Dosimetric assessment of bolus for postmastectomy radiotherapy

There remains wide variation in the use of chest wall boluses for postmastectomy radiotherapy, which may result from the need for 2 treatment plans with the commonly used half-time tissue-equivalent 5-mm-thick bolus to achieve a full surface dose. To establish a bolus method requiring one treatment plan, we assessed the surface dose of a thinner daily bolus for all treatment fractions and compared it against the half-time 5-mm-thick bolus. In this basic study, we specifically investigated dosage achieved when using the following: (1) the existing bolus protocol, a half-time 5-mm-thick tissue-equivalent Clearfit bolus (Fujidenolo Inc., Aichi, JP); (2) no bolus; and (3) daily 1-, 2-, and 3-mm-thick Clearfit boluses at 4 and 6 MV photons. Dosimetric measurements were then taken in an anthropomorphic phantom to study the effect of each regimen on the surface doses, and the mean surface doses of the daily thinner boluses were compared with the existing bolus protocol by the Welch 2-sample t test. The mean surface doses for the existing bolus protocol, no bolus, and daily 1-, 2-, and 3-mm-thick boluses were 68% (range, 59% to 77%), 53% (41% to 66%), 73% (60% to 83%), 77% (66% to 87%), and 82% (75% to 91%) of the prescription dose at 4 MV, respectively; the corresponding values at 6 MV were 71% (63% to 79%), 50% (39% to 60%), 72% (56% to 83%), 81% (68% to 90%), and 89% (80 to 97%) of the prescription dose. The mean surface doses were comparable between the existing bolus protocol and the 1-mm-thick daily bolus at 4 and 6 MV. In conclusion, the mean surface dose of a 1-mm-thick bolus approximate that of a half-time 5-mm-thick bolus at 4 and 6 MV. As such, we have started a prospective clinical study on the safety and efficacy of a 1-mm-thick bolus for postmastectomy radiotherapy.