Katharine L. Aitken

Dr. Katharine L. Aitken

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2021 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
FSFinbar Slevin
Finbar Slevin
KAKatharine L. Aitken
Katharine L. Aitken
Filippo AlongiFilippo Alongi
Filippo Alongi
SASTEFANO ARCANGELI
STEFANO ARCANGELI
ECEliot Chadwick
Eliot Chadwick
LMLouise Murray
Louise Murray

1 July 2015 in Clinical Oncology
Verified
Journal Article
Closed access
KAKatharine L. Aitken
Katharine L. Aitken
ATA. Tree
A. Tree
KTK. Thomas
K. Thomas
CNC. Nutting
C. Nutting
MHMaria Hawkins
Maria Hawkins
NAN. van As
N. van As

16 March 2022 in Clinical Oncology
Verified
Journal Article
Closed access
KAKatharine L. Aitken
Katharine L. Aitken
SMS. Mukherjee
S. Mukherjee

1 May 2019 in Clinical and Translational Radiation Oncology
Verified
Journal Article
Open access
JBJenny Bertholet
Jenny Bertholet
AHArabella Hunt
Arabella Hunt
ADAlex Dunlop
Alex Dunlop
TBThomas Bird
Thomas Bird
RMRobert Adam Mitchell
Robert Adam Mitchell
KAKatharine L. Aitken
Katharine L. Aitken
To determine the potential for dose escalation to a biological equivalent dose BED10 ≅ 100 Gy in hypofractionated radiotherapy for locally advanced pancreatic cancer (LAPC). Ten unselected LAPC patients were retrospectively included in the study. Two fractionation regimens were compared (5 and 15 fractions). The aim was to cover 95% of the Planning Target Volume (PTV) with a BED10 = 54 Gy (base dose = 33 Gy in 5 fractions, 42.5 Gy in 15 fractions) whilst respecting organs-at-risk (OAR) constraints. Once the highest PTV coverage was achieved dose escalation to a BED10 ≅ 100 Gy (escalated dose = 50 Gy in 5 fractions, 67.5 Gy in 15 fractions) was attempted, limiting the PTV maximum dose to 130% of the escalated dose. In 5 fractions, 95% PTV coverage by both base and escalated doses could be achieved for one patient with PTV more than 1 cm away from OAR. 95% and 90% PTV coverage by the base dose was achieved in one and two patients respectively. In all other patients, coverage even by the base dose had to be compromised to comply with OAR constraints. In 15 fractions, 95% PTV coverage by the base dose was feasible for all patients except one. Dose escalation allowed improvement in target coverage by the base dose in both fractionation regimen whilst covering a sub-volume of the PTV with a BED10 ≅ 100 Gy. Both fractionation schemes were equivalent in terms of dose escalation potential. LAPC patients with OAR close to the PTV are generally not eligible for hypofractionation with dose escalation. However, this planning study shows that it is possible to cover PTV sub-volumes with a BED10 ≅ 100 Gy in addition to delivering a BED10 = 54 Gy to 90-95% of the PTV as commonly prescribed to this population. Combined with an adaptive approach, this may maximize PTV coverage by a high BED on days with favourable anatomy.

1 July 2018 in Physics and Imaging in Radiation Oncology
Verified
Journal Article
Open access
TWThomas Woolcot
Thomas Woolcot
EKEvanthia Kousi
Evanthia Kousi
EWEmma Wells
Emma Wells
KAKatharine L. Aitken
Katharine L. Aitken
HTHelen Taylor
Helen Taylor
MSMaria A. Schmidt
Maria A. Schmidt
We demonstrated a general method to evaluate systematic errors related to Magnetic Resonance (MR) imaging sequences in marker-based co-registration of MR and Computed Tomography (CT) images, and investigated the effect of MR image quality in the co-registration process using clinical MR and CT protocols for stereotactic ablative body radiotherapy (SABR) planning of the liver. Small systematic errors (under 1.6 mm) were detected, unlikely to be a clinical risk to liver SABR. The least favourable marker configuration was found to be a co-planar arrangement parallel to the transaxial image plane.

27 November 2025 in Clinical Oncology
Verified
Journal Article
Closed access
PDP. Díez
P. Díez
RPR. Patel
R. Patel
AHAnoop Haridass
Anoop Haridass
MKM. Kroiss
M. Kroiss
CCC.H. Clark
C.H. Clark
FMF. McDonald
F. McDonald