Evaluating pre-operative therapy effects in breast cancer

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the impact of pre-operative therapy on response rates and survival outcomes in patients with breast cancer. It will analyze both prospective and retrospective data to compare the effectiveness of different pre-operative regimens based on patients' clinicopathological characteristics. The study will include women aged 18 and older who have been histologically confirmed to have primary breast cancer and are scheduled to receive pre-operative therapy.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Female, Aged ≥18 years
* Histologically confirmed primary breast cancer
* Plan to receive pre-operative therapy
* Adequate organ function

Exclusion Criteria:

* History of neurological or psychological disease, including epilepsy or dementia
* Not suitable to participate in this study judged by investigators

Where it's running

• Renji Hospital, School of Medicine, Shanghai Jiaotong University
  Shanghai, China Recruiting

Study contacts

• Study coordinator: Wenjin Yin
• Email: yinwenjin@renji.com
• Phone: 86(21)68385569

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.