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Effect of Circulating Tumor Cell Detection in Patients with Luminal A Breast Cancer without Lymph Node Metastasis Instead of Conventional Imaging Examination after Operation: Non-inferiority Randomized Controlled Clinical Trials

Effect of Circulating Tumor Cell Detection in Patients with Luminal A Breast Cancer without Lymph Node Metastasis Instead of Conventional Imaging Examination after Operation: Non-inferiority Randomized Controlled Clinical Trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025362
Enrollment
Unknown
Registered
2019-08-25
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast neoplasms

Interventions

Group 1:PET-CT
Group 2:Circulating tumor cell detection by collecting peripheral blood

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. estrogen receptor >=10%, progesterone receptor >= 10% and epidermal growth factor receptor 2 negative; 2. proliferation index Ki-67 < 14%; 3. systemic therapy (chemotherapy, radiotherapy and endocrine therapy) in accordance with the National Comprehensive Cancer Network guidelines; 4. provision of informed consent of patients and their families.

Exclusion criteria

Exclusion criteria: 1. Bilateral breast cancer; 2. inflammatory breast cancer; 3. pregnancy or lactation; 4. history of other cancers or chest radiotherapy; 5. lymph node metastasis.

Design outcomes

Primary

MeasureTime frame
Disease-free survival;

Secondary

MeasureTime frame
Overall survival;Total length of hospital stay;Average length of hospital stay per reexamination;Total cost of reexaminations;Average cost per reexamination;

Countries

China

Contacts

Public ContactJianyi Li

Shengjing Hospital of China Medical University

sjbreast@yeah.net+86 18940257177

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026