1. Needle use and dosimetric evaluation in cervical cancer brachytherapy using the Utrecht applicator
- Author
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Monique C.W.M. Bloemers, Cherita Sombroek, Anton Mans, Baukelien van Triest, Marlies E. Nowee, and Milena Smolic
- Subjects
medicine.medical_treatment ,Brachytherapy ,Uterine Cervical Neoplasms ,Dose distribution ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Radiation treatment planning ,Cervical cancer ,business.industry ,Radiotherapy Planning, Computer-Assisted ,Radiotherapy Dosage ,Hematology ,medicine.disease ,Intensity (physics) ,Tumor Burden ,Oncology ,Needles ,030220 oncology & carcinogenesis ,Female ,business ,Nuclear medicine - Abstract
Background and purpose To analyse the clinical use of needles and examine the feasibility to meet the planning criteria in three fractions of cervical cancer brachytherapy. Furthermore, to investigate whether the needles with the largest discrepancy between application and loading are essential to treatment planning. Materials and methods For 22 patients we analysed the applied and loaded needle patterns, and examined the dosimetric results for small ( Results On average 5.8 needles were applied and 4.8 loaded per fraction, with average intensity 22% (17% for small, 29% for large CTVHR). Mid-lateral needles were applied and loaded most frequently and intensely. The average CTVHR D90% prescribed dose was 88.8 Gy (SD 4.2) EQD210, the average OAR D 2 cm 3 limit was respected. Omitting the mid-ventral needles, minimal statistically significant differences were found in dose distributions between RP and CP. Conclusions Applying on average 5.8 needles per fraction it was possible to meet the planning criteria for targets and OARs in three BT fractions for both small and large CTVHR. The mid-ventral needles were not essential in treatment planning, unless situated in the vicinity of the GTVres.
- Published
- 2017