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An Exploratory Study of Neoadjuvant Cetuximab Followed by Cetuximab and Chemoradiotherapy in Women With Newly Diagnosed Locally Advanced Cervical Cancer.
Fracasso, Paula M; Duska, Linda R; Thaker, Premal H; Gao, Feng; Zoberi, Imran; Dehdashti, Farrokh; Siegel, Barry A; Uliel, Livnat; Menias, Christine O; Rehm, Patrice K; Goodner, Sherry A; Creekmore, Allison N; Lothamer, Heather L; Rader, Janet S.
Afiliación
  • Fracasso PM; UVA Cancer Center.
  • Duska LR; Departments of Medicine.
  • Thaker PH; UVA Cancer Center.
  • Gao F; Obstetrics and Gynecology.
  • Zoberi I; Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.
  • Dehdashti F; Departments of Obstetrics and Gynecology.
  • Siegel BA; Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.
  • Uliel L; Department of Surgery, Division of Public Health Sciences, Washington University School of Medicine.
  • Menias CO; Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.
  • Rehm PK; Radiation Oncology.
  • Goodner SA; Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.
  • Creekmore AN; Division of Nuclear Medicine.
  • Lothamer HL; Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.
  • Rader JS; Division of Nuclear Medicine.
Am J Clin Oncol ; 45(7): 286-293, 2022 07 01.
Article en En | MEDLINE | ID: mdl-35696702
OBJECTIVES: This study explored the feasibility of cetuximab with chemoradiation in women with cervical carcinoma and evaluated fluorine-18 fluorodeoxyglucose-positron emission tomography/computed tomography (18F-FDG-PET/CT) to assess early response to cetuximab (NCT00292955). PATIENTS AND METHODS: Eligible patients with International Federation of Gynecology and Obstetrics (FIGO) stage IB-IVB invasive carcinoma of the uterine cervix were treated on 1 of 3 dose levels (DL). DL1 consisted of neoadjuvant cetuximab, then concurrent radiotherapy with cetuximab 250 mg/m2/cisplatin 40 mg/m2, followed by weekly cetuximab. DL2 consisted of radiotherapy with cetuximab 200 mg/m2 and cisplatin 30 mg/m2. DL3 consisted of radiotherapy with cetuximab 250 mg/m2 and cisplatin 30 mg/m2. Patients underwent 18F-FDG-PET/CT before treatment, after neoadjuvant cetuximab, and at the end of treatment. RESULTS: Of the 21 patients enrolled, 9, 3, and 9 were treated in DL1, DL2, and DL3, respectively. DL1 required dose reductions due to gastrointestinal toxicities. DL2 and 3 were tolerated with 1 dose-limiting toxicity (grade 4 renal failure) at DL3. Following 3 weekly treatments of neoadjuvant cetuximab in DL1, 7 patients had maximum standardized uptake value changes on 18F-FDG-PET/CT consistent with response to cetuximab. Of the 12 patients with locally advanced disease, eleven evaluable patients had no evidence of disease on 18F-FDG-PET/CT at treatment end. Five-year progression-free survival and overall survival rates for all patients were 57.5% and 58.5%, respectively. CONCLUSIONS: Cetuximab with cisplatin 30 mg/m2 and radiotherapy was tolerated. 18F-FDG-PET/CT demonstrated early evidence of response to neoadjuvant cetuximab. With advances in precision oncology and the recent approval of pembrolizumab in metastatic cervical cancer, dual-target inhibition with an epidermal growth factor receptor inhibitor may be a promising treatment in the future.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Am J Clin Oncol Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Am J Clin Oncol Año: 2022 Tipo del documento: Article