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  1. No Access

    Chapter and Conference Paper

    Sequential Chemotherapy with Mitoxantrone, Etoposide and Cytarabine for Previously Treated Acute Myeloid Leukemia: EMA 86 Regimen

    EMA 86 regimen, associating mitoxantrone, 12 mg/m2/day on days 1–3, etoposide, 200 mg/m2/day as a continuous infusion on days 8–10 and cytarabine, 500 mg/m2/day as a continuous infusion on days 1–3 and 8–10, was ...

    Eric Archimbaud, Xavier Thomas, Véronique Leblond in Acute Leukemias V (1996)

  2. No Access

    Article

    Chromosome and Molecular Abnormalities in Myelodysplastic Syndromes

    Cytogenetic abnormalities are seen in approximately 50% of cases of myelodysplastic syndrome (MDS) and 80% of cases of secondary MDS (following chemotherapy or radiotherapy). These abnormalities generally cons...

    Pierre Fenaux in International Journal of Hematology (2001)

  3. No Access

    Article

    Mesenchymal cells generated from patients with myelodysplastic syndromes are devoid of chromosomal clonal markers and support short- and long-term hematopoiesis in vitro

    Myelodysplastic syndromes (MDS) are clonal malignant stem cell disorders characterized by inefficient hematopoiesis. The role of the marrow microenvironment in the pathogenesis of the disease has been controve...

    Valérie Soenen-Cornu, Cristina Tourino, Marie-Laure Bonnet, Martine Guillier in Oncogene (2005)

  4. No Access

    Article

    Inhibitors of DNA methylation: beyond myelodysplastic syndromes

    DNA methyltransferase (DNMT) inhibitors, azacitidine (Vidaza®, Pharmion, Boulder, CO, USA) and decitabine (Dacogen™; SuperGen Inc, Dublin, CA, USA, and MGI Pharma Inc, Bloomington, MN, USA), have had a significan...

    Pierre Fenaux in Nature Clinical Practice Oncology (2005)

  5. No Access

    Article

    Differentiating megakaryocytes in myelodysplastic syndromes succumb to mitochondrial derangement without caspase activation

    Myelodysplastic syndromes (MDS) constitute a preneoplastic condition in which potentially malignant cancer stem cells continuously die during differentiation. This MDS-associated cell death often involves casp...

    Thorsten Braun, Gabrielle Carvalho, Jennifer Grosjean, Lionel Ades in Apoptosis (2007)

  6. No Access

    Chapter

    Burkitt’s Acute Lymphoblastic Leukemia (L3ALL) in Adults

    Accounting for 1–3% of all cases of acute lymphoblastic leukemias (ALL), Burkitt cell ALL (L3ALL) is characterized by the morphology of blast cells, the presence of monoclonal surface immunoglobulins (sIg), and b...

    Vincent Ribrag, Philippe Casassus, Pierre Fenaux in Acute Leukemias (2008)

  7. Article

    Open Access

    Practical recommendations on the use of lenalidomide in the management of myelodysplastic syndromes

    Lenalidomide, an oral immunomodulatory agent, has received approval in the USA from the Food and Drug Administration (FDA) for the management of myelodysplastic syndromes (MDS) classified by the International ...

    Aristoteles Giagounidis, Pierre Fenaux, Ghulam J. Mufti, Petra Muus in Annals of Hematology (2008)

  8. No Access

    Article

    Flt3 receptor inhibition reduces constitutive NFκB activation in high-risk myelodysplastic syndrome and acute myeloid leukemia

    High-risk myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) are characterized by the activation of the anti-apoptotic transcription factor NFκB, via the IKK complex. Here, we show that constituti...

    Jennifer Grosjean-Raillard, Lionel Adès, Simone Boehrer, Maximilien Tailler in Apoptosis (2008)

  9. Article

    Open Access

    Valuation of transfusion-free living in MDS: results of health utility interviews with patients

    This study measured how myelodysplastic syndrome (MDS) patients value transfusion independence (TI), reduced transfusions (RT) and transfusion-dependence (TD) using health utility assessment methodology.

    Agota Szende, Caroline Schaefer, Thomas F Goss in Health and Quality of Life Outcomes (2009)

  10. Article

    Open Access

    A European survey on the detection and management of iron overload in transfusion-dependent patients with MDS

    To better understand the detection and management of iron overload in transfusion-dependent patients with myelodysplastic syndromes (MDS), a 15-min web- or paper-based survey was conducted among 338 European p...

    Aristoteles Giagounidis, Susanna Leto di Priolo, Susanne Ille in Annals of Hematology (2011)

  11. No Access

    Article

    Treatment of myelodysplastic syndromes with excess of blasts by bevacizumab is well tolerated and is associated with a decrease of VEGF plasma level

    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 ...

    Laurence Legros, Bohrane Slama, Jean-Michel Karsenti, Norbert Vey in Annals of Hematology (2012)

  12. Article

    Open Access

    Lenalidomide as a disease-modifying agent in patients with del(5q) myelodysplastic syndromes: linking mechanism of action to clinical outcomes

    Deletion of the long arm of chromosome 5, del(5q), is the most prevalent cytogenetic abnormality in patients with myelodysplastic syndromes (MDS). In isolation, it is traditionally associated with favorable pr...

    Aristoteles Giagounidis, Ghulam J. Mufti, Pierre Fenaux in Annals of Hematology (2014)

  13. No Access

    Article

    Aseptic muscular abscesses associated with myelodysplastic syndrome

    Adrien Mirouse, Alexandre Virone, Delphine Gobert in European Journal of Dermatology (2014)

  14. Article

    Erratum to: Flt3 receptor inhibition reduces constitutive NFκB activation in high-risk myelodysplastic syndrome and acute myeloid leukemia

    Jennifer Grosjean-Raillard, Lionel Adès, Simone Boehrer, Maximilien Tailler in Apoptosis (2015)

  15. Article

    Open Access

    GEP analysis validates high risk MDS and acute myeloid leukemia post MDS mice models and highlights novel dysregulated pathways

    In spite of the recent discovery of genetic mutations in most myelodysplasic (MDS) patients, the pathophysiology of these disorders still remains poorly understood, and only few in vivo models are available to...

    Laura Guerenne, Stéphanie Beurlet, Mohamed Said in Journal of Hematology & Oncology (2016)

  16. Article

    Open Access

    Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents

    The cytidine analogues azacytidine and 5-aza-2’-deoxycytidine (decitabine) are commonly used to treat myelodysplastic syndromes, with or without a myeloproliferative component. It remains unclear whether the r...

    Jane Merlevede, Nathalie Droin, Tingting Qin, Kristen Meldi in Nature Communications (2016)

  17. Article

    Open Access

    Clinical characteristics and outcomes according to age in lenalidomide-treated patients with RBC transfusion-dependent lower-risk MDS and del(5q)

    Particularly since the advent of lenalidomide, lower-risk myelodysplastic syndromes (MDS) patients with del(5q) have been the focus of many studies; however, the impact of age on disease characteristics and re...

    Pierre Fenaux, Aristoteles Giagounidis in Journal of Hematology & Oncology (2017)

  18. Article

    Open Access

    Cytomorphology review of 100 newly diagnosed lower-risk MDS patients in the European LeukemiaNet MDS (EUMDS) registry reveals a high inter-observer concordance

    The European LeukemiaNet MDS (EUMDS) registry is collecting data of myelodysplastic syndrome (MDS) patients belonging to the IPSS low or intermediate-1 category, newly diagnosed by local cytologists. The diagn...

    Louise de Swart, Alex Smith, Marius MacKenzie, Argiris Symeonidis in Annals of Hematology (2017)

  19. Article

    Open Access

    Validation of a post-hypomethylating agent failure prognostic model in myelodysplastic syndromes patients treated in a randomized controlled phase III trial of rigosertib vs. best supportive care

    Aziz Nazha, Mikkael A. Sekeres, Rami Komrokji, David P. Steensma in Blood Cancer Journal (2017)

  20. No Access

    Chapter

    Treatment with Hypomethylating Agents (HMA)

    In 1993 Silverman and coworkers [1] reported on a phase 2 trial on 43 patients with higher-risk MDS (medullary blast count >10%) using 75 mg/m2 5-Azacytidine (5-Aza) for 7 days every 28 days for 6 cycles. Forty-n...

    Ulrich Germing, Pierre Fenaux in Myelodysplastic Syndromes (2018)

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