PET to assess early metabolic response and to guide treatment of adenocarcinoma of the oesophagogastric junction: the MUNICON phase II trial.
By F. Lordick, K. Ott, B. Krause, W. Weber, K. Becker, H. Stein, S. Lorenzen, T. Schuster, H. Wieder, K. Herrmann and 6 more. The Lancet Oncology, 2007
814 citations recorded by the source corpus.
Subfields: Oncology, Pulmonary and Respiratory Medicine, Surgery
View Paper: https://www.semanticscholar.org/paper/935871cfa36e0c3756806517aff89cb4d6c1cb33
How researchers see this paper
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In Oncology
In Pulmonary and Respiratory Medicine
- Ralph Weissleder
- Lee Josephson
- Isaac Koh
- Vasilis Ntziachristos
- D. Hanahan
- Lisa M. Coussens
- Ron M. A. Heeren
- Liam A. McDonnell
Citations in the corpus
- Imaging in the era of molecular oncology (2008, methodology): “In the clinic, analysing glucose metabolism by using PET (after administering the probe [ 18 F] fluorodeoxyglucose, which is preferentially taken up by metabolically active cells) is progressively being used as a surrogate for treatment efficacy75,76.”
- A systematic review of the factors affecting accuracy of SUV measurements. (2010, background): “Quantification such as SUV plays a more important role in this scenario; clinical studies to date indicate that most tumors responding to therapy show a 20–40% decrease in SUV early in the treatment course [11–15].”