The anti-tumor activity of cetuximab prior to chemoradiotherapy and the safety and tolerability of cetuximab with concurrent chemoradiation will be determined in women with locally advanced or metastatic cervical carcinoma.
- Women with Federation of Gynecology and Obstetrics (FIGO) Clinical Stage IB2-IVB carcinoma of the cervix - Baseline cervical biopsy, blood samples, and FDG-PET/computed tomography (CT) scan - Cetuximab 400 mg/m2 on day 1 followed by cetuximab 250 mg/m2 on days 8 and 15 - Repeat cervical biopsy and FDG-PET/CT scan following cetuximab monotherapy - Radiation and weekly cisplatin 40 mg/m2 and cetuximab 250 mg/2 for 6 weeks - Cetuximab 250 mg/m2 weekly for 12 weeks - Repeat cervical biopsy (if tumor present) and FDG-PET/CT scan after completion of therapy - Follow for tumor recurrence and survival
| Condition | Cancer of the Cervix |
|---|---|
| Treatment | Cetuximab |
| Clinical Study Identifier | NCT00292955 |
| Sponsor | University of Virginia |
| Last Modified on | 22 January 2022 |
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