Publications by authors named "Espadana A"

Article Synopsis
  • This study examines the impact of next-generation sequencing (NGS) on the risk assessment of acute myeloid leukemia (AML) patients, focusing on a cohort of 268 newly diagnosed individuals.
  • Initially, 23% of patients could not be categorized into risk groups, but this number dropped to 10% after incorporating NGS data, highlighting NGS's role in improving risk stratification.
  • The findings reveal not only a refinement in risk classifications—resulting in 62 patients being better assessed—but also unexpected clinical outcomes tied to specific gene mutations, emphasizing the need for further research in this area.
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This retrospective study investigated outcomes of 404 patients with relapsed/refractory (R/R) FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) acute myeloid leukemia (AML) enrolled in the PETHEMA registry, pre-approval of tyrosine kinase inhibitors. Most patients (63%) had received first-line intensive therapy with 3 + 7. Subsequently, patients received salvage with intensive therapy (n = 261), non-intensive therapy (n = 63) or supportive care only (n = 80).

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Secondary acute myeloid leukemia (sAML) comprises a heterogeneous group of patients and is associated with poor overall survival (OS). We analyze the characteristics, treatment patterns, and outcomes of adult patients with sAML in the Programa Español de Tratamientos en Hematología (PETHEMA) registry. Overall, 6211 (72.

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Selection of elderly patients (aged ≥60 years) for intensive chemotherapy treatment of acute myeloblastic leukaemia (AML) remains challenging. Several cooperative groups such as Acute Leukaemia French Association (ALFA), Haematological Oncology Clinical Studies Group (HOCSG) and MD Anderson Cancer Center (MDACC) have developed predictive models to select those patients who can benefit from intensive chemotherapy. Our purpose is to validate and compare these three models in a cohort of patients treated in real-life setting.

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Oxidative stress and abnormal DNA methylation have been implicated in some types of cancer, namely in myelodysplastic syndromes (MDS). Since both mechanisms are observed in MDS patients, we analyzed the correlation of intracellular levels of peroxides, superoxide anion, and glutathione (GSH), as well as ratios of peroxides/GSH and superoxide/GSH, with the methylation status of P15 and P16 gene promoters in bone marrow leukocytes from MDS patients. Compared to controls, these patients had lower GSH content, higher peroxide levels, peroxides/GSH and superoxide/GSH ratios, as well as higher methylation frequency of P15 and P16 gene promoters.

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Article Synopsis
  • Oxidative stress results from an imbalance of reactive oxygen species (ROS) and antioxidants, which can lead to either cell death (apoptosis) or increased cell growth in myelodysplastic syndrome (MDS) patients.
  • Researchers studied oxidative stress and mitochondrial dysfunction in bone marrow samples from MDS patients, finding significant differences in ROS and antioxidant levels compared to healthy controls.
  • Their findings indicate that oxidative stress markers may serve as potential diagnostic and prognostic biomarkers for MDS, as higher ROS and lower antioxidant levels were associated with poorer survival outcomes.
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Central diabetes insipidus, is a syndrome characterized by the excretion of abnormally elevated volumes of diluted urine, due to the diminution of reabsorption of water in the collecting ducts, induced by the diminution of production of antidiuretic hormone. The involvement of the central nervous system in the leukaemia is frequent, but the association leukaemia/diabetes insipidus is rare. We describe a clinical case of a 40 years old female, whose first manifestation of leukaemia was diabetes insipidus; we discuss the difficulties of diagnosis, the particularities of the case and its evolution.

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The authors describe a clinical case of chronic myeloid leukemia with a typical presentation (massive splenomegaly and marked leucocytosis), but with a complex translocation--t (7; 9; 22) (q11; q34; q11). The evolution was rather atypical with a lymphoblastic crisis in association with osteolytic lesions and with parenchymal and soft tissue lymphoblastic tumours.

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