Judith E. Karp

ORCID: 0000-0003-4754-127X
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About
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Research Areas
  • Acute Myeloid Leukemia Research
  • Acute Lymphoblastic Leukemia research
  • Chronic Myeloid Leukemia Treatments
  • Chronic Lymphocytic Leukemia Research
  • Histone Deacetylase Inhibitors Research
  • Retinoids in leukemia and cellular processes
  • Neutropenia and Cancer Infections
  • PARP inhibition in cancer therapy
  • Protein Degradation and Inhibitors
  • Cancer therapeutics and mechanisms
  • Cancer-related Molecular Pathways
  • DNA Repair Mechanisms
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Hematopoietic Stem Cell Transplantation
  • Multiple Myeloma Research and Treatments
  • Cancer-related gene regulation
  • Cell death mechanisms and regulation
  • Antifungal resistance and susceptibility
  • RNA Interference and Gene Delivery
  • Cancer Genomics and Diagnostics
  • Epigenetics and DNA Methylation
  • Cancer Treatment and Pharmacology
  • Lung Cancer Treatments and Mutations
  • Fungal Infections and Studies
  • Lymphoma Diagnosis and Treatment

Johns Hopkins University
2014-2024

Sidney Kimmel Comprehensive Cancer Center
2015-2024

Sidney Kimmel Cancer Center
2008-2023

Johns Hopkins Hospital
1989-2021

Johns Hopkins Medicine
1985-2021

Northwestern University
2009-2020

Klinik und Poliklinik für Kinder- und Jugendmedizin
2019

National Heart Lung and Blood Institute
2013-2016

National Institutes of Health
1993-2016

Georgia Regents Medical Center
2016

In early 1990 fluconazole was introduced as a prophylactic antifungal agent after bone marrow transplantation. During the same year Candida krusei emerged chief candida pathogen among patients with transplants.

10.1056/nejm199110313251803 article EN New England Journal of Medicine 1991-10-31

Abstract Optimal reexpression of most genes silenced through promoter methylation requires the sequential application DNA methyltransferase inhibitors followed by histone deacetylase in tumor cell cultures. Patients with myelodysplastic syndrome or acute myeloid leukemia (AML) were treated inhibitor 5-azacitidine (aza-CR) sodium phenylbutyrate. Major responses associated cytogenetic complete response developed patients receiving prolonged dosing schedules aza-CR. Bisulfite sequencing p15...

10.1158/0008-5472.can-06-0080 article EN Cancer Research 2006-06-15

We studied 25 patients with acute nonlymphocytic leukemia in second remission (20 patients) or third (5 whom autologous bone marrow transplantation was performed use of incubated ex vivo the alkylating agent 4-hydroperoxycyclophosphamide. Patients received intensive cytoreductive therapy busulfan and cyclophosphamide total body irradiation, followed by an infusion that had been collected remission, treated 4-hydroperoxycyclophosphamide, cryopreserved. Four died from bacterial fungal sepsis...

10.1056/nejm198607173150301 article EN New England Journal of Medicine 1986-07-17

Patients with cancer are at increased risk for developing infectious complications during the course of their disease and treatment. The following sections NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) Prevention Treatment Cancer-Related Infections provide an overview factors complications, recommendations categorization, strategies prevention infections high-risk patient populations cancer. Individualized evaluation incorporation preventative measures essential components...

10.6004/jnccn.2012.0146 article EN Journal of the National Comprehensive Cancer Network 2012-11-01

Our understanding of phenotypic and functional signatures CD8+ T cell dysfunction in acute myeloid leukemia (AML) is limited. Deciphering these deranged states how they are impacted by induction chemotherapy essential for incorporation novel immune-based strategies to restore maintain antileukemia immunity.We utilized high-dimensional immunophenotyping, gene expression, studies characterize peripheral blood bone marrow cells 72 AML patients at diagnosis after chemotherapy.Our data suggest...

10.1172/jci.insight.120974 article EN JCI Insight 2018-11-01

Because the use of fluconazole prophylaxis had been associated with an increased rate Candida krusei infections at The John Hopkins Oncology Center, early empiric amphotericin B plus flucytosine were given to febrile neutropenic patients colonized by C. krusei. By this practice, proportion fungemias attributable was low (12.5%) in receiving over a 6-month interval. However, Torulopsis (Candida) glabrata assumed much higher (75%) among fluconazole. In vitro susceptibility testing combined...

10.1128/aac.37.9.1847 article EN Antimicrobial Agents and Chemotherapy 1993-09-01

We evaluated the effect of norfloxacin, 400 mg given orally every 12 hours, on prevention bacterial infections in 68 adult patients who had acute leukemia throughout prolonged courses granulocytopenia (median, 32 days). Gram-negative were documented 13 33 receiving placebo, but only 4 35 norfloxacin; no frequency gram-positive or fungal was noted. Norfloxacin administration resulted suppression gastrointestinal tract colonization by aerobic bacteria without development norfloxacin...

10.7326/0003-4819-106-1-1 article EN Annals of Internal Medicine 1987-01-01

• We prospectively examined the eyes of 120 patients with leukemia. Only 38% had normal results examination. Leukemic infiltrates were present in 3% patients, other findings related to leukemia seen 39% and 20% unrelated abnormalities. Visual loss was at least 5% this study.

10.1001/archopht.1989.01070010715033 article EN Archives of Ophthalmology 1989-05-01

During a 2-year period, 15 of 110 patients (14%) admitted for intensive therapy acute leukemia associated with prolonged deep granulocytopenia developed documented invasive aspergillosis (IA). Antemortem diagnosis was accomplished in 14, and 13 (87%) survived the infection. Because high success rate, we reviewed courses to assess factors this favorable outcome. Eleven presented pulmonary IA; early symptoms occurred at mean 21.6 days (less than 100/muL) included refractory fever 14 signs or...

10.1200/jco.1987.5.12.1985 article EN Journal of Clinical Oncology 1987-12-01

Abstract Purpose: Vascular endothelial growth factor (VEGF) promotes acute myelogenous leukemia (AML) cell and survival may contribute to drug resistance. bevacizumab, an anti-VEGF monoclonal antibody, exhibits clinical activity against diverse malignancies when administered with cytotoxic chemotherapy. We conducted a Phase II trial of bevacizumab after chemotherapy adults refractory or relapsed AML, using timed sequential therapy (TST) approach. Experimental Design: 10 mg/kg was on day 8...

10.1158/1078-0432.ccr-03-0627 article EN Clinical Cancer Research 2004-06-01
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