Jeffrey J. Raizer

ORCID: 0009-0003-8469-2509
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About
Contact & Profiles
Research Areas
  • Glioma Diagnosis and Treatment
  • Brain Metastases and Treatment
  • Meningioma and schwannoma management
  • Chromatin Remodeling and Cancer
  • Fibroblast Growth Factor Research
  • Cancer, Hypoxia, and Metabolism
  • Neuroblastoma Research and Treatments
  • Sarcoma Diagnosis and Treatment
  • Lung Cancer Research Studies
  • Cancer Immunotherapy and Biomarkers
  • CNS Lymphoma Diagnosis and Treatment
  • Cancer Treatment and Pharmacology
  • Retinoids in leukemia and cellular processes
  • Neurofibromatosis and Schwannoma Cases
  • Management of metastatic bone disease
  • Histone Deacetylase Inhibitors Research
  • Pancreatic and Hepatic Oncology Research
  • Lymphoma Diagnosis and Treatment
  • Radiopharmaceutical Chemistry and Applications
  • Radiomics and Machine Learning in Medical Imaging
  • Gastric Cancer Management and Outcomes
  • Cancer Research and Treatments
  • Cancer Mechanisms and Therapy
  • Immune cells in cancer
  • ATP Synthase and ATPases Research

Takeda (United States)
2023-2025

Northwestern University
2014-2024

Astellas Pharma (United States)
2021-2023

Midwestern University
2007-2022

Northwestern Medicine
2012-2022

Robert H. Lurie Comprehensive Cancer Center of Northwestern University
2006-2022

University Medical Center
2020

Abbott (United States)
2005-2018

Agenus (United States)
2016-2018

Memorial Sloan Kettering Cancer Center
2002-2017

Michael Weller Nicholas Butowski David Tran Lawrence D. Recht Michael Lim and 95 more Hal W. Hirte Lynn S. Ashby Laszlo Mechtler Samuel Goldlust Fábio M. Iwamoto Jan Drappatz Donald M. O’Rourke Mark Wong Mark G. Hamilton Gaetano Finocchiaro James Perry Wolfgang Wick Jennifer Green Yi He Christopher D. Turner Michael Yellin Tibor Keler Thomas A. Davis Roger Stupp John H. Sampson Nicholas Butowski Jian L. Campian Lawrence D. Recht Michael Lim Lynn S. Ashby Jan Drappatz Hal W. Hirte Fábio M. Iwamoto Laszlo Mechtler Samuel Goldlust Kevin Becker Gene H. Barnett Garth Nicholas Annick Desjardins Tara Benkers Naveed Wagle Morris D. Groves Santosh Kesari Zsolt Horváth Ryan Merrell Richard Curry James O’Rourke David M. Schuster Mark Wong Maciej M. Mrugała Randy Jensen John Trusheim Glenn J. Lesser Karl Bélanger Andrew E. Sloan Benjamin Purow Karen Fink Jeffrey J. Raizer Michael Schulder Suresh Nair Scott Peak James Perry Alba A. Brandes Michael Weller Nimish Mohile Joseph Landolfi Jon Olson Gaetano Finocchiaro Ross Jennens Paul DeSouza Bridget A. Robinson Marka R. Crittenden Kent C. Shih Alexandra Flowers Shirley Ong Jennifer Connelly Costas G. Hadjipanayis Pierre Giglio Frank E. Mott David Mathieu N. Lessard Sanchez Juan Sepulveda József Lövey Helen Wheeler Po-Ling Inglis Claire Hardie Daniela A. Bota Maciej S. Lesniak Jana Portnow Bruce Frankel Larry Junck Reid C. Thompson Lawrence Berk John Paul McGhie David Macdonald Frank Saran Riccardo Soffietti Deborah T. Blumenthal Sá Barreto Costa Marcos André de Anna K. Nowak

10.1016/s1470-2045(17)30517-x article EN The Lancet Oncology 2017-08-23

NovoTTF-100A is a portable device delivering low-intensity, intermediate frequency electric fields via non-invasive, transducer arrays. Tumour Treatment Fields (TTF), completely new therapeutic modality in cancer treatment, physically interfere with cell division.Phase III trial of chemotherapy-free treatment NovoTTF (20-24h/day) versus active chemotherapy the patients recurrent glioblastoma. Primary end-point was improvement overall survival.Patients (median age 54 years (range 23-80),...

10.1016/j.ejca.2012.04.011 article EN cc-by-nc-nd European Journal of Cancer 2012-05-18

Cilengitide, an inhibitor of alphavbeta3 and alphavbeta5 integrin receptors, demonstrated minimal toxicity durable activity across a wide range doses administered to adults with recurrent glioblastoma multiforme (GBM) in prior phase I study. The current multicenter II study was conducted evaluate the safety cilengitide GBM patients at first recurrence.Eligible were randomly assigned receive either 500 or 2,000 mg twice weekly on continuous basis. Patients assessed every 4 weeks. primary end...

10.1200/jco.2008.16.7510 article EN Journal of Clinical Oncology 2008-11-04

A multicenter phase II study was conducted to assess the efficacy of rituximab, methotrexate, procarbazine, and vincristine (R-MPV) followed by consolidation reduced-dose whole-brain radiotherapy (rdWBRT) cytarabine in primary CNS lymphoma.Patients received induction chemotherapy with R-MPV (five seven cycles); those achieving a complete response (CR) rdWBRT (23.4 Gy), otherwise, standard WBRT offered (45 Gy). Consolidation given after radiotherapy. The end point 2-year progression-free...

10.1200/jco.2013.50.4910 article EN Journal of Clinical Oncology 2013-10-08

Phase I: To determine the maximum tolerated doses, toxicities, and pharmacokinetics of imatinib mesylate (Gleevec) in patients with malignant gliomas taking enzyme-inducing antiepileptic drugs (EIAED) or not EIAED. II: therapeutic efficacy imatinib.Phase I component used an interpatient dose escalation scheme. End points phase II were 6-month progression-free survival response.Fifty enrolled (27 EIAED 23 non-EIAED). The for non-EIAED was 800 mg/d. Dose-limiting toxicities neutropenia, rash,...

10.1158/1078-0432.ccr-06-0773 article EN Clinical Cancer Research 2006-08-15

Our goals were to evaluate the safety of adding rituximab methotrexate (MTX)-based chemotherapy for primary CNS lymphoma, determine whether additional cycles induction improve complete response (CR) rate, and examine effectiveness toxicity reduced-dose whole-brain radiotherapy (WBRT) after CR.Thirty patients (17 women; median age, 57 years; Karnofsky performance score, 70) treated with five seven (rituximab, MTX, procarbazine, vincristine [R-MPV]) as follows: day 1, 500 mg/m2; 2, MTX 3.5...

10.1200/jco.2007.12.5062 article EN Journal of Clinical Oncology 2007-10-18

PURPOSE To assess whether reirradiation (re-RT) and concurrent bevacizumab (BEV) improve overall survival (OS) and/or progression-free (PFS), compared with BEV alone in recurrent glioblastoma (GBM). The primary objective was OS, secondary objectives included PFS, response rate, treatment adverse events (AEs) including delayed CNS toxicities. METHODS NRG Oncology/RTOG1205 is a prospective, phase II, randomized trial of re-RT versus alone. Stratification factors age, resection, Karnofsky...

10.1200/jco.22.00164 article EN Journal of Clinical Oncology 2022-10-19

Abstract Metastases to the spine represent a challenging problem in an oncology practice. Treatment decisions require multidisciplinary review. Radiation therapy remains primary treatment for metastatic spinal tumor, but advances radiation therapy, chemotherapy, and surgery have changed roles of each lead improved patient outcomes. Regardless treatment, diagnosis before development significant neurologic functional deficits improve Physician awareness appropriate imaging greatly assist early...

10.1634/theoncologist.4-6-459 article EN The Oncologist 1999-12-01

Brain metastases (BM) are among the most devastating and debilitating complications of melanoma. This retrospective study was conducted to gain a better understanding patient disease characteristics that have greatest impact on overall survival in melanoma patients with BM; therapeutic interventions were also assessed. The records all diagnosed cutaneous BM who seen at Memorial Sloan-Kettering Cancer Center between 1991 2001 retrospectively reviewed. A variety factors, including age...

10.1215/15228517-2007-058 article EN Neuro-Oncology 2008-02-21

Retrospective review of prospectively maintained institutional spine database.To assess the pain, neurologic, and functional outcome patients with metastatic spinal cord compression using a posterolateral transpedicular approach circumferential fusion.Patients metastases often have patterns disease requiring both an anterior posterior surgical decompression fusion. For whose concurrent illness or previous surgery makes difficult, was used to resect involved vertebral bodies, elements,...

10.1097/00007632-200009010-00016 article EN Spine 2000-09-01

This phase II study evaluated the efficacy and safety of AMG 102 (rilotumumab), a fully human monoclonal antibody against hepatocyte growth factor/scatter factor (HGF/SF), in patients with recurrent glioblastoma (GBM). Patients histologically confirmed, measurable GBM or gliosarcoma (World Health Organization grade 4) ≤3 relapses prior systemic therapies received (10 20 mg/kg) by infusion every 2 weeks. The primary endpoint was best confirmed objective response rate (central assessment) per...

10.1093/neuonc/noq198 article EN Neuro-Oncology 2011-02-04

Abstract BACKGROUND: The authors evaluated a 3‐week schedule of bevacizumab in patients with recurrent high‐grade glioma (HGG). METHODS: Patients received 15 mg/kg every 3 weeks and were 6 until tumor progression. Tissue correlates used to quantify content vascular endothelial growth factor A (VEGFA) receptor‐2 (VEGFR2). RESULTS: Of 61 who treated (35 men 26 women; median age, 52 years; age range, 21‐78 years), 50 had glioblastoma multiforme (GBM), 11 anaplastic (AG). number previous...

10.1002/cncr.25462 article EN Cancer 2010-07-27

The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Central Nervous System (CNS) Cancers provide interdisciplinary recommendations managing adult CNS cancers. Primary and metastatic brain tumors are a heterogeneous group of neoplasms with varied outcomes management strategies. These Insights summarize the Panel's discussion highlight notable changes 2015 update. This article outlines data provides insight into panel decisions regarding adjuvant radiation chemotherapy...

10.6004/jnccn.2015.0148 article EN Journal of the National Comprehensive Cancer Network 2015-10-01

Increased mitogenic signaling and angiogenesis, frequently facilitated by somatic activation of EGF receptor (EGFR; ErbB1) and/or loss PTEN, VEGF overexpression, respectively, drive malignant glioma growth. We hypothesized that patients with recurrent glioblastoma would exhibit differential antitumor benefit based on tumor PTEN/EGFRvIII status when treated the antiangiogenic agent pazopanib ErbB inhibitor lapatinib.A phase II study evaluated activity 400 mg/d plus lapatinib 1,000 in grade 4...

10.1158/1078-0432.ccr-12-1707 article EN Clinical Cancer Research 2013-01-31

Panobinostat is a histone deacetylase inhibitor with antineoplastic and antiangiogenic effects in glioma that may work synergistically bevacizumab. We conducted multicenter phase II trial of panobinostat combined bevacizumab patients recurrent high-grade (HGG). Patients HGG were treated oral 30 mg 3 times per week, every other combination 10 mg/kg week. The primary endpoint was 6-month progression-fee survival (PFS6) rate for participants glioblastoma (GBM). anaplastic (AG) evaluated as an...

10.1093/neuonc/nou350 article EN Neuro-Oncology 2015-01-07

In 2010, an estimated 22,020 new cases of primary brain and other nervous system neoplasms were diagnosed in the United States, 1 approximately 13,140 deaths occurred from these tumors.The incidence malignant tumors has been increasing over past 30 years, especially elderly persons. 2 Metastatic disease to central (CNS) occurs much more frequently, with 10 times that tumors.Between 20% 40% patients systemic cancer will develop metastases.

10.6004/jnccn.2011.0036 article EN Journal of the National Comprehensive Cancer Network 2011-04-01
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