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Study identifier: NCT03561740 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Recruiting

A Study of the Addition of Metronomic Capecitabine to Standard Adjuvant Therapy in High Risk HER2+ BC paTients

Condition: Breast Cancer  ·  Sponsor: Sun Yat-sen University

PhasePhase 3
Planned participants794
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

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About this study

Breast cancer is the most common malignant tumor in women. Recurrent or metastatic breast cancer is incurable. High risk patients usually have the following characteristics, such as, non-pCR after neoadjuvant therapy, lymph nodes positive, \>2cm tumor size, HER2 overexpression, etc. Intensive targeted or chemo therapy could improve prognosis. Previous studies have shown the efficacy and feasibility of intensive treatment of capecitabine in non-pCR breast cancer patients. Given the metronomic capecitabine therapy is well tolerated, we designed this study to compare the efficacy and safety of adding metronomic capecitabine to standard adjuvant therapy for high risk HER2+ breast cancer patients.

This description comes directly from the study's public registry record.

Talk to the study team

Shusen Wang, MD  ·  +86-13926168469  ·  wangshs@sysucc.org.cn

Wen Xia, MD  ·  +86-18565557603  ·  xiawen@sysucc.org.cn

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Locations (1)

Shusen WangGuangzhou, Guangdong, ChinaRecruiting

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