To analyze the
dose&n
dash;volu
me histogra
m of the central shiel
ding technique for cervical cancer ra
diotherapy by co
mputing the co
mposite three-
di
mensional EQD2
dose
distributions of external-bea
m ra
diotherapy plus intracavitary brachytherapy.
d="absSec_2">Methods and Materials
d="abspara0015">On a phantom, three patterns of high-risk clinical target volume (HR-CTV) with right–left diameters of 3, 4, and 5 cm were created using clinical data. Four patterns of combinations of whole-pelvis irradiation plus “pelvis irradiation using the central shielding technique” (CS) (shielding width, 3 or 4 cm) were created: 20 Gy/10 fractions + 30 Gy/15 fractions, 30 Gy/15 fractions + 20 Gy/10 fractions, 40 Gy/20 fractions + 10 Gy/5 fractions, and 50 Gy/25 fractions + 0 Gy. The intracavitary brachytherapy plan was set as 24 Gy/4 fractions prescribed to the Point A. The HR-CTV m>Dm>90/m>Dm>98 and modeled bladder/rectum m>Dm>2cc were computed using the composite EQD2 dose distributions of all the treatment combinations.
d="absSec_3">Results
d="abspara0020">If appropriate combinations of the treatment plans were selected on the basis of the CS doses and the HR-CTV sizes, the m>Dm>90/m>Dm>98 of HR-CTV 3 cm, HR-CTV 4 cm, and HR-CTV 5 cm were 89.7 Gy/80.6 Gy, 77.3 Gy/72.0 Gy, and 73.0 Gy/69.2 Gy in the case of CS width 3 cm, respectively; and 86.2 Gy/76.0 Gy, 73.3 Gy/67.6 Gy, and 70.9 Gy/67.1 Gy in the case of CS width 4 cm, respectively. The contributions of CS to the HR-CTV m>Dm>90/bladder m>Dm>2cc/rectum m>Dm>2cc values were 24–56%/28–32%/9% of the CS plan doses for shielding width of 3 cm and were 13–35%/11–16%/5–6% for shielding width of 4 cm.
d="absSec_4">Conclusion
d="abspara0025">The dose contributions of CS were variable but not negligible when analyzing the total doses delivered to the HR-CTV.