Purpose: To evaluate the dosimetric benefits of MRI-based brachytherapy in small and large high-risk clinical target volume (HR-CTV) in cervical cancer.

Methods And Materials: Twenty-eight fractions obtained from sixteen cervical cancer patients treated with MRI-based high-dose-rate brachytherapy with standard tandem and ovoid applicators were used; original fractions were optimized to HR-CTV D. Fractions were separated based on the median volume into small and large (HR-CTV <25 cm or >25 cm) lesion groups. Retrospective plans prescribed to Point A were created for each fraction. D, D, and International Commission of Radiation Unit and Measurements (ICRU) points were used to compare Point A vs. HR-CTV D plans for bladder, rectum, and sigmoid.

Results: In the small lesion group, Point A plans vs. HR-CTV D plans had significantly higher D, D, and ICRU points for bladder, rectum, and sigmoid (p < 0.05). In the large lesion group, there was no significant difference between Point A and HR-CTV D plans for D, D, and ICRU points to the organs at risk (OARs).

Conclusions: The dosimetric advantages to OARs offered by MRI-based brachytherapy with prescription to HR-CTV D compared to Point A is most distinct for patients with smaller HR-CTV (<25 cm). This study demonstrates sufficient tumor coverage with lower doses to OARs in HR-CTV D vs. Point A plans in the small lesion group. These improvements were not seen in the large lesion group, indicating a lesser dosimetric advantage of HR-CTV D compared to Point A planning when the cervical lesion is >25 cm. Incorporation of interstitial needles for patients with larger HR-CTV is likely the best method to decrease dose to OARs and improve tumor coverage.

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Source
http://dx.doi.org/10.1016/j.brachy.2016.08.010DOI Listing

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