK; ADENOCARCINOMA; EXERCISE; SAFETY; CARE; METAANALYSIS; OVERWEIGHT;
D O I
10.1016/j.cct.2014.06.014
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: Endometrial adenocarcinoma (EC) is the most common gynaecologic cancer. Up to 90% of EC patients are obese which poses a health threat to patients post-treatment. Standard treatment for EC includes hysterectomy, although this has significant side effects for obese women at high risk of surgical complications and for women of childbearing age. This trial investigates the effectiveness of non-surgical or conservative treatment options for obese women with early stage EC. The primary aim is to determine the efficacy of: levonorgestrel intrauterine device (LNG-IUD); with or without metformin (an antidiabetic drug); and with or without a weight loss intervention to achieve a pathological complete response (pCR) in EC at six months from study treatment initiation. The secondary aim is to enhance understanding of the molecular processes and to predict a treatment response by investigating EC biomarkers. Methods: An open label, three-armed, randomised, phase-II, multi-centre trial of LNG-IUD +/- metformin +/- weight loss intervention. 165 participants from 28 centres are randomly assigned in a 3:3:5 ratio to the treatment arms. Clinical, quality of life and health behavioural data will be collected at baseline, six weeks, three and six months. EC biomarkers will be assessed at baseline, three and six months. Conclusions: There is limited prospective evidence for conservative treatment for EC. Trial results could benefit patients and reduce health system costs through a reduction in hospitalisations and through lower incidence of adverse events currently observed with standard treatment. Crown Copyright (C) 2014 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 21
页数:8
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