Repopulation of cancer cells during therapy: an important cause of treatment failure
By John J. Kim, I. Tannock. Nature Reviews. Cancer, 2005
690 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/da07705be3ceae0715e2223f64eed2082bc3e1c5
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The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- Rakesh K. Jain
- N. Ferrara
- D. Duda
- R. Kerbel
- Subash C. Gupta
- A. Minchinton
- I. Tannock
- Jay S. Loeffler
Citations in the corpus
- Lessons from phase III clinical trials on anti-VEGF therapy for cancer (2006, background): “Whereas none of the successful phase III trials of bevacizumab to date used dose-dens”
- Angiogenesis as a therapeutic target (2005, background): “Furthermore, it has been proposed that progressively accelerated proliferation and repopulation of cancer cells during intervals of radiotherapy or chemotherapy is an important cause of treatment failur”
- Strategies to improve radiotherapy with targeted drugs (2011, background): “; the ability of the surviving cells to repopulate within a treatment time of 6–7 week”
- Oxidative stress, inflammation, and cancer: how are they linked? (2010, background): “Acquired tumor radioresistance can be induced during radiotherapy owing to tumor repopulation [272].”
- Drug penetration in solid tumours (2006, background): “, leads to the effective exposure of cells distal from blood vessels (although it seems probable that rapid clearance from plasma limits the amount of drug that penetrates into tumour tissue); second, sequential cycles of doxorubicin-based chemotherapy lead to the sequential killing of cells at incr”