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Neoadjuvant presurgical PD-1 inhibition in oral cavity squamous cell carcinoma.
Knochelmann, Hannah M; Horton, Joshua D; Liu, Sixue; Armeson, Kent; Kaczmar, John M; Wyatt, Megan M; Richardson, Mary S; Lomeli, Shirley H; Xiong, Ying; Graboyes, Evan M; Lentsch, Eric J; Hornig, Joshua D; Skoner, Judith; Stalcup, Seth; Spampinato, Maria V; Garrett-Mayer, Elizabeth; O'Quinn, Elizabeth C; Timmers, Cynthia D; Romeo, Martin J; Wrangle, John M; Young, M Rita I; Rubinstein, Mark P; Day, Terry A; Lo, Roger S; Paulos, Chrystal M; Neskey, David M.
Afiliação
  • Knochelmann HM; Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
  • Horton JD; Department of Surgery - Oncology, Emory University, Atlanta, GA, USA.
  • Liu S; Department of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
  • Armeson K; Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Kaczmar JM; Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
  • Wyatt MM; Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
  • Richardson MS; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • Lomeli SH; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • Xiong Y; Division of Medical Oncology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.
  • Graboyes EM; Department of Surgery - Oncology, Emory University, Atlanta, GA, USA.
  • Lentsch EJ; Department of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
  • Hornig JD; Department of Pathology, Medical University of South Carolina, Charleston, SC, USA.
  • Skoner J; Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
  • Stalcup S; Department of Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Spampinato MV; Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Garrett-Mayer E; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • O'Quinn EC; Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Timmers CD; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • Romeo MJ; Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Wrangle JM; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • Young MRI; Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
  • Rubinstein MP; Department of Radiology, Medical University of South Carolina, Charleston, SC, USA.
  • Day TA; Department of Radiology, Medical University of South Carolina, Charleston, SC, USA.
  • Lo RS; American Society of Clinical Oncology, Alexandria, VA, USA.
  • Paulos CM; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
  • Neskey DM; Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
Cell Rep Med ; 2(10): 100426, 2021 10 19.
Article em En | MEDLINE | ID: mdl-34755137
Oral cavity squamous cell carcinoma (OCSCC) is a prevalent surgically treated subset of head and neck cancer with frequent recurrence and poor survival. Immunotherapy has demonstrated efficacy in recurrent/metastatic head and neck cancer. However, whether antitumor responses could be fostered by neoadjuvant presurgical immunotherapy remains unclear. Using a Simon's two-stage design, we present results of a single-arm phase-II trial where 12 patients with stage II-IVA OCSCC received 3 to 4 biweekly doses of 3 mg/kg nivolumab followed by definitive surgical resection with curative intent. Presurgical nivolumab therapy in this cohort shows an overall response rate of 33% (n = 4 patients; 95% CI: 12%-53%). With a median follow up of 2.23 years, 10 out of 12 treated patients remain alive. Neoadjuvant nivolumab is safe, well-tolerated, and is not associated with delays in definitive surgical treatment in this study. This work demonstrates feasibility and safety for incorporation of nivolumab in the neoadjuvant setting for OCSCC (ClinicalTrials.gov: NCT03021993).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Receptor de Morte Celular Programada 1 / Nivolumabe / Recidiva Local de Neoplasia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cell Rep Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Receptor de Morte Celular Programada 1 / Nivolumabe / Recidiva Local de Neoplasia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cell Rep Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos