Nimotuzumab is a humanized monoclonal antibody against epidermal growth factor receptor (EGFR). Clinical trials are ongoing globally to evaluate Nimotuzumab in different indications. Nimotuzumab has been approved to treat squamous cell carcinoma of head and neck (SCCHN), glioma and nasopharyngeal carcinoma in different countries. The clinical phaseⅡtrial is designed to assess the resection rate and pathological complete response of nimotuzumab plus carboplatin and paclitaxel in patients with cervical cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
200mg/w,weekly, 6 weeks
AUC 6, d1,1 cycle/21d, 2 cycles
175 mg/m2, d1 1 cycle/21d, 2 cycles.
Shanghai first people's hospital
Shanghai, Shanghai Municipality, China
resection rate
Time frame: the day right after surgery
Pathological response rate
Time frame: the day right after surgery
objective response rate(ORR)
Time frame: The first seven weeks after the end of treatment
Progression free survival progression-free survival (PFS)
Time frame: Follow-up is for three consecutive years after surgery. Once every three months in the first year, and then once every six months in the second and third year.
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