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Treatment of adult ALL patients with third-generation CD19-directed CAR T cells: results of a pivotal trial.
Schubert, Maria-Luisa; Schmitt, Anita; Hückelhoven-Krauss, Angela; Neuber, Brigitte; Kunz, Alexander; Waldhoff, Philip; Vonficht, Dominik; Yousefian, Schayan; Jopp-Saile, Lea; Wang, Lei; Korell, Felix; Keib, Anna; Michels, Birgit; Haas, Dominik; Sauer, Tim; Derigs, Patrick; Kulozik, Andreas; Kunz, Joachim; Pavel, Petra; Laier, Sascha; Wuchter, Patrick; Schmier, Johann; Bug, Gesine; Lang, Fabian; Gökbuget, Nicola; Casper, Jochen; Görner, Martin; Finke, Jürgen; Neubauer, Andreas; Ringhoffer, Mark; Wolleschak, Denise; Brüggemann, Monika; Haas, Simon; Ho, Anthony D; Müller-Tidow, Carsten; Dreger, Peter; Schmitt, Michael.
Affiliation
  • Schubert ML; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Schmitt A; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Hückelhoven-Krauss A; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Neuber B; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Kunz A; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Waldhoff P; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Vonficht D; Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH), Heidelberg, Germany.
  • Yousefian S; Division of Stem Cells and Cancer, Deutsches Krebsforschungszentrum (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Jopp-Saile L; Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.
  • Wang L; Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Korell F; Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Keib A; Department of Hematology, Oncology and Tumor Immunology, Charité University Medicine, Berlin, Germany.
  • Michels B; Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH), Heidelberg, Germany.
  • Haas D; Division of Stem Cells and Cancer, Deutsches Krebsforschungszentrum (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Sauer T; Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.
  • Derigs P; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Kulozik A; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Kunz J; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Pavel P; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Laier S; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Wuchter P; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Schmier J; Department of Internal Medicine V, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
  • Bug G; Department of Pediatric Hematology, Oncology and Immunology, University Hospital Heidelberg, Heidelberg, Germany.
  • Lang F; Department of Pediatric Hematology, Oncology and Immunology, University Hospital Heidelberg, Heidelberg, Germany.
  • Gökbuget N; Institute for Clinical Transfusion Medicine and Cell Therapy (IKTZ), German Red Cross Blood Service Baden-Württemberg-Hessen, Heidelberg, Germany.
  • Casper J; Institute for Clinical Transfusion Medicine and Cell Therapy (IKTZ), German Red Cross Blood Service Baden-Württemberg-Hessen, Heidelberg, Germany.
  • Görner M; Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, of the Heidelberg University, German Red Cross Blood Service Baden-Württemberg - Hessen, Mannheim, Germany.
  • Finke J; GRN MVZ Sinsheim, Sinsheim, Germany.
  • Neubauer A; Department of Internal Medicine II, University Hospital Frankfurt, Frankfurt, Germany.
  • Ringhoffer M; Department of Internal Medicine II, University Hospital Frankfurt, Frankfurt, Germany.
  • Wolleschak D; Department of Internal Medicine II, University Hospital Frankfurt, Frankfurt, Germany.
  • Brüggemann M; Department of Hematology and Oncology, University Hospital Oldenburg, Oldenburg, Germany.
  • Haas S; Department of Hematology and Oncology, Hospital Bielefeld, Bielefeld, Germany.
  • Ho AD; Department of Internal Medicine I, University Hospital Freiburg, Freiburg, Germany.
  • Müller-Tidow C; Department of Hematology, Oncology and Immunology, University Hospital Giessen und Marburg, Marburg, Germany.
  • Dreger P; Städtisches Klinikum Karlsruhe, Karlsruhe, Germany.
  • Schmitt M; Department of Hematology and Oncology, Center of Internal Medicine, Otto-von-Guericke University Medical Center, Magdeburg, Germany.
J Hematol Oncol ; 16(1): 79, 2023 07 22.
Article in En | MEDLINE | ID: mdl-37481608
ABSTRACT

BACKGROUND:

Third-generation chimeric antigen receptor (CAR)-engineered T cells (CARTs) might improve clinical outcome of patients with B cell malignancies. This is the first report on a third-generation CART dose-escalating, phase-1/2 investigator-initiated trial treating adult patients with refractory and/or relapsed (r/r) acute lymphoblastic leukemia (ALL).

METHODS:

Thirteen patients were treated with escalating doses of CD19-directed CARTs between 1 × 106 and 50 × 106 CARTs/m2. Leukapheresis, manufacturing and administration of CARTs were performed in-house.

RESULTS:

For all patients, CART manufacturing was feasible. None of the patients developed any grade of Immune effector cell-associated neurotoxicity syndrome (ICANS) or a higher-grade (≥ grade III) catokine release syndrome (CRS). CART expansion and long-term CART persistence were evident in the peripheral blood (PB) of evaluable patients. At end of study on day 90 after CARTs, ten patients were evaluable for response Eight patients (80%) achieved a complete remission (CR), including five patients (50%) with minimal residual disease (MRD)-negative CR. Response and outcome were associated with the administered CART dose. At 1-year follow-up, median overall survival was not reached and progression-free survival (PFS) was 38%. Median PFS was reached on day 120. Lack of CD39-expression on memory-like T cells was more frequent in CART products of responders when compared to CART products of non-responders. After CART administration, higher CD8 + and γδ-T cell frequencies, a physiological pattern of immune cells and lower monocyte counts in the PB were associated with response.

CONCLUSION:

In conclusion, third-generation CARTs were associated with promising clinical efficacy and remarkably low procedure-specific toxicity, thereby opening new therapeutic perspectives for patients with r/r ALL. Trial registration This trial was registered at www. CLINICALTRIALS gov as NCT03676504.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurotoxicity Syndromes Limits: Adult / Humans Language: En Journal: J Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2023 Document type: Article Affiliation country: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurotoxicity Syndromes Limits: Adult / Humans Language: En Journal: J Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2023 Document type: Article Affiliation country: Alemania