1. Intensity-modulated arc therapy with simultaneous integrated boost in the treatment of primary irresectable cervical cancer. Treatment planning, quality control, and clinical implementation.
- Author
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Vandecasteele K, De Neve W, De Gersem W, Delrue L, Paelinck L, Makar A, Fonteyne V, De Wagter C, Villeirs G, and De Meerleer G
- Subjects
- Adenocarcinoma pathology, Adult, Aged, Carcinoma, Squamous Cell pathology, Cervix Uteri radiation effects, Dose Fractionation, Radiation, Female, Film Dosimetry, Humans, Image Processing, Computer-Assisted, Intestines radiation effects, Lymphatic Irradiation, Middle Aged, Neoplasm Invasiveness, Neoplasm Staging, Positron-Emission Tomography, Quality Control, Radiotherapy Dosage, Radiotherapy Planning, Computer-Assisted standards, Radiotherapy, Intensity-Modulated standards, Tomography, X-Ray Computed, Urinary Bladder radiation effects, Uterine Cervical Neoplasms pathology, Adenocarcinoma radiotherapy, Carcinoma, Squamous Cell radiotherapy, Radiotherapy Planning, Computer-Assisted methods, Radiotherapy, Intensity-Modulated methods, Uterine Cervical Neoplasms radiotherapy
- Abstract
Purpose: To report on the planning procedure, quality control, and clinical implementation of intensity-modulated arc therapy (IMAT) delivering a simultaneous integrated boost (SIB) in patients with primary irresectable cervix carcinoma., Patients and Methods: Six patients underwent PET-CT (positron emission tomography-computed tomography) and MRI (magnetic resonance imaging) before treatment planning. Prescription (25 fractions) was (1) a median dose (D(50)) of 62, 58 and 56 Gy to the primary tumor (GTV_cervix), primary clinical target volume (CTV_cervix) and its planning target volume (PTV_cervix), respectively; (2) a D(50) of 60 Gy to the PET-positive lymph nodes (GTV_nodes); (3) a minimal dose (D(98)) of 45 Gy to the planning target volume of the elective lymph nodes (PTV_nodes). IMAT plans were generated using an anatomy-based exclusion tool with the aid of weight and leaf position optimization. The dosimetric delivery of IMAT was validated preclinically using radiochromic film dosimetry., Results: Five to nine arcs were needed to create valid IMAT plans. Dose constraints on D(50) were not met in two patients (both GTV_cervix: 1 Gy and 3 Gy less). D(98) for PTV_nodes was not met in three patients (1 Gy each). Film dosimetry showed excellent gamma evaluation. There were no treatment interruptions., Conclusion: IMAT allows delivering an SIB to the macroscopic tumor without compromising the dose to the elective lymph nodes or the organs at risk. The clinical implementation is feasible.
- Published
- 2009
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