Rectum Protection by Rectal Gel Injection in Cervical Cancer Brachytherapy: A Dosimetric Study Deformable Surface Dose Accumulation and Machine-Learning-Based Discriminative Modeling.

PURPOSE

This retrospective study aimed to evaluate the dosimetric effects of a rectal insertion of on rectal protection using deformable dose accumulation and machine learning-based discriminative modelling.

MATERIALS AND METHODS

Sixty-two patients with cervical cancer enrolled in a clinical trial, who received a injection of 20 g into their rectum for rectal protection high-dose rate brachytherapy (HDR-BT, 6 Gy/f), were studied. The cumulative equivalent 2-Gy fractional rectal surface dose was deformably summed using an in-house-developed topography-preserved point-matching deformable image registration method. The cumulative three-dimensional (3D) dose was flattened and mapped to a two-dimensional (2D) plane to obtain the rectal surface dose map (RSDM). For analysis, the rectal dose (RD) was further subdivided as follows: whole, anterior, and posterior 3D-RD and 2D-RSDM. The dose-volume parameters (DVPs) were extracted from the 3D-RD, while the dose geometric parameters (DGPs) and textures were extracted from the 2D-RSDM. These features were fed into 192 classification models (built with 8 classifiers and 24 feature selection methods) for discriminating the dose distributions between pre- and pro-.

RESULTS

The rectal insertion of dialated the rectum in the ambilateral direction, with the rectal column increased from pre- 15 cm to post- 18 cm ( < 0.001). The characteristics of DGPs accounted for the largest portions of the top-ranked features. The top-ranked dosimetric features extracted from the posterior rectum were more reliable indicators of the dosimetric effects/changes introduced by the rectal insertion of . A significant dosimetric impact was found on the dose-volume parameters D-D extracted on the posterior rectal wall.

CONCLUSIONS

The rectal insertion of incurs significant dosimetric changes on the posterior rectal wall. Whether this effect is eventually translated into clinical gains requires further long-term follow-up and more clinical data for confirmation.