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A brain metastasis therapy tweak, for the better? Concomitant stereotactic radiotherapy and molecular-targeted therapy

Abstract:
The most common cause of cancer demise is the metastasis to distant organs. In particular, brain metastasis represents one of the highest mortality rates in the oncology field. Some of the reasons for the meagre advance in the treatment of this disease are the limited conditions for favourable surgical debulking of tumour, off-target effects of conventional treatments and the limited efficacy of delivery into the brain for currently available drugs. Contrary to those conventional strategies, targeted anticancer therapies exploit molecules that act on specific mechanisms that may disturb the malignant process, whilst minimising adverse effects on healthy tissues. Based on that approach, we have been working on novel anti-cell adhesion molecule (CAM) therapies.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1093/neuonc/now292.008

Authors

More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Oncology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Oncology
Sub department:
CRUK/MRC Ox Inst Radiation Oncology
Role:
Author
ORCID:
0000-0002-4169-8447
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Oncology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Sub department:
CRUK/MRC Ox Inst for Radiation Oncology
Role:
Author
ORCID:
0000-0003-1211-2766


Publisher:
Oxford University Press
Host title:
Neuro-Oncology
Journal:
2016 British Neuro-Oncology Society Meeting (BNOS 2016) More from this journal
Volume:
19
Pages:
126
Publication date:
2017-03-02
Acceptance date:
2016-06-27
DOI:
EISSN:
1523-5866
ISSN:
1522-8517


Pubs id:
pubs:719630
UUID:
uuid:41a21992-b867-4671-a907-3a77bdc09c9c
Local pid:
pubs:719630
Source identifiers:
719630
Deposit date:
2018-10-30
ARK identifier:

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