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MRD combined with CTC for postcontamental evaluation and dynamic monitoring

MRD combined with CTC for postcontamental evaluation and dynamic monitoring

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096946
Enrollment
Unknown
Registered
2025-02-10
Start date
2025-02-15
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Esophageal malignancy

Interventions

Patients with locally advanced esophageal squamous cell carcinoma:None

Sponsors

Beijing Friendship Hospital affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age > 18 years old; 2) Patients with cT2N+M0 or cT3-cT4NanyM0 esophageal squamous cell carcinoma; 3) Patients who have not received any anti-tumor treatment in the past, including but not limited to surgery, radiotherapy, chemotherapy, immunotherapy, targeted therapy, etc.; 4) Able to provide tissue and blood samples for biological analysis; 5) Voluntarily sign the informed consent form (or signed by the legal representative) to prove that they understand the purpose of the study and the operations required for the study and are willing to participate in the study

Exclusion criteria

Exclusion criteria: 1) Aged > 70 years, or with severe comorbidities, such as cardiovascular and cerebrovascular diseases that affect surgery; 2) Previous history of malignant tumors, or received chemotherapy, radiotherapy, molecular targeted therapy, or Chinese medicine treatment and other anti-tumor treatments before enrollment; 3) Preoperative examinations indicate that the tumor may invade the main trachea, heart or large blood vessels; 4) Allergic to the active ingredients or excipients of the drug in this study; 5) Pregnant or lactating patients. 6) Other situations that the researchers believe are not suitable for enrollment

Design outcomes

Primary

MeasureTime frame
Overall survival;Disease-free survival;

Secondary

MeasureTime frame
pCR;MPR;

Countries

China

Contacts

Public ContactYong Cui

Beijing Friendship Hospital affiliated to Capital Medical University

cywork1@sina.com+86 136 9369 3620

Outcome results

None listed

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