Unknown,Transcriptomics,Genomics,Proteomics

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Expression data for Cediranib in Metastatic ASPS


ABSTRACT: Gene expression from pre- and post- Cediranib treated patients with metastatic Alveolar Soft Part Sarcoma (ASPS) Paired tumor biopsies from 6 patients were collected. Samples were collected at baseline and 3 to 5 days following treatment. The patients are all enrolled in the replicate cohort of a National Cancer Institute (NCI)-sponsered investigational new drug application with institutional review board approval, and all participants provided written informed consent. ClinicalTrials.gov number, NCT00942877. The timing of the tumor biopsies was based on clinical observations of increased tumor pain associated with an inflammatory-like response in peripheral tumor lesions, usually within the second week of treatment. Tumor biopsies were obtained in the first week of treatment before the development of clinical signs and symptoms to evaluate gene expression changes. The time points are labeled "pre" and "post" to denote their relationship to treatment.

ORGANISM(S): Homo sapiens

SUBMITTER: Eric Polley 

PROVIDER: E-GEOD-32569 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Cediranib for metastatic alveolar soft part sarcoma.

Kummar Shivaani S   Allen Deborah D   Monks Anne A   Polley Eric C EC   Hose Curtis D CD   Ivy S Percy SP   Turkbey Ismail B IB   Lawrence Scott S   Kinders Robert J RJ   Choyke Peter P   Simon Richard R   Steinberg Seth M SM   Doroshow James H JH   Helman Lee L  

Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20130429 18


<h4>Purpose</h4>Alveolar soft part sarcoma (ASPS) is a rare, highly vascular tumor, for which no effective standard systemic treatment exists for patients with unresectable disease. Cediranib is a potent, oral small-molecule inhibitor of all three vascular endothelial growth factor receptors (VEGFRs).<h4>Patients and methods</h4>We conducted a phase II trial of once-daily cediranib (30 mg) given in 28-day cycles for patients with metastatic, unresectable ASPS to determine the objective response  ...[more]

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