Search Results - "RUBIN, Eric H"
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Tumor mutational burden predicts the efficacy of pembrolizumab monotherapy: a pan-tumor retrospective analysis of participants with advanced solid tumors
Published in Journal for immunotherapy of cancer (01-01-2022)“…BackgroundSeveral studies have evaluated the relationship between tumor mutational burden (TMB) and outcomes of immune checkpoint inhibitors. In the phase II…”
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Drug development and clinical trials—the path to an approved cancer drug
Published in Nature reviews. Clinical oncology (01-04-2012)“…The current system for the development of anticancer drugs is not fit for purpose. In this Review article, this system is examined from the perspective of the…”
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Rendering the 3 + 3 Design to Rest: More Efficient Approaches to Oncology Dose-Finding Trials in the Era of Targeted Therapy
Published in Clinical cancer research (01-06-2016)“…Selection of the maximum tolerated dose (MTD) as the recommended dose for registration trials based on a dose-escalation trial using variations of an MTD/3 + 3…”
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4
Antitumor activity in RAS-driven tumors by blocking AKT and MEK
Published in Clinical cancer research (15-02-2015)“…KRAS is the most commonly mutated oncogene in human tumors. KRAS-mutant cells may exhibit resistance to the allosteric MEK1/2 inhibitor selumetinib (AZD6244;…”
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5
Epothilones: Mechanism of Action and Biologic Activity
Published in Journal of clinical oncology (15-05-2004)“…Drugs that target microtubules are among the most commonly prescribed anticancer therapies. Although the mechanisms by which perturbation of microtubule…”
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Phase I Study of Eribulin Mesylate Administered Once Every 21 Days in Patients with Advanced Solid Tumors
Published in Clinical cancer research (15-06-2009)“…Purpose: To evaluate the maximum tolerated dose (MTD), dose-limiting toxicities (DLT), and pharmacokinetics of eribulin mesylate (E7389), a halichondrin B…”
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From Famine to Feast: Developing Early-Phase Combination Immunotherapy Trials Wisely
Published in Clinical cancer research (01-09-2017)“…Not until the turn of this century has immunotherapy become a fundamental component of cancer treatment. While monotherapy with immune modulators, such as…”
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Clinical pharmacology profile of vorinostat, a histone deacetylase inhibitor
Published in Cancer chemotherapy and pharmacology (01-09-2013)“…Purpose Vorinostat is a histone deacetylase inhibitor that has demonstrated preclinical activity in numerous cancer models. Clinical activity has been…”
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Selective Oral Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor ZD1839 Is Generally Well-Tolerated and Has Activity in Non–Small-Cell Lung Cancer and Other Solid Tumors: Results of a Phase I Trial
Published in Journal of clinical oncology (15-09-2002)“…To investigate safety, tolerability, dose-related pharmacologic properties, and pharmacodynamics of ZD1839 (gefinitib, Iressa; AstraZeneca Pharmacueticals,…”
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Mechanisms of resistance to topoisomerase I-targeting drugs
Published in Oncogene (20-10-2003)“…DNA topoisomerases are a class of enzymes that alter the topology of DNA and are targets of several anticancer drugs. Camptothecins (CPTs) are a relatively new…”
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Topors Functions as an E3 Ubiquitin Ligase with Specific E2 Enzymes and Ubiquitinates p53
Published in The Journal of biological chemistry (27-08-2004)“…The human topoisomerase I- and p53-binding protein topors contains a highly conserved, N-terminal C3HC4-type RING domain that is homologous to the RING domains…”
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Pharmacokinetic/Pharmacodynamic Modeling and Simulation of Neutropenia during Phase I Development of Liposome-Entrapped Paclitaxel
Published in Clinical cancer research (15-09-2008)“…Purpose: To evaluate the maximum tolerated dose (MTD), dose-limiting toxicities (DLT), and pharmacokinetics of liposome-entrapped paclitaxel easy-to-use…”
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Pharmacokinetics of Cetuximab After Administration of Escalating Single Dosing and Weekly Fixed Dosing in Patients with Solid Tumors
Published in Clinical cancer research (01-11-2006)“…Purpose: Previous studies of cetuximab pharmacokinetics did not fully characterize its elimination phase. The purpose of this trial was to evaluate the…”
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A Study to Determine the Effects of Food and Multiple Dosing on the Pharmacokinetics of Vorinostat Given Orally to Patients with Advanced Cancer
Published in Clinical cancer research (01-12-2006)“…Purpose: This phase I study, conducted in advanced-stage cancer patients, assessed the safety and tolerability of oral vorinostat (suberoylanilide hydroxamic…”
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A Single Supratherapeutic Dose of Vorinostat Does Not Prolong the QTc Interval in Patients with Advanced Cancer
Published in Clinical cancer research (15-11-2009)“…Purpose: This dedicated QTc phase I study, conducted in advanced-stage cancer patients, assessed the effect of a single supratherapeutic dose (800 mg) of…”
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Phase I Dose-Finding Study of Weekly Single-Agent Patupilone in Patients With Advanced Solid Tumors
Published in Journal of clinical oncology (20-12-2005)“…To evaluate the safety and maximum-tolerated dose (MTD) of weekly patupilone, a natural epothilone B, in patients with advanced solid tumors. Patients were…”
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The BATTLE trial: a bold step toward improving the efficiency of biomarker-based drug development
Published in Cancer discovery (01-06-2011)“…Successful completion of the Biomarker-integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE) trial, reported in this issue of Cancer…”
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Adaptive phase 2/3 designs for oncology drug development – Time to hedge
Published in Contemporary clinical trials (01-02-2023)“…Randomized-controlled Phase 2 trials are routinely skipped in oncology drug development in favor of directly going to confirmatory Phase 3 after…”
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Ubiquitination by TOPORS Regulates the Prostate Tumor Suppressor NKX3.1
Published in The Journal of biological chemistry (22-02-2008)“…The NKX3.1 gene located at 8p21.2 encodes a homeodomain-containing transcription factor that acts as a haploinsufficient tumor suppressor in prostate cancer…”
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Finding the Right Dose for Cancer Therapeutics—Can We Do Better?
Published in Clinical cancer research (15-02-2010)“…Unlike other diseases, dose-selection for cancer therapeutics is often based on the maximum-tolerated dose in phase 1 studies involving relatively few…”
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