Priscilla K. Brastianos

ORCID: 0000-0003-4470-8425
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About
Contact & Profiles
Research Areas
  • Brain Metastases and Treatment
  • Glioma Diagnosis and Treatment
  • Lung Cancer Research Studies
  • Meningioma and schwannoma management
  • Lung Cancer Treatments and Mutations
  • Pituitary Gland Disorders and Treatments
  • Cancer Immunotherapy and Biomarkers
  • Neurofibromatosis and Schwannoma Cases
  • Radiopharmaceutical Chemistry and Applications
  • Cancer Genomics and Diagnostics
  • Advanced Breast Cancer Therapies
  • Chemical Reactions and Isotopes
  • Head and Neck Surgical Oncology
  • Ferroptosis and cancer prognosis
  • Bone Tumor Diagnosis and Treatments
  • Melanoma and MAPK Pathways
  • Click Chemistry and Applications
  • Radiomics and Machine Learning in Medical Imaging
  • Nanoplatforms for cancer theranostics
  • Chromatin Remodeling and Cancer
  • Synthesis and Biological Evaluation
  • Adrenal and Paraganglionic Tumors
  • CNS Lymphoma Diagnosis and Treatment
  • Immune cells in cancer
  • Cancer therapeutics and mechanisms

Massachusetts General Hospital
2016-2025

Harvard University
2016-2025

Broad Institute
2014-2025

Dana-Farber Cancer Institute
2013-2024

Center for Neuro-Oncology
2012-2024

MGH Institute of Health Professions
2019-2024

Brigham and Women's Hospital
2011-2023

Dana-Farber Brigham Cancer Center
2009-2023

Ludwig-Maximilians-Universität München
2023

Woman's Hospital
2023

Abstract Brain metastases are associated with a dismal prognosis. Whether brain harbor distinct genetic alterations beyond those observed in primary tumors is unknown. We performed whole-exome sequencing of 86 matched metastases, tumors, and normal tissue. In all clonally related cancer samples, we branched evolution, where metastatic sites shared common ancestor yet continued to evolve independently. 53% cases, found potentially clinically informative the not detected primary-tumor sample....

10.1158/2159-8290.cd-15-0369 article EN Cancer Discovery 2015-09-27

Tumor subclasses differ according to the genotypes and phenotypes of malignant cells as well composition tumor microenvironment (TME). We dissected these influences in isocitrate dehydrogenase (IDH)-mutant gliomas by combining 14,226 single-cell RNA sequencing (RNA-seq) profiles from 16 patient samples with bulk RNA-seq 165 samples. Differences between IDH-mutant astrocytoma oligodendroglioma can be primarily explained distinct TME signature genetic events, whereas both types share similar...

10.1126/science.aai8478 article EN cc-by Science 2017-03-30
Floris P Barthel Kevin C. Johnson Frederick S. Varn Anzhela D. Moskalik Georgette Tanner and 95 more Emre Kocakavuk Kevin Anderson Olajide Abiola Kenneth Aldape Kristin Alfaro-Munoz Donát Alpár Samirkumar B. Amin David M. Ashley Pratiti Bandopadhayay Jill S. Barnholtz‐Sloan Rameen Beroukhim Christoph Bock Priscilla K. Brastianos Daniel J. Brat Andrew Brodbelt Alexander Bruns Ketan R. Bulsara Aruna Chakrabarty Arnab Chakravarti Jeffrey H. Chuang Elizabeth B. Claus Elizabeth J. Cochran Jennifer Connelly J Costello Gaetano Finocchiaro Michael Fletcher Pim J. French Hui Gan Mark R. Gilbert Peter V. Gould Matthew Grimmer Antonio Iavarone Azzam Ismail Michael D. Jenkinson Mustafa Khasraw Hoon Kim Mathilde C.M. Kouwenhoven Peter S. LaViolette Ho‐Keung Ng Peter Lichter Keith L. Ligon Allison Lowman Tathiane M. Malta Tali Mazor Kerrie L. McDonald Annette M. Molinaro Do‐Hyun Nam Naema Nayyar Ho‐Keung Ng Chew Yee Ngan Simone P. Niclou Johanna M. Niers Houtan Noushmehr Javad Noorbakhsh D. Ryan Ormond Chul‐Kee Park Laila Poisson Raúl Rabadán Bernhard Radlwimmer Hui Gan Guido Reifenberger K. Jason Michael Schuster Brian Shaw Susan Short Peter A. Sillevis Smitt Andrew E. Sloan Marion Smits Hiromichi Suzuki Ghazaleh Tabatabai Erwin G. Van Meir Colin Watts Michael Weller Pieter Wesseling Bart A. Westerman Georg Widhalm Adelheid Wöehrer W. K. Alfred Yung Gelareh Zadeh Jason T. Huse John de Groot Lucy F. Stead Roel G.W. Verhaak Floris P Barthel Kevin C. Johnson Frederick S. Varn Anzhela D. Moskalik Georgette Tanner Emre Kocakavuk Kevin Anderson Kenneth Aldape Kristin Alfaro-Munoz Samirkumar B. Amin David M. Ashley Pratiti Bandopadhayay

10.1038/s41586-019-1775-1 article EN Nature 2019-11-20

Meningiomas are the most common primary intracranial tumor in adults. Identification of SMO and AKT1 mutations meningiomas has raised possibility targeted therapies for some patients. The frequency such clinical cohorts presence other actionable important to define.We used high-resolution array-comparative genomic hybridization prospectively characterize copy-number changes 150 then characterized these samples AKT1, KLF4, NF2, PIK3CA, SMO, TRAF7.Similar prior reports, we identified a subset...

10.1093/neuonc/nov316 article EN Neuro-Oncology 2016-01-28

We recently reported that BRAF V600E is the principal oncogenic driver of papillary craniopharyngioma, a highly morbid intracranial tumor commonly refractory to treatment. Here, we describe our treatment man age 39 years with multiply recurrent craniopharyngioma using dabrafenib (150mg, orally twice daily) and trametinib (2mg, daily). After 35 days treatment, volume was reduced by 85%. Mutations mediate resistance MAPK pathway inhibition were not detected in post-treatment sample whole exome...

10.1093/jnci/djv310 article EN JNCI Journal of the National Cancer Institute 2015-10-23

Abstract Background Variability in standard-of-care classifications precludes accurate predictions of early tumor recurrence for individual patients with meningioma, limiting the appropriate selection who would benefit from adjuvant radiotherapy to delay recurrence. We aimed develop an individualized prediction model risk combining clinical and molecular factors meningioma. Methods DNA methylation profiles clinically annotated samples across multiple institutions were used a methylome 5-year...

10.1093/neuonc/noz061 article EN public-domain Neuro-Oncology 2019-04-12

Pediatric low-grade gliomas (PLGGs) are among the most common solid tumors in children but, apart from BRAF kinase mutations or duplications specific subclasses, few genetic driver events known. Diffuse PLGGs comprise a set of uncommon subtypes that exhibit invasive growth and therefore especially challenging clinically. We performed high-resolution copy-number analysis on 44 formalin-fixed, paraffin-embedded diffuse to identify recurrent alterations. exhibited fewer such alterations than...

10.1073/pnas.1300252110 article EN Proceedings of the National Academy of Sciences 2013-04-30

A recent meeting was held on March 22, 2019, among the FDA, clinical scientists, pharmaceutical and biotech companies, trials cooperative groups, patient advocacy groups to discuss challenges potential solutions for increasing development of therapeutics central nervous system metastases. key issue identified at this need consistent tumor measurement reliable response assessment, including first step standardized image acquisition with an MRI protocol that could be implemented in multicenter...

10.1093/neuonc/noaa030 article EN Neuro-Oncology 2020-02-07

Expanding the US Food and Drug Administration-approved indications for immune checkpoint inhibitors in patients with cancer has resulted therapeutic success immune-related adverse events (irAEs). Neurologic irAEs (irAE-Ns) have an incidence of 1%-12% a high fatality rate relative to other irAEs. Lack standardized disease definitions accurate phenotyping leads syndrome misclassification impedes development evidence-based treatments translational research. The objective this study was develop...

10.1136/jitc-2021-002890 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2021-07-01

Abstract Purpose: Patients with KRAS-mutant non–small cell lung cancer (NSCLC) brain metastases (BM) have a poor prognosis. Adagrasib (MRTX849), potent oral small-molecule KRASG12C inhibitor, irreversibly and selectively binds KRASG12C, locking it in its inactive state. has been optimized for favorable pharmacokinetic properties, including long half-life (∼24 hours), extensive tissue distribution, dose-dependent pharmacokinetics, central nervous system penetration; however, BM-specific...

10.1158/1078-0432.ccr-22-0383 article EN cc-by-nc-nd Clinical Cancer Research 2022-04-11

Craniopharyngiomas, primary brain tumors of the pituitary-hypothalamic axis, can cause clinically significant sequelae. Treatment with use surgery, radiation, or both is often associated substantial morbidity related to vision loss, neuroendocrine dysfunction, and memory loss. Genotyping has shown that more than 90% papillary craniopharyngiomas carry

10.1056/nejmoa2213329 article EN New England Journal of Medicine 2023-07-12
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