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Neoadjuvant Radiotherapy in Treating Patients With Stage II, III, IV Esophageal Cancer That Can Be Removed by Surgey

Neoadjuvant Radiotherapy on the Immune Microenvironment in Treating Patients With Stage II, III, IV Esophageal Cancer That Can Be Removed by Surgey

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024237
Enrollment
Unknown
Registered
2019-07-02
Start date
2019-07-15
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

esophageal cancer

Interventions

1:neoadjuvant radiotherapy

Sponsors

Wang Wei
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of thoracic esophageal cancer (cT1b-T4a,N-N+) as determined by clinical staging,required to undergo neoadjuvant radiotherapy and following resection according to the routine procedures. (1) Bulk of gastroesophageal junction tumor should be in the esophagus. (2) Bronchoscopy with biopsy and cytology required if primary esophageal cancer is 3 months; 3. WBC > 4,000/mm3; ANC > 1,500/mm3; Platelet count > 100,000/mm3; Hemoglobin > 9 g/dL; Bilirubin normal; Creatinine normal; AST <=3 times upper limit of normal (ULN); Alkaline phosphatase <= 3 times ULN. 4. Able to take oral medication or undergo enteral administration of medication; 5. Fertile patients must use effective contraception during and for 90 days after completion of study treatment; 6. No concurrent uncontrolled illness, including, but not limited to, any of the following: (1) Ongoing or active infection; (2) Symptomatic congestive heart failure; (3) Unstable angina pectoris; (4) Cardiac arrhythmia;; (5) Psychiatric illness or social situation that would preclude study compliance; 7. No known HIV or hepatitis B or C (active and/or previously treated).

Exclusion criteria

Exclusion criteria: 1. Pregnancy or lactation; 2. There are not enough specimens of tumor tissue or they can not be used for analysis and detection; 3. Refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
gene expression;

Countries

China

Contacts

Public ContactWang Wei

Nanfang Hospital of Southern Medical University

wangwei9500@hotmail.com+86 18520529179

Outcome results

None listed

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