Clinical trial · Observational
Definitive Radiotherapy for Cervical and Upper Thoracic Esophageal Cancer (ChC&UES): A Multi-center Real World Study
NCT06481449CI-TRIAL-00078447unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Cervical and upper thoracic esophageal cancer (ESCA) presents treatment challenges due to limited clinical evidence. This multi-center study (ChC\&UES) explores radical radio(chemo)therapy efficacy and safety
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Esophageal Neoplasm | Esophageal Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (2)
- label
- High dose radiotherapy (≥60Gy)
- description
- Patients who received 60 Gy or more than 60Gy radiation dose for radical radiation therapy for the primary tumor.
- label
- Low dose radiotherapy (50-<60Gy)
- description
- Patients who received 50-\<60Gy radiation dose for radical radiation therapy for the primary tumor.
Primary outcomes (2)
- measure
- Overall survival time (OS)
- timeFrame
- 2000.1.1-2024.6.20
- description
- Compared the differences in overall survival (OS) between low dose radiation and high dose radiation group after definitive radiotherapy. OS is defined as time from start of enrollment to death from any cause.
- measure
- progression-free survival (PFS)
- timeFrame
- 2000.1.1-2024.6.20
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age 18 and older. 2. Confirmation of esophageal cancer through histopathology or cytology. 3. Primary tumor location within the cervical or upper thoracic segment, extending from the upper esophageal sphincter to the azygos vein. 4. Absence of distant metastasis. 5. Patients unable or unwilling to undergo surgical treatment for various reasons. 6. Receipt of radical radiotherapy as the first-line treatment, with or without chemotherapy, immunotherapy, or targeted therapy. 7. Undergoing conventional radiation therapy (1.8-2.0Gy per session, once per day). 8. Receiving 3DCRT or IMRT radiotherapy. 9. Availability of complete radiotherapy prescription dose information and follow-up records. Exclusion Criteria: 1. Receipt of radiation dose below 50Gy. 2. History of other malignancies (except for cured cancer in situ and malignancies cured for over 5 years) or laryngeal invasion. 3. Diagnosis of double primary esophageal cancer. 4. Prior chest radiation therapy within the past 5 years. 5. Recurrent or metastatic esophageal cancer. 6. Receipt of 2D radiotherapy, large fractionation, or hyper-fractionation radiotherapy. 7. Patients with incomplete radiotherapy dose and follow-up data.
References
Publications (0)
Data not yet available
No reference posted for this study.