Search Results - "Sargas, Claudia"
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Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene
Published in Cancers (08-03-2020)“…Although acute promyelocytic leukemia (APL) is one of the most characterized forms of acute myeloid leukemia (AML), the molecular mechanisms involved in the…”
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Validation of mutated CEBPA bZIP as a distinct prognosis entity in acute myeloid leukemia: a study by the Spanish PETHEMA registry
Published in Haematologica (Roma) (18-04-2024)Get full text
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Prognostic significance of FLT3-ITD length in AML patients treated with intensive regimens
Published in Scientific reports (20-10-2021)“…FLT3- ITD mutations are detected in approximately 25% of newly diagnosed adult acute myeloid leukemia (AML) patients and confer an adverse prognosis. The FLT3…”
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Design and Validation of a Custom Next-Generation Sequencing Panel in Pediatric Acute Lymphoblastic Leukemia
Published in International journal of molecular sciences (23-02-2023)“…The molecular landscape of acute lymphoblastic leukemia (ALL) is highly heterogeneous, and genetic lesions are clinically relevant for diagnosis, risk…”
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Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype
Published in Scientific reports (03-04-2020)“…Nearly 50% of patients with de novo acute myeloid leukemia (AML) harbor an apparently normal karyotype (NK) by conventional cytogenetic techniques showing a…”
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The Q-LAMP Method Represents a Valid and Rapid Alternative for the Detection of the BCR-ABL1 Rearrangement in Philadelphia-Positive Leukemias
Published in International journal of molecular sciences (04-12-2019)“…Molecular detection of the fusion transcripts is necessary for the genetic confirmation of a chronic myeloid leukemia diagnosis and for the risk classification…”
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The role of next-generation sequencing in acute myeloid leukemia
Published in Current opinion in oncology (15-09-2022)Get full text
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The role of next-generation sequencing in acute myeloid leukemia
Published in Current opinion in oncology (01-11-2022)“…Purpose of review The development of high-throughput techniques like next-generation sequencing (NGS) has unraveled the genetic profile of cancer. In this…”
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Correction: Liquori et al. Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene. Cancers 2020, 12, 624
Published in Cancers (09-07-2021)“…The authors wish to make the following corrections to this paper [...]…”
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Treatment Outcomes in Unfit Patients with Newly Acute Myeloid Leukemia According to IDH1 Mutational Status: Real World Evidence from the Pethema Epidemiologic Registry
Published in Blood (02-11-2023)“…Background: Current treatment of unfit acute myeloid leukemia (AML) patients include hypomethylating agents (HMA) with or without venetoclax, low-dose…”
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Networking for advanced molecular diagnosis in acute myeloid leukemia patients is possible: the PETHEMA NGS-AML project
Published in Haematologica (Roma) (01-12-2021)“…Next-Generation Sequencing has recently been introduced to efficiently and simultaneously detect genetic variations in acute myeloid leukemia. However, its…”
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Pethema NGS-AML Project. Final Analysis and Clinical Validation of New Genomic Classifications
Published in Blood (15-11-2022)Get full text
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Author Correction: Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA
Published in Scientific reports (28-03-2024)Get full text
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Improving the prediction of acute myeloid leukaemia outcomes by complementing mutational profiling with ex vivo chemosensitivity
Published in British journal of haematology (01-05-2020)“…Summary Refractoriness to induction therapy and relapse after complete remission are the leading causes of death in patients with acute myeloid leukaemia…”
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Nationwide Laboratory Network for AML Cross-Validated NGS Studies: Results from a Real-Life Cohort of the Pethema Group
Published in Blood (23-11-2021)“…Next-Generation Sequencing (NGS) has recently been introduced to efficiently and simultaneously detect genetic variations in acute myeloid leukemia (AML)…”
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Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA
Published in Scientific reports (29-07-2022)“…The screening of the BCR::ABL1 kinase domain (KD) mutation has become a routine analysis in case of warning/failure for chronic myeloid leukemia (CML) and…”
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Clinical Utility of a Next-Generation Sequencing Panel for Acute Myeloid Leukemia Diagnostics
Published in The Journal of molecular diagnostics : JMD (01-03-2019)“…Next-generation sequencing (NGS) has redefined the genetic landscape of acute myeloid leukemia (AML), providing new molecular markers for diagnostic and…”
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A phase I trial of selinexor plus FLAG-Ida for the treatment of refractory/relapsed adult acute myeloid leukemia patients
Published in Annals of hematology (01-06-2021)“…Prognosis for relapsed or refractory (R/R) acute myeloid leukemia (AML) despite salvage therapy is dismal. This phase I dose-escalation trial assessed the…”
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Molecular Landscape and Validation of New Genomic Classification in 2668 Adult AML Patients: Real Life Data from the PETHEMA Registry
Published in Cancers (10-01-2023)“…Next-Generation Sequencing (NGS) implementation to perform accurate diagnosis in acute myeloid leukemia (AML) represents a major challenge for molecular…”
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