Abstract

Purpose : To explain a possible association between treatment technique and postoperative mortality adter preoperative radiotherapy of rectal carcinoma, the dose distributions were compared in model experiments. Methods and Materials : Preoperative radiotherapy with a three-beam technique delivered in five fractions to 25 effects of this treatment, both acute and late, have been low. In a parallel trial using an identical fractionation schedule and total dose but with a two-beam technique, the postoperative mortality was higher. Two-, three-, and four-beam techniques were analyzed in 20 patients with computed tomography based, three-dimensional dose planning. Dose distributions and dose-volume histograms in the planning target volume (PTV) and in the organs at risk were considered. A numerical “biological” model was used to compare the techniques. Results : The two-beam and the four-beam box techniques give the most homogeneous distributions in the PTV, although all techniques results in dose distributions that would be considered adequate, provided 16 MV or higher photon energies are used. Three- and four-beam techniques show advantages over the two-beam technique with respect to organs at risk, particularly the small bowel. With the two-beam technique and the upper beam limit at mid-L4, the volume of the bowel that receives >95% of the prescribed dose, and hence, is included in the treated volume (TV), is more twice as large as that with three- and four-beam techniques, and that of the total body between 1.5 and 2 times as large. The results of the analyses using the biological model indicate that the three- and four-beam techniques result in less small bowel complication rates than the two-bowel technique. The integral energy to the total body is similar for all treatment modalities compared. Conclusions : The volume of bowel included in the TV, rather than the energy imparted to the body, influences postoperative mortality, and emphasizes the importance of precise radiotherapy planing to minimize normal tissue toxicity.

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