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ORIGINAL ARTICLES |
From the Departments of Abdominal Surgery (GB, FP), Radiobiology/Radiotherapy (WL, JF, KH, WVdB, PL), Pathology (KG), and Hepatology (SHY), University Hospital Gasthuisberg, Katholieke Universiteit Leuven, Belgium; and Department of Experimental Therapy (DV), The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Correspondence: Address correspondence and reprint requests to: Freddy Penninckx, MD, PhD, Department of Abdominal Surgery, University Hospital Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium; Fax: 32-1-634-4832; E-mail: freddy.penninckx{at}uz.kuleuven.ac.be
Background: We investigated the degree of tumor cell killing after radiotherapy regimens commonly used in clinical practice in comparison with an accelerated schedule.
Methods: Mtln3 mammary adenocarcinoma tumor cells were inoculated subcutaneously in the hind leg of syngeneic Fischer 344 rats. Tumors were irradiated with 5 x 5 Gy in 5 days, 10 x 3 Gy over 10 days, or 5 x (2 x 3) Gy in 5 days. After excision of the irradiated tumors, the dye exclusion, a tetrazolium-based colorimetric and the clonogenic assays were used to determine tumor cell viability and surviving fractions.
Results: Estimated potential doubling time values indicate a rapid proliferation capacity, comparable with potential doubling time values in human rectal cancer. The dye exclusion and clonogenic assays revealed a significantly higher degree of cell killing after the hypofractionated and the accelerated regimens of, respectively, 5 x 5 Gy and 5 x (2 x 3) Gy over 5 days compared with 10 x 3 Gy over 10 days.
Conclusions: A shorter treatment time offered the best therapeutic efficacy. The schedule involving two daily fractions of 3 Gy over 5 days should be less toxic than 5 x 5 Gy and may therefore provide a therapeutic advantage.
Key Words: Rectal carcinoma Preoperative irradiation Total treatment time Fractionation Tumor cell proliferation
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