Michael Byrne

ORCID: 0000-0002-2966-4877
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About
Contact & Profiles
Research Areas
  • Acute Myeloid Leukemia Research
  • Hematopoietic Stem Cell Transplantation
  • Chronic Myeloid Leukemia Treatments
  • Acute Lymphoblastic Leukemia research
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Multiple Myeloma Research and Treatments
  • Immune Cell Function and Interaction
  • CAR-T cell therapy research
  • Chronic Lymphocytic Leukemia Research
  • Cancer Treatment and Pharmacology
  • Eosinophilic Disorders and Syndromes
  • Protein Degradation and Inhibitors
  • RNA regulation and disease
  • interferon and immune responses
  • Neutropenia and Cancer Infections
  • Histone Deacetylase Inhibitors Research
  • Cancer therapeutics and mechanisms
  • Childhood Cancer Survivors' Quality of Life
  • Lymphoma Diagnosis and Treatment
  • Cytomegalovirus and herpesvirus research
  • RNA Interference and Gene Delivery
  • Cancer Genomics and Diagnostics
  • Corneal Surgery and Treatments
  • Mesenchymal stem cell research
  • RNA Research and Splicing

Tennessee Oncology
2024-2025

Rutgers, The State University of New Jersey
2025

Vanderbilt University Medical Center
2015-2024

Vanderbilt University
2016-2023

United States Marine Corps
2022

Partners In Care
2022

University of Newcastle Australia
2022

Vanderbilt-Ingram Cancer Center
2016-2021

Patient Advocate Foundation
2020

University of Florida
2012-2018

A minimally invasive diagnostic assay for early detection of Alzheimer's disease (AD) is required to select optimal patient groups in clinical trials, monitor progression and response treatment, better plan care. Blood an attractive source biomarkers due minimal discomfort the patient, encouraging greater compliance trials frequent testing. MiRNAs belong class non-coding regulatory RNA molecules ∼22 nt length are now recognized regulate ∼60% all known genes through post-transcriptional gene...

10.1371/journal.pone.0069807 article EN cc-by PLoS ONE 2013-07-29

Outcomes are poor in TP53-mutant (mTP53) acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), even after allogeneic hematopoietic stem-cell transplant (HCT). Eprenetapopt (APR-246) is a first-in-class, small-molecule p53 reactivator.We conducted phase II, multicenter, open-label trial to assess efficacy safety of eprenetapopt combined with azacitidine as maintenance therapy HCT (ClinicalTrials.gov identifier: NCT03931291). Patients mTP53 MDS or AML received up 12 cycles 3.7 g...

10.1200/jco.22.00181 article EN Journal of Clinical Oncology 2022-07-11
Mark J. Levis Mehdi Hamadani Brent R. Logan Richard J. Jones Anurag K. Singh and 95 more Mark R. Litzow John R. Wingard Esperanza B. Papadopoulos Alexander E. Perl Robert J. Soiffer Celalettin Üstün Masumi Ueda Geoffrey L. Uy Edmund K. Waller Sumithra Vasu Melhem Solh Asmita Mishra Lori Muffly Hee‐Je Kim Jan‐Henrik Mikesch Yuho Najima Masahiro Onozawa Kirsty Thomson Arnon Nagler Andrew H. Wei Guido Marcucci Nancy L. Geller Nahla Hasabou David Delgado Matt Rosales Jason E. Hill Stanley C. Gill Rishita Nuthethi Denise King Heather Wittsack Adam Mendizabal Steven M. Devine Mary M. Horowitz Yi‐Bin Chen Ed Agura Jessica K. Altman Αchilles Anagnostopoulos Sarah Anand Andrew Artz Walter E. Aulitzky Sophia Balderman Karen K. Ballen Michael W. Becker Yves Béguin Leanne Berkahn Zwi Berneman Vijaya Raj Bhatt Ian Bilmon Francesca Bonifazi Adrienne Briggs Benedetto Bruno Claudio G. Brunstein Michael Byrne Jenny Byrne Mónica Cabrero Roberto Cairoli George Carrum Jan Černý Yi‐Bin Chen June‐Won Cheong Fabio Ciceri Mercedes Colorado Rachel J. Cook Daniel R. Couriel Charles Craddock Lloyd E. Damon Abhinav Deol Yohan Desbrosses Steve Devine Carmen Di Grazia Antonio Di Stasi Ajoy Dias Kathy Dorritie James Essell Tetsuya Eto Sherif Farag Édouard Forcade Olga Frankfurt Shin‐ichiro Fujiwara Takahiro Fukuda Kentaro Fukushima Sabine Fürst Tatsunori Goto Aric C. Hall Shunsuke Hatta Yosr Hicheri Mitchell E. Horwitz Hsin‐An Hou Jonathan How Dianna S. Howard Wei‐Hsun Hsu Anne Huynh David Irvine Takayuki Ishikawa Katarzyna Jamieson

Allogeneic hematopoietic cell transplantation (HCT) improves outcomes for patients with AML harboring an internal tandem duplication mutation of

10.1200/jco.23.02474 article EN cc-by-nc-nd Journal of Clinical Oncology 2024-03-12

Abstract HLA-haploidentical hematopoietic cell transplantation (Haplo-HCT) using posttransplantation cyclophosphamide (PT-Cy) has improved donor availability. However, a matched sibling (MSD) is still considered the optimal donor. Using Center for International Blood and Marrow Transplant Research database, we compared outcomes after Haplo-HCT vs MSD in patients with acute myeloid leukemia (AML) first complete remission (CR1). Data from 1205 adult CR1 AML (2008-2015) were analyzed. A total...

10.1182/bloodadvances.2019000050 article EN cc-by-nc-nd Blood Advances 2019-06-14

Abstract Allogeneic hematopoietic cell transplant is a potential curative therapy for acute lymphoblastic leukemia (ALL). Delineating the graft-versus-leukemia (GVL) effect as function of graft-versus-host disease (GVHD) offers to improve survival. We examined 5215 recipients with ALL reported Center International Blood and Marrow Transplant Research registry. Overall survival (OS) was compared according presence severity GVHD evaluated in 3 cohorts: 2593 adults first or second complete...

10.1182/bloodadvances.2018027003 article EN cc-by-nc-nd Blood Advances 2019-02-26

Advanced hepatocellular cancer (HCC) is an incurable disease with limited options for systemic treatment. Sorafenib was approved advanced HCC based on trials in patients Child-Pugh class A. We reviewed our experience retrospectively who were treated sorafenib a focus B (CP-B) liver cirrhosis and effect of hypertension (HTN) survival.We medical charts documented received since 2007. Survival data plotted according to HTN.Results 41 39% had CP-B. Eighty-five percent male 67% due viral...

10.1097/coc.0b013e3182468039 article EN American Journal of Clinical Oncology 2012-05-01

For patients with high risk myeloid disease, allogeneic hematopoietic cell transplantation (HCT) is the only potentially curative therapy. Unfortunately, many of these relapse after HCT and have a limited survival. The recent approval venetoclax, an orally bioavailable BCL-2 inhibitor, resulted in significant responses treatment naïve acute leukemia (AML), off-label use relapsed/refractory setting increasing. We report outcomes 21 who underwent for relapsed AML, were treated venetoclax....

10.1002/ajh.25859 article EN American Journal of Hematology 2020-05-11

Post-transplant cyclophosphamide (PTCy) has significantly increased the successful use of haploidentical donors with a relatively low incidence graft-versus-host disease (GVHD). Given its increasing use, we sought to determine risk factors for GVHD after hematopoietic cell transplantation (haplo-HCT) using PTCy. Data from Center International Blood and Marrow Transplant Research on adult patients acute myeloid leukemia, lymphoblastic myelodysplastic syndrome, or chronic leukemia who...

10.1016/j.bbmt.2020.05.001 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2020-05-17

The purpose of this study was to determine whether laser Doppler skin perfusion pressure (LD-SPP) could accurately predict amputation wound healing.We studied a total 62 limbs in 52 patients (28 men and 24 women) with mean age 62.2 years (range 34 93 years). From this, 39 underwent major (15 above-the-knee, below-the-knee), 23 minor amputations (4 transmetatarsal 19 toes). There were five postoperative deaths, leaving 57 available for analysis.Three 13 above-knee failed heal. Twenty-one...

10.1016/s0741-5214(05)80014-x article EN cc-by-nc-nd Journal of Vascular Surgery 1995-05-01

The application of machine learning in medicine has been productive multiple fields, but not previously applied to analyze the complexity organ involvement by chronic graft-versus-host disease. Chronic disease is classified an overall composite score as mild, moderate or severe, which may overlook clinically relevant patterns involvement. Here we a novel computational approach with goal identifying phenotypic groups based on subcomponents National Institutes Health Consensus Criteria....

10.3324/haematol.2018.193441 article EN cc-by-nc Haematologica 2018-09-20

Autologous stem cell transplantation (ASCT) can be curative for patients with relapsed/refractory Hodgkin lymphoma (HL). Based on studies suggesting that anti-PD-1 monoclonal antibodies (mAbs) sensitize to subsequent chemotherapy, we hypothesized therapy before ASCT would result in acceptable outcomes among high-risk who progressed or responded insufficiently ≥1 salvage regimen, including chemorefractory are traditionally considered poor candidates. We retrospectively identified 78 HL...

10.1182/bloodadvances.2020003556 article EN cc-by-nc-nd Blood Advances 2021-03-12

Post-transplantation cyclophosphamide (PTCy) has been shown to effectively control graft-versus-host disease (GvHD) in haploidentical (Haplo) transplantations. In this retrospective registry study, we compared GvHD organ distribution, severity, and outcomes patients with occurring after Haplo transplantation PTCy prophylaxis (Haplo/PTCy) versus HLA-matched unrelated donor conventional (MUD/conventional). We evaluated 2 cohorts: grade 4 acute (aGvHD) including 264 1163 recipients of MUD...

10.1016/j.jtct.2022.07.013 article EN cc-by-nc-nd Transplantation and Cellular Therapy 2022-07-17

Guadecitabine is a novel hypomethylating agent (HMA) resistant to deamination by cytidine deaminase. Patients with relapsed/refractory acute myeloid leukemia (AML) were randomly assigned guadecitabine or preselected treatment choice (TC) of high-intensity chemotherapy, low-intensity HMAs low-dose cytarabine, best supportive care (BSC). The primary end point was overall survival (OS). A total 302 patients (n = 148) TC 154). Preselected TCs 233 [77%; mainly HMAs]), chemotherapy 63 [21%]), and...

10.1182/bloodadvances.2023012062 article EN cc-by-nc-nd Blood Advances 2024-01-17

The toxicity of chimeric antigen receptor-natural killer (CAR-NK) therapy has not been tested in solid tumors, compared with CAR-T side by side. To address this, we investigated the CD147-CAR-NK "on-target/off-tumor" and neurotoxicity human CD147-transgenic (hCD147TG) mice hepatocellular carcinoma (HCC). We first vitro cytotoxicity against CD147+ tumor healthy cells. Both cells CD147-IL15-CAR-NK (autocrine expressing interleukin [IL]-15) can kill specifically but lung spleen tissue from...

10.1016/j.omton.2025.200957 article EN cc-by Deleted Journal 2025-02-26

This Viewpoint discusses the need to bring chimeric antigen receptor T-cell (CAR-T) therapy community oncology, which will allow an uninterrupted continuum of care for patients.

10.1001/jamaoncol.2025.0042 article EN JAMA Oncology 2025-03-06
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