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2020 | 1 |
2022 | 1 |
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HYPORT adjuvant acute toxicity and patient dosimetry quality assurance results - Interim analysis.
Radiother Oncol. 2022 Sep;174:59-68. doi: 10.1016/j.radonc.2022.07.003. Epub 2022 Jul 9.
Radiother Oncol. 2022.
PMID: 35817323
Clinical Trial.
Hypofractionated radiation therapy comparing a standard radiotherapy schedule (over 3 weeks) with a novel 1-week schedule in adjuvant breast cancer: an open-label randomized controlled study (HYPORT-Adjuvant)-study protocol for a multicentre, randomized phase III trial.
Chatterjee S, Chakraborty S; HYPORT Adjuvant Author Group.
Chatterjee S, et al.
Trials. 2020 Sep 30;21(1):819. doi: 10.1186/s13063-020-04751-y.
Trials. 2020.
PMID: 32998747
Free PMC article.
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