Publications by authors named "Antonio Medina Almeida"

Myelodysplastic syndromes (MDSs) represent a heterogeneous group of hematological stem cell disorders with an increasing burden on health care systems. Evidence-based MDS guidelines and recommendations (G/Rs) are published but do not necessarily translate into better quality of care if adherence is not maintained in daily clinical practice. Guideline-based indicators (GBIs) are measurable elements for the standardized assessment of quality of care and, thus far, have not been developed for adult MDS patients.

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  • - Ruxolitinib has been approved for treating polycythemia vera patients who can't tolerate or are resistant to hydroxyurea, based on findings from the RESPONSE studies.
  • - In a phase 3b study involving 161 patients, nearly 38% experienced adverse events that required dose adjustments, with anemia and thrombocytosis as the most common issues.
  • - After 24 weeks, 45.3% of participants achieved hematocrit control, 18% had hematologic remission, and 86.7% saw a significant reduction in spleen size, with safety and efficacy similar to previous studies.
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  • Iron overload from red blood cell transfusions can lead to serious health issues in lower-risk myelodysplastic syndrome (MDS) patients, with iron chelation therapy (ICT) potentially improving survival rates.
  • This study analyzed data from the European MDS registry to compare patients who received ICT with those who did not, using various statistical models to assess overall survival.
  • The results indicated that patients receiving ICT had significantly better survival rates and about 39% showed improvement in blood cell production, suggesting ICT could benefit transfused MDS patients.
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Progression-free survival (PFS) of patients with lower-risk myelodysplastic syndromes (MDS) treated with red blood cell transfusions is usually reduced, but it is unclear whether transfusion dose density is an independent prognostic factor. The European MDS Registry collects prospective data at 6-monthly intervals from newly diagnosed lower-risk myelodysplastic syndromes patients in 16 European countries and Israel. Data on the transfusion dose density - the cumulative dose received at the end of each interval divided by the time since the beginning of the interval in which the first transfusion was received - were analyzed using proportional hazards regression with time-varying co-variates, with death and progression to higher-risk MDS/acute myeloid leukemia as events.

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Prognosis of lower-risk (International Prognostic Scoring System [IPSS] low/intermediate-1) myelodysplastic syndrome (MDS) is heterogeneous and relies on steady-state assessment of cytopenias. We analyzed relative drops in neutrophil and platelet counts during the first 6 months of follow-up of lower-risk MDS patients. We performed a landmark analysis of overall survival (OS) of lower-risk MDS patients prospectively included in the European LeukaemiaNet MDS registry having a visit at 6 ± 1 month from inclusion to assess the prognostic relevance of relative drops in neutrophils and platelets, defined as (count at landmark - count at inclusion)/count at inclusion.

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Conventional karyotype is one of the most relevant prognostic factors in MDS. However, about 50% of patients with MDS have a normal karyotype. Usually, 20-25 normal metaphases (nMP) are considered to be optimal to exclude small abnormal clones which might be associated with poor prognosis.

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Background: Aberrant epigenetic patterns are central in the pathogenesis of haematopoietic diseases such as myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML). Vorinostat is a HDACi which has produced responses in these disorders. The purpose of this study was to address the functional effects of vorinostat in leukemic cell lines and primary AML and MDS myeloid cells and to dissect the genetic and molecular mechanisms by which it exerts its action.

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