Repeated peripheral infusions of anti-EGFRvIII CAR T cells in combination with pembrolizumab show no efficacy in glioblastoma: a phase 1 trial

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作者
Stephen J. Bagley
Zev A. Binder
Lamia Lamrani
Eliana Marinari
Arati S. Desai
MacLean P. Nasrallah
Eileen Maloney
Steven Brem
Robert A. Lustig
Goldie Kurtz
Michelle Alonso-Basanta
Pierre-Emmanuel Bonté
Christel Goudot
Wilfrid Richer
Eliane Piaggio
Shawn Kothari
Lea Guyonnet
Coralie L. Guerin
Joshua J. Waterfall
Suyash Mohan
Wei-Ting Hwang
Oliver Y. Tang
Meghan Logun
Meghna Bhattacharyya
Kelly Markowitz
Devora Delman
Amy Marshall
E. John Wherry
Sebastian Amigorena
Gregory L. Beatty
Jennifer L. Brogdon
Elizabeth Hexner
Denis Migliorini
Cecile Alanio
Donald M. O’Rourke
机构
[1] Perelman School of Medicine at the University of Pennsylvania,Department of Medicine
[2] Perelman School of Medicine at the University of Pennsylvania,Department of Neurosurgery
[3] Perelman School of Medicine at the University of Pennsylvania,Center for Cellular Immunotherapies
[4] Perelman School of Medicine at the University of Pennsylvania,GBM Translational Center of Excellence, Abramson Cancer Center
[5] Clinical Immunology Laboratory,Center for Translational Research in Onco
[6] Institut Curie,Hematology
[7] INSERM U932,Department of Oncology
[8] PSL University,Department of Pathology and Laboratory Medicine
[9] Immunity and Cancer,Department of Radiation Oncology
[10] Institut Curie Research Center,Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine
[11] Parker Institute for Cancer Immunotherapy,undefined
[12] Agora Cancer Research Center,undefined
[13] University of Geneva,undefined
[14] Swiss Cancer Center Léman,undefined
[15] Lausanne and Geneva,undefined
[16] University Hospital of Geneva,undefined
[17] Perelman School of Medicine at the University of Pennsylvania,undefined
[18] Perelman School of Medicine at the University of Pennsylvania,undefined
[19] Department of Translational Research,undefined
[20] PSL Research University,undefined
[21] Institut Curie Research Center,undefined
[22] Department of Hematology and Medical Oncology,undefined
[23] Emory University,undefined
[24] Cytometry Platform,undefined
[25] CurieCoreTech,undefined
[26] Institut Curie,undefined
[27] INSERM U830,undefined
[28] PSL University,undefined
[29] Institut Curie Research Cente,undefined
[30] Department of Radiology,undefined
[31] Perelman School of Medicine at the University of Pennsylvania,undefined
[32] Department of Biostatistics,undefined
[33] Epidemiology,undefined
[34] and Informatics,undefined
[35] Perelman School of Medicine at the University of Pennsylvania,undefined
[36] Warren Alpert Medical School of Brown University,undefined
[37] Cooper Medical School of Rowan University,undefined
[38] University of Pennsylvania,undefined
[39] Institute for Immunology and Immune Health,undefined
[40] Novartis Institutes for BioMedical Research,undefined
来源
Nature Cancer | 2024年 / 5卷
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摘要
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.
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页码:517 / 531
页数:14
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