scholarly journals PO-1100 Implementation of FAST-Forward during COVID19: Report of acute skin toxicity /resource implications

2021 ◽  
Vol 161 ◽  
pp. S915-S916
Author(s):  
K. Nugent ◽  
E. Quinlan ◽  
S. Cleary ◽  
H. O’Driscoll ◽  
J. Trousdell ◽  
...  
2015 ◽  
Vol 88 (1055) ◽  
pp. 20150414 ◽  
Author(s):  
Benoîte Méry ◽  
Alexis Vallard ◽  
Jane-Chloé Trone ◽  
Cécile Pacaut ◽  
Jean-Baptiste Guy ◽  
...  

BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Huayong Jiang ◽  
Lingling Meng ◽  
Huijuan Zhang ◽  
Xiangkun Dai ◽  
Qian Zhang ◽  
...  

Abstract Background The purpose of this phase II study was to evaluate the feasibility of hypofractionated radiotherapy (HFRT) with a dose of 36.5 Gy in 10 fractions in postmastectomy patients. Methods From March 2014 to December 2015, 85 patients with locally advanced breast cancer were eligible to participate in this study with a schedule of 36.5 Gy in 10 fractions. Intensity-modulated radiation therapy (IMRT) was delivered to the chest wall with or without the supraclavicular region. The primary endpoint was radiation-related toxicities. The secondary endpoints were locoregional failure-free survival (LRFFS), disease-free survival (DFS) and overall survival (OS). And the outcomes were compared with our retrospective study of 72 patients with 42.5 Gy in 16 fractions. Results The median follow-up was 69.0 (range 66.5-71.5) months in the 36.5 Gy group and 93.0 (range 91.9-94.1) months in the 42.5 Gy group, respectively. Radiation-related toxicities were mainly grade 1, although a few patients had grade 2 plexopathy (1.2%) and acute skin toxicity (1.2%) in the 36.5 Gy group, and grade 2 acute skin toxicity (5.6%) and lymphedema (4.2%) in the 42.5 Gy group. There were no significant differences between the groups in acute and late toxicities. For all the patients, the 5-year LRFFS, DFS and OS were 97.7 and 100.0%, 93.1 and 90.3%, 98.8 and 97.2%, respectively, without significant differences between the groups. Conclusion Postmastectomy HFRT with a schedule of 36.5 Gy in 10 fractions was feasible, with mild toxicities and excellent 5-year clinical outcome. Trial registration Trial registration number: ChiCTR-ONRC-14004391. Date of registration: 9/3/2014.


2020 ◽  
Vol 9 (S1) ◽  
pp. S8-S11
Author(s):  
Daniel Sampaio Vieira ◽  
Marcio Lemberg Reisner ◽  
Juliana Depra Panichella ◽  
Isabella Peixoto Barbosa

2006 ◽  
Vol 33 (6Part8) ◽  
pp. 2067-2067
Author(s):  
JS Li ◽  
G Freedman ◽  
S Stathakis ◽  
P Anderson ◽  
C-M Ma

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