Skip to main content
Clinical Trials/RBR-5pygzhj
RBR-5pygzhj
Recruiting
Phase 2

A phase II single-arm clinical trial to evaluate the feasibility and efficacy of Neoadjuvant Anastrozole in luminal, low proliferative index Breast Cancer patients at TNM stages II and III

Hospital de Câncer de Barretos0 sitesJuly 18, 2022

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Malignant neoplasm of breast
Sponsor
Hospital de Câncer de Barretos
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 18, 2022
End Date
December 31, 2024
Last Updated
2 years ago
Study Type
Intervention
Sex
Female

Investigators

Sponsor
Hospital de Câncer de Barretos

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older; histologically confirmed unilateral primary invasive carcinoma of the breast;
  • estrogen receptor positive (Allread \=6\); progesterone receptor positive (any percentage value); HER\-2 negative; histological grade according to Scarf\-Bloom\-Richardson 1 or 2; Ki\-67 antigen \<50% on immunohistochemistry; TNM staging by 8th Edition cT2\-4c cNqq M0; tumor clinically palpable and larger than 2cm on palpation and/or imaging examination; functional capacity assessed by Eastern Cooperative Oncology Group Performance Status (ECOG\-PS) of 0 \- 2; adequate hematologic, renal, and hepatic function; absence of any psychological, familial, sociological, or geographic condition that would potentially hinder adherence to the study protocol and follow\-up schedule; patient agreeent to provide the required research biopsies from baseline, week 4 (re\-biopsy) and surgery for biomarker and biorepository research.

Exclusion Criteria

  • Inflammatory breast cancer defined as clinically significant erythema of the breast and/or documented dermal lymphatic invasion; excisional biopsy of current breast cancer; hormone replacement therapy of any kind, megestrol acetate or raloxifene within one week prior to inclusion; axillary staging surgical procedure prior to study entry; clinical or radiographic evidence of metastatic disease; skin implants in the breast that prevent the required research biopsies or may interfere with palpation of the breast lesion; treatment for cancer, including surgery, radiation therapy, chemotherapy, biotherapy, hormone therapy, or any investigational product prior to study entry; history of previous invasive breast cancer; patient with any other concomitant serious and/or uncontrolled medical condition that may, in the opinion of the Investigator, cause unacceptable safety risks, contraindicate the patient's participation in the clinical trial or compromise adherence to the protocol (e.g. chronic pancreatitis, chronic active hepatitis, liver cirrhosis or any other significant liver disease, active, untreated or uncontrolled fungal, bacterial or viral infections, active infection requiring systemic antibacterial therapy, etc.) or limit life expectancy to \= 5 years.

Outcomes

Primary Outcomes

Not specified

Similar Trials