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Is ENI Necessary For Patients With Thoracic Esophageal Cancer After Esophagectomy And With Pathological Stage Of T1-2,N+,M0

Is Elective Nodal Irradiation (ENI) Necessary For Patients With Thoracic Esophageal Squamous Cell Carcinoma Who Undergo Esophagectomy And With Pathological Stage Of T1-2,N+,M0 -- A Randomized Phase Ⅲ Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01398449
Enrollment
874
Registered
2011-07-20
Start date
2011-04-30
Completion date
2017-12-31
Last updated
2011-07-20

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

Conditions

Esophageal Squamous Cell Carcinoma

Keywords

thoracic esophageal squamous cell carcinoma, esophagectomy, elective nodal irradiation, adjuvant chemotherapy

Brief summary

Is elective nodal irradiation (ENI) necessary for patients with thoracic esophageal cancer after esophagectomy and with pathological stage of T1-2,N+,M0?

Detailed description

Patient Population: Thoracic esophageal squamous cell carcinoma after esophagectomy with at least 15 lymph nodes removed for adequate nodal staging. R0 resection; T1-2, N+, M0. Scheme: After esophagectomy, patients are firstly stratified by numbers of lymph node metastasis (\<3 or \>=3). Then patients are randomized to 2 arms: Arm A: Adjuvant chemotherapy (4 cycles). Arm B: Adjuvant chemotherapy (4 cycles) + Elective Nodal Irradiation (bilateral supraclavicular fossa and mediastinum).

Interventions

OTHERAdjuvant chemotherapy only

Sponsors

The First Affiliated Hospital of Soochow University
CollaboratorOTHER
The Affiliated Tumor Hospital of Nantong University, Nantong, Jiangsu Province, China
CollaboratorOTHER
Jiangsu Cancer Institute & Hospital
CollaboratorOTHER
Affiliated Hospital of Jiangsu University
CollaboratorOTHER
Zhejiang Cancer Hospital
CollaboratorOTHER
First Affiliated Hospital of Wenzhou Medical University
CollaboratorOTHER
Zhejiang University
CollaboratorOTHER
The First Affiliated Hospital of Anhui Medical University
CollaboratorOTHER
Anhui Provincial Hospital
CollaboratorOTHER_GOV
Fujian Cancer Hospital
CollaboratorOTHER_GOV
Shanghai Chest Hospital
CollaboratorOTHER
Shanghai Pulmonary Hospital, Shanghai, China
CollaboratorOTHER
RenJi Hospital
CollaboratorOTHER
Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 and ≤70 2. ECOG performance status 0-1 3. Weight is not less than 90% of it before operation 4. Registration within 8 weeks after esophagectomy 5. Histologically proven primary thoracic esophageal squamous cell carcinoma 6. R0 resection and number of lymph nodes dissected ≥15 after esophagectomy 7. Stage T1-2N1-3M0 based pathological diagnosis 8. Chest and abdominal contrast enhanced CT within 6 weeks prior to registration(PET/CT scan is selective) 9. Without supraclavicular nodes and abdominal regions nodes existed after surgery 10. Without neo-adjuvant chemotherapy and radiotherapy 11. WBC≥ 4.0X109/L ,Absolute neutrophil count (ANC) ≥ 2.0X109/L 12. Platelets ≥ 100X109/L 13. Hemoglobin ≥ 90g/L(without blood transfusion) 14. AST (SGOT)/ALT (SGPT) ≤ 2.5 x upper limit of normal, Bilirubin ≤ 1.5 x upper limit of normal 15. Creatinine ≤ 1.5 x upper limit of normal 16. Sign study-specific informed consent prior to study entry

Exclusion criteria

1. Multiple primary esophageal tumors 2. Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years (For example, carcinoma in situ of the breast, oral cavity, or cervix are all permissible). 3. Severe, active comorbidity, defined as follows: 3.1 Unstable angina and/or congestive heart failure requiring hospitalization within the last 3 months 3.2 Transmural myocardial infarction within the last 6 months 3.3 Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration 3.4 Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration 3.5 Acquired immune deficiency syndrome (AIDS) based upon current CDC definition; note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatments involved in this protocol may be significantly immunosuppressive. 4. Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception. 5. Prior systemic chemotherapy, prior radiation therapy or prior target drug therapy

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalTo evaluate elective nodal irradiation (ENI) is better for the overall survival of patients with thoracic esophageal cancer after esophagectomy who with pathological stage of T1-2, N positive, M0

Secondary

MeasureTime frameDescription
Locoregional control rate
Safety and Tolerability (incidence rate of adverse events)the incidence rate of adverse events, especially radiation-induced lung toxicity
Failure patternTo evaluate the rationality of ENI after esophagectomy by analyzing the therapeutic failure patterns especially by comparing the in-field and out-of-field recurrences

Countries

China

Contacts

Primary ContactXu-Wei Cai, M.D., Ph.D.
birdhome2000@hotmail.com8621-64175590

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026