Clinical trial · Interventional
Exemestane Versus Anastrozole as First Line Hormone Therapy in Postmenopausal Metastatic Breast Cancer Patients
Phase II Randomized, Multicenter, Crossover Clinical Trial for Administration of Exemestane vs. Anastrozole as First Line Treatment for Postmenopausal Patients With Hormone Receptor Positive Advanced Breast Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a pivotal phase II, multicenter, open-label trial, designed to compare the efficacy of exemestane versus anastrozole as a first line treatment for advanced breast cancer. One hundred postmenopausal patients, with metastatic, positive hormone receptor breast cancer will be enrolled in this trial.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Anastrozole | Drug | Anastrozole | ALIAS |
| Exemestane | Drug | Exemestane | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Exemestane
- description
- 25mg/day per VO until progression disease, after this progression the patient could receive the another drug (comparator arm) ie Anastrozole by investigator decision
- interventionNames
- Drug: Anastrozole
- type
- ACTIVE_COMPARATOR
- label
- Anastrozole
- description
- 1mg/day per VO until progression disease, after this progression the patient could receive the another drug (experimental arm) ie Exemestane by investigator decision
- interventionNames
- Drug: Exemestane
Primary outcomes (1)
- measure
- Overall Response Rate (ORR) in both arms
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: * Pathological diagnoses of breast cancer. * Postmenopausal women, defined as: * Bilateral surgical oophorectomy or amenorrhoea \>= 5 years; * Age \>= 56 years old and amenorrhoea \>= 1 year; * Chemotherapy induced amenorrhoea \>= 2 years; * Radiotherapy induced amenorrhoea at least 3 months before: * Age \< 56 and \< 5 years of amenorrhoea: follicle-stimulating hormone (FSH) levels to confirm postmenopausal status. * Metastatic breast cancer (stage IV) or non-operable locally advanced breast cancer (stage IIIB). * Positive estrogen and/or progesterone receptors as \>10% cells or \>10fmol/mg. * Measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST) criteria. * Patients who have received adjuvant tamoxifen are eligible, if progression has been established at least 24 months since treatment start. * Neoadjuvant chemotherapy is allowed if progression has been established at least 12 months after end of treatment. * Patients may have received a first line of chemotherapy for advanced disease, but treatment must have ended at least 4 weeks before enrolment, and all acute toxicities must be resolved. Previous treatment with Herceptin is allowed. * Normal haematological, hepatic and renal functions. * Performance status ECOG of 0, 1, 2. * Life expectancy superior to 3 months. * Written informed consent. Exclusion Criteria: * Previous hormone treatment for metastatic disease. * Previous treatment with aromatase inhibitors. * Inflammatory breast cancer, or aggressive metastatic disease, or visceral lesions, or metastasis in the central nervous system (CNS). * Non-measurable disease. * Second malignancy except for basal skin carcinoma or cervical in situ carcinoma adequately treated. If other malignancies, patient must have a disease-free period superior to 5 years. * Treatment with any investigational product in the 4 previous weeks. * Patients with negative estrogen and progesterone receptor tumours.
References
Publications (1)
- RESULTLlombart-Cussac A, Ruiz A, Anton A, Barnadas A, Antolin S, Ales-Martinez JE, Alvarez I, Andres R, Garcia Saenz JA, Lao J, Carrasco E, Camara C, Casas I, Martin M. Exemestane versus anastrozole as front-line endocrine therapy in postmenopausal patients with hormone receptor-positive, advanced breast cancer: final results from the Spanish Breast Cancer Group 2001-03 phase 2 randomized trial. Cancer. 2012 Jan 1;118(1):241-7. doi: 10.1002/cncr.26299. Epub 2011 Jun 29. PMID 21717449