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    • Attilio Orazi
    • Attilio Orazi

      Attilio Orazi

      Department of Pathology, Texas Tech University Health Sciences Center, El Paso, TX, USA. | Department of Pathology, Texas Tech University Health Sciences Center El Paso, 4800 ...

       

       

      KOL Resume for Attilio Orazi

      Year
      2022

      Department of Pathology, Texas Tech University Health Sciences Center, El Paso, TX, USA.

      Texas Tech University Health Sciences Center, El Paso, Texas, United States.

      2021

      Departments of Pathology, Texas Tech University Health Sciences Center, PL Foster School of Medicine, El Paso, TX, USA

      Department of Pathology, Texas Tech University Health Sciences Center El Paso, United States of America

      2020

      Department of Pathology, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas

      2019

      Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA;

      Dept. Pathology and Laboratory Medicine,Weill Cornell Medical College/New York Presbyterian Hospital

      2018

      Division of Hematopathology, Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA

      Pathology, Weill Cornell Medical College, New York, NY

      2017

      Department of Pathology and Laboratory Medicine Weill Cornell Medical College/New York Presbyterian Hospital New York New York

      2016

      Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue, 10065, New York, NY, USA

      Weill Medical College of Cornell University, New York, New York.

      2015

      From the Division of Hematopathology, Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.

      Weill Cornell Medical College, New York, NY;

      2014

      Weill Medical College of Cornell University, New York, NY

      2013

      Department of Pathology and Laboratory Medicine, New York Presbyterian Hospital, Weill Cornell Medical Center, New York, NY, USA

      Weill Medical College of Cornell University, New York, NY;

      2012

      Division of Hematopathology, Weill Cornell Medical College, New York, NY

      Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York

      2011

      Hematopathology Division, Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, 1300 York Avenue, 10065, New York, NY, USA

      Weill Cornell Medical College/New York Presbyterian Hospital, New York, New York

      2010

      Department of Pathology; Indiana University School of Medicine, Indianapolis, IN; and

      Division of Hematopathology, Weill Cornell Medical Center-New York Presbyterian Hospital, New York, NY

      2009

      Weill Medical College of Cornell University, Department of Pathology and Laboratory Medicine, New York, NY, USA

      2008

      Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Clarian Pathology Laboratory, Room 5044, 350 West 11th Street, Indianapolis, IN 46202-5200, USA

      William Beaumont Hospital, Royal Oak, MI Indiana University School of Medicine, Indianapolis, IN William Beaumont Hospital, Royal Oak, MI Indiana University School of Medicine, Indianapolis, IN William Beaumont Hospital, Royal Oak, MI Indiana University School of Medicine, Indianapolis, IN

       

       

      Attilio Orazi: Influence Statistics

      Sample of concepts for which Attilio Orazi is among the top experts in the world.
      Concept World rank
      cases mlib #1
      97 patients dlbcl #1
      brain neoplasms cd56 #1
      cases overt mds #1
      cases megakaryocytes #1
      controls pinp #1
      rcm jak2 #1
      cr51 rcm #1
      term mpd #1
      bmb specimens #1
      amlmpn cases amldn #1
      immune response haemophilus #1
      patients mf2 3 #1
      differentiation infant leukemia #1
      bone marrows #1
      mf2 3 patients #1
      cd34 immunohistochemistry cases #1
      absolute monocytosis #1
      v617f‐positive #1
      primary myelofibrosis cmml #1
      pfpmf #1
      antigens biopsy bone #1
      tumor biopsy myelogenous #1
      blast cells conditions #1
      post polycythemic #1
      2 large institutions #1
      marrow fibrosis jak2 #1
      cases primary testicular #1
      diagnostic approach mds #1
      specificity myeloid leukemia #1
      classification jak2 #1
      differences cd34microvessel density #1
      underlying mpn amlmpn #1
      presence gamnagandy bodies #1
      enlarged mass #1
      operative hyperleukocytosis #1
      knockout protein kras #1
      mpns myelodysplastic #1
      rare patients features #1
      defined myeloid #1
      fibrosis cd4 count #1
      83 93 patients #1
      fibrosis normal controls #1
      cytogenetics mdss #1
      pmf myelodysplastic syndrome #1
      postoperative hyperleukocytosis leukostasis #1
      hpf pfpmf #1
      term mds mpd #1
      cellularity megakaryocyte #1
      myeloid progenitor numbers #1

       

      Prominent publications by Attilio Orazi

      KOL-Index: 17220

      Acute myeloid leukemia arising from chronic myelomonocytic leukemia is currently classified as acute myeloid leukemia with myelodysplasia-related changes, a high-risk subtype. However, the specific features of these cases have not been well described. We studied 38 patients with chronic myelomonocytic leukemia who progressed to acute myeloid leukemia. We compared the clinicopathologic and genetic features of these cases with 180 patients with de novo acute myeloid leukemia and 34 ...

      Known for Myeloid Leukemia | Chronic Myelomonocytic | Myelodysplastic Syndromes | Npm1 Mutation | Bone Marrow
      KOL-Index: 17141

      Double-hit B-cell lymphoma is a common designation for a group of tumors characterized by concurrent translocations of MYC and BCL2, BCL6, or other genes. The prognosis of concurrent MYC and BCL6 translocations is not well known. In this study, we assessed rearrangements and expression of MYC, BCL2 and BCL6 in 898 patients with de novo diffuse large B-cell lymphoma treated with standard chemotherapy (cyclophosphamide, doxorubicin, vincristine, and prednisone plus rituximab). Neither BCL6 ...

      Known for Cell Lymphoma | Diffuse Large | Myc Bcl6 | Protooncogene Proteins | Prognostic Impact
      KOL-Index: 16425

      Diffuse large B-cell lymphoma (DLBCL) is stratified into prognostically favorable germinal center B-cell (GCB)-like and unfavorable activated B-cell (ABC)-like subtypes based on gene expression signatures. In this study, we analyzed 893 de novo DLBCL patients treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone). We show that MYC/BCL2 protein coexpression occurred significantly more commonly in the ABC subtype. Patients with the ABC or GCB subtype of ...

      Known for Gene Expression | Inferior Survival | Patients Dlbcl | Cell Subtype | Diffuse Large
      KOL-Index: 16421

      PURPOSE: Approximately 5% of diffuse large B-cell lymphomas (DLBCLs) are double-hit lymphomas (DHLs) with translocations of both MYC and BCL2. DHLs are characterized by poor outcome. We tested whether DLBCLs with high expression of MYC protein and BCL2 protein share the clinical features and poor prognosis of DHLs.

      PATIENTS AND METHODS: Paraffin-embedded lymphoma samples from 193 patients with de novo DLBCL who were uniformly treated with rituximab, cyclophosphamide, doxorubicin, ...

      Known for Lymphoma Treated | Strong Predictor | Doxorubicin Vincristine | Myc Bcl2 | Diffuse Large
      KOL-Index: 14913

      Acute myeloid leukemia and myelodysplastic syndrome with inv(3)(q21q26.2)/t(3;3)(q21;q26.2) have a poor prognosis. Indeed, the inv(3)(q21q26.2)/t(3;3)(q21;q26.2) has been recognized as a poor risk karyotype in the revised International Prognostic Scoring System. However, inv(3)(q21q26.2)/t(3;3)(q21;q26.2) is not among the cytogenetic abnormalities pathognomonic for diagnosis of acute myeloid leukemia irrespective of blast percentage in the 2008 WHO classification. This multicenter study ...

      Known for Acute Myeloid Leukemia | Myelodysplastic Syndrome | Inv3q21q262 T33q21q262 | Blast Percentage | Bone Marrow
      KOL-Index: 14741

      In spite of the impressive advances in the area of molecular pathology, bone marrow morphology remains the diagnosis cornerstone to identify the various subtypes of myeloid neoplasms. Morphological examination of the bone marrow requires both bone marrow aspirate and bone marrow trephine biopsy. Immunohistochemistry of bone marrow biopsy with markers reactive in paraffin-embedded tissues represents a powerful diagnostic tool; its results can be easily correlated with those obtained by ...

      Known for Myelodysplastic Syndromes | Acute Myeloid | Bone Marrow | Flow Cytometry | Biopsy Immunohistochemistry
      KOL-Index: 14416

      Abnormal expression of the chemokine receptor CXCR4 plays an essential role in tumor cell dissemination and disease progression. However, the significance of CXCR4 overexpression in de novo diffuse large B cell lymphoma (DLBCL) is unknown. In 743 patients with de novo diffuse large B cell lymphoma (DLBCL) who received standard Rituximab-CHOP immunochemotherapy, we assessed the expression of CXCR4 and dissected its prognostic significance in various DLBCL subsets. Our results showed that ...

      Known for Cell Lymphoma | Cxcr4 Expression | Diffuse Large | Germinal Center | Prognostic Significance
      KOL-Index: 14323

      PURPOSE: Activated signal transducer and activator of transcription 3 (STAT3) regulates tumor growth, invasion, cell proliferation, angiogenesis, immune response, and survival. Data regarding expression of phosphorylated (activated) STAT3 in diffuse large B-cell lymphoma (DLBCL) and the impact of phosphorylated STAT3 (pSTAT3) on prognosis are limited.

      EXPERIMENTAL DESIGN: We evaluated expression of pSTAT3 in de novo DLBCL using immunohistochemistry, gene expression profiling (GEP), and ...

      Known for Stat3 Expression | Cell Lymphoma | Novo Diffuse | Clinical Implications | Jakstat Pathway
      KOL-Index: 14144

      Diffuse large B-cell lymphoma can be classified by gene expression profiling into germinal center and activated B-cell subtypes with different prognoses after rituximab-CHOP. The importance of previously recognized prognostic markers, such as Bcl-2 protein expression and BCL2 gene abnormalities, has been questioned in the new therapeutic era. We analyzed Bcl-2 protein expression, and BCL2 and MYC gene abnormalities by interphase fluorescence in situ hybridization in 327 patients with de ...

      Known for Germinal Center | Bcl2 Translocations | Poor Outcome | Cell Lymphoma | Diffuse Large
      KOL-Index: 14055

      The World Health Organization criteria for diagnosing chronic myelomonocytic leukemia (CMML) are largely based on findings observed in the peripheral blood and bone marrow aspirate. A specific diagnostic role for the bone marrow biopsy has not been adequately explored. We examined whether bone marrow biopsy supplemented by immunohistochemistry may be helpful in distinguishing CMML from cases of chronic myelogenous leukemia and atypical chronic myeloid leukemia (aCML). We immunostained 25 ...

      Known for Bone Marrow | Chronic Myelomonocytic Leukemia | Cases Cmml | Tumor Biopsy | Antigens Biomarkers
      KOL-Index: 13991

      Bevacizumab is a humanized monoclonal antibody directed against vascular endothelial growth factor (VEGF-A). Non-Hodgkin's lymphoma patients with high serum VEGF levels have an inferior survival compared to patients with low VEGF levels. Bevacizumab was administered through a central line at 15 mg kg(-1) IV on day 1 followed by rituximab (R) and CHOP on day 2 for cycle 1 and day 1 for cycles 2 - 8. Serum levels of bevacizumab and R were measured at specified time points to assess ...

      Known for Monoclonal Antibodies | Bevacizumab Chop | Diffuse Large | Cell Lymphoma | Vegf Levels
      KOL-Index: 13685

      CD30, originally identified as a cell-surface marker of Reed-Sternberg and Hodgkin cells of classical Hodgkin lymphoma, is also expressed by several types of non-Hodgkin lymphoma, including a subset of diffuse large B-cell lymphoma (DLBCL). However, the prognostic and biological importance of CD30 expression in DLBCL is unknown. Here we report that CD30 expression is a favorable prognostic factor in a cohort of 903 de novo DLBCL patients. CD30 was expressed in ∼14% of DLBCL patients. ...

      Known for Cd30 Expression | Diffuse Large | Cell Lymphoma | Favorable Prognosis | Dlbcl Patients
      KOL-Index: 13307

      Interdigitating dendritic cell sarcoma (IDCS) is a rare tumor derived from interdigitating dendritic cells. Three cases of IDCS associated with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) have been described, but no clonal relationship between the 2 neoplasms was demonstrated. We present a detailed case analysis of a CLL/SLL with metachronous IDCS and demonstrate that these 2 neoplasms are clonally related. The IDCS and CLL cells had trisomy 12 and identical ...

      Known for Chronic Lymphocytic Leukemia | Small Lymphocytic Lymphoma | Dendritic Cell | Cll Sll | 2 Neoplasms
      KOL-Index: 13133

      Chronic myelomonocytic leukemia is characterized by persistent absolute monocytosis (≥1 × 109/l) in the peripheral blood and dysplasia in ≥1 lineages. In the absence of dysplasia, an acquired clonal genetic abnormality is required or causes for reactive monocytosis have to be excluded. Oligomonocytic chronic myelomonocytic leukemia showing increased monocytes but no absolute monocytosis in the peripheral blood occurs occasionally. These cases are likely classified as myelodysplastic ...

      Known for Chronic Myelomonocytic | Absolute Monocytosis | Peripheral Blood | Myelodysplastic Syndrome | Clinicopathologic Features
      KOL-Index: 12664

      Gene expression profiling (GEP) has stratified diffuse large B-cell lymphoma (DLBCL) into molecular subgroups that correspond to different stages of lymphocyte development–namely germinal center B-cell like and activated B-cell like. This classification has prognostic significance, but GEP is expensive and not readily applicable into daily practice, which has lead to immunohistochemical algorithms proposed as a surrogate for GEP analysis. We assembled tissue microarrays from 475 de novo ...

      Known for Gene Expression | Dlbcl Rituximab | Diffuse Large | Cell Lymphoma | Bcl6 Cases

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      Attilio Orazi:Expert Impact

      Concepts for whichAttilio Orazihas direct influence:Bone marrow,  Acute myeloid leukemia,  Myelodysplastic syndromes,  Myeloid leukemia,  Primary myelofibrosis,  Cell lymphoma,  Myeloproliferative neoplasms,  Chronic myelomonocytic leukemia.

      Attilio Orazi:KOL impact

      Concepts related to the work of other authors for whichfor which Attilio Orazi has influence:Bone marrow,  Acute myeloid leukemia,  Myelodysplastic syndromes,  Cell lymphoma,  Myeloproliferative neoplasms,  Polycythemia vera,  Essential thrombocythemia.


       

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      Department of Pathology, Texas Tech University Health Sciences Center, El Paso, TX, USA. | Department of Pathology, Texas Tech University Health Sciences Center El Paso, 4800 Alberta Avenue, 79905, El Paso, TX, USA | Texas Tech University Health Scie

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