Jochen Buechner

ORCID: 0000-0001-5848-4501
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About
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Research Areas
  • Acute Lymphoblastic Leukemia research
  • CAR-T cell therapy research
  • Hematopoietic Stem Cell Transplantation
  • DNA Repair Mechanisms
  • Childhood Cancer Survivors' Quality of Life
  • Acute Myeloid Leukemia Research
  • Neuroblastoma Research and Treatments
  • CRISPR and Genetic Engineering
  • Virus-based gene therapy research
  • Chronic Myeloid Leukemia Treatments
  • Immunodeficiency and Autoimmune Disorders
  • Lymphoma Diagnosis and Treatment
  • Carcinogens and Genotoxicity Assessment
  • Cancer-related Molecular Pathways
  • Signaling Pathways in Disease
  • Cancer-related molecular mechanisms research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Cancer Genomics and Diagnostics
  • Polyomavirus and related diseases
  • RNA modifications and cancer
  • Epigenetics and DNA Methylation
  • Mesenchymal stem cell research
  • Genomics and Rare Diseases
  • Oral health in cancer treatment
  • Single-cell and spatial transcriptomics

Oslo University Hospital
2016-2025

Université de Montréal
2018

University Hospital of North Norway
2009-2013

UiT The Arctic University of Norway
2010-2011

University of Freiburg
2003

In a single-center phase 1-2a study, the anti-CD19 chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel produced high rates of complete remission and was associated with serious but mainly reversible toxic effects in children young adults relapsed or refractory B-cell acute lymphoblastic leukemia (ALL).We conducted 2, single-cohort, 25-center, global study pediatric adult patients CD19+ ALL. The primary end point overall rate (the incomplete hematologic recovery) within 3...

10.1056/nejmoa1709866 article EN New England Journal of Medicine 2018-01-31

Total body irradiation (TBI) before allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with acute lymphoblastic leukemia (ALL) is efficacious, but long-term side effects are concerning. We investigated whether preparative combination chemotherapy could replace TBI such patients.FORUM a randomized, controlled, open-label, international, multicenter, phase III, noninferiority study. Patients ≤ 18 years at diagnosis, 4-21 HSCT, complete remission pre-HSCT, and an...

10.1200/jco.20.02529 article EN cc-by Journal of Clinical Oncology 2020-12-17

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary point, may be published when key planned co-primary or secondary analyses are not yet available. Trial Updates provide an opportunity to disseminate additional results from studies, in JCO elsewhere, for which point has already been reported. In analysis of global phase II ELIANA trial (ClinicalTrials.gov identifier: NCT02435849), tisagenlecleucel provided...

10.1200/jco.22.00642 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-11-18
Sushree Sangita Sahoo Victor B. Pastor Charnise Goodings Rebecca Voss Emilia J. Kozyra and 91 more Amina Szvetnik Peter Noellke Michael Dworzak Jan Starý Franco Locatelli Riccardo Masetti Markus Schmugge Barbara De Moerloose Albert Catalá Krisztián Kállay Dominik Turkiewicz Henrik Hasle Jochen Buechner Kirsi Jahnukainen Marek Ussowicz Sophia Polychronopoulou Owen P. Smith Oksana Fabri Shlomit Barzilai Válerie de Haas Irith Baumann Stephan Schwarz‐Furlan Jan Starý Barbara De Moerloose Krisztián Kállay Owen P. Smith Válerie de Haas Gudrun Göhring Charlotte M. Niemeyer Karin Nebral Ingrid Simonitsch-Kluppp Pascale De Paepe Nadine Van Roy Vít Campr Zuzana Zemanová Erik Clasen‐Linde Tine Plesner Brigitte Schlegelberger Martina Rudelius Kalliopi N. Manola Kalliopi Stefanaki Judit Csomor Hajnalka Andrikovics David R. Betts Maureen J. O’Sullivan Yaniv Zohar Marta Jeison Rita De Vito Francesco Pasquali Jadwiga Małdyk Olga Haus Helena Alaiz Paula Kjöllerström Luís Mascarenhas‐Lemos Ivana Boďová Martin Čermák Lukáš Plank Barbara Gazić Marko Kavčič Helena Podgornik Margarita Llavador Ros José Cervera Carole Gengler Joëlle Tchinda Berna Beverloo Roos J. Leguit Marena R. Niewisch Martin G. Sauer Birgit Burkhardt Peter Lang Peter Bader Rita Beier Ingo Müller Michael H. Albert Roland Meisel Ansgar Schulz Gunnar Cario Pritam Kumar Panda Julius Wehrle Shinsuke Hirabayashi Marta Derecka Robert Durruthy-Durruthy Gudrun Göhring Ayami Yoshimi‐Noellke Manching Ku Dirk Lebrecht Miriam Erlacher Christian Flotho Brigitte Strahm Charlotte M. Niemeyer Marcin W. Włodarski

10.1038/s41591-021-01511-6 article EN Nature Medicine 2021-10-01

MicroRNAs (miRNAs) regulate expression of many cancer-related genes through posttranscriptional repression their mRNAs. In this study we investigate the proto-oncogene MYCN as a target for miRNA regulation. A luciferase reporter assay was used to software-predicted sites in 3′-untranslated region (3′UTR) MYCN. The miRNAs were overexpressed cell lines by transfection mimics or miRNA-expressing plasmids. Mutation validate 3′UTR direct several miRNAs. To measure miRNA-mediated suppression...

10.1038/bjc.2011.220 article EN cc-by-nc-sa British Journal of Cancer 2011-06-07

The inability to generate mesenchymal stromal cells (MSCs) of consistent potency likely is responsible for inconsistent clinical outcomes patients with aGvHD receiving MSC products. We developed a novel manufacturing protocol characterized by high in vitro and near-identity individual doses, referred as "MSC-Frankfurt am Main (MSC-FFM)". Herein, we report the 69 who have received MSC-FFM. These were 51 children 18 adults refractory grade II (4%), III (36%) or IV (59%). Patients either...

10.1038/s41409-018-0102-z article EN cc-by Bone Marrow Transplantation 2018-01-23

We assessed minimal residual disease (MRD) detection and B-cell aplasia after tisagenlecleucel therapy for acute lymphoblastic leukemia (ALL) to define biomarkers predictive of relapse (N = 143). Next-generation sequencing (NGS) MRD >0 in bone marrow (BM) was highly associated with relapse. recovery [signifying loss functional chimeric antigen receptor (CAR) T cells] within the first year treatment a hazard ratio (HR) 4.5 [95% confidence interval (CI), 2.03-9.97; P < 0.001]. Multivariate...

10.1158/2643-3230.bcd-21-0095 article EN cc-by-nc-nd Blood Cancer Discovery 2021-12-01

Abstract Background Neuroblastoma is a childhood cancer derived from immature cells of the sympathetic nervous system. The disease clinically heterogeneous, ranging neuronal differentiated benign ganglioneuromas to aggressive metastatic tumours with poor prognosis. Amplification MYCN oncogene well established prognostic factor found in up 40% high risk neuroblastomas. Using neuroblastoma cell lines study differentiation vitro now established. Several protocols, including exposure various...

10.1186/1471-213x-11-1 article EN cc-by BMC Developmental Biology 2011-01-03

Abstract Atypical teratoid rhabdoid tumors ( AT / RT ) are characterized by mutations and subsequent inactivation of SMARCB 1 INI 1, hSNF 5 ), a predilection for very young children an unfavorable outcome. The European Registry EU ‐ RHAB was established to generate common database establish standardized treatment regimen as the basis phase I/ II trials. Thus, genetic analyses, neuropathologic radiologic diagnoses, consensus were prospectively evaluated. From 2005 2009, 31 patients with from...

10.1002/cam4.741 article EN cc-by Cancer Medicine 2016-05-26

Abstract Although most children with acute lymphoblastic leukemia (ALL) receive fractionated total body irradiation (FTBI) as myeloablative conditioning (MAC) for allogeneic hematopoietic stem cell transplantation (allo-HSCT), it is an important matter of debate if chemotherapy can effectively replace FTBI. To compare outcomes after FTBI versus chemotherapy-based (CC), we performed a retrospective EBMT registry study. Children aged 2–18 years MAC first allo-HSCT bone marrow (BM) or...

10.1038/s41409-020-0854-0 article EN cc-by Bone Marrow Transplantation 2020-03-17

Background Tisagenlecleucel, an anti-CD19 chimeric antigen receptor T cell therapy, has demonstrated efficacy in children and young adults with relapsed/refractory B acute lymphoblastic leukemia (B-ALL) two multicenter phase 2 trials (ClinicalTrials.gov, NCT02435849 (ELIANA) NCT02228096 (ENSIGN)), leading to commercialization of tisagenlecleucel for the treatment patients up age 25 years B-ALL that is refractory or second greater relapse. Methods A pooled analysis 137 from these (ELIANA:...

10.1136/jitc-2020-002287 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2021-08-01

Abstract Cytokine release syndrome (CRS) is a systemic inflammatory response associated with chimeric antigen receptor T-cell (CAR-T) therapies. In severe cases, CRS can be coagulopathy and hypofibrinogenemia. We present our global multicenter experience CRS-associated after tisagenlecleucel therapy in 137 patients relapsed or refractory B-cell acute lymphoblastic leukemia from the ELIANA ENSIGN trials. These trials included clinical guidelines for fibrinogen replacement during coagulopathy....

10.1182/bloodadvances.2020002757 article EN cc-by-nc-nd Blood Advances 2021-01-25

The MYCN oncogene is frequently amplified in neuroblastoma. It one of the most consistent markers bad prognosis for this disease. Dickkopf-3 (DKK3) a secreted protein DKK family Wnt regulators. functions as tumor suppressor range cancers, including was recently found to downregulate DKK3 mRNA. In study, we show that knockdown MYCN-amplified (MNA) neuroblastoma cell lines increases secretion endogenous culture media. MicroRNAs (miRNAs) are ∼20 nt long single-stranded RNA molecules messenger...

10.1093/carcin/bgr073 article EN Carcinogenesis 2011-05-13

We performed molecular, enzyme, and metabolic studies in 50 patients with D-2-hydroxyglutaric aciduria (D-2-HGA) who accumulated D-2-hydroxyglutarate (D-2-HG) physiological fluids. Presumed pathogenic mutations were detected 24 of the dehydrogenase (D2HGDH) gene, which encodes (D-2-HGDH). Enzyme assay D-2-HGDH confirmed that all had impaired enzyme activity, whereas D-2-HGA whose activity was normal did not have mutations. Significantly lower D-2-HG concentrations body fluids observed...

10.1002/humu.21186 article EN Human Mutation 2009-12-18

(1) Background: Refractory acute graft-versus-host disease (R-aGvHD) remains a leading cause of death after allogeneic stem cell transplantation. Survival rates 15% four years are currently achieved; deaths only in part due to aGvHD itself, but mostly adverse effects R-aGvHD treatment with immunosuppressive agents as these predispose patients opportunistic infections and loss graft-versus-leukemia surveillance resulting relapse. Mesenchymal stromal cells (MSC) from different tissues those...

10.3390/cells8121577 article EN cc-by Cells 2019-12-05
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