Abstract
Purpose
The present study compared the complications associated with hypofractionated intensity-modulated radiation therapy (Hypo-IMRT) of prostate cancer to conventionally fractionated IMRT (Conv-IMRT).
Materials and methods
Hypo-IMRT delivered 70 Gy in 28 fractions, whereas Conv-IMRT delivered 78 Gy in 39 fractions. Toxicity was graded with the Common Terminology Criteria for Adverse Events, version 4.0, weekly during radiotherapy, 1 month after radiotherapy, and annually in both patient groups.
Results
The median follow-ups were 39.1 and 38.7 months for patients in the Hypo- and Conv-IMRT groups, respectively. There was no significant difference in rates of acute and late adverse events. The proportions of grade 2 acute genitourinary complications were 48.4 and 51.2% in the Hypo- and Conv-IMRT groups, respectively. The presence of a baseline International Prostate Symptom Score (IPSS) of ten or more was the only significant prognostic factor for grade 2 acute genitourinary toxicity. The incidence of grade 2 late rectal hemorrhage at 3 years was 3.2 and 3.5% in the Hypo- and Conv-IMRT groups, respectively. Small rectal volume was significantly associated with grade 2 late rectal hemorrhage.
Conclusion
Regarding acute and late adverse events, hypofractionated IMRT for prostate cancer was well tolerated and comparable with conventionally fractionated IMRT.
Clinical trial registration no. UMIN000003218.
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Acknowledgements
We gratefully acknowledge the assistance of Yuko Ohtomo and other members of the Department of Radiation Oncology at the Cancer Institute Hospital of the Japanese Foundation for Cancer Research. This work was supported by Health and Labour Sciences Research Grants (H26-Cancer Policy-General-014).
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This study was funded by Health and Labour Sciences Research Grants (H26-Cancer Policy-General-014).
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Kozuka, T., Nakano, M., Hashimoto, M. et al. Acute and late complications after hypofractionated intensity modulated radiotherapy in prostate cancer. Jpn J Radiol 35, 269–278 (2017). https://doi.org/10.1007/s11604-017-0630-2
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DOI: https://doi.org/10.1007/s11604-017-0630-2