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Prospective clinical trial of PET/MRI combined with chest enhanced CT in evaluating the efficacy of neoadjuvant chemoradiotherapy for esophageal squamous cell carcinoma

Prospective clinical trial of PET/MRI combined with chest enhanced CT in evaluating the efficacy of neoadjuvant chemoradiotherapy for esophageal squamous cell carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065360
Enrollment
Unknown
Registered
2022-11-03
Start date
2022-11-13
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

esophageal squamous cell carcinoma

Interventions

Group of PET/CT + chest CT enhanced examination:Nil

Sponsors

Renji Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The AJCC staging of the 8th edition suggests that patients of thoracic esophageal squamous cell carcinoma of cT1-2N+M0 or cT3-4aNanyM0; 2. Aged 18-75 years, regardless of gender; 3. Patients with thoracic esophageal squamous cell carcinoma confirmed by cell/tissue pathological biopsy have not previously received systemic anti-tumor therapy; 4. Patients with cT1-2N+M0 or cT3-4aNanyM0 evaluated by imaging examiation will accept the neoadjuvant therapy; 5. KPS is greater than 90 points; 6. Through the discussion by MDT, the general condition can meet the requirements of neoadjuvant therapy; 7. Reproductive age women must finish the pregnant text within 7 days before enroll in the study. Only those with negative result can be included in this trial. Reproductive age patients and their sexual partners should take reasonable contraceptive measures until at least 180 days after the end of the study; 8. Voluntarily enrolled in the trial and signed the consent form.

Exclusion criteria

Exclusion criteria: 1. Combined with the second primary tumor; 2. Cases with previous thoracic and abdominal surgery; 3. Previous history of radiotherapy and chemotherapy; 4. Previous history of esophageal endoscopic treatment; 5. People who are allergic to drugs used in clinical trials, allergic constitution or allergic to multiple drugs; 6. Female patients who plan to become pregnant within 6 months, or are in pregnancy or lactation; 7. Patients who can't or refuse surgical treatment after new adjuvant therapy; 8. Claustrophobic patients; 9. Those who can't stand lifting with both arms and lying down for 15-30 minutes; 10. Those who have participated in clinical trials or are participating in other clinical trials in the past 1 month.

Design outcomes

Primary

MeasureTime frame
Parameters of PET/CT for tumor T staging and N staging;

Countries

China

Contacts

Public ContactZhiyong Sun

Renji Hospital, Shanghai Jiaotong University School of Medicine

sunzhiyong@renji.com+86 13917529020

Outcome results

None listed

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