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Repeated peripheral infusions of anti-EGFRvIII CAR T cells in combination with pembrolizumab show no efficacy in glioblastoma: a phase 1 trial.
Bagley, Stephen J; Binder, Zev A; Lamrani, Lamia; Marinari, Eliana; Desai, Arati S; Nasrallah, MacLean P; Maloney, Eileen; Brem, Steven; Lustig, Robert A; Kurtz, Goldie; Alonso-Basanta, Michelle; Bonté, Pierre-Emmanuel; Goudot, Christel; Richer, Wilfrid; Piaggio, Eliane; Kothari, Shawn; Guyonnet, Lea; Guerin, Coralie L; Waterfall, Joshua J; Mohan, Suyash; Hwang, Wei-Ting; Tang, Oliver Y; Logun, Meghan; Bhattacharyya, Meghna; Markowitz, Kelly; Delman, Devora; Marshall, Amy; Wherry, E John; Amigorena, Sebastian; Beatty, Gregory L; Brogdon, Jennifer L; Hexner, Elizabeth; Migliorini, Denis; Alanio, Cecile; O'Rourke, Donald M.
Afiliación
  • Bagley SJ; Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. sbagley@pennmedicine.upenn.edu.
  • Binder ZA; Department of Neurosurgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Lamrani L; Center for Cellular Immunotherapies, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Marinari E; GBM Translational Center of Excellence, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Desai AS; Clinical Immunology Laboratory, Institut Curie, Paris, France.
  • Nasrallah MP; INSERM U932, PSL University, Immunity and Cancer, Institut Curie Research Center, Paris, France.
  • Maloney E; Parker Institute for Cancer Immunotherapy, San Francisco, CA, USA.
  • Brem S; Agora Cancer Research Center, Lausanne, Switzerland.
  • Lustig RA; Center for Translational Research in Onco-Hematology, University of Geneva, Geneva, Switzerland.
  • Kurtz G; Swiss Cancer Center Léman, Lausanne and Geneva, Geneva, Switzerland.
  • Alonso-Basanta M; Department of Oncology, University Hospital of Geneva, Geneva, Switzerland.
  • Bonté PE; Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Goudot C; GBM Translational Center of Excellence, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Richer W; Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Piaggio E; Department of Neurosurgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Kothari S; Department of Neurosurgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Guyonnet L; GBM Translational Center of Excellence, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Guerin CL; Department of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Waterfall JJ; Department of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Mohan S; Department of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Hwang WT; INSERM U932, PSL University, Immunity and Cancer, Institut Curie Research Center, Paris, France.
  • Tang OY; INSERM U932, PSL University, Immunity and Cancer, Institut Curie Research Center, Paris, France.
  • Logun M; INSERM U932, PSL University, Immunity and Cancer, Institut Curie Research Center, Paris, France.
  • Bhattacharyya M; Department of Translational Research, PSL Research University, Institut Curie Research Center, Paris, France.
  • Markowitz K; INSERM U932, PSL University, Immunity and Cancer, Institut Curie Research Center, Paris, France.
  • Delman D; Department of Hematology and Medical Oncology, Emory University, Atlanta, GA, USA.
  • Marshall A; Cytometry Platform, CurieCoreTech, Institut Curie, Paris, France.
  • Wherry EJ; Cytometry Platform, CurieCoreTech, Institut Curie, Paris, France.
  • Amigorena S; Department of Translational Research, PSL Research University, Institut Curie Research Center, Paris, France.
  • Beatty GL; INSERM U830, PSL University, Institut Curie Research Cente, Paris, France.
  • Brogdon JL; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Hexner E; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Migliorini D; GBM Translational Center of Excellence, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Alanio C; Warren Alpert Medical School of Brown University, Providence, RI, USA.
  • O'Rourke DM; Department of Neurosurgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Nat Cancer ; 5(3): 517-531, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38216766
ABSTRACT
We previously showed that chimeric antigen receptor (CAR) T-cell therapy targeting epidermal growth factor receptor variant III (EGFRvIII) produces upregulation of programmed death-ligand 1 (PD-L1) in the tumor microenvironment (TME). Here we conducted a phase 1 trial (NCT03726515) of CAR T-EGFRvIII cells administered concomitantly with the anti-PD1 (aPD1) monoclonal antibody pembrolizumab in patients with newly diagnosed, EGFRvIII+ glioblastoma (GBM) (n = 7). The primary outcome was safety, and no dose-limiting toxicity was observed. Secondary outcomes included median progression-free survival (5.2 months; 90% confidence interval (CI), 2.9-6.0 months) and median overall survival (11.8 months; 90% CI, 9.2-14.2 months). In exploratory analyses, comparison of the TME in tumors harvested before versus after CAR + aPD1 administration demonstrated substantial evolution of the infiltrating myeloid and T cells, with more exhausted, regulatory, and interferon (IFN)-stimulated T cells at relapse. Our study suggests that the combination of CAR T cells and PD-1 inhibition in GBM is safe and biologically active but, given the lack of efficacy, also indicates a need to consider alternative strategies.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glioblastoma / Anticuerpos Monoclonales Humanizados Límite: Humans Idioma: En Revista: Nat Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glioblastoma / Anticuerpos Monoclonales Humanizados Límite: Humans Idioma: En Revista: Nat Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos