• Hitoshi Ishikawa, Hiroshi Tsuji, Tadashi Kamada, Naoki Hirasawa, Takeshi Yanagi, Jun-Etsu Mizoe, Koichiro Akakura, Hiroyoshi Suzuki, Jun Shimazaki, and Hirohiko Tsujii.
• Research Center for Charged Particle Therapy, National Institute of Radiological Sciences, Chiba, Japan.
• Int. J. Radiat. Oncol. Biol. Phys. 2006 Nov 15; 66 (4): 1084-91.

PurposeThe aim of this study was to determine the risk factors for late gastrointestinal (GI) morbidity after hypofractionated carbon ion radiotherapy (C-ion RT) for prostate cancer.Methods And MaterialsBetween April 2000 and November 2003, a Phase II clinical trial of C-ion RT with a total dose of 66 GyE in 20 fractions was performed on 175 patients with prostate cancer, and the correlations of clinical and dosimetric parameters with the incidence of late GI toxicity in 172 patients who survived for more than 18 months were investigated.ResultsAlthough no Grade 3-4 late morbidities of the rectum were observed, Grade 1 and 2 morbidities developed in 23 (13%) and 4 (2%) patients, respectively. Dose-volume histogram analysis revealed that the percentage of rectal volume receiving 50% of the prescribed dose (V50) was significantly higher in patients with rectal toxicity than without toxicity (13.2 +/- 5.6% with toxicity; 11.4 +/- 4.0% without toxicity, p = 0.046). Multivariate analysis demonstrated that the use of anticoagulation therapy (p = 0.010) and rectal V50 (p = 0.012) were significant risk factors for the occurrence of Grade 1-2 late GI toxicity.ConclusionsAlthough C-ion RT with hypofractionation yielded favorable results regarding late GI complication, dosimetric parameter was a very important factor in the occurrence of rectal bleeding after C-ion RT as well as photon beam RT. Our results provide useful information for physicians applying charged particle RT in the treatment of prostate cancer.

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