Clinical Trials

JBCRG-14

Phase II study of Letrozole combined with Cyclophosphamide and Capecitabine(LCX) for Hormone-Sensitive advanced breast cancer(age over 65)

Status
Study Closed

Objectives
First: Evaluation of the response rate and the pathological response for primary site , and the safety of Letrozole combined with Cyclophosphamide and Capecitabine (LCX) for Hormone-Sensitive advanced breast cancer(age over 65) . At the same time, the breast-conserving surgery rate, relapse-free survival and overall survival will be assessed. In addition, the clinical efficacy as well as biological properties of the cancer tissue will be investigated using molecular biological and biochemical techniques. Second: Safety,Efficacy

Subjects

Endpoints
First: Overall Response Rate Second: Pathological Complete Response, Safety, Breast Conserving Rate, Disease-free Survival

Trial Period
Oct. 2011~Sep.2018 (Entry:2years, Follow up:5years)

Lead Principal Investigator
Takahiro Nakayama (Department of breast and endocrine surgery, Osaka Medical Center for Cancer and Cardiovascular Disease)

Target Sample Size
32

Regimen
Letrozole, Cyclophosphamide and Capecitabine

Source of Funding
JBCRG(Japan Breast Cancer Research Group)

Conference Presentation

Articles and Publications

UMIN-ID
UMIN000006708

jRCT

Memo

COI Disclosure

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