Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT04353557

ctDNA Monitoring in Early Breast Cancer

Led by Geneplus-Beijing Co. Ltd. · Updated on 2024-07-18

200

Participants Needed

1

Research Sites

365 weeks

Total Duration

On this page

Sponsors

G

Geneplus-Beijing Co. Ltd.

Lead Sponsor

A

Army Medical University, China

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a observational, single center study, monitoring the circulating tumor DNA (ctDNA) in patients with early breast cancer and assessing the prognostic value and treatment outcome monitoring of ctDNA.

CONDITIONS

Official Title

ctDNA Monitoring in Early Breast Cancer

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 80 years old
  • Histologically proven primary breast cancer with clinical stage I-III
  • Patients with neoadjuvant therapy, and/or radical surgery/breast conserving surgery, adjuvant chemotherapy and target therapy (Her2+), radiotherapy (if indicated)
  • Expected to achieve R0 resection
  • Estimated lifetime is more than 3 months
  • Signed Informed Consent Form
  • Consent to provide research blood samples
Not Eligible

You will not qualify if you...

  • Patients intended to receive adjuvant chemotherapy with Eastern Cooperative Oncology Group (ECOG) performance status 3, 4 or 5
  • Patients intended to receive postoperative radiotherapy with Eastern Cooperative Oncology Group (ECOG) performance status 5
  • Prior diagnosis of cancer in the previous 5 years, other than for basal cell carcinoma of the skin or cervical carcinoma in situ
  • Presence of any systemic illness incompatible with participation in the clinical trial or inability to provide written informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Army Medical Center of PLA, China

Chongqing, Chongqing Municipality, China, 400042

Actively Recruiting

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Research Team

Y

Yan Xu, M.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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