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Trial of Low Dose Tamoxifen in Women With Breast Intraepithelial Neoplasia - Long Term Follow-up
Sponsor: Andrea DeCensi
Summary
The aim of the study is to evaluate whether tamoxifen at a low dose of 5mg/d reduces in the long term the incidence of invasive breast cancer and ductal carcinoma in situ, DCIS (DIN 1c, 2, 3) of the breast, in woman operated for lobular intraepithelial neoplasia (LIN1, 2 and 3) or ER-positive ductal intraepithelial neoplasia (DIN 1b, DIN2, DIN3, 1a excluded) of the breast. To improve the risk-benefit ratio, the use of lower doses of the drug has been proposed. Biomarker trials revealed that 5 mg/d was noninferior to 20 mg/d in inhibiting proliferation of breast cancer and normal endometrial tissue. By contrast, the risk of endometrial cancer si dose-dependent, and the dose reduction can lead a substantial decrease. Morover a dose of 5 mg/day is associated with an overall decrease of the estrogenic activity of tamoxifen on insulin like growth factor (IGF-I), sex hormone-binding globulin (SHBG) and antithrombin-III, with a decrease of venous thromboembolic events. Moreover, tamoxifen exhibits a high tissue distribution, so that a dose of 5 mg/day attains at the breast tissue level a concentration 10 times higher than that needed to inhibit cell growth in vitro. A prospective cohort study also showed that 10 mg on alternate days halves recurrence of DCIS in postmenopausal women. It has been shown that the treatment of dysplasia or pre-cancer drives the reduction of the invasive neoplasms onset. This is a chemoprevention trial designed to validatate the low-dose Tamoxifen in women with diseases at high evolutionary risk. The demonstration of efficacy and safety of such a treatment for the prevention of the invasive breast cancer would lead improvements in term of survival and quality of life for the patients at increased risk.
Official title: Randomized Placebo-controlled Phase III Trial of Low Dose Tamoxifen in Women With Breast Intraepithelial Neoplasia - Long Term Follow-up
Key Details
Gender
FEMALE
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
500
Start Date
2008-11-12
Completion Date
2028-12-31
Last Updated
2023-07-17
Healthy Volunteers
No
Conditions
Interventions
Tamoxifen
placebo
Locations (14)
Ospedali riuniti ASL AL - Ospedale SS. Antonio e Margherita
Tortona, Alessandria, Italy
Istituto Scientifico Romagnolo per lo studio e la cura dei tumori
Meldola, Forlì-Cesena, Italy
Ospedale di Carpi "Bernardino Ramazzini"
Carpi, Modena, Italy
IRCCS Istituto Tumori Giovanni Paolo II
Bari, Italy
Azienda Ospedaliera Mater Domini Catanzaro
Catanzaro, Italy
E.O. Ospedali Galliera
Genoa, Italy
IEO - European Institute of Oncology IRCCS
Milan, Italy
Azienda Ospedaliera-Universitaria Policlinico di Modena
Modena, Italy
Istituto Nazionale Tumori IRCCS Fondazione G. Pascale
Naples, Italy
ICS Maugeri -Centro Medico di Pavia
Pavia, Italy
AUSL - Oncologia Medica
Ravenna, Italy
Azienda Ospedaliera-Universitaria Città della Salute e della Scienza di Torino
Torino, Italy
Azienda Socio-Sanitaria Territoriale Sette Laghi, Varese
Varese, Italy
Azienda ULSS8 Berica
Vicenza, Italy