TY - JOUR
T1 - Intensity-modulated adjuvant whole breast radiation delivered with static angle tomotherapy (TomoDirect)
T2 - A prospective case series
AU - Franco, Pierfrancesco
AU - Zeverino, Michele
AU - Migliaccio, Fernanda
AU - Sciacero, Piera
AU - Cante, Domenico
AU - Borca, Valeria Casanova
AU - Torielli, Paolo
AU - Arrichiello, Cecilia
AU - Girelli, Giuseppe
AU - Numico, Gianmauro
AU - La Porta, Maria Rosa
AU - Tofani, Santi
AU - Ricardi, Umberto
PY - 2013/11
Y1 - 2013/11
N2 - Purpose To report the 2-year outcomes of whole breast intensity-modulated radiotherapy (IMRT) after conserving surgery for early breast cancer (EBC) delivered with static angle tomotherapy (TomoDirect) (TD). Methods A prospective cohort of 120 EBC patients underwent whole breast IMRT with TD between 2010 and 2012. Radiation was delivered to a conventionally fractionated whole breast total dose of 50 Gy with TD, followed by a sequential conventionally fractionated tumor bed boost dose of 10-16 Gy with helical tomotherapy (HT). Clinical endpoints include acute and late toxicity, cosmesis, quality of life and local control. Results Median follow-up was 24 months (range 12-36 months); maximum detected acute skin toxicity was G0 22 %; G1 63 %; G2 12 % and G3 3 %. Predictors of acute dermatitis were as follows: volume of the whole breast minus boost volume receiving 105, 110 and 115 % of prescription dose, whole breast and boost volume, breast thickness and soft tissue thickness. Late skin toxicity was mild with no[G2 events. Cosmesis was good/excellent in 91.7 %of patients and fair/poor in 8.3 %. Quality of life was preserved over time, but for fatigue, transiently increased. Conclusion Adjuvant whole breast IMRT delivered sequentially with both TD and HT provides consistent clinical results. An observed unintended excessive dose outside the tumor bed might increase acute toxicity and eventually affect long-term clinical endpoints. The incorporation of the boost dose within the whole breast phase employing a simultaneous integrated boost (SIB) approach might mitigate this issue.
AB - Purpose To report the 2-year outcomes of whole breast intensity-modulated radiotherapy (IMRT) after conserving surgery for early breast cancer (EBC) delivered with static angle tomotherapy (TomoDirect) (TD). Methods A prospective cohort of 120 EBC patients underwent whole breast IMRT with TD between 2010 and 2012. Radiation was delivered to a conventionally fractionated whole breast total dose of 50 Gy with TD, followed by a sequential conventionally fractionated tumor bed boost dose of 10-16 Gy with helical tomotherapy (HT). Clinical endpoints include acute and late toxicity, cosmesis, quality of life and local control. Results Median follow-up was 24 months (range 12-36 months); maximum detected acute skin toxicity was G0 22 %; G1 63 %; G2 12 % and G3 3 %. Predictors of acute dermatitis were as follows: volume of the whole breast minus boost volume receiving 105, 110 and 115 % of prescription dose, whole breast and boost volume, breast thickness and soft tissue thickness. Late skin toxicity was mild with no[G2 events. Cosmesis was good/excellent in 91.7 %of patients and fair/poor in 8.3 %. Quality of life was preserved over time, but for fatigue, transiently increased. Conclusion Adjuvant whole breast IMRT delivered sequentially with both TD and HT provides consistent clinical results. An observed unintended excessive dose outside the tumor bed might increase acute toxicity and eventually affect long-term clinical endpoints. The incorporation of the boost dose within the whole breast phase employing a simultaneous integrated boost (SIB) approach might mitigate this issue.
KW - Adjuvant whole breast radiotherapy
KW - IGRT
KW - IMRT
KW - Radiotherapy
KW - TomoDirect
KW - Tomotherapy
UR - http://www.scopus.com/inward/record.url?scp=84892675392&partnerID=8YFLogxK
U2 - 10.1007/s00432-013-1515-0
DO - 10.1007/s00432-013-1515-0
M3 - Review article
SN - 0171-5216
VL - 139
SP - 1927
EP - 1936
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
IS - 11
ER -