TY - JOUR
T1 - Moderate hypofractionation remains the standard of care for whole-breast radiotherapy in breast cancer: Considerations regarding FAST and FAST-Forward
AU - Breast Cancer Expert Panel of the German Society of Radiation Oncology (DEGRO)
AU - Krug, David
AU - Baumann, René
AU - Combs, Stephanie E.
AU - Duma, Marciana Nona
AU - Dunst, Jürgen
AU - Feyer, Petra
AU - Fietkau, Rainer
AU - Haase, Wulf
AU - Harms, Wolfgang
AU - Hehr, Thomas
AU - Piroth, Marc D.
AU - Sedlmayer, Felix
AU - Souchon, Rainer
AU - Strnad, Vratislav
AU - Budach, Wilfried
N1 - Funding Information:
D. Krug has received honoraria from Merck Sharp & Dome, outside of the submitted work. J. Dunst is the principal investigator of the HYPOSIB trial. F. Sedlmayer is the principal investigator of the HIOB trial and has received a research grant from IntraOP Medical for the conduct of the trial. All authors, D. Krug, R. Baumann, S.E. Combs, M.N. Duma, J. Dunst, P. Feyer, R. Fietkau, W. Haase, W. Harms, T. Hehr, M.D. Piroth, F. Sedlmayer, R. Souchon, V. Strnad and W. Budach, are members of the German Society for Radiation Oncology (DEGRO).
Publisher Copyright:
© 2021, The Author(s).
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/4
Y1 - 2021/4
N2 - Moderate hypofractionation is the standard of care for adjuvant whole-breast radiotherapy after breast-conserving surgery for breast cancer. Recently, 10-year results from the FAST and 5‑year results from the FAST-Forward trial evaluating adjuvant whole-breast radiotherapy in 5 fractions over 5 weeks or 1 week have been published. This article summarizes recent data for moderate hypofractionation and results from the FAST and FAST-Forward trial on ultra-hypofractionation. While the FAST trial was not powered for comparison of local recurrence rates, FAST-Forward demonstrated non-inferiority for two ultra-hypofractionated regimens in terms of local control. In both trials, the higher-dose experimental arms resulted in elevated rates of late toxicity. For the lower dose experimental arms of 28.5 Gy over 5 weeks and 26 Gy over 1 week, moderate or marked late effects were similar in the majority of documented items compared to the respective standard arms, but significantly worse in some subdomains. The difference between the standard arm and the 26 Gy of the FAST-Forward trial concerning moderate or marked late effects increased with longer follow-up in disadvantage of the experimental arm for most items. For now, moderate hypofractionation with 40–42.5 Gy over 15–16 fractions remains the standard of care for the majority of patients with breast cancer who undergo whole-breast radiotherapy without regional nodal irradiation after breast-conserving surgery.
AB - Moderate hypofractionation is the standard of care for adjuvant whole-breast radiotherapy after breast-conserving surgery for breast cancer. Recently, 10-year results from the FAST and 5‑year results from the FAST-Forward trial evaluating adjuvant whole-breast radiotherapy in 5 fractions over 5 weeks or 1 week have been published. This article summarizes recent data for moderate hypofractionation and results from the FAST and FAST-Forward trial on ultra-hypofractionation. While the FAST trial was not powered for comparison of local recurrence rates, FAST-Forward demonstrated non-inferiority for two ultra-hypofractionated regimens in terms of local control. In both trials, the higher-dose experimental arms resulted in elevated rates of late toxicity. For the lower dose experimental arms of 28.5 Gy over 5 weeks and 26 Gy over 1 week, moderate or marked late effects were similar in the majority of documented items compared to the respective standard arms, but significantly worse in some subdomains. The difference between the standard arm and the 26 Gy of the FAST-Forward trial concerning moderate or marked late effects increased with longer follow-up in disadvantage of the experimental arm for most items. For now, moderate hypofractionation with 40–42.5 Gy over 15–16 fractions remains the standard of care for the majority of patients with breast cancer who undergo whole-breast radiotherapy without regional nodal irradiation after breast-conserving surgery.
UR - http://www.scopus.com/inward/record.url?scp=85099972614&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/a7c36cb7-fb82-3605-9c43-595650d51447/
U2 - 10.1007/s00066-020-01744-3
DO - 10.1007/s00066-020-01744-3
M3 - Scientific review articles
C2 - 33507331
AN - SCOPUS:85099972614
SN - 0179-7158
VL - 197
SP - 269
EP - 280
JO - Strahlentherapie und Onkologie
JF - Strahlentherapie und Onkologie
IS - 4
ER -