2016
DOI: 10.1016/j.radonc.2016.02.027
|View full text |Cite
|
Sign up to set email alerts
|

Acute skin toxicity associated with a 1-week schedule of whole breast radiotherapy compared with a standard 3-week regimen delivered in the UK FAST-Forward Trial

Abstract: Background and purposeFAST-Forward is a phase 3 clinical trial testing a 1-week course of whole breast radiotherapy against the UK standard 3-week regimen after primary surgery for early breast cancer. Two acute skin toxicity substudies were undertaken to test the safety of the test schedules with respect to early skin reactions.Material and methodsPatients were randomly allocated to 40 Gy/15 fractions (F)/3-weeks, 27 Gy/5F/1-week or 26 Gy/5F/1-week. Acute breast skin reactions were graded using RTOG (first su… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

7
133
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 184 publications
(140 citation statements)
references
References 3 publications
7
133
0
Order By: Relevance
“…Results from FAST‐Forward UK phase III study are also awaited as the regimens of 5 or 15 days were compared. The first outcomes showed mild acute skin reactions with 1‐week schedules …”
Section: Discussionmentioning
confidence: 99%
“…Results from FAST‐Forward UK phase III study are also awaited as the regimens of 5 or 15 days were compared. The first outcomes showed mild acute skin reactions with 1‐week schedules …”
Section: Discussionmentioning
confidence: 99%
“…Establishing the toxicities patterns and aesthetics changes through clinical trials is a fundamental step for the possible future use of adjuvant whole breast irradiation in 5 fractions, either once a week or in consecutive days, as in the FAST‐Forward protocol …”
Section: Discussionmentioning
confidence: 99%
“…Fast‐Forward is a step further and is a phase 3 trial comparing 1‐week course with current UK 3‐week regimen. Early skin toxicity (grade >3 as assessed with the RT Oncology Group [RTOG], and the Common Terminology Criteria for Adverse Events [CTCAE] criteria) safety substudies revealed a maximum of up to 9.8% incidence in 1‐week course vs up to 13.6% in the 3‐week course . Long‐term outcomes are awaited with interest and potentially practice‐changing.…”
Section: Modifications Of Dose and Delivery Of Rtmentioning
confidence: 99%