Nimotuzumab (hR3) is an IgG1 humanized monoclonal antibody that recognized an epitope located in the extra cellular domain of the human epidermal growth factor receptor (EGFR). Clinical efficacy has been shown in adult with head and neck cancer. The phase I study assessed the safety, and efficacy of the combination of Nimotuzumab administered concomitantly with chemo-radiotherapy in patients with locally advanced esophageal cancer tumours.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
11
Fudan University Cancer Hospital
Shanghai, Shanghai Municipality, China
Safety and toxicity of this new treatment. Both acute and chronic toxicity will be evaluated.
Time frame: within study period
To determine the complete response rate、partial rate、disease responserate、disease control rate in the patients subject to treatment
Time frame: 6 months
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