Clinical trial · Interventional
Postoperative Concurrent Chemoradiotherapy Versus Radiotherapy Alone for Patients With Locoregionally Advanced Esophageal Squamous Cell Carcinoma
A Randomized Phase Ⅱ/Ⅲ Trial of Postoperative Concurrent Chemoradiotherapy Versus Radiotherapy Alone for Patients With Locoregionally Advanced Esophageal Squamous Cell Carcinoma
NCT03600831CI-TRIAL-00072856completedPhase 2 / Phase 3ClinicalTrials.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)
The aim of this study is to investigate the effect of postoperative concurrent chemoradiotherapy versus radiotherapy alone for patients with locally advanced esophageal squamous cell carcinoma.
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 Squamous Cell Carcinoma | Esophageal Squamous Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Docetaxel plus cisplatin | Drug | — | UNRESOLVED |
| radiotherapy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- concurrent chemoradiotherapy group
- description
- All patients in this group will receive concurrent chemoradiotherapy with DP regimen (docetaxel plus cisplatin).
- interventionNames
- Drug: Docetaxel plus cisplatin
- Radiation: radiotherapy
- type
- ACTIVE_COMPARATOR
- label
- radiotherapy group
- description
- All patients in this group will receive radiotherapy alone 50Gy (2.0 Gy/fraction, 5 days a week).
- interventionNames
- Radiation: radiotherapy
Primary outcomes (1)
- measure
- Disease-free survival (DFS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. biopsy-confirmed esophageal squamous cell carcinoma 2. age ≤ 70 years old, 3. Karnofsky performance status ≥ 70, 4. R0 esophagectomy according to the pathological examination of the resected specimens, 5. postoperative stage Ⅱ-Ⅳa according to the AJCC 7th edition of tumor-node-metastasis (TNM) classification for esophageal carcinoma 6. Adequate organ functions (1).white blood cell (WBC) ≥3×109⁄L; (2).Absolute neutrophil counts (ANC) ≥1.5×109⁄L; (3).Hemoglobin (Hb) ≥10g⁄dl; (4).Platelet (Plt) ≥100×109⁄L; (5).Total bilirubin \<1.5 upper limit of normal (ULN); (6).Aspartate transaminase (AST) ≤2.5 ULN; (7).Alanine aminotransferase (ALT) ≤2.5 ULN; (8).Creatinine ≤1.5 ULN; (9).adequate pulmonary function (FEV1\>0.8 L;. 7. no previous treatment or severe complications 8. Written informed consent Exclusion Criteria: 1. previous treatment with chemotherapy or radiotherapy 2. greater than 3 months after surgery 3. complete esophageal obstruction after surgery, esophageal perforation; 4. other malignant tumors, except for skin basal cell carcinoma, or cervical carcinoma in situ, who survived with no evidence disease for over 3 years; 5. pregnant or breast-feeding women; 6. patients with any serious concurrent disease, such as severe diabetes, uncontrolled hypertension, serious chronic obstructive pulmonary disease; 7. drug addiction, Alcoholism or AIDS; 8. uncontrolled seizures or psychiatric diseases, loss of control over their own behavior; 9. with clear chemotherapy drug allergy 10. participation in other interventional clinical trials within 30 days;
References
Publications (0)
Data not yet available
No reference posted for this study.