Morton Coleman

ORCID: 0000-0002-8516-2513
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About
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Research Areas
  • Lymphoma Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Multiple Myeloma Research and Treatments
  • Protein Degradation and Inhibitors
  • Cancer Treatment and Pharmacology
  • Lung Cancer Treatments and Mutations
  • Monoclonal and Polyclonal Antibodies Research
  • Chronic Myeloid Leukemia Treatments
  • CAR-T cell therapy research
  • Viral-associated cancers and disorders
  • Peptidase Inhibition and Analysis
  • Acute Myeloid Leukemia Research
  • CNS Lymphoma Diagnosis and Treatment
  • Cancer therapeutics and mechanisms
  • Acute Lymphoblastic Leukemia research
  • Cutaneous lymphoproliferative disorders research
  • Ubiquitin and proteasome pathways
  • Medical Imaging Techniques and Applications
  • Immunodeficiency and Autoimmune Disorders
  • Hematopoietic Stem Cell Transplantation
  • Immunotherapy and Immune Responses
  • Multiple and Secondary Primary Cancers
  • Hematological disorders and diagnostics
  • Cancer Mechanisms and Therapy
  • Ovarian cancer diagnosis and treatment

Weill Cornell Medicine
2017-2024

Cornell University
2015-2024

Clinical Research Associates
2017-2024

TB Alliance
2023

New York Hospital Queens
2009-2021

NewYork–Presbyterian Hospital
2010-2021

Presbyterian Hospital
2009-2021

Charles University
2019

Lymphoma Research Foundation
2007-2017

Boston Children's Museum
2014

The treatment of relapsed chronic lymphocytic leukemia (CLL) has resulted in few durable remissions. Bruton's tyrosine kinase (BTK), an essential component B-cell-receptor signaling, mediates interactions with the tumor microenvironment and promotes survival proliferation CLL cells.We conducted a phase 1b-2 multicenter study to assess safety, efficacy, pharmacokinetics, pharmacodynamics ibrutinib (PCI-32765), first-in-class, oral covalent inhibitor BTK designed for B-cell cancers, patients...

10.1056/nejmoa1215637 article EN New England Journal of Medicine 2013-06-19

Treatment of mantle-cell lymphoma (MCL) is nonstandardized, though patients are commonly treated immediately at diagnosis. Because data on observation, or "watch and wait," have not been previously reported, we analyzed the outcome deferred initial therapy.Inclusion criteria in this retrospective analysis were a diagnosis MCL between 1997 2007 known date first treatment. Hospital research charts reviewed for prognostic treatment-related information. Date death was derived from hospital...

10.1200/jco.2008.19.6121 article EN Journal of Clinical Oncology 2009-02-03

Human babesiosis is a tickborne malaria-like illness that generally resolves without complication after administration of atovaquone and azithromycin or clindamycin quinine. Although patients experiencing unresponsive to standard antimicrobial therapy have been described, the pathogenesis, clinical course, optimal treatment regimen such cases remain uncertain.We compared immunologic status, 14 case who experienced morbidity death persistence Babesia microti infection, despite repeated...

10.1086/525852 article EN Clinical Infectious Diseases 2007-12-20

The proteasome inhibitor bortezomib may enhance activity of chemoimmunotherapy in lymphoma. We evaluated dose-escalated plus standard cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) rituximab (R) patients with diffuse large B-cell lymphoma (DLBCL) mantle cell (MCL).Seventy-six subjects untreated DLBCL (n = 40) MCL 36) received CHOP every 21 days (CHOP-21) R at 0.7 mg/m(2) 4), 1.0 9), or 1.3 63) on 1 4 for six cycles.Median age was 63 years (range, 20 to 87), International...

10.1200/jco.2010.31.1142 article EN Journal of Clinical Oncology 2010-12-29

Mantle-cell lymphoma is generally incurable. Initial treatment not standardized but usually includes cytotoxic chemotherapy. Lenalidomide, an immunomodulatory compound, and rituximab, anti-CD20 antibody, are active in patients with recurrent mantle-cell lymphoma. We evaluated lenalidomide plus rituximab as a first-line therapy.We conducted single-group, multicenter, phase 2 study induction maintenance phases. During the phase, was administered at dose of 20 mg daily on days 1 through 21...

10.1056/nejmoa1505237 article EN New England Journal of Medicine 2015-11-04
Saad Z. Usmani Fredrik Schjesvold Albert Oriol Lionel Karlin Michèle Cavo and 95 more Robert M. Rifkin Habte A. Yimer Richard LeBlanc Naoki Takezako Robert McCroskey Andrew Lim Kenshi Suzuki Hiroshi Kosugi George Grigoriadis Irit Avivi Thierry Façon Sundar Jagannath Sagar Lonial Razi Ghori Mohammed Z.H. Farooqui Patricia Marinello Jesús F. San Miguel Andrew Lim George Grigoriadis Trish Walker Andrew J. Nicol Richard LeBlanc Donna Reece Mohamed Elemary Jean Samuel Boudreault Pedneault Lionel Karlin Thierry Façon Michel Attal Katja Weisel Monika Engelhardt Andréas Mackensen John Quinn Irit Avivi Amos Cohen Hila Magen‐Nativ Noam Benyamini Michèle Cavo Alessandra Larocca Naoki Takezako Kenshi Suzuki Hiroshi Kosugi Morio Matsumoto Shinsuke Iida Takayuki Ishikawa Yukio Kondo Kazutaka Sunami Kiyoshi Ando Takanori Teshima Takaaki Chou Hiromi Iwasaki Hirokazu Miki Itaru Matsumura Yasushi Onishi Koji Izutsu Masahiro Kizaki Anupkumar George Hillary Blacklock David Simpson Fredrik Schjesvold Anders Waage Olga Samoilova Evgeniy Nikitin Tatiana Chagorova Andrew M. McDonald Moosa Patel Albert Oriol Jesus San Miguel Izquierdo María‐Victoria Mateos Matthew Streetly Peter Forsyth Graham Jackson Stephen J. Jenkins Robert M. Rifkin Habte A. Yimer Robert McCroskey Danko Martincic Stefano Tarantolo Sarah Larson Yacoub Faroun Jennifer Vaughn Rachid Baz Gene Saylors Amarendra Neppalli Anastasios Raptis Henry C. Fung Maxwell Janosky Don A. Stevens Morton Coleman Dennis Costa Scott Cross Suzanne Fanning Daniel Farray Berges Thomas M. Harris Ira Zackon Djordje Atanackovic

10.1016/s2352-3026(19)30109-7 article EN The Lancet Haematology 2019-07-18

This single-center, dose-escalation study examines the safety, efficacy, and pharmacokinetics of epratuzumab (anti-CD22 humanized monoclonal antibody) in patients with recurrent indolent non-Hodgkin's lymphoma (NHL).Patients had NHL disease after at least one chemotherapy regimen. Epratuzumab was administered intravenously 120 to 1,000 mg/m2 over 30 60 minutes weekly for four treatments.Fifty-five received were assessable safety; 51 response. Patients heavily pretreated (50% prior regimens)...

10.1200/jco.2003.01.082 article EN Journal of Clinical Oncology 2003-07-08

The hallmark of chronic myelocytic leukemia is the presence Philadelphia chromosome (Ph1). In recent studies, we obtained data that strongly suggested involvement an oncogene, c-abl, in this type leukemia. This normally located on 9, translocated to 22 as a result Ph1 translocation. addition, identified region 22, breakpoint cluster (bcr), which contains chromosomal all patients with who are positive for Ph1. Recent studies have bcr part gene truncated consequence deleted could be replaced...

10.1056/nejm198512053132301 article EN New England Journal of Medicine 1985-12-05

This study is an integrated efficacy analysis of the five clinical trials tositumomab and iodine-131 in patients with relapsed or refractory low-grade, follicular, transformed low-grade non-Hodgkin's lymphoma (NHL) that resulted regulatory approval by US Food Drug Administration.This included 250 patients. Patients received a single course tositumomab. Responses were assessed independent panel radiologists oncologists.Response rates ranged from 47% to 68%; complete response 20% 38%. With...

10.1200/jco.2004.00.9217 article EN Journal of Clinical Oncology 2005-09-27

Abstract Purpose: We conducted a single-center, dose-escalation study evaluating the safety, pharmacokinetics, and efficacy of epratuzumab, an anti-CD22 humanized monoclonal antibody, in patients with aggressive non-Hodgkin’s lymphoma. Experimental Design: Epratuzumab was administered once weekly for 4 weeks at 120-1000-mg/m2 doses to 56 [most (n = 35) diffuse large B-cell lymphoma]. Results: Patients were heavily pretreated (median, prior therapies), 25% received high-dose chemotherapy stem...

10.1158/1078-0432.ccr-04-0294 article EN Clinical Cancer Research 2004-08-15

Abstract BACKGROUND The accuracy of fluorodeoxyglucose positron emission tomography (FDG‐PET; dual‐head camera with attenuation correction) and Ga‐67 scintigraphy was compared to identify disease sites in patients Hodgkin (HD) intermediate high‐grade non‐Hodgkin lymphoma (NHL) at initial diagnosis or clinical recurrence. METHODS Fifty‐one contemporaneous FDG‐PET scintigraphies were performed on NHL (35 grade, 3 high grade) HD (13 patients). Sites correlated a site‐by‐site basis images....

10.1002/cncr.10336 article EN Cancer 2002-02-15

Early prediction of response to therapy may offer the potential identify patients who will benefit from standard conventional therapy. The objective this study was determine predictive value FDG-PET as an early indicator after 1 cycle chemotherapy for progression-free survival (PFS) in diffuse large cell lymphoma (DLCL) and classic Hodgkin disease (HD).FDG-PET performed before, cycle, completion 47 patients. were followed with a median follow-up 21 months (range, 3-47 months). PFS compared...

10.1002/cncr.22276 article EN Cancer 2006-10-24

This is a multicenter phase I/II dose-finding study in relapsed/refractory B-cell non-Hodgkin's lymphoma (NHL) evaluating veltuzumab, humanized anti-CD20 antibody with structure-function differences from chimeric rituximab.Eighty-two patients (median age, 64 years; 79% stage III/IV, one to nine prior treatments) received four once-weekly doses of 80 750 mg/m(2) veltuzumab and were assessed for safety, efficacy, pharmacodynamics, pharmacokinetics, immunogenicity.Veltuzumab was well tolerated,...

10.1200/jco.2008.19.9117 article EN Journal of Clinical Oncology 2009-05-19

Abstract Advanced marginal zone lymphoma (MZL) is an incurable B-cell malignancy dependent on receptor signaling. The phase 2 PCYC-1121 study demonstrated the safety and efficacy of single-agent ibrutinib 560 mg/d in 63 patients with relapsed/refractory MZL treated prior rituximab (RTX) or rituximab-based chemoimmunotherapy (RTX-CIT). We report final analysis median follow-up 33.1 months (range: 1.4-44.6). Overall response rate (ORR) was 58%; duration (DOR) 27.6 (95% confidence interval...

10.1182/bloodadvances.2020003121 article EN cc-by-nc-nd Blood Advances 2020-11-23
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