Everolimus in Breast Cancer Patients After Pre-operative Chemotherapy

Phase 2

• Conditions: Breast Neoplasms
• Interventions: Drug: Everolimus

• Registration Number: NCT01088893
• Lead Sponsor: Organisation for Oncology and Translational Research

Brief Summary

This is a randomized controlled pilot study investigating signals involved in drug resistance to chemotherapy.

Patient will be randomized to undergo observation or to receive Everolimus after completion of neoadjvuant treatment (anthracycline and/or taxane-based) and before surgery. The patients will be monitored for efficacy and safety.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2009-08-11
• Study Start: 2009-11
• Study First Submitted QC: 2010-03-16
• Study First Posted: 2010-03-17
• Status Verified: 2012-05
• Last Update Submitted: 2012-05-22
• Last Update Posted: 2012-05-24
• Primary Completion: 2012-12
• Study Completion: 2013-03

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

• Women aged ≥ 18 years;
• Histologically and/or cytologically confirmed invasive ductal or lobular breast cancer;
• Tumor of 3 cm or greater at time of diagnosis
• Measurable primary tumor after neoadjuvant treatment before randomization
• No prior chemotherapy for breast cancer;
• ECOG performance status ≤1 or Karnofsky performace status ≥ 70%
• Adequate liver/renal function
• Able to swallow whole tablets.
• Able to give written informed consent
• Able to follow prescription instructions reasonably well

Exclusion Criteria

• Male patient
• Prior history of other malignancy within 5 years of study entry, aside from contralateral breast carcinoma, appropriately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin
• Distant metastasis, including skin involvement beyond the breast area
• Other severe acute or chronic medical or psychiatric condition, or laboratory abnormality that would impart, in the judgment of the investigator, excess risk associated with study participation or study drug administration, or which, in the judgment of the investigator, would make the patient inappropriate for entry into this study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Everolimus	Everolimus	-

Primary Outcome Measures

Name	Time	Method
measure change of biomarkers in pre- and post- surgery samples	baseline and 1 month

Trial Locations

Locations (1)

Unimed Medical Institute; 🇨🇳 Hong Kong, China