Sally Louise Trent

Dr. Sally Louise Trent

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

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

Representative Publications

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9 April 2018 in Clinical Sarcoma Research
Verified
Journal Article
Open access
PDF file
RMRuth E. Macpherson
Ruth E. Macpherson
SPSarah Pratap
Sarah Pratap
HTHelen Tyrrell
Helen Tyrrell
MKMehrdad Khonsari
Mehrdad Khonsari
SWShaun Wilson
Shaun Wilson
BHBass Hassan
Bass Hassan
The use of 18F-FDG PET–CT (PET–CT) is widespread in many cancer types compared to sarcoma. We report a large retrospective audit of PET–CT in bone and soft tissue sarcoma with varied grade in a single multi-disciplinary centre. We also sought to answer three questions. Firstly, the correlation between sarcoma sub-type and grade with 18FDG SUVmax, secondly, the practical uses of PET–CT in the clinical setting of staging (during initial diagnosis), restaging (new baseline prior to definitive intervention) and treatment response. Finally, we also attempted to evaluate the potential additional benefit of PET–CT over concurrent conventional CT and MRI. A total of 957 consecutive PET–CT scans were performed in a single supra-regional centre in 493 sarcoma patients (excluding GIST) between 2007 and 2014. We compared, PET–CT SUVmax values in relation to histology and FNCCC grading. We compared PET–CT findings relative to concurrent conventional imaging (MRI and CT) in staging, restaging and treatment responses. High-grade (II/III) bone and soft tissue sarcoma correlated with high SUVmax, especially undifferentiated pleomorphic sarcoma, leiomyosarcoma, translocation induced sarcomas (Ewing, synovial, alveolar rhabdomyosarcoma), de-differentiated liposarcoma and osteosarcoma. Lower SUVmax values were observed in sarcomas of low histological grade (grade I), and in rare subtypes of intermediate grade soft tissue sarcoma (e.g. alveolar soft part sarcoma and solitary fibrous tumour). SUVmax variation was noted in malignant peripheral nerve sheath tumours, compared to the histologically benign plexiform neurofibroma, whereas PET–CT could clearly differentiate low from high-grade chondrosarcoma. We identified added utility of PET–CT in addition to MRI and CT in high-grade sarcoma of bone and soft tissues. An estimated 21% overall potential benefit was observed for PET–CT over CT/MRI, and in particular, in ‘upstaging’ of high-grade disease (from M0 to M1) where an additional 12% of cases were deemed M1 following PET–CT. PET–CT in high-grade bone and soft tissue sarcoma can add significant benefit to routine CT/MRI staging. Further prospective and multi-centre evaluation of PET–CT is warranted to determine the actual predictive value and cost-effectiveness of PET–CT in directing clinical management of clinically complex and heterogeneous high-grade sarcomas.

24 August 2022 in Cancers
Verified
Journal Article
Open access
PDF file
ZOZhengxiao Ouyang
Zhengxiao Ouyang
STSally Louise Trent
Sally Louise Trent
CMCatherine McCarthy
Catherine McCarthy
TCThomas Cosker
Thomas Cosker
DWDuncan Whitwell
Duncan Whitwell
CGChristopher L.Max H. Gibbons
Christopher L.Max H. Gibbons
Preoperative radiotherapy increases the risk of postoperative wound complication in the treatment of soft tissue sarcoma (STS). This study aims to develop a nomogram for predicting major wound complication (MaWC) after surgery. Using the Oxford University Hospital (OUH) database, a total of 126 STS patients treated with preoperative radiotherapy and surgical resection between 2007 and 2021 were retrospectively reviewed. MaWC was defined as a wound complication that required secondary surgical intervention. Univariate and multivariate regression analyses on the association between MaWC and risk factors were performed. A nomogram was formulated and the areas under the Receiver Operating Characteristic Curves (AUC) were adopted to measure the predictive value of MaWC. A decision curve analysis (DCA) determined the model with the best discriminative ability. The incidence of MaWC was 19%. Age, tumour size, diabetes mellitus and metastasis at presentation were associated with MaWC in the univariate analysis. Age, tumour size, and metastasis at presentation were independent risk factors in the multivariate analysis. The sensitivity and specificity of the predictive model is 0.90 and 0.76, respectively. The AUC value was 0.86. The nomogram constructed in the study effectively predicts the risk of MaWC after preoperative radiotherapy and surgery for STS patients.

11 February 2023 in European Journal of Obstetrics & Gynecology and Reproductive Biology
Verified
Journal Article
Closed access
SESally S. El-Tawab
Sally S. El-Tawab
JFJulia Fox
Julia Fox
STSally Louise Trent
Sally Louise Trent
SKSean Kehoe
Sean Kehoe

17 August 2024 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
ZOZhengxiao Ouyang
Zhengxiao Ouyang
TWTianyu Wang
Tianyu Wang
JBJennifer Brown
Jennifer Brown
ZOZsolt Orosz
Zsolt Orosz
STSally Louise Trent
Sally Louise Trent
CGChristopher Leonard Maxime Gibbons
Christopher Leonard Maxime Gibbons

2 July 2025 in Clinical Oncology
Verified
Journal Article
Closed access
JMJ. McGrane
J. McGrane
LELeonie Eastlake
Leonie Eastlake
DHD. Hadjiyiannakis
D. Hadjiyiannakis
SLSusan Lalondrelle
Susan Lalondrelle
RBR. Bowen
R. Bowen
GMG.J. Melendez-Torres
G.J. Melendez-Torres

10 March 2023 in Clinical Oncology
Verified
Journal Article
Closed access
PDF file
SEShawn David Ponniah Ellis
Shawn David Ponniah Ellis
CHCharles Hamilton
Charles Hamilton
BHBass Hassan
Bass Hassan
SPSarah Pratapa
Sarah Pratapa
STSally Louise Trent
Sally Louise Trent