Skip to content

Retrospective Analysis of Different Treatment Methods for Patients with Synchronous Esophageal Cancer

Retrospective Analysis of Different Treatment Methods for Patients with Synchronous Esophageal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122207
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-10
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Esophageal Cancer

Interventions

Observation group (including 1. Surgery group: Patients who received surgery as the main treatment method
2. Chemotherapy group: Patients who received chemotherapy as the main treatment mode
3. Radiotherapy group: patients who received radiotherapy as the main treatment method
4. Comprehensive treatment group: patients who received combined treatment of multiple treatment methods.):None

Sponsors

Meishan City People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Inclusion Criteria: Age >=40 and =4 cycles of platinum-based chemotherapy. Radiotherapy group: Received radical radiotherapy (dose >=50 Gy). Multimodality group: Completed neoadjuvant therapy followed by surgery, or concurrent chemoradiotherapy. 3.Data Integrity: Complete baseline data (including imaging reports for TNM staging). At least 1 year of regular follow-up (outpatient/telephone).

Exclusion criteria

Exclusion criteria: 1.Clinical Characteristics: History of other malignant tumors. Severe cardiac dysfunction (NYHA Class III–IV) or hepatic/renal insufficiency (Child-Pugh Grade C). 2.Treatment-Related: Received palliative treatment or non-standard regimens. Treatment interruption (chemotherapy 30% (e.g., staging, treatment regimen). Lost to follow-up or incomplete follow-up data. Concurrent participation in other interventional clinical trials.

Design outcomes

Primary

MeasureTime frame
Overall Survival;Disease-Free Survival;Local Control Rate;Postoperative Recovery Duration;Hospital Stay Duration;Incidence of Adverse Events (including anastomotic leakage, pulmonary infection, incisional infection, etc.);Chemotherapy-Related Adverse Effects (including myelosuppression, nausea and vomiting, alopecia, etc.);Radiotherapy-Related Adverse Effects (including esophageal perforation, radiation pneumonitis, etc.);

Countries

China

Contacts

Public ContactShi Yong

Meishan City People's Hospital

3265664178@qq.com+86 28 38025162

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026