1 -1.8 -2.4 0.26 Bladder            ICRU-D2 -3.1 -2.3 -3.8 0.01    ICRU-D5 -1.7 -1.1 -2.3 0.01 * Abbreviations: Group 1 = CTV coverage > 95% isodose line prescribed

to Point A, Group 2 = CTV coverage < 95% isodose line prescribed to Point A. D2 = the minimum dose value in the 2.0-cc volume receiving the highest dose, D5 = the minimum dose value in the 5.0-cc volume receiving the highest dose. Bladder doses The mean ICRU bladder dose and D2 and D5 of the bladder for all patients were 6.1 Gy (2.9–8.7 Gy), 9.2 Gy (7.6–12.9 Gy), MK-0457 in vivo and 7.2 Gy (3.4–10.9 Gy), respectively. The mean D2 and D5 of the bladder were 1.51 and 1.28 times higher than the mean ICRU bladder dose (6.1 Gy and 5.6 Gy). The differences of means between the ICRU bladder dose points from the conventional plan and the D2 (p < 0.001) and D5 (p < 0.001) of the bladder from the CT plan were statistically significant. The mean ICRU bladder doses did not differ between groups 1 and 2. However, D2 and D5 values were significantly higher in group 2 than in group 1 (Table 5). Likewise, there were significant differences between ICRU bladder and D2 values (p < 0.001) and D5 values (p < 0.001) for groups 1 and 2. The difference in the ICRU bladder point dose and D2, and the ICRU bladder point dose and D5 was significantly higher in group 2 than in group 1 (Table

5). Comparison of sigmoid colon and small bowel doses The mean sigmoid colon and small bowel doses for all patients were 6.5 Gy (2.6–11.2 Gy) and 5.1 Gy (2.1–9.8 Gy), respectively, for D2; and 6.8 Gy (2.0–11.5 Gy) and 5.6 Gy (1.8–9.7 selleck kinase inhibitor Gy), respectively, for D5. The D2 and D5 values for sigmoid colon were significantly higher in group 2 than in group 1 (up to 15%) (Table 4). Although the D2 and D5 values for the small bowel were also higher in group 2 than in group 1,

the difference did not reach BVD-523 clinical trial statistical significance. Discussion In the current study, we assessed the conventional BRT plan based on ICRU reference points and the CT-based BRT plan in patients with cervical cancer. We clearly demonstrated that tumor volume coverage was inadequate in the conventional plan compared to the CT-plan, and was inversely related with the volume of the target and the extension of tumor. With the conventional plan, the ICRU rectum and bladder point doses underestimated Florfenicol the actual rectum and bladder doses obtained from the CT-plan. Additionally, we demonstrated that more precise analysis of the dose received by certain volume of OARs can be accomplished by utilizing the DVHs on CT-plans, which may be of critical importance in regard to normal tissue tolerance limits. After publication of ICRU 38 report, ICRU reference points for tumors, and reference dose points for bladder and rectum were used for defining the doses in conventional plans.