Frontiers in Oncology | 2021

The Relationship Between Late Morbidity and Dose–Volume Parameter of Rectum in Combined Intracavitary/Interstitial Cervix Cancer Brachytherapy: A Mono-Institutional Experience

 
 
 
 
 
 
 

Abstract


Purpose To establish a dose volume–effect relationship for predicting late rectal complication (LRC) in locally advanced cervical cancer patients treated with external beam radiotherapy (EBRT) followed by combined intracavitary/interstitial brachytherapy (IC/IS-BT). Materials and Methods A retrospective analysis was performed in 110 patients with locally advanced cervical cancer who underwent definitive radiotherapy combined with IC/IS-BT from July 2010 to September 2018. We report the 90% of the target volume receiving the minimum dose for high risk clinical target volume (HR-CTV D90) and intermediate risk clinical target volume (IR-CTV D90), and the minimum doses to the most exposed 0.1, 1, and 2 cm³ D 0.1 c m 3 , D 1 c m 3 , D 2 c m 3 doses at the International Commission on Radiation Units and Measurements (DICRU) for organs at risk (OARs). The total dose of EBRT plus brachytherapy was transformed to the biologically equivalent dose in 2 Gy fractions (EQD2) with α/β value of 10 Gy for target, 3 Gy for organs at risk using the linear quadratic model. The morbidity was scored according to the Radiation Therapy Oncology Group (RTOG) criteria. The Probit model was used to establish a prediction model on rectum between the organs at risk for dose and LRC. The receiver operating characteristic (ROC) curve was used to evaluate the predictive value of dose volume parameters for LRC. Results The median follow-up time was 72.3 months. The mean ( ± standard deviation) D 2 c m 3 , D 1 c m 3 , D 0.1 c m 3 , and DICRU values of rectum were 64.72 ± 7.47 GyEQD2, 70.18 ± 5.92 GyEQD2, 79.32 ± 7.86 GyEQD2, and 67.22 ± 7.87 GyEQD2, respectively. The Probit model showed significant relationships between D 1 c m 3 or D 0.1 c m 3 , and the probability of grade1–4, grade 2–4 rectal events at 1 year, and between D 1 c m 3 and the probability of grade2–4 rectal events at 3 and 5 years. The dose values for 10% complication rates (ED10) of D 1 c m 3 were 74.18 (70.42–76.71) GyEQD2, 67.80 (59.91, 71.08) GyEQD2, 66.37 (52.00, 70.27) GyEQD2 for grade 2–4 with rectal morbidity at 1, 3, and 5 years, respectively. Conclusion Our study proved that D 1 c m 3 and D 0.1 c m 3 were considered as useful dosimetric parameters for predicting the risk of grade1–4 and grade2–4 LRC at 1-year, and D 1 c m 3 might be an indicator for predicting grade2-4 LRC at 3/5years. The patients with rectal D 1 c m 3 >66.37–74.18 GyEQD2 should be closely observed for grade2–4 LRC.

Volume 11
Pages None
DOI 10.3389/fonc.2021.693864
Language English
Journal Frontiers in Oncology

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