Nimotuzumab Combined With Neoadjuvant Chemotherapy in the Treatment of Resectable LA HNSCC (NCT05351762) | Clinical Trial Compass
UnknownPhase 2
Nimotuzumab Combined With Neoadjuvant Chemotherapy in the Treatment of Resectable LA HNSCC
55 participantsStarted 2022-07-01
Plain-language summary
This study is a prospective, open-label, single-arm study. The trial will be divided into 3 phases: screening/baseline, treatment and follow-up. To initially explore the efficacy and safety of nimotuzumab combined with neoadjuvant chemotherapy (TPF regimen) in the treatment of resectable locally advanced head and neck tumors. Targeted therapy: Nimotuzumab injection 400 mg, once on the 1st day and once on the 21st day, for a total of 2 times. It should be administered by intravenous infusion 1 hour before chemotherapy, and the administration process should last for more than 60 minutes. Chemotherapy (TPF regimen): nab-paclitaxel 175mg/m2, on the 1st day; nedaplatin 100mg/m2, on the 1st day; oral administration of Sigirone on the 1st-14th day, 2/day; a treatment cycle of 21 days, a total of 2 a treatment cycle. After two cycles of chemotherapy, all patients underwent radical surgery according to whether the throat could be preserved and the patient's own wishes. The primary endpoint of the study is the tumor objective response rate (ORR), and the secondary endpoints are the primary tumor pathological complete response (pCR) rate, organ preservation rate, 1-year overall survival (OS) rate, and 1-year disease-free survival (DFS) rate. , quality of life, safety evaluation.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion criteria
✓. 18-80 years old, including 18 and 80 years old;
✓. Resectable stage III to IVa head and neck squamous cell carcinoma (including oropharyngeal carcinoma, laryngeal carcinoma and hypopharyngeal carcinoma) was confirmed by histopathology or cytology by MRI imaging;
✓. ECOG PS score 0-2;
✓. Histopathological immunohistochemical test indicated positive EGFR expression
✓. Histopathological immunohistochemical tests were P16 negative and EBER negative
✓. Lymph nodes have signs of extraperitoneal invasion (MRI, CT or pathology)
✓. At least one measurable lesion according to RECIST 1.1 evaluation criteria;
✓. Expected survival time ≥6 months;
Exclusion criteria
✕. Received PD-1 inhibitor, EGFR mab, EGFR-TKI and anti-angiogenic drugs within 4 weeks before enrollment;
. Participating in other interventional clinical trials within 30 days prior to screening;
✕. History of other malignant tumors (except cured basal cell carcinoma of the skin)
✕. there are serious and poorly controlled concurrent diseases (such as heart failure, diabetes, hypertension, liver failure, renal failure, thyroid disease, mental illness, etc.);
✕. known to be infected with HIV or active viral hepatitis or tuberculosis;
✕. Major surgical or planned surgery within 30 days of the first administration of the investigational drug;
✕. Allergic to drugs or ingredients used in the program;
✕. Women who are pregnant (as confirmed by blood or urine HCG testing) or who are lactating, or subjects of childbearing age are unwilling or unable to use effective contraceptive methods (for both male and female subjects) until at least 6 months after the last trial treatment;