Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Emma Sturgill"'
Autor:
Denise A. Yardley, Carissa Jones, Daniel Schlauch, David R. Spigel, Rebecca Lachs, Erika Hamilton, Andrew J. McKenzie, Howard A. Burris, Emma Sturgill, Mythili Shastry, Amanda Misch, Suzanne F. Jones
Publikováno v:
JCO Precision Oncology. :1297-1311
PURPOSE Molecular biomarkers informing disease diagnosis, prognosis, and treatment decisions in patients with breast cancer are being uncovered by next-generation sequencing (NGS) technologies. In this study, we survey how NGS is used for patients wi
Autor:
Rebecca Lachs, Carissa Jones, Erika Hamilton, Andrew J. McKenzie, Mythili Shastry, Amanda Misch, Emma Sturgill, Suzanne F. Jones, Denise A. Yardley, David R. Spigel, Daniel Schlauch, Howard A. Burris
Publikováno v:
Cancer Research. 81:PS18-34
Background: Molecular biomarkers such as the expression status of hormone receptors (HR) and HER2 influence disease diagnosis, prognosis, and treatment decisions in breast cancer patients. Recent advances in genetic sequencing technologies and target
Autor:
Andrew Jacob McKenzie, Carissa Jones, Emma Sturgill, Mary Lynne Capps, Larry Edward Bilbrey, David R. Spigel, Meredith McKean, Stephen Matthew Schleicher
Publikováno v:
Journal of Clinical Oncology. 40:96-96
96 Background: Despite the availability of molecularly-targeted agents for the treatment of many cancer types, gaps remain in integrating comprehensive precision oncology decision support tools and services into routine clinical practice. Molecular T
Autor:
Emma Sturgill, Jessica Correia, Cooper Schumacher, Daniel Luckett, Suzanne Fields Jones, Howard A. Burris III, David R. Spigel, Andrew Jacob McKenzie
Publikováno v:
Journal of Clinical Oncology. 40:3116-3116
3116 Background: Molecular landscape studies are critical to biomarker discovery and precision oncology research. However, non-White patients (pts) have historically been under-represented. In this study, we examine clinico-genomic data from a networ
Autor:
Marilyn Elaine Holt, Amanda Misch, Smita K. Rao, Emma Sturgill, Carissa Jones, Daniel Schlauch, Daniel Luckett, David R. Spigel, Suzanne Fields Jones, Andrew Jacob McKenzie
Publikováno v:
Journal of Clinical Oncology. 40:3146-3146
3146 Background: With the 2018 FDA approval of osimertinib for first-line treatment in EGFR-mutated lung cancers, the prevalence of acquired EGFR T790M mutations is expected to decrease, heightening the significance of de novo T790M mutations. Previo
Autor:
Emma Sturgill, Amanda Misch, Carissa Jones, Daniel Luckett, Xiaotong Fu, Suzanne Jones, Howard Burris, David Spigel, Andrew McKenzie
Publikováno v:
Cancer Genetics. :18
Autor:
Howard A. Burris, Andrew J. McKenzie, Xiaotong Fu, Suzanne F. Jones, David R. Spigel, Daniel Luckett, Emma Sturgill, Amanda Misch, Carissa Jones
Publikováno v:
Journal of Clinical Oncology. 39:2540-2540
2540 Background: Tumor mutational burden (TMB) detected by tissue-based Next Generation Sequencing (NGS) is a biomarker for immunotherapy (IO) response. Plasma-based NGS vendors have developed methods for quantifying TMB from circulating tumor DNA; h
Autor:
Caressa Lietman, Melissa Lynne Johnson, Emma Sturgill, Rebecca Lachs, Andrew J. McKenzie, David R. Spigel, Carissa Jones, Amanda Misch, Suzanne F. Jones
Publikováno v:
Journal of Clinical Oncology. 39:9099-9099
9099 Background: The development of CPIs and driver-targeted TKIs has transformed the treatment of NSCLC and increased survival rates. However, the role of CPIs in patients with oncogenic-driven NSCLC remains an area of investigation. We sought to ex
Autor:
Carissa Jones, Rebecca Lachs, Emma Sturgill, Amanda Misch, Caressa Lietman, Suzanne Fields Jones, Howard A. Burris III, Shiraj Sen, Johanna C. Bendell
Publikováno v:
Journal of Clinical Oncology. 39:113-113
113 Background: Checkpoint inhibitor (CPI) therapies have shown prolonged survival in patients (pts) with microsatellite instability (MSI). Tumor mutation burden (TMB) has also been associated with benefit from CPIs, with pembrolizumab recently appro
Autor:
Andrew McKenzie, Arielle Fisher, Mick Correll, Carissa Jones, Jessica Correia, James Thurber, Amanda Misch, Jessica Heritage, Emma Sturgill, Suzanne Fields Jones, Melissa Lynne Johnson, David R. Spigel
Publikováno v:
Journal of Clinical Oncology. 38:9613-9613
9613 Background: MET is a validated oncogene for molecular targeted therapy in non-small-cell lung cancer (NSCLC), and METex14 mutations result in MET overexpression. Studies with MET-targeting therapies have demonstrated high objective response rate