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PREOPERATIVE TREATMENT OF POSTMENOPAUSAL BREAST CANCER PATIENTS WITH LETROZOLE: A RANDOMIZED DOUBLE-BLIND MULTICENTER STUDY

Not Applicable
Registration Number
PER-019-99
Lead Sponsor
OVARTIS BIOSCIENSES PERÚ S.A.,
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. were poslmenopausal women with untreated primary
breast cancer, confirmed by core needle biopsy, with 10% nuclear Postmenopausal breast cancer patients with ER and/or PgR positive tumors,
2.Clinical staging mandated T2-4a-c,NO-2, MO tumors.
3.defined postmenopausal status
4. Tumors, measurable by clinical examination, mammography and ultrasound.
5. Proper functioning of bone marrow(RC >3.5 x109/L . plaquetes >100.0 x109/L, and Hb 11.0 g/dL).
6. Adequate renal founction (<120 umol/L ) and liver function (bilirrubine < 25 :umol/L, AST (SGOT <60 U/L).
7. a life expectancy of at least six months
8. written informed consent

Exclusion Criteria

1. prior exposure to letrozole or tamoxifen.
2. . endocrine pathology: DM, confirmed hypothyroidism, sd. Cushing, Addison´s disease (treated or not).
3. Patients with unstable angina or uncontrolled heart disease (Class III / IV)
4. Patients with bilateral breast tumors
5. candidates for conservative surgery
6. evidence of inflammatory breast cancer or metastasis
7. any other neoplasm, except ca uterine cervix treated with conization or basal or squamous cell carcinoma of adequately treated skin or other cancer curable as hodking lymphoma and not hodking if more than 5 years have passed and there has been no recurrence.
8. Concomitant antineoplastic treatment QT, immunotherapy, MRB, endocrine therapy, bisphosphonates and radiotherapy. Patients who have received THR will not be excluded if it is found to have been discontinued 2 weeks before the trial.
9. Concomitant treatment with steroids for other indications than cancer, with the exception of aerosols for COPD and intra-articular injection as an anti-inflammatory treatment.
10. Other experimental drugs.
11. History of non-compliance with medical treatment or unreliable patients.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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