Miguel Á. Sanz

ORCID: 0000-0003-1489-1177
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About
Contact & Profiles
Research Areas
  • Acute Myeloid Leukemia Research
  • Retinoids in leukemia and cellular processes
  • Acute Lymphoblastic Leukemia research
  • Hematopoietic Stem Cell Transplantation
  • Chronic Myeloid Leukemia Treatments
  • Multiple Myeloma Research and Treatments
  • Neutropenia and Cancer Infections
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Blood groups and transfusion
  • Polyomavirus and related diseases
  • Platelet Disorders and Treatments
  • Hematological disorders and diagnostics
  • Antifungal resistance and susceptibility
  • Lymphoma Diagnosis and Treatment
  • Fungal Infections and Studies
  • Histone Deacetylase Inhibitors Research
  • Protein Degradation and Inhibitors
  • Antioxidant Activity and Oxidative Stress
  • Blood disorders and treatments
  • Bone and Joint Diseases
  • Cancer Treatment and Pharmacology
  • Drug-Induced Ocular Toxicity
  • Cancer Genomics and Diagnostics
  • Hemoglobinopathies and Related Disorders

Universitat de València
2016-2025

Instituto de Investigación Sanitaria La Fe
2005-2025

Hospital Universitari i Politècnic La Fe
2015-2024

Centro de Investigación Biomédica en Red de Cáncer
2017-2024

Vall d'Hebron Hospital Universitari
1990-2024

Hospital San Pedro de Alcántara
2010-2024

Instituto Politécnico Nacional
2014-2024

Weatherford College
2024

Aurora Medical Center
2024

Centre Hospitalier Universitaire de Toulouse
2012-2024

Patients with acute myeloid leukemia (AML) and a FLT3 mutation have poor outcomes. We conducted phase 3 trial to determine whether the addition of midostaurin - an oral multitargeted kinase inhibitor that is active in patients standard chemotherapy would prolong overall survival this population.We screened 3277 patients, 18 59 years age, who had newly diagnosed AML for mutations. were randomly assigned receive (induction therapy daunorubicin cytarabine consolidation high-dose cytarabine)...

10.1056/nejmoa1614359 article EN New England Journal of Medicine 2017-06-23

Blinatumomab, a bispecific monoclonal antibody construct that enables CD3-positive T cells to recognize and eliminate CD19-positive acute lymphoblastic leukemia (ALL) blasts, was approved for use in patients with relapsed or refractory B-cell precursor ALL on the basis of single-group trials showed efficacy manageable toxic effects.In this multi-institutional phase 3 trial, we randomly assigned adults heavily pretreated ALL, 2:1 ratio, receive either blinatumomab standard-of-care...

10.1056/nejmoa1609783 article EN New England Journal of Medicine 2017-03-01

Retrospective studies have shown that adolescents and young adults with acute lymphoblastic leukemia (ALL) treated pediatric protocols better outcomes than similarly aged patients adult protocols, but prospective comparing using schedules are scarce. The ALL-96 protocol was addressed to compare the toxicity results of a pediatric-based in (age 15-18 years) 19-30 standard-risk (SR) ALL.Adolescents (n = 35) 46) received standard five-drug/5-week induction course followed by two cycles early...

10.1200/jco.2007.13.7265 article EN Journal of Clinical Oncology 2008-04-08
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