Exemestane, Letrozole, or Anastrozole in Treating Postmenopausal Women Who Are Undergoing Surgery for Stage II or Stage III Breast Cancer

NCT00265759 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 622

Last updated 2025-04-23

Study results available
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Summary

RATIONALE: Estrogen can cause the growth of breast cancer cells. Hormone therapy using exemestane, letrozole, or anastrozole, may fight breast cancer by lowering the amount of estrogen the body makes. Giving exemestane, letrozole, or anastrozole before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. It is not yet known whether exemestane, letrozole, or anastrozole is more effective in treating breast cancer.

PURPOSE: This randomized phase III trial is studying exemestane, letrozole, and anastrozole to compare how well they work in treating postmenopausal women who are undergoing surgery for stage II or stage III breast cancer.

Conditions

Interventions

DRUG

anastrozole

Given PO

DRUG

exemestane

Given PO

DRUG

letrozole

Given PO

PROCEDURE

Therapeutic Conventional Surgery

Undergo partial or radical mastectomy or lumpectomy with or without lymph node dissection

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Cancer and Leukemia Group B

    collaborator NETWORK
  • Alliance for Clinical Trials in Oncology

    lead OTHER

Principal Investigators

  • Matthew J. Ellis, MD, PhD, FRCP · Washington University Siteman Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2012-08-31
Completion
2019-11-27

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00265759 on ClinicalTrials.gov