Mustafa Khasraw

ORCID: 0000-0003-3249-9849
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About
Contact & Profiles
Research Areas
  • Glioma Diagnosis and Treatment
  • Brain Metastases and Treatment
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Genomics and Diagnostics
  • Lung Cancer Research Studies
  • Lung Cancer Treatments and Mutations
  • Epigenetics and DNA Methylation
  • CAR-T cell therapy research
  • Neuroblastoma Research and Treatments
  • Cancer Research and Treatments
  • Neuroendocrine Tumor Research Advances
  • Radiomics and Machine Learning in Medical Imaging
  • ATP Synthase and ATPases Research
  • PARP inhibition in cancer therapy
  • Heat shock proteins research
  • Mitochondrial Function and Pathology
  • Cancer Treatment and Pharmacology
  • Cancer, Hypoxia, and Metabolism
  • Colorectal Cancer Treatments and Studies
  • Ferroptosis and cancer prognosis
  • Pancreatic and Hepatic Oncology Research
  • Health Systems, Economic Evaluations, Quality of Life
  • Statistical Methods in Clinical Trials

Duke University Hospital
2020-2025

Duke Medical Center
2020-2025

Duke University
2020-2025

Duke Cancer Institute
2021-2025

The Royal Melbourne Hospital
2012-2024

Duke University Health System
2024

The University of Sydney
2014-2023

National Health and Medical Research Council
2009-2023

Royal North Shore Hospital
2009-2022

Hudson Institute
2022

•TMB-H failed to predict improved or clinically relevant response ICB in all cancer types.•Cancer types where TMB-H does not generally show no relationship between tumor neoantigen load and CD8 T-cell infiltration.•Further studies should be carried out before application of as a biomarker for types. BackgroundHigh mutation burden (TMB-H) has been proposed predictive immune checkpoint blockade (ICB), largely due the potential mutations generate immunogenic neoantigens. Despite recent...

10.1016/j.annonc.2021.02.006 article EN cc-by Annals of Oncology 2021-03-18
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

Abstract Immune checkpoint inhibitors, including antibodies that block programmed cell death protein-1 (PD-1) and PD-L1, have transformed the management of many cancers. However, majority patients primary or acquired resistance to these immunotherapies. There is a significant unmet need for predictive biomarkers can reliably identify who derive clinically meaningful response from PD-1/PD-L1 blockade. High tumor mutational burden (TMB-H) has shown promise as biomarker in lung cancer, but...

10.1158/1078-0432.ccr-20-3054 article EN Clinical Cancer Research 2020-11-16
Frederick S. Varn Kevin C. Johnson Jan Martínek Jason T. Huse MacLean P. Nasrallah and 95 more Pieter Wesseling Lee Cooper Tathiane M. Malta Taylor Wade Thaís S. Sabedot Daniel J. Brat Peter V. Gould Adelheid Wöehrer Kenneth Aldape Azzam Ismail Santhosh Sivajothi Floris P Barthel Hoon Kim Emre Kocakavuk Nazia Ahmed Kieron White Indrani Datta Hyo-Eun Moon Steven Pollock Christine N. Goldfarb Ga-Hyun Lee Luciano Garofano Kevin Anderson Djamel Nehar-Belaid Jill S. Barnholtz‐Sloan Spyridon Bakas Annette T. Byrne Fulvio D’Angelo Hui Gan Mustafa Khasraw Simona Migliozzi D. Ryan Ormond Sun Ha Paek Erwin G. Van Meir Annemiek Walenkamp Colin Watts Tobias Weiß Michael Weller Karolina Palucka Lucy F. Stead Laila Poisson Houtan Noushmehr Antonio Iavarone Roel G.W. Verhaak Frederick S. Varn Kevin C. Johnson Jan Martínek Jason T. Huse MacLean P. Nasrallah Pieter Wesseling Lee Cooper Tathiane M. Malta Taylor Wade Thaís S. Sabedot Daniel J. Brat Peter V. Gould Adelheid Wöehrer Kenneth Aldape Azzam Ismail Santhosh Sivajothi Floris P Barthel Hoon Kim Emre Kocakavuk Nazia Ahmed Kieron White Indrani Datta Hyo-Eun Moon Steven Pollock Christine N. Goldfarb Ga-Hyun Lee Luciano Garofano Kevin Anderson Djamel Nehar-Belaid Jill S. Barnholtz‐Sloan Spyridon Bakas Annette T. Byrne Fulvio D’Angelo Hui Gan Mustafa Khasraw Simona Migliozzi D. Ryan Ormond Sun Ha Paek Erwin G. Van Meir Annemiek Walenkamp Colin Watts Tobias Weiß Michael Weller Kristin Alfaro-Munoz Samirkumar B. Amin David M. Ashley Christoph Bock Andrew Brodbelt Ketan R. Bulsara Ana Valéria Castro Jennifer Connelly

10.1016/j.cell.2022.04.038 article EN publisher-specific-oa Cell 2022-05-31

Addition of temozolomide (TMZ) to radiotherapy (RT) improves overall survival (OS) in patients with glioblastoma (GBM), but previous studies suggest that tumors harboring an unmethylated MGMT promoter derive minimal benefit. The aim this open-label, phase III CheckMate 498 study was evaluate the efficacy nivolumab (NIVO) + RT compared TMZ newly diagnosed GBM promoter.Patients were randomized 1:1 standard (60 Gy) NIVO (240 mg every 2 weeks for eight cycles, then 480 4 weeks) or (75 mg/m2...

10.1093/neuonc/noac099 article EN cc-by-nc Neuro-Oncology 2022-04-14

Background: PET scans using FDG and somatostatin receptor imaging agents have both been used to study neuroendocrine tumours.Most reports documented the sensitivity specificity of each radiopharmaceutical independently, even suggested superiority one over other for different grades disease.Aim: The aim this work was develop a grading scheme that describes joint results in staging subjects with tumours single combined parameter.The has developed is referred as NETPET grade.Methods: This...

10.7150/thno.18068 article EN cc-by Theranostics 2017-01-01

Spinal ependymal tumors form a histologically and molecularly heterogeneous group of with generally good prognosis. However, their treatment can be challenging if infiltration the spinal cord or dissemination throughout central nervous system (CNS) occurs and, in these cases, clinical outcome remains poor. Here, we describe new relatively rare subgroup identified using DNA methylation profiling that is distinct from other molecular subgroups ependymoma. Copy number variation plots derived...

10.1007/s00401-019-02056-2 article EN cc-by Acta Neuropathologica 2019-08-14

Expression of programmed cell death protein 1 (PD-1)/programmed ligand (PD-L1) across glioma grades is undocumented, and their interactions with commonly expressed genetic epigenetic alterations are undefined but nonetheless highly relevant to combinatorial treatments. Patients CNS malignancies were profiled by Caris Life Sciences from 2009 2016. Immunohistochemistry findings for PD-1 on tumor-infiltrating lymphocytes (TIL) PD-L1 tumor cells available 347 cases. Next-generation sequencing,...

10.1093/neuonc/now132 article EN Neuro-Oncology 2016-07-01

<h3>Objectives</h3> Using the prediction of cancer outcome as a model, we have tested hypothesis that through analysing routinely collected digital data contained in an electronic administrative record (EAR), using machine-learning techniques, could enhance conventional methods predicting clinical outcomes. <h3>Setting</h3> A regional centre Australia. <h3>Participants</h3> Disease-specific from purpose-built registry (Evaluation Cancer Outcomes (ECO)) 869 patients were used to predict...

10.1136/bmjopen-2013-004007 article EN cc-by-nc BMJ Open 2014-03-01

Abstract Several immunotherapy clinical trials in recurrent glioblastoma have reported long-term survival benefits 10–20% of patients. Here we perform genomic analysis tumor tissue from WHO grade IV patients acquired prior to intervention. We report that very low mutation burden is associated with longer after recombinant polio virotherapy or immune checkpoint blockade A relationship between and not observed cohorts naïve newly diagnosed Transcriptomic analyses reveal an inverse enrichment...

10.1038/s41467-020-20469-6 article EN cc-by Nature Communications 2021-01-13

Understanding the molecular basis of drug resistance and utilising this information to overcome chemoresistance remains a key challenge in oncology.Here we report that survivin, protein implicated resistance, is overexpressed cancer stem cell pool doxorubicin-resistant breast cells.Moreover, by an active targeting system consisting RNA aptamer targeted against epithelial adhesion molecule Dicer substrate survivin siRNA, could deliver high dose siRNA cells xenograft tumours.Importantly,...

10.7150/thno.11692 article EN cc-by Theranostics 2015-01-01

Abstract Background Temozolomide offers minimal benefit in patients with glioblastoma unmethylated O6-methylguanine-DNA methyltransferase (MGMT) promoter status, hence, the need for novel therapies. This study evaluated whether veliparib, a brain-penetrant poly(ADP-ribose) polymerase (PARP) inhibitor, acts synergistically radiation and temozolomide. Methods VERTU was multicenter 2:1 randomized phase II trial newly diagnosed MGMT-unmethylated promotor status. The experimental arm consisted of...

10.1093/neuonc/noab111 article EN cc-by-nc Neuro-Oncology 2021-05-06
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