A Phase II Study of Chemoradiotherapy With Nimotuzumab in Unresectable Esophageal Cancer

• Status: Recruiting
• Trial end date: 2022-08-01
• Target enrollment: 0
• Participant gender: All

Summary

This phase II clinical study is designed to evaluate the 1 year local tumor control rates after the targeted therapy of intensity-modulated radiation therapy synchronized chemotherapy with nimotuzumab combined with S-1 in local advanced esophageal squamous cell carcinomas based on Nutritional Risk Screening NRS2002.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Chinese Academy of Medical Sciences
• Treatments: Nimotuzumab

Criteria

Inclusion Criteria:

• ≥18 years

• Pathologically or cytologically proven esophageal squamous cell carcinomas in patients staged as T2-4N0-1M0-1b (AJCC 6th TNM staging, M1b limited to clavicular or celiac lymph node metastasis)

• Primary treatment accepted in Chinese Academy of Medical Sciences

• KPS ≥70

• NRS score ≥2

• Cervical or thoracic esophageal cancer histologically proved esophageal cell carcinoma

• Normal organ and marrow function as defined below:

Hemoglobin: greater than or equal to 100g/L ;Leukocytes: greater than or equal to 3,500 G/L; Neutrophil: greater than or equal to 1,500 G/L; Platelets: greater than or equal to 100,000/mm3 ; Creatinine within normal upper limits; BUN within normal upper limits; AST/ALT: less than or equal to 1.5 times the upper limit; Total bilirubin: less than or equal to 1.5 times the upper limit; Alkaline phosphatase :less than or equal to 1.5 times the upper limit

• Informed consent

Exclusion Criteria:

• Patients with other cancer history in 5 years except cervical carcinoma in situ and non-malignant melanoma skin cancer

• Any prior chemotherapy or other cancer treatment prior to this protocol

• With any distant metastasis in liver, lung, bone, CNS or peritoneal transplantation

• History of allergic reactions attributed to contrast medium, similar chemical or biologic complex

• Existing esophageal fistula, perforation and cachexia

• Existing active infection such as active tuberculosis and hepatitis

• Uncontrolled illness including, but not limited to, active infection, symptomatic heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness

• History of myocardial infarction within the past 6 months or history of ventricular arrhythmia

• Participation in other clinical trials currently or within 4 weeks of selection

• Pregnant or lactating females