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“Background Intracavitary brachytherapy (ICBT) with external radiotherapy (ERT) is
an essential component of cervical cancer management and has a high therapeutic index by delivering a high dose to the primary cervical lesion and lower doses to adjacent organs, resulting in increased local control and survival without increased in toxicity [1–4]. However the doses delivered to tumor and normal tissues from ICBT are difficult to quantify accurately in conventional Terminal deoxynucleotidyl transferase brachytherapy (BRT) planning. To ensure consistency in the reporting of ICBT applications in cervical cancer, the International Commission on Radiation Units and Measurement (ICRU) recommended a number of parameters for doses and volumes to be considered. These include points A and B, representing the doses in the parametria and the pelvic wall, and the rectal and bladder points representing the organs at risk (OARs), respectively [5]. Physicians have used these reference point doses to report treatment intensity and to estimate the maximal dose to normal tissues, which can predict late complications.