Christoph Mann

ORCID: 0000-0002-7823-8428
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About
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Research Areas
  • Multiple Myeloma Research and Treatments
  • Protein Degradation and Inhibitors
  • Peptidase Inhibition and Analysis
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Treatment and Pharmacology
  • Chronic Lymphocytic Leukemia Research
  • Cancer Mechanisms and Therapy
  • Quinazolinone synthesis and applications
  • Cancer therapeutics and mechanisms
  • CAR-T cell therapy research
  • Antifungal resistance and susceptibility
  • Glycosylation and Glycoproteins Research
  • Molecular Junctions and Nanostructures
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • MicroRNA in disease regulation
  • Fungal Infections and Studies
  • Medieval European History and Architecture
  • Insurance, Mortality, Demography, Risk Management
  • Phytochemical compounds biological activities
  • Neutropenia and Cancer Infections
  • HIV/AIDS drug development and treatment
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Renal and related cancers
  • Historical Influence and Diplomacy

Universitätsklinikum Gießen und Marburg
2019-2024

Philipps University of Marburg
2019-2024

Azienda Ospedaliera Citta' della Salute e della Scienza di Torino
2022

The GMMG-CONCEPT trial investigated isatuximab, carfilzomib, lenalidomide, and dexamethasone (Isa-KRd) in transplant-eligible (TE) transplant-noneligible (TNE) patients with newly diagnosed multiple myeloma (NDMM) exclusively high-risk disease for whom prospective trials are limited, aiming to induce minimal residual (MRD) negativity.This academic, investigator-initiated, multicenter, phase II enrolled NDMM (HRNDMM) defined by mandatory International Staging System stage II/III combined...

10.1200/jco.23.01696 article EN cc-by-nc-nd Journal of Clinical Oncology 2023-09-27

The aim of this trial was to investigate the addition anti-SLAMF7 monoclonal antibody elotuzumab lenalidomide, bortezomib, and dexamethasone (RVd) in induction consolidation therapy as well lenalidomide maintenance treatment transplant-eligible patients with newly diagnosed multiple myeloma.

10.1016/s2352-3026(23)00366-6 article EN cc-by The Lancet Haematology 2024-01-30
Elias Karl Uta Bertsch Ema Požek Roland Fenk Britta Besemer and 95 more Christine Hanoun Roland Schroers Ivana von Metzler Mathias Hänel Christoph Mann Lisa Leypoldt Bernhard Heilmeier Stefanie Huhn Sabine Vogel Michael Hundemer Christof Scheid Igor Wolfgang Blau Steffen Luntz Niels Weinhold Diana Tichy Tobias A.W. Holderried Karolin Trautmann‐Grill Deniz Gezer Maika Klaiber-Hakimi Martin Müller Evgenii Shumilov Wolfgang Knauf Christian Michel Thomas Geer Hendrik Riesenberg Christoph Lutz Marc S. Raab Axel Benner Martin Hoffmann Katja Weisel Hans Salwender Hartmut Goldschmidt Miriam Ahlborn Joachim Behringer Helga Bernhard Britta Besemer Joerg Thomas Bittenbring Igor Wolfgang Blau Claus Bolling Amelie Boquoi Daniel Debatin Gerlinde Egerer Roland Fenk Barbara Ferstl Stefan Fronhoffs Tobias Gaska Thomas Geer Deniz Gezer Hartmut Goldschmidt Martin Görner Ullrich Graeven Mathias Hänel Bernhard Heilmeier Michael Heinsch Martin Hoffmann Tobias A.W. Holderried Olaf Hopfer Snjezana Janjetovic Maika Klaiber-Hakimi Martine Klausmann Stefan Klein Wolfgang Knauf Yon‐Dschun Ko Doris Kraemer Martin Kropff Paul La Rosée Rolf Mahlberg Christoph Mann Uwe M. Martens Ivana von Metzler Christian Michel Martin Müller Wolfram Pönisch Peter Reimer Claudia Riechel Mark Ringhoffer Mathias Rummel Volker Runde Hans Salwender Markus Schaich Christoph Scheid Martin Schmidt‐Hieber Daniel Schöndube Roland Schroers Heinrich Schutte Evgenii Shumilov Peter Staib Dirk Strumberg Hans‐Joachim Tischler Karolin Trautmann‐Grill Walter Verbeek Rudolf Weide Eckhart Weidmann Katja Weisel Maike de Wit

Previously, addition of isatuximab (Isa) to standard-of-care lenalidomide-bortezomib-dexamethasone (RVd) in transplant-eligible patients with newly diagnosed multiple myeloma the GMMG-HD7 trial (ClinicalTrials.gov identifier: NCT03617731) resulted a significant increase minimal residual disease negativity (MRD-) rates after induction therapy. A total 662 were randomly assigned receive therapy Isa-RVd (n = 331) or RVd 329), followed by single tandem autologous stem-cell transplant and second...

10.1200/jco-24-02266 article EN Journal of Clinical Oncology 2024-12-09

With the advent of novel, highly effective therapies for multiple myeloma (MM), classical serologic monitoring appears insufficient response assessment and prediction relapse. Moreover, studies in MM are hampered by interference therapeutic antibodies. The detection malignant plasma cell clones next generation sequencing (NGS) or multiparameter flow cytometry (MFC) circumvents these difficulties can be performed peripheral blood (pB) targeting circulating cell-free DNA (cfDNA) cells (CPCs),...

10.1007/s00277-022-04771-5 article EN cc-by Annals of Hematology 2022-02-01

8508 Background: High-risk (HR) multiple myeloma (MM) still has a significant impaired prognostic outcome. Addition of CD38 monoclonal antibodies to standard-of-care regimens significantly improved response rates and depth in newly diagnosed (ND) relapsed/refractory MM patients (pts). Here, we report the prespecified end induction interim analysis (IA) investigator-initiated GMMG-CONCEPT trial (NCT03104842), evaluating quadruplet regimen isatuximab plus carfilzomib, lenalidomide...

10.1200/jco.2020.38.15_suppl.8508 article EN Journal of Clinical Oncology 2020-05-20

In the battle against multiple myeloma (MM), T cell strategies have emerged as crucial, exploiting their natural tumor-cell targeting ability to enhance patient outcomes.Recent studies underscore dual roles of cells in MM: while specific can effectively target and destroy MM cells, regulatory may block this response, highlighting complexity immune environment [1,2].Elotuzumab, SLAM family member 7 (SLAMF7) protein, represents a promising advance enhancing killer (NK) activity modulating...

10.1038/s41375-024-02290-y article EN cc-by Leukemia 2024-06-03

<b><i>Background/Aims:</i></b> Activated fibroblasts are key controllers of extracellular matrix turnover in kidney fibrosis, the pathophysiological end stage chronic disease. The proliferation activated depends on expression calcium-dependent potassium channel KCNN4. Expression this ion is upregulated fibrotic kidneys. Genetic and pharmacological blockade KCNN4 inhibits fibrosis <i>in vitro</i> vivo</i>....

10.1159/000498875 article EN cc-by-nc-nd Kidney & Blood Pressure Research 2019-01-01

10.1038/s41409-022-01815-2 article EN Bone Marrow Transplantation 2022-11-01

Background: The multicenter phase III trial GMMG-HD7 (NCT03617731) demonstrated superior minimal residual disease (MRD) negativity rate after induction therapy in patients with transplant-eligible newly-diagnosed multiple myeloma (NDMM) by addition of the anti-CD38 monoclonal antibody isatuximab (Isa) to lenalidomide / bortezomib dexamethasone (Isa-RVd), as compared RVd alone (Goldschmidt H et al., 2021, ASH Annual Meeting). Aims: Here we present a subgroup analysis on high-risk...

10.1097/01.hs9.0000846588.94000.04 article EN cc-by-nc-nd HemaSphere 2022-06-01
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