Michael Robert Horsman

Michael Robert Horsman

orcid

Research Focus & Metrics

Academic Career Length

47Years (1980-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 November 2012 in Nature Reviews Clinical Oncology
Verified
Journal Article
Closed access
MHMichael Robert Horsman
Michael Robert Horsman
LMLise Saksø Mortensen
Lise Saksø Mortensen
JPJørgen B. Petersen
Jørgen B. Petersen
MBMorten Busk
Morten Busk
JOJens Overgaard
Jens Overgaard

3 May 2005 in British Journal of Cancer
Verified
Journal Article
Open access
PDF file
MLMartin Leach
Martin Leach
KBK M Brindle
K M Brindle
JEJ L Evelhoch
J L Evelhoch
JGJ R Griffiths
J R Griffiths
MHMichael Robert Horsman
Michael Robert Horsman
PWP Workman
P Workman
Vascular and angiogenic processes provide an important target for novel cancer therapeutics. Dynamic contrast-enhanced magnetic resonance imaging is being used increasingly to noninvasively monitor the action of these therapeutics in early-stage clinical trials. This publication reports the outcome of a workshop that considered the methodology and design of magnetic resonance studies, recommending how this new tool might best be used.

1 August 2007 in Clinical Oncology
Verified
Journal Article
Closed access
MHMichael Robert Horsman
Michael Robert Horsman
JOJ. Overgaard
J. Overgaard

1 January 1996 in Seminars in Radiation Oncology
Verified
Journal Article
Closed access
JOJens Overgaard
Jens Overgaard
MHMichael Robert Horsman
Michael Robert Horsman

16 March 2016 in Journal of Radiation Research
Verified
Journal Article
Open access
PDF file
MHMichael Robert Horsman
Michael Robert Horsman
JOJens Overgaard
Jens Overgaard
Since the initial observations made at the beginning of the last century, it has been established that solid tumors contain regions of low oxygenation (hypoxia). Tumor cells can survive in these hypoxic conditions and are a major factor in tumor radioresistance. This significance has resulted in hypoxia becoming the most cited biological topic in translational radiation oncology. Identifying hypoxic cells in human tumors has become paramount, and the ability to do this has been improved by the help of new imaging techniques and the use of predictive gene profiles. Substantial data confirm the presence of hypoxia in many types of human tumors, although with considerable heterogeneity among individual tumors. Various approaches have been investigated for eliminating the hypoxic population. These include increasing oxygen availability, directly radiosensitizing or killing the hypoxic cells, indirectly affecting them by targeting the tumor vascular supply, increasing the radiation dose to this resistant population, or by using radiation with a high linear energy transfer, for which hypoxia is believed to be less of an issue. Many of these approaches have undergone controlled clinical trials during the last 50 years, and the results have shown that hypoxic radiation resistance can indeed be overcome. Thus, ample data exists to support a high level of evidence for the benefit of hypoxic modification. However, such hypoxic modification still has no impact on general clinical practice. In this review we summarize the biological rationale, and the current activities and trials, related to identifying and overcoming hypoxia in modern radiotherapy.

2 June 2004 in Cancer
Verified
Journal Article
Closed access
PDF file
DSDietmar W. Siemann
Dietmar W. Siemann
DCDavid J. Chaplin
David J. Chaplin
MHMichael Robert Horsman
Michael Robert Horsman