Myelodysplastic syndrome (MDS) defines a group of heterogeneous hematologic malignancies that often progresses to acute myeloid leukemia (AML). The leading treatment for high-risk MDS patients is azacitidine (Aza, Vidaza®), but a significant proportion of patients are refractory and all patients eventually relapse after an undefined time...
-
January 2020 (v1)Journal articleUploaded on: October 14, 2023
-
July 2012 (v1)Journal article
Marrow cells from patients with higher-risk myelodysplastic syndrome (MDS) exhibit constitutive nuclear factor (NF)-κB activation. The proteasome inhibitor, bortezomib, has limited efficacy as a single agent in acute myeloid leukaemia. Its activity on leukaemic cell lines is potentiated by chemotherapy. We treated 43 higher-risk MDS patients...
Uploaded on: December 2, 2022 -
December 13, 2012 (v1)Journal article
International audience
Uploaded on: December 2, 2022 -
May 7, 2011 (v1)Journal article
Myelodysplastic syndromes (MDS) are associated with increased bone marrow vascularity and increased levels of various angiogenic factors including Vascular Endothelial Growth Factor (VEGF) which is implicated in the proliferation and survival of leukemic cells. Before the approval of hypomethylating agents in this indication, the GFM conducted...
Uploaded on: December 3, 2022 -
September 26, 2013 (v1)Journal article
International audience
Uploaded on: December 2, 2022 -
September 26, 2013 (v1)Journal article
International audience
Uploaded on: October 11, 2023 -
November 15, 2022 (v1)Journal article
No description
Uploaded on: March 25, 2023 -
2017 (v1)Journal article
Background: Systemic inflammatory and autoimmune diseases (SIADs) associated with myelodysplastic syndromes are often difficult to treat. Corticosteroids are efficient but only usually at high doses. The use of biologics needs to be specified.Methods: In a French multicenter retrospective study, we analyzed the efficacy and safety of biologics...
Uploaded on: February 28, 2023