Katherine Peters

Overview:

Dr. Katy Peters, MD Ph.D. FAAN is an associate professor of neurology and neurosurgery at the Preston Robert Tisch Brain Tumor Center (PRTBTC) at Duke.   Her academic medical career started at Stanford University School of Medicine, receiving an MD and Ph.D. in Cancer Biology.  After completing a neurology residency at Johns Hopkins University and a fellowship in cognitive neurosciences, Katy joined the PRTBTC as a neuro-oncology fellow.  In 2009, she became a faculty member at PRTBTC.  With a fantastic team of nursing and advanced practice providers, she actively sees and cares for patients with primary brain tumors.  Her research interests include supportive care for brain cancer patients, cognitive dysfunction in cancer patients, and physical function and activity of brain cancer patients.   While she runs clinical trials to treat primary brain tumors, her key interest is on clinical trials that focus on improving brain tumor patients' quality of life and cognition.   In 2019, the PRTBTC designated her as the Director of Supportive Care, thus furthering the PRTBTC and her committee to better the quality of life for brain tumor patients.   She is active in teaching medical school students, residents, fellows, and advanced practice providers and is the Program Director of the PRTBRC neuro-oncology fellowship.     She is board certified by the American Board of Psychiatry and Neurology and the United Council of Neurologic Subspecialties for neuro-oncology.

Positions:

Associate Professor of Neurosurgery

Neurosurgery, Neuro-Oncology
School of Medicine

Vice Chair for Education in the Department of Neurology

Neurology
School of Medicine

Associate Professor in Neurology

Neurology
School of Medicine

Member of the Duke Cancer Institute

Duke Cancer Institute
School of Medicine

Education:

M.D. 2003

Stanford University

Ph.D. 2003

Stanford University

Intern, Medicine

Johns Hopkins University

Resident and Fellow in Neurology, Neurology

Johns Hopkins University

Fellow in Neuro-Oncology, Surgery

Duke University

Grants:

Ph 1/2 Trial for Patients with Newly Diagnosed High Grade Glioma Treated with Concurrent Radiation Therapy, Temozolomide, and BMX-001

Administered By
Neurosurgery, Neuro-Oncology
Awarded By
BioMimetix JV LLC
Role
Principal Investigator
Start Date
End Date

A Phase 1, Multicenter, Randomized, Controlled, Open-label, Perioperative Study of AG-120 and AG-881 in Subjects with Recurrent, Non-enhancing, IDH1 Mutant, Low-grade Glioma. (AG120-881-C-001)

Administered By
Duke Cancer Institute
Awarded By
Agios Pharmaceuticals, Inc.
Role
Principal Investigator
Start Date
End Date

Functional Capacity and Physical Function in Glioblastoma Patients Treated with or without Tumor-Treating Fields

Administered By
Duke Cancer Institute
Awarded By
Novocure
Role
Principal Investigator
Start Date
End Date

A Study for Management of Ocular Side Effects in Subjects with EGFR-Amplified Glioblastoma receiving Depatuxizumab Mafodotin

Administered By
Duke Cancer Institute
Awarded By
AbbVie Inc.
Role
Principal Investigator
Start Date
End Date

A randomized phase 2 single blind study of temozolomide plus radiation therapy combined with nivolumab or placebo in newly diagnosed adult subjects with MGMT-methylated glioblastoma (BMS CA209-548)

Administered By
Duke Cancer Institute
Awarded By
Bristol-Myers Squibb Company
Role
Principal Investigator
Start Date
End Date

Publications:

Ibrutinib in primary central nervous system diffuse large B-cell lymphoma.

The standard regimen for the treatment of newly diagnosed primary CNS lymphoma (PCNSL) remains regimens that contain high-dose methotrexate (MTX). While these regimens can provide control for some patients, there is a dearth of options for the treatment of patients with PCNSL who cannot tolerate MTX-containing regimens, or whose cancers are refractory to MTX. In this article, we review a promising new option; ibrutinib, a Bruton tyrosine kinase inhibitor, for patients with relapsed and refractory PCNSL.
Authors
T Low, J; B Peters, K
MLA Citation
T Low, Justin, and Katherine B Peters. “Ibrutinib in primary central nervous system diffuse large B-cell lymphoma.Cns Oncol, vol. 9, no. 1, Mar. 2020, p. CNS51. Pubmed, doi:10.2217/cns-2019-0022.
URI
https://scholars.duke.edu/individual/pub1570175
PMID
32141313
Source
pubmed
Published In
Cns Oncology
Volume
9
Published Date
Start Page
CNS51
DOI
10.2217/cns-2019-0022

PHASE I STUDY OF VANDETANIB, IMATINIB MESYLATE, AND HYDROXYUREA FOR RECURRENT MALIGNANT GLIOMA

Authors
Reardon, DA; Vredenburgh, JL; Desjardins, A; Gururangan, S; Peters, KB; Boulton, ST
MLA Citation
Reardon, David A., et al. “PHASE I STUDY OF VANDETANIB, IMATINIB MESYLATE, AND HYDROXYUREA FOR RECURRENT MALIGNANT GLIOMA.” Neuro Oncology, vol. 11, no. 6, OXFORD UNIV PRESS INC, 2009, pp. 946–946.
URI
https://scholars.duke.edu/individual/pub874915
Source
wos
Published In
Neuro Oncology
Volume
11
Published Date
Start Page
946
End Page
946

Bevacizumab plus etoposide among recurrent malignant glioma patients: Phase II study final results.

2046 Background: Significant therapeutic benefit has been observed among recurrent malignant glioma (MG) patients treated with bevacizumab (BV), a neutralizing monoclonal antibody to vascular endothelial growth factor (VEGF) with or without chemotherapy. In this study, we evaluate the efficacy of BV plus etoposide (E), a topoisomerase inhibitor, among recurrent MG patients. METHODS: Recurrent patients with no more than three prior episodes of recurrence are eligible, while those with prior BV treatment or prior intracranial hemorrhage are excluded. The primary outcome measure is 6 month progression-free survival (6-PFS). BV is dosed at 10 mg/kg intravenously every other week. Etoposide is orally administered daily (50 mg/m2) for days 1-21 of each 28-day cycle. RESULTS: Fifty-nine patients (GBM, n = 27; grade 3 MG, n = 32) with a median of 2 prior progressions have enrolled. With a median follow-up of 45 weeks, median overall survival (OS) for GBM and grade 3 MG patients were 46 and 47 weeks, while the 6-PFS is 44% and 40.6%, respectively. The most common toxicities were neutropenia (41%), fatigue (22%), and infection (20%) and were grade 2 in most cases. One patient developed grade 1 intracranial hemorrhage and 1 patient had a grade 4 GI perforation. CONCLUSIONS: Combination of bevacizumab and etoposide is well tolerated in recurrent MG patients and is associated with encouraging anti-tumor benefit. Accrual is complete and an update of further treatment and follow-up will be presented. No significant financial relationships to disclose.
Authors
Reardon, D; Desjardins, A; Vredenburgh, JJ; Gururangan, S; Peters, KB; Norfleet, JA
MLA Citation
Reardon, D., et al. “Bevacizumab plus etoposide among recurrent malignant glioma patients: Phase II study final results.J Clin Oncol, vol. 27, no. 15_suppl, May 2009, p. 2046.
URI
https://scholars.duke.edu/individual/pub1162964
PMID
27964642
Source
pubmed
Published In
Journal of Clinical Oncology
Volume
27
Published Date
Start Page
2046

LONG-TERM FOLLOW-UP OF A PHASE II TRIAL OF UPFRONT BEVACIZUMAB WITH TEMOZOLOMIDE AND RADIATION THERAPY FOLLOWED BY BEVACIZUMAB, TEMOZOLOMIDE, AND IRINOTECAN FOR NEWLY DIAGNOSED GLIOBLASTOMA MULTIFORME (GBM)

Authors
Ranjan, T; Desjardins, A; Peters, KB; Alderson, L; Kirkpatrick, J; Herndon, J; Bailey, L; Sampson, J; Friedman, AH; Friedman, H; Vredenburgh, J
URI
https://scholars.duke.edu/individual/pub929129
Source
wos
Published In
Neuro Oncology
Volume
14
Published Date
Start Page
81
End Page
82

Bevacizumab plus etoposide among recurrent malignant glioma patients: Phase II study final results

Authors
Reardon, D; Desjardins, A; Vredenburgh, JJ; Gururangan, S; Peters, KB; Norfleet, JA
MLA Citation
Reardon, D., et al. “Bevacizumab plus etoposide among recurrent malignant glioma patients: Phase II study final results.” Journal of Clinical Oncology, vol. 27, no. 15, AMER SOC CLINICAL ONCOLOGY, 2009.
URI
https://scholars.duke.edu/individual/pub874869
Source
wos
Published In
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
Volume
27
Published Date

Research Areas:

Brain--Tumors
Cancer
Cognition
Quality of Life
Supratentorial brain tumors