Dosimetric analysis of tomotherapy-based intensity-modulated radiotherapy with and without bone marrow sparing for the treatment of cervical cancer
Objective The aim of the study was to compare tomotherapy-based bone marrow-sparing intensity-mod-ulated radiotherapy (BMS-IMRT) with intensity-modulated radiotherapy (IMRT) without entering the pelvic bone marrow as a planning constraint in the treatment of cervical cancer after hysterectomy. Metho...
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Veröffentlicht in: | Oncology and translational medicine 2015-06, Vol.1 (3), p.135-139 |
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Sprache: | eng |
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Zusammenfassung: | Objective The aim of the study was to compare tomotherapy-based bone marrow-sparing intensity-mod-ulated radiotherapy (BMS-IMRT) with intensity-modulated radiotherapy (IMRT) without entering the pelvic bone marrow as a planning constraint in the treatment of cervical cancer after hysterectomy. Methods BMS-IMRT and IMRT plans were designed for a cohort of nine patients. The prescribed dose was 45 Gy in 1.8 Gy daily fractions, and 95% of the planned target volume received this dose. The doses were computed using a commercial y available treatment planning system with the convolution/superposi-tion algorithm. Plans were compared according to dose-volume histogram analysis in terms of planning target volume homogeneity and conformity indices (HI and CI) as wel as organ at risk dose and volume parameters. Results BMS-IMRT had advantages over IMRT in terms of CI, but was equivalent to the latter in HI. V5, V10, V20, V30, and V40 of pelvic bone marrow in BMS-IMRT decreased by 0.06%, 17.33%, 22.19%, 13.85%, and 16.46%, respectively, compared with IMRT. Except for V30 of the smal bowel and V30 and V40 of the bladder, no statistical y significant dif erences were found between BMS-IMRT and IMRT in the smal bowel, bladder, and rectum. Conclusion For cervical cancer patients receiving tomotherapy-based radiotherapy after hysterectomy, BMS-IMRT reduced pelvic bone marrow volume receiving low-dose radiation, and it may be conducive to preventing acute hematologic toxicity. |
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ISSN: | 2095-9621 1610-1979 |
DOI: | 10.1007/s10330-014-1434-9 |