
Jenny Byrne
Articles
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Sep 1, 2024 |
onlinelibrary.wiley.com | Jenny Byrne |Frédéric Baron |Myriam Labopin |Sorbonne Paris France
CONFLICT OF INTEREST STATEMENT FB has received travel grants and/or speaker honoraria from Pfizer, Celgene, Abbvie, Novartis, and Sanofi. JV has received speaker honoraria from AbbVie and ExCellThera. The other authors declare that they have no relevant conflict of interest. REFERENCES 1, , , et al. Impact of the type of anthracycline and of stem cell transplantation in younger patients with acute myeloid leukemia: long-term follow up of a phase III study. Am J Hematol. 2020; 95: 749-758.
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Aug 23, 2024 |
digitalcommons.library.tmc.edu | Jenny Byrne |Stephane de Botton |Pau Montesinos |Andre C Schuh
This open-label, randomized, phase 3 trial (NCT02577406) compared enasidenib, an oral IDH2 (isocitrate dehydrogenase 2) inhibitor, with conventional care regimens (CCRs) in patients aged ≥60 years with late-stage, mutant-IDH2 acute myeloid leukemia (AML) relapsed/refractory (R/R) to 2 or 3 prior AML-directed therapies.
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Jul 17, 2024 |
fis.uke.de | Jenny Byrne |Romain Guièze |Linda Koster |Diderik-Jan Eikema
Research ExplorerPublicationsAllogeneic hematopoietic stem-cell transplantation for patie... Abstract Bibliographical data
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Mar 11, 2024 |
onlinelibrary.wiley.com | Jenny Byrne |Corinne De Lord |Gwynn Matthias
INTRODUCTION Next-generation targeted sequencing (NGS) is an established diagnostic tool for haematological malignancies. NGS is performed by aligning the sequenced reads to the genome reference sequence and reporting discovered differences. One limitation of this approach is the inherent heterogeneity of germline genetics, which results in the inability to unambiguously determine whether any differences detected between tumour and reference are germline or somatic in origin.
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Mar 11, 2024 |
pericles.pericles-prod.literatumonline.com | Jenny Byrne |Corinne De Lord |Gwynn Matthias
INTRODUCTION Next-generation targeted sequencing (NGS) is an established diagnostic tool for haematological malignancies. NGS is performed by aligning the sequenced reads to the genome reference sequence and reporting discovered differences. One limitation of this approach is the inherent heterogeneity of germline genetics, which results in the inability to unambiguously determine whether any differences detected between tumour and reference are germline or somatic in origin.
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