Search Results - "Lowder, James N"
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Safety and tolerability of guadecitabine (SGI-110) in patients with myelodysplastic syndrome and acute myeloid leukaemia: a multicentre, randomised, dose-escalation phase 1 study
Published in The lancet oncology (01-09-2015)“…Summary Background Hypomethylating agents are used to treat cancers driven by aberrant DNA methylation, but their short half-life might limit their activity,…”
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Immunomodulatory Properties of DNA Hypomethylating Agents: Selecting the Optimal Epigenetic Partner for Cancer Immunotherapy
Published in Frontiers in pharmacology (07-12-2018)“…DNA hypomethylating agents (DHAs) play a well-acknowledged role in potentiating the immunogenicity and the immune recognition of neoplastic cells. This…”
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SPIRE - combining SGI-110 with cisplatin and gemcitabine chemotherapy for solid malignancies including bladder cancer: study protocol for a phase Ib/randomised IIa open label clinical trial
Published in Current controlled trials in cardiovascular medicine (03-04-2018)“…Urothelial bladder cancer (UBC) accounts for 10,000 new diagnoses and 5000 deaths annually in the UK (Cancer Research UK,…”
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Dose, schedule, safety, and efficacy of guadecitabine in relapsed or refractory acute myeloid leukemia
Published in Cancer (15-01-2018)“…BACKGROUND Outcomes for patients with relapsed or refractory acute myeloid leukemia (AML) are poor. Guadecitabine, a next‐generation hypomethylating agent,…”
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Contemporary experience with high-dose interleukin-2 therapy and impact on survival in patients with metastatic melanoma and metastatic renal cell carcinoma
Published in Cancer Immunology, Immunotherapy (01-12-2016)“…High-dose interleukin-2 (HD IL-2) was approved for treatment of metastatic renal cell carcinoma (mRCC) in 1992 and for metastatic melanoma (mM) in 1998, in an…”
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High dose interleukin-2 (Aldesleukin) - expert consensus on best management practices-2014
Published in Journal for Immunotherapy of Cancer (16-09-2014)“…Interleukin-2 (IL-2) was historically one of the few treatments for adults with stage IV solid tumors that could produce complete responses (CRs) that were…”
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Journal Article Book Review -
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Abstract 2325: Immune checkpoint(s) expression in AML patients enrolled in a phase 1-2 study with guadecitabine
Published in Cancer research (Chicago, Ill.) (15-07-2016)“…Abstract Immune checkpoint(s) blockade is becoming the therapeutic mainstay in melanoma and lung cancer. Based on these important clinical achievements,…”
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Anti-CD3 antibody visilizumab is not effective in patients with intravenous corticosteroid-refractory ulcerative colitis
Published in Gut (01-11-2010)“…Pilot studies with visilizumab, a humanised monoclonal antibody to CD3, suggest efficacy for corticosteroid-refractory ulcerative colitis (UC). A…”
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Will next-generation agents deliver on the promise of epigenetic hypomethylation therapy?
Published in Epigenomics (01-10-2015)“…Longer exposure would logically affect more cells and enhance efficacy. [...]the clinical activity of these agents is highly dose- and schedule-sensitive (5)…”
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Prospective randomized open‐label multicenter phase I/II dose escalation trial of visilizumab (HuM291) in severe steroid‐refractory ulcerative colitis
Published in Inflammatory bowel diseases (01-04-2010)“…Background: Visilizumab is a humanized IgG2 monoclonal anti‐CD3 antibody. We evaluated its safety and dose response in severe intravenous steroid‐refractory…”
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Simultaneous Modeling of Biomarker and Toxicity Response Predicted Optimal Regimen of Guadecitabine (SGI‐110) in Myeloid Malignancies
Published in CPT: pharmacometrics and systems pharmacology (01-10-2017)“…Guadecitabine (SGI‐110) is a novel next‐generation hypomethylating agent (HMA) administered as s.c. injection with extended decitabine exposure…”
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Transient cytokine-induced liver injury following administration of the humanized anti-CD3 antibody visilizumab (HuM291) in Crohn's disease
Published in The American journal of gastroenterology (01-04-2009)“…Monoclonal antibodies to CD3 and CD4 T-cell receptors are evolving for Crohn's disease (CD) and ulcerative colitis. Their administration is often associated…”
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The Use of Registries to Improve Cancer Treatment: A National Database for Patients Treated with Interleukin-2 (IL-2)
Published in Journal of personalized medicine (07-03-2014)“…Registries evaluating un-randomized patients have provided valuable information with respect to a therapy's utility, treatment practices, and evolution over…”
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Implementation of an Interleukin-2 National Registry: an opportunity to improve cancer outcomes
Published in Journal for immunotherapy of cancer (18-06-2014)“…Cancer registries have proven valuable with respect to validating therapeutic safety and drug efficacy, uncovering real-world implementation practices, and…”
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Abstract CT059: Epigenetic tumor remodelling to improve the efficacy of immune checkpoint blockade: the NIBIT-M4 clinical trial
Published in Cancer research (Chicago, Ill.) (01-07-2018)“…Abstract Introduction: The anti-CTLA-4 monoclonal antibody (mAb) ipilimumab (Ipi) has firstly shown the therapeutic potential of targeting immune checkpoints…”
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Safety and immunobiological activity of guadecitabine sequenced with ipilimumab in metastatic melanoma patients: The phase Ib NIBIT-M4 study
Published in Journal of clinical oncology (20-05-2019)“…Abstract only 2549 Background: DNA hypomethylating agents show broad immuno-modulatory activity in neoplastic cells, and may improve the effectiveness of…”
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A phase Ib study combining the second-generation DNA hypomethylating agent (DHA) guadecitabine (SGI-110) and ipilimumab in patients with metastatic melanoma: The NIBIT-M4 study
Published in Journal of clinical oncology (20-05-2016)“…Abstract only…”
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Successful Emulation of IV Decitabine Pharmacokinetics with an Oral Fixed-Dose Combination of the Oral Cytidine Deaminase Inhibitor (CDAi) E7727 with Oral Decitabine, in Subjects with Myelodysplastic Syndromes (MDS): Final Data of Phase 1 Study
Published in Blood (02-12-2016)“…▪ Introduction: Patients with International Prognostic Scoring System (IPSS) intermediate 1 and 2 (Int) and high risk (HR) MDS benefit from therapy with…”
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A Phase 2 Dose-Confirmation Study of Oral ASTX727, a Combination of Oral Decitabine with a Cytidine Deaminase Inhibitor (CDAi) Cedazuridine (E7727), in Subjects with Myelodysplastic Syndromes (MDS)
Published in Blood (08-12-2017)“…Aims: A combination of oral decitabine (DAC), a drug normally parenterally administered, with an oral cytidine deaminase inhibitor (CDAi), enhances its…”
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Improved median overall survival (OS) in patients with metastatic melanoma (mM) treated with high-dose (HD) IL-2: Analysis of the PROCLAIM 2007-2012 national registry
Published in Journal of clinical oncology (20-05-2014)“…Abstract only…”
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