Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer
Integrating immunotherapy, proton therapy and biological dose escalation into the definitive chemoradiation of oropharyngeal cancer poses several challenges. Reliable and reproducible data must be obtained in a timely fashion. However, despite recent international radiotherapy contouring guidelines,...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2018-06-01
|
Series: | Medicines |
Subjects: | |
Online Access: | http://www.mdpi.com/2305-6320/5/3/65 |
id |
doaj-ace8e4883096419c86c91a85b01e1468 |
---|---|
record_format |
Article |
spelling |
doaj-ace8e4883096419c86c91a85b01e14682020-11-24T23:18:30ZengMDPI AGMedicines2305-63202018-06-01536510.3390/medicines5030065medicines5030065Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal CancerAgostino Cristaudo0Mitchell Hickman1Charles Fong2Paul Sanghera3Andrew Hartley4Department of Radiation Oncology, University of Pisa, 56100 Pisa PI, ItalyHall-Edwards Radiotherapy Research Group, Queen Elizabeth Hospital, Birmingham B15 2TH, UKHall-Edwards Radiotherapy Research Group, Queen Elizabeth Hospital, Birmingham B15 2TH, UKHall-Edwards Radiotherapy Research Group, Queen Elizabeth Hospital, Birmingham B15 2TH, UKHall-Edwards Radiotherapy Research Group, Queen Elizabeth Hospital, Birmingham B15 2TH, UKIntegrating immunotherapy, proton therapy and biological dose escalation into the definitive chemoradiation of oropharyngeal cancer poses several challenges. Reliable and reproducible data must be obtained in a timely fashion. However, despite recent international radiotherapy contouring guidelines, controversy persists as to the applicability of such guidelines to all cases. Similarly, a lack of consensus exists concerning both the definition of the organ at risk for oral mucositis and the most appropriate endpoint to measure for this critical toxicity. Finally, the correlation between early markers of efficacy such as complete response on PET CT following treatment and subsequent survival needs elucidation for biological subsets of oropharyngeal cancer.http://www.mdpi.com/2305-6320/5/3/65clinical target volume (CTV)mucositisorgan at risk (OAR)intensity modulated proton therapy (IMPT)PET/CT |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Agostino Cristaudo Mitchell Hickman Charles Fong Paul Sanghera Andrew Hartley |
spellingShingle |
Agostino Cristaudo Mitchell Hickman Charles Fong Paul Sanghera Andrew Hartley Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer Medicines clinical target volume (CTV) mucositis organ at risk (OAR) intensity modulated proton therapy (IMPT) PET/CT |
author_facet |
Agostino Cristaudo Mitchell Hickman Charles Fong Paul Sanghera Andrew Hartley |
author_sort |
Agostino Cristaudo |
title |
Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer |
title_short |
Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer |
title_full |
Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer |
title_fullStr |
Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer |
title_full_unstemmed |
Assessing Novel Drugs and Radiation Technology in the Chemoradiation of Oropharyngeal Cancer |
title_sort |
assessing novel drugs and radiation technology in the chemoradiation of oropharyngeal cancer |
publisher |
MDPI AG |
series |
Medicines |
issn |
2305-6320 |
publishDate |
2018-06-01 |
description |
Integrating immunotherapy, proton therapy and biological dose escalation into the definitive chemoradiation of oropharyngeal cancer poses several challenges. Reliable and reproducible data must be obtained in a timely fashion. However, despite recent international radiotherapy contouring guidelines, controversy persists as to the applicability of such guidelines to all cases. Similarly, a lack of consensus exists concerning both the definition of the organ at risk for oral mucositis and the most appropriate endpoint to measure for this critical toxicity. Finally, the correlation between early markers of efficacy such as complete response on PET CT following treatment and subsequent survival needs elucidation for biological subsets of oropharyngeal cancer. |
topic |
clinical target volume (CTV) mucositis organ at risk (OAR) intensity modulated proton therapy (IMPT) PET/CT |
url |
http://www.mdpi.com/2305-6320/5/3/65 |
work_keys_str_mv |
AT agostinocristaudo assessingnoveldrugsandradiationtechnologyinthechemoradiationoforopharyngealcancer AT mitchellhickman assessingnoveldrugsandradiationtechnologyinthechemoradiationoforopharyngealcancer AT charlesfong assessingnoveldrugsandradiationtechnologyinthechemoradiationoforopharyngealcancer AT paulsanghera assessingnoveldrugsandradiationtechnologyinthechemoradiationoforopharyngealcancer AT andrewhartley assessingnoveldrugsandradiationtechnologyinthechemoradiationoforopharyngealcancer |
_version_ |
1725581263750823936 |