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Ross C. Donehower

Researcher at Johns Hopkins University

Publications -  233
Citations -  32588

Ross C. Donehower is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Pharmacokinetics & Chemotherapy. The author has an hindex of 72, co-authored 229 publications receiving 28457 citations. Previous affiliations of Ross C. Donehower include Johns Hopkins University School of Medicine & National Institutes of Health.

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A Phase I study of the oral antimetabolite, CS-682, administered once daily 5 days per week in patients with refractory solid tumor malignancies

TL;DR: A Phase I study of CS-682, administered orally five days per week in patients with refractory solid tumor malignancies, found that the recommended phase II dose, given the ease of administration and tolerability, was well tolerated.
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Reversibility of High-Affinity Binding of Methotrexate in L1210 Murine Leukemia Cells

TL;DR: The experiments demonstrate the reversibility of methotrexate binding to high-affinity intracellular sites in vitro and are consistent with the hypothesis that residual [ 3 H]-methotrexate persisted in a tightly bound complex with dihydrofolate reductase.
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Preliminary results of a phase II trial of gefitinib in progressive metastatic neuroendocrine tumors (NET): A Phase II Consortium (P2C) study

TL;DR: 6 month progression-free survival (PFS) rates at 6 months of 30% (carcinoid and ICC) and 10% (ICC) were considered promising and Gefitinib is a small-molecule inhibitor of the EGFR tyrosine kinase domain.
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Immune-Related Adverse Events Requiring Hospitalization: Spectrum of Toxicity, Treatment, and Outcomes

TL;DR: A notable proportion of ICI-treated patients are hospitalized for irAEs, and these patients have a high demand for multidisciplinary management, which has important implications for inpatient service planning and risk stratification.
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A Phase I Study of EKB-569 in Combination with Capecitabine in Patients with Advanced Colorectal Cancer

TL;DR: In advanced colorectal cancer, 50 mg E KB-569 daily can be safely combined with 1,000 mg/m2 capecitabine twice a day, and a statistically significant increase in plasma levels of 5-fluorouracil for the combination of EKB- 569 and cape citabine may be due to the single-dose versus multiple-dose exposure difference, variability in exposure or a potential drug interaction.