Search Results - "Supko, Jeffrey"
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Ricolinostat, the First Selective Histone Deacetylase 6 Inhibitor, in Combination with Bortezomib and Dexamethasone for Relapsed or Refractory Multiple Myeloma
Published in Clinical cancer research (01-07-2017)“…Histone deacetylase (HDAC) inhibition improves the efficacy of proteasome inhibition for multiple myeloma but adds substantial toxicity. Preclinical models…”
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Ricolinostat plus lenalidomide, and dexamethasone in relapsed or refractory multiple myeloma: a multicentre phase 1b trial
Published in The lancet oncology (01-11-2016)“…Summary Background Histone deacetylase (HDAC) inhibitors are an important new class of therapeutics for treating multiple myeloma. Ricolinostat (ACY-1215) is…”
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Postinduction Dexamethasone and Individualized Dosing of Escherichia Coli L-Asparaginase Each Improve Outcome of Children and Adolescents With Newly Diagnosed Acute Lymphoblastic Leukemia: Results From a Randomized Study—Dana-Farber Cancer Institute ALL Consortium Protocol 00-01
Published in Journal of clinical oncology (20-03-2013)“…We assessed the toxicity and efficacy of dexamethasone and a novel dosing method of Escherichia coli L-asparaginase (EC-Asnase) in children and adolescents…”
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A phase I/II trial of hydroxychloroquine in conjunction with radiation therapy and concurrent and adjuvant temozolomide in patients with newly diagnosed glioblastoma multiforme
Published in Autophagy (01-08-2014)“…Preclinical studies indicate autophagy inhibition with hydroxychloroquine (HCQ) can augment the efficacy of DNA-damaging therapy. The primary objective of this…”
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5
Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic
Published in Proceedings of the National Academy of Sciences - PNAS (10-08-2010)“…The pharmacologic utility of lengthy peptides can be hindered by loss of bioactive structure and rapid proteolysis, which limits bioavailability. For example,…”
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Acoustic feedback enables safe and reliable carboplatin delivery across the blood-brain barrier with a clinical focused ultrasound system and improves survival in a rat glioma model
Published in Theranostics (01-01-2019)“…The blood-brain barrier (BBB) restricts delivery of most chemotherapy agents to brain tumors. Here, we investigated a clinical focused ultrasound (FUS) device…”
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Blood-brain barrier disruption and delivery of irinotecan in a rat model using a clinical transcranial MRI-guided focused ultrasound system
Published in Scientific reports (29-05-2020)“…We investigated controlled blood-brain barrier (BBB) disruption using a low-frequency clinical transcranial MRI-guided focused ultrasound (TcMRgFUS) device and…”
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Molecular and Clinical Effects of Notch Inhibition in Glioma Patients: A Phase 0/I Trial
Published in Clinical cancer research (01-10-2016)“…High-grade gliomas are associated with a dismal prognosis. Notch inhibition via the gamma-secretase inhibitor RO4929097 has emerged as a potential therapeutic…”
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Identification of a Benzoisoxazoloazepine Inhibitor (CPI-0610) of the Bromodomain and Extra-Terminal (BET) Family as a Candidate for Human Clinical Trials
Published in Journal of medicinal chemistry (25-02-2016)“…In recent years, inhibition of the interaction between the bromodomain and extra-terminal domain (BET) family of chromatin adaptors and acetyl-lysine residues…”
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A Phase I First-in-Human Trial of Bardoxolone Methyl in Patients with Advanced Solid Tumors and Lymphomas
Published in Clinical cancer research (15-06-2012)“…Bardoxolone methyl, a novel synthetic triterpenoid and antioxidant inflammation modulator, potently induces Nrf2 and inhibits NF-κB and Janus-activated…”
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Activating mTOR mutations in a patient with an extraordinary response on a phase I trial of everolimus and pazopanib
Published in Cancer discovery (01-05-2014)“…Understanding the genetic mechanisms of sensitivity to targeted anticancer therapies may improve patient selection, response to therapy, and rational treatment…”
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Intravenous pegylated asparaginase versus intramuscular native Escherichia coli l -asparaginase in newly diagnosed childhood acute lymphoblastic leukaemia (DFCI 05-001): a randomised, open-label phase 3 trial
Published in The lancet oncology (01-12-2015)“…Summary Background l -asparaginase is a universal component of treatment for childhood acute lymphoblastic leukaemia, and is usually administered…”
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13
Chemical genetics identify eIF2α kinase heme-regulated inhibitor as an anticancer target
Published in Nature chemical biology (01-09-2011)“…Overabundance of the eIF2–GTP–Met-tRNAi translational initiation complex has been linked to malignant transformation. N , N '-diarylurea chemical probes that…”
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A phase I study of erlotinib and hydroxychloroquine in advanced non-small-cell lung cancer
Published in Journal of thoracic oncology (01-10-2012)“…This investigator-initiated study explores the safety, maximum tolerated dose, clinical response, and pharmacokinetics of hydroxychloroquine (HCQ) with and…”
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Efficacy and Toxicity of Pegaspargase and Calaspargase Pegol in Childhood Acute Lymphoblastic Leukemia: Results of DFCI 11-001
Published in Journal of clinical oncology (01-11-2021)“…Dana-Farber Cancer Institute Acute Lymphoblastic Leukemia (ALL) Consortium Protocol 11-001 assessed efficacy and toxicity of calaspargase pegol (calaspargase),…”
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Current Perspectives on the Clinical Experience, Pharmacology, and Continued Development of the Camptothecins
Published in Clinical cancer research (01-03-2002)“…The camptothecins are a maturing class of anticancer agents. In this article, we review the pharmacology and antitumor activity of the camptothecin analogues…”
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Activating Mutations in the Epidermal Growth Factor Receptor Underlying Responsiveness of Non–Small-Cell Lung Cancer to Gefitinib
Published in The New England journal of medicine (20-05-2004)“…Gefitinib, an inhibitor of the tyrosine kinase of the epidermal growth factor receptor (EGFR), is effective in less than 20 percent of patients with…”
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Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling
Published in Proceedings of the National Academy of Sciences - PNAS (11-12-2007)“…Kinase inhibitors constitute an important new class of cancer drugs, whose selective efficacy is largely determined by underlying tumor cell genetics. We…”
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Phase I study of RO4929097 with bevacizumab in patients with recurrent malignant glioma
Published in Journal of neuro-oncology (01-12-2016)“…Antiangiogenic therapies for malignant gliomas often result in transient response, and recurrent disease is characterized by adoption of invasive and hypoxic…”
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Combined PARP and HSP90 inhibition: preclinical and Phase 1 evaluation in patients with advanced solid tumours
Published in British journal of cancer (01-04-2022)“…Purpose PARP inhibitor resistance may be overcome by combinatorial strategies with agents that disrupt homologous recombination repair (HRR). Multiple HRR…”
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