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Articles by Michael Rade
MyCARdiac score: integrating cardiac imaging and biomarkers to predict outcomes in RRMM patients receiving cilta-cel - Leukemia
To the Editor Chimeric antigen receptor (CAR) T-cell therapy has transformed treatment for relapsed and refractory multiple myeloma (RRMM), but its wider use has renewed attention to off-target toxicities.
A longitudinal single-cell atlas to predict outcome and toxicity after BCMA-directed CAR T cell therapy in multiple myeloma
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Results We recruited a real-world cohort of 61 RRMM patients treated with BCMA-directed CAR T cells at our center. Samples of 57 patients were available for single-cell multi-omics profiling: A total of 135 peripheral blood mononuclear cell (PBMC) samples at 3 different time points were collected for single cell RNA, B cell receptor (BCR), TCR and surface protein profiling.
By Michael Rade, David Fandrei, Markus Kreuz, Sabine Seiffert, Anja Grahnert, Maik Friedrich, Thomas C. Wiemers, Patrick Born, Luise Fischer, Heike Weidner, Lorenz C. Hofbauer, Ronny Baber, Song Wang, Enrica Bach, Sandra Hoffmann, Jonathan Scolnick, Mirco Friedrich, Farid Keramati, Peter Brazda, Zsolt Sebestyen, Jürgen Kuball, Miriam Alb, Lukas Scheller, Michael Hudecek, Hermann Einsele, Klaus H. Metzeler, Marco Herling, Carmen Diana Herling, Madlen Jentzsch, Georg-Nikolaus Franke, Andreas Boldt, Ulrike Kohl, Uwe Platzbecker, Vladan Vucinic, Kristin Reiche, Maximilian Merz
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Cell Press
Verified
ROR2-specific CAR T cells are effective against hematologic and solid tumors and well tolerated in mice
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Keywords receptor tyrosine kinase-like orphan receptor 2 ROR2 CAR T cell immunotherapy multiple myeloma clear cell renal cell carcinoma Introduction The receptor tyrosine kinase (RTK)-like orphan receptor 2 (ROR2) has been nominated as a target for RTK inhibitors due to its role in oncogenic signaling.1 ROR2 expression has been associated with cancer invasiveness and the formation of metastases,2,3,4 and several studies have suggested that ROR2 expression is a genetic disease and prognostic...
By Justus Weber, Michael Rade, Peter Spieler, Claudia Müller, Charis Kalogirou, Laura Mainz, Jörg Lehmann, Robert Klopfleisch, Mathias Rosenfeldt, Sophia Danhof, K. Martin Kortüm, Ulrike Kohl, Hermann Einsele, Christoph Rader, Kristin Reiche, Thomas Nerreter, Michael Hudecek, Josefine Michael, Liz Therese Tony, Fabian Freitag
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Cell Reports Medicine
Verified
Bispecific Antibodies as Bridging to BCMA CAR-T Cell Therapy for Relapsed/Refractory Multiple Myeloma
Abstract Externe IDs PubMedCentral PMC11707513 Schlagworte Humans, Multiple Myeloma/therapy, Antibodies, Bispecific/therapeutic use, Immunotherapy, Adoptive/methods, B-Cell Maturation Antigen/immunology, Middle Aged, Male, Female, Aged, Adult, Receptors, Chimeric Antigen/immunology, Neoplasm Recurrence, Local/therapy, T-Lymphocytes/immunology
Single-cell multiomic dissection of response and resistance to chimeric antigen receptor T cells against BCMA in relapsed multiple myeloma - Nature Cancer
Abstract Markers that predict response and resistance to chimeric antigen receptor (CAR) T cells in relapsed/refractory multiple myeloma are currently missing. We subjected mononuclear cells isolated from peripheral blood and bone marrow before and after the application of approved B cell maturation antigen-directed CAR T cells to single-cell multiomic analyses to identify markers associated with resistance and early relapse.
A reliable transcriptomic risk-score applicable to formalin-fixed paraffin-embedded biopsies improves outcome prediction in localized prostate cancer
BACKGROUND: Clinical manifestation of prostate cancer (PCa) is highly variable. Aggressive tumors require radical treatment while clinically non-significant ones may be suitable for active surveillance. We previously developed the prognostic ProstaTrend RNA signature based on transcriptome-wide microarray and RNA-sequencing (RNA-Seq) analyses, primarily of prostatectomy specimens.
A time-resolved meta-analysis of consensus gene expression profiles during human T-cell activation
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