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ACTIVE NOT RECRUITING
NCT01357772
PHASE3

Trial of Low Dose Tamoxifen in Women With Breast Intraepithelial Neoplasia - Long Term Follow-up

Sponsor: Andrea DeCensi

View on ClinicalTrials.gov

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

Interventions

DRUG

Tamoxifen

DRUG

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